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2. Cell shape sensing licenses dendritic cells for homeostatic migration to lymph nodes

Author

Alraies, Zahraa, Rivera, Claudia A., Delgado, Maria-Graciela, Sanséau, Doriane, Maurin, Mathieu, Amadio, Roberto, Maria Piperno, Giulia, Dunsmore, Garett, Yatim, Aline, Lacerda Mariano, Livia, Kniazeva, Anna, Calmettes, Vincent, Sáez, Pablo J., Williart, Alice, Popard, Henri, Gratia, Matthieu, Lamiable, Olivier, Moreau, Aurélie, Fusilier, Zoé, Crestey, Lou, Albaud, Benoit, Legoix, Patricia, Dejean, Anne S., Le Dorze, Anne-Louise, Nakano, Hideki, Cook, Donald N., Lawrence, Toby, Manel, Nicolas, Benvenuti, Federica, Ginhoux, Florent, Moreau, Hélène D., P. F. Nader, Guilherme, Piel, Matthieu, and Lennon-Duménil, Ana-Maria

Published
2024
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4. Dendritic cell-targeted therapy expands CD8 T cell responses to bona-fide neoantigens in lung tumors

Author

López, Lucía, Morosi, Luciano Gastón, La Terza, Federica, Bourdely, Pierre, Rospo, Giuseppe, Amadio, Roberto, Piperno, Giulia Maria, Russo, Valentina, Volponi, Camilla, Vodret, Simone, Joshi, Sonal, Giannese, Francesca, Lazarevic, Dejan, Germano, Giovanni, Stoitzner, Patrizia, Bardelli, Alberto, Dalod, Marc, Pace, Luigia, Caronni, Nicoletta, Guermonprez, Pierre, and Benvenuti, Federica

Published
2024
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5. Che-1/miR-590-3p/TAZ axis sustains multiple myeloma disease

Author

Bruno, Tiziana, Catena, Valeria, Corleone, Giacomo, Cortile, Clelia, Cappelletto, Maria Chiara, Bellei, Barbara, De Nicola, Francesca, Amadio, Bruno, Gumenyuk, Svitlana, Marchesi, Francesco, Annibali, Ombretta, Blandino, Giovanni, Fanciulli, Maurizio, and Di Agostino, Silvia

Published
2024
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6. ALCAM-mediated cDC1 CD8 T cells interactions are suppressed in advanced lung tumors

Author

Luciano G. Morosi, Giulia M. Piperno, Lucía López, Roberto Amadio, Sonal Joshi, Alessandra Rustighi, Giannino Del Sal, and Federica Benvenuti

Subjects
ALCAM, cDC1, immunological synapse, lung cancer, NSCLC, Immunologic diseases. Allergy, RC581-607, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract

Conventional type 1 dendritic cells (cDC1) are critical regulators of anti-tumoral T-cell responses. The structure and abundance of intercellular contacts between cDC1 and CD8 T cells in cancer tissues is important to determine the outcome of the T-cell response. However, the molecular determinants controlling the stability of cDC1–CD8 interactions during cancer progression remain poorly investigated. Here, we generated a genetic model of non-small cell lung cancer crossed to a fluorescent cDC1 reporter (KP-XCR1venus) to allow the detection of cDC1-CD8T cell clusters in tumor tissues across tumor stages. We found that cDC1-CD8 clusters are abundant and productive at the early stages of tumor development but progressively diminish in advanced tumors. Transcriptional profiling and flow cytometry identified the adhesion molecule ALCAM/CD166 (Activated Leukocyte Cell Adhesion Molecule, ligand of CD6) as highly expressed by lung cDC1 and significantly downregulated in advanced tumors. Analysis of human datasets indicated that ALCAM is downregulated in non-small cell lung cancer and its expression correlates to better prognosis. Mechanistically, triggering ALCAM on lung cDC1 induces cytoskeletal remodeling and contact formation whereas its blockade prevents T-cell activation. Together, our results indicate that ALCAM is important to stabilize cDC1–CD8 interactions at early tumor stages, while its loss in advanced tumors contributes to immune evasion.

Published
2024
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7. VEGF and ELAVL1/HuR protein levels are increased in dry and wet AMD patients. A new tile in the pathophysiologic mechanisms underlying RPE degeneration?

Author

Giorgia Bresciani, Federico Manai, Szabolcs Felszeghy, Adrian Smedowski, Kai Kaarniranta, and Marialaura Amadio

Subjects
Retina, HuR, VEGF, Nrf2, RPE, AMD, Therapeutics. Pharmacology, RM1-950
Abstract

Age-related macular degeneration (AMD) is a common retinal pathology characterized by degeneration of macula’s retinal pigment epithelium (RPE) and photoreceptors, visual impairment, or loss. Compared to wet AMD, dry AMD is more common, but lacks cures; therefore, identification of new potential therapeutic targets and treatments is urgent. Increased oxidative stress and declining antioxidant, detoxifying systems contribute to the pathophysiologic mechanisms underlying AMD. The present work shows that the Embryonic Lethal Abnormal Vision-Like 1/Human antigen R (ELAVL1/HuR) and the Vascular Endothelial Growth Factor (VEGF) protein levels are higher in the RPE of both dry and wet AMD patients compared to healthy subjects. Moreover, increased HuR protein levels are detected in the retina, and especially in the RPE layer, of a dry AMD model, the nuclear factor erythroid 2-related factor 2 (Nrf2) / peroxisome proliferator-activated receptor gamma coactivator-1α (PGC-1α) double knock-out mouse. The crosstalk among Nrf2, HuR and VEGF has been also studied in ARPE-19 cells in basal and stressful conditions related to the AMD context (i.e., oxidative stress, autophagy impairment, Nrf2 deficit), offering new evidence of the mutual influence between Nrf2 and HuR, of the dependence of VEGF expression and secretion by these two factors, and of the increased susceptibility of cells to stressful conditions in Nrf2- or HuR-impaired contexts. Overall, this study shows evidence of the interplay among Nrf2, HuR and VEGF, essential factors for RPE homeostasis, and represents an additional piece in the understanding of the complex pathophysiologic mechanisms underlying AMD.

Published
2024
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8. Combining neural networks and data assimilation to enhance the spatial impact of Argo floats in the Copernicus Mediterranean biogeochemical model

Author

C. Amadio, A. Teruzzi, G. Pietropolli, L. Manzoni, G. Coidessa, and G. Cossarini

Subjects
Geography. Anthropology. Recreation, Environmental sciences, GE1-350
Abstract

Biogeochemical-Argo (BGC-Argo) float profiles provide substantial information on key vertical biogeochemical dynamics and have been successfully integrated in biogeochemical models via data assimilation approaches. Although BGC-Argo assimilation results have been encouraging, data scarcity remains a limitation with respect to their effective use in operational oceanography. To address availability gaps in the BGC-Argo profiles, an observing system experiment (OSE) that combines a neural network (NN) and data assimilation (DA) was performed here. A NN was used to reconstruct nitrate profiles, starting from oxygen profiles and associated Argo variables (pressure, temperature, and salinity), while a variational data assimilation scheme (3DVarBio) was upgraded to integrate BGC-Argo and reconstructed observations in the Copernicus Mediterranean operational forecast system (MedBFM). To ensure the high quality of oxygen data, a post-deployment quality control method was developed with the aim of detecting and eventually correcting potential sensors drift. The Mediterranean OSE features three different set-ups: a control run without assimilation; a multivariate run with assimilation of BGC-Argo chlorophyll, nitrate, and oxygen; and a multivariate run that also assimilates reconstructed observations. The general improvement in the skill performance metrics demonstrated the feasibility of integrating new variables (oxygen and reconstructed nitrate). Major benefits have been observed with respect to reproducing specific biogeochemical-process-based dynamics such as the nitracline dynamics, primary production, and oxygen vertical dynamics. The assimilation of BGC-Argo nitrate corrects a generally positive bias of the model in most of the Mediterranean areas, and the addition of reconstructed profiles makes the corrections even stronger. The impact of enlarged nitrate assimilation propagates to ecosystem processes (e.g. primary production) at a basin-wide scale, demonstrating the importance of the assimilation of BGC-Argo profiles in forecasting the biogeochemical ocean state.

Published
2024
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9. Theater as a means of communicating research on climate change: The case of 'Cambiare il clima'

Author

Elisa Vanin, Costantino Manes, Alvise Mattozzi, Lara Giordana, Micol Rispoli, Marco Andorno, and Sebastiano Amadio

Subjects
Science
Abstract

Between 2018 and 2023, the Department of Environmental, Land and Infrastructure Engineering (DIATI) at the Polytechnic University of Turin (PoliTo) implemented a project to advance research and education on climate change monitoring, adaptation and mitigation solutions. As part of their communication efforts, DIATI partnered with Faber Teater to create the play “Cambiare il clima” (in Italian, this means “Change the Climate”).This involved a collaboration between DIATI researchers, communication officers, and Faber Teater. The documentary theater that resulted was premiered at Biennale Tecnologia in 2020 and performed at various venues in Northern Italy, targeting both the general public and students.

Published
2024
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10. Dendritic cell-targeted therapy expands CD8 T cell responses to bona-fide neoantigens in lung tumors

Author

Lucía López, Luciano Gastón Morosi, Federica La Terza, Pierre Bourdely, Giuseppe Rospo, Roberto Amadio, Giulia Maria Piperno, Valentina Russo, Camilla Volponi, Simone Vodret, Sonal Joshi, Francesca Giannese, Dejan Lazarevic, Giovanni Germano, Patrizia Stoitzner, Alberto Bardelli, Marc Dalod, Luigia Pace, Nicoletta Caronni, Pierre Guermonprez, and Federica Benvenuti

Subjects
Science
Abstract

Abstract Cross-presentation by type 1 DCs (cDC1) is critical to induce and sustain antitumoral CD8 T cell responses to model antigens, in various tumor settings. However, the impact of cross-presenting cDC1 and the potential of DC-based therapies in tumors carrying varied levels of bona-fide neoantigens (neoAgs) remain unclear. Here we develop a hypermutated model of non-small cell lung cancer in female mice, encoding genuine MHC-I neoepitopes to study neoAgs-specific CD8 T cell responses in spontaneous settings and upon Flt3L + αCD40 (DC-therapy). We find that cDC1 are required to generate broad CD8 responses against a range of diverse neoAgs. DC-therapy promotes immunogenicity of weaker neoAgs and strongly inhibits the growth of high tumor-mutational burden (TMB) tumors. In contrast, low TMB tumors respond poorly to DC-therapy, generating mild CD8 T cell responses that are not sufficient to block progression. scRNA transcriptional analysis, immune profiling and functional assays unveil the changes induced by DC-therapy in lung tissues, which comprise accumulation of cDC1 with increased immunostimulatory properties and less exhausted effector CD8 T cells. We conclude that boosting cDC1 activity is critical to broaden the diversity of anti-tumoral CD8 T cell responses and to leverage neoAgs content for therapeutic advantage.

Published
2024
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11. Pentamidine-loaded gelatin decreases adhesion formation of flexor tendon

Author

Guidong Shi, Nakagawa Koichi, Rou Wan, Yicun Wang, Ramona Reisdorf, Abigayle Wilson, Tony C.T. Huang, Peter C. Amadio, Alexander Meves, Chunfeng Zhao, and Steven L. Moran

Subjects
Adhesion, Flexor tendon repair, Gelatin, Pentamidine, Turkey model, Diseases of the musculoskeletal system, RC925-935
Abstract

Background: Prevention of adhesion formation following flexor tendon repair is essential for restoration of normal finger function. Although many medications have been studied in the experimental setting to prevent adhesions, clinical application is limited due to the complexity of application and delivery in clinical translation. Methods: In this study, optimal dosages of gelatin and pentamidine were validated by gelatin concentration test. Following cell viability, cell migration, live and dead cell, and cell adhesion assay of the Turkey tenocytes, a model of Turkey tendon repair was established to evaluate the effectiveness of the Pentamidine-Gelatin sheet. Results: Pentamidine carried with gelatin, a Food and drug administration (FDA) approved material for drug delivery, showed good dynamic release, biocompatibility, and degradation. The optimal dose of pentamidine (25ug) was determined in the in vivo study using tenocyte viability, migration, and cell adhesion assays. Further biochemical analyses demonstrated that this positive effect may be due to pentamidine downregulating the Wnt signaling pathway without affecting collagen expression. Conclusions: We tested a FDA-approved antibiotic, pentamidine, for reducing adhesion formation after flexor tendon repair in both in vitro and in vivo using a novel turkey animal model. Compared with the non-pentamidine treatment group, pentamidine treated turkeys had significantly reduced adhesions and improved digit function after six weeks of tendon healing. The translational potential of this article: This study for the first time showed that a common clinical drug, pentamidine, has a potential for clinical application to reduce tendon adhesions and improve tendon gliding function without interfering with tendon healing.

Published
2024
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12. Towards a Taxonomy of Industrial Challenges and Enabling Technologies in Industry 4.0

Author

Roberto Figlie, Riccardo Amadio, Marios Tyrovolas, Chrysostomos Stylios, Lukasz Pasko, Dorota Stadnicka, Anna Carreras-Coch, Agustin Zaballos, Joan Navarro, and Daniele Mazzei

Subjects
Business challenges, enabling technologies, Industry 4.0, taxonomy, web platform, Electrical engineering. Electronics. Nuclear engineering, TK1-9971
Abstract

In the era of Industry 4.0 (I4.0), a significant challenge hindering digital transformation is the lack of mutual understanding between academia—particularly within engineering and computer science—and the industrial sector, especially small to medium-sized enterprises (SMEs). This gap can result in industries missing out on the potential benefits of cutting-edge scientific research and innovations that can address their daily concerns. At the same time, academics may struggle to identify real-world application areas for their emerging technological solutions. Moreover, the ever-increasing complexity of industrial challenges and technologies has widened the hiatus. To address this issue, our study introduces a comprehensive taxonomy, developed through a transparent, iterative process and presented via a user-centric web platform. Distinct from existing taxonomies, ours emphasizes practical applicability by categorizing and connecting industrial challenges with I4.0 technologies using articles, best practices, and use cases from academic and grey literature, thereby effectively bridging the academic-industrial communication gap. Its effectiveness and practical utility were validated in a workshop as part of the Erasmus+ project PLANET4, where industry professionals provided positive feedback after applying it to real-world challenges. Future work will include expanding the taxonomy, developing an Industry 4.0 ontology, and further enhancing the usability and maintainability of the developed web platform.

Published
2024
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14. Standing on Elevated Platform Changes Postural Reactive Responses during Arm Movement

Author

Luis Mochizuki, Juliana Pennone, Aline Bigongiari, Renata Garrido Cosme, Marcelo Massa, Alessandro Hervaldo Nicolai Ré, Ricardo Pereira Alcântaro, and Alberto Carlos Amadio

Subjects
posture, EMG, fear of falling, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
Abstract

Background/Objectives: This study investigated the behavior of postural adjustments throughout the entire action: from the preparatory phase (anticipatory postural adjustment, APA), the focal movement phase (online postural adjustments, OPA), to the compensatory phase (compensatory postural adjustment, CPA) while raising the arms in a standing position, both with eyes opened and closed. The goal was to analyze the effects of reduced sensorial information and different heights on postural muscle activity during these three phases. Methods: Eight young women performed rapid shoulder flexion while standing on the ground and on a 1-m elevated platform. The EMG activity of the trunk and lower limb muscles was recorded during all three phases. Results: Although average muscle activity was similar on the ground and the elevated platform, the pattern of postural muscle activation varied across the motor action. During OPA, all postural muscle activity was the highest, while it was the lowest during APA. On the elevated platform postural muscles have increased their activation during APA. In the most stable condition (standing on the ground with eyes opened), muscle activity showed a negative correlation between APA and OPA, but there was no correlation between OPA and CPA. Conclusions: Our results suggest postural control adapts to sensory, motor, and cognitive conditions. Therefore, the increased demand for postural control due to the height of the support base demands greater flexibility in postural synergies and alters muscle activity.

Published
2024
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15. Designing an effective dissolution test for bilayer tablets tailored for optimal melatonin release in sleep disorder management

Author

Rebecca Bassetto, Emanuele Amadio, Francesco Ciampanelli, Stefano Perin, Pietro Ilari, Paolo Gaballo, Martina Callegari, Sara Feltrin, Jacopo Gobbo, Samuele Zanatta, and Walter Bertin

Subjects
dissolution, SIFC system, biorelevant media, melatonin, bioaccessibility, modulated release, Nutrition. Foods and food supply, TX341-641
Abstract

This project aims to investigate the release performance of bilayer tablet (BL-Tablet) designed with both fast and slow-release technology, targeting sleep disorders. The tablet incorporates Melatonin, extracts of Eschscholzia californica and Melissa officinalis. In order to validate the effectiveness of the extended-release profile, an advanced dissolution test was herein proposed. This new method utilizes biorelevant intestinal fluid media and incorporates a stomach-to-intestine fluid changing (SIFC) system. To demonstrate the advantages of employing this method for assessing the controlled release profile of active ingredients, the dissolution results were compared with those obtained using the conventional EU Pharmacopoeia approach. Furthermore, the comparative analysis was extended to include a monolayer tablet version (ML-Tablet) lacking the slow-release technology. Technological characterization and bioaccessibility studies, including intestinal permeability test, were conducted as well to assess the pharmacological performance and bioavailability of active ingredients. The dissolution data recovered revealed that the two dissolution methods did not exhibit any significant differences in the release of ML-Tablet’s. However, the dissolution profile of the BL-Tablet exhibited notable differences between the two methods particularly when assessing the behavior of the slow-release layer. In this scenario, both methods initially exhibited a similar release pattern within the first approximately 0.5 h, driven by the fast-release layer of the tablet. Following this, distinct gradual and sustained releases were observed, spanning 2.5 h for the EU Pharmacopoeia method and 8 h for the new SIFC-biorelevant dissolution method, respectively. Overall, the novel method demonstrated a substantial improvement compared to conventional EU Pharmacopoeia test in evaluating the performance of a controlled slow-release technology. Remarkably, the prolonged release technology did not have an adverse impact on melatonin intestinal absorption, and, consequently, maintaining its potential bioavailability of around 78%. Concluding, this research provides valuable insights into how the innovative dissolution test can assist formulators in developing controlled release formulations.

Published
2024
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16. Tim4 enables large peritoneal macrophages to cross-present tumor antigens at early stages of tumorigenesis

Author

Sonal Joshi, Lucía López, Luciano Gastón Morosi, Roberto Amadio, Manendra Pachauri, Marco Bestagno, Ironya Paul Ogar, Mauro Giacca, Giulia Maria Piperno, Daan Vorselen, and Federica Benvenuti

Subjects
CP: Immunology, CP: Cancer, Biology (General), QH301-705.5
Abstract

Summary: Receptors controlling the cross-presentation of tumor antigens by macrophage subsets in cancer tissues are poorly explored. Here, we show that TIM4+ large peritoneal macrophages efficiently capture and cross-present tumor-associated antigens at early stages of peritoneal infiltration by ovarian cancer cells. The phosphatidylserine (PS) receptor TIM4 promotes maximal uptake of dead cells or PS-coated artificial targets and triggers inflammatory and metabolic gene programs in combination with cytoskeletal remodeling and upregulation of transcriptional signatures related to antigen processing. At the cellular level, TIM4-mediated engulfment induces nucleation of F-actin around nascent phagosomes, delaying the recruitment of vacuolar ATPase, acidification, and cargo degradation. In vivo, TIM4 deletion blunts induction of early anti-tumoral effector CD8 T cells and accelerates the progression of ovarian tumors. We conclude that TIM4-mediated uptake drives the formation of specialized phagosomes that prolong the integrity of ingested antigens and facilitate cross-presentation, contributing to immune surveillance of the peritoneum.

Published
2024
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17. NADPH-oxidases as potential pharmacological targets for thrombosis and depression comorbidity

Author

Patrizia Amadio, Leonardo Sandrini, Marta Zarà, Silvia S. Barbieri, and Alessandro Ieraci

Subjects
NOX, Platelets, Endothelium, Neurons, Microglia, Psychiatry disorders, Medicine (General), R5-920, Biology (General), QH301-705.5
Abstract

There is a complex interrelationship between the nervous system and the cardiovascular system. Comorbidities of cardiovascular diseases (CVD) with mental disorders, and vice versa, are prevalent. Adults with mental disorders such as anxiety and depression have a higher risk of developing CVD, and people with CVD have an increased risk of being diagnosed with mental disorders.Oxidative stress is one of the many pathways associated with the pathophysiology of brain and cardiovascular disease. Nicotinamide adenine dinucleotide phosphate oxidase (NOX) is one of the major generators of reactive oxygen species (ROS) in mammalian cells, as it is the enzyme that specifically produces superoxide.This review summarizes recent findings on the consequences of NOX activation in thrombosis and depression. It also discusses the therapeutic effects and pharmacological strategies of NOX inhibitors in CVD and brain disorders. A better comprehension of these processes could facilitate the development of new therapeutic approaches for the prevention and treatment of the comorbidity of thrombosis and depression.

Published
2024
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18. Erratum to: Search for exclusive Higgs and Z boson decays to ϕγ and ργ with the ATLAS detector

Author

The ATLAS collaboration, M. Aaboud, G. Aad, B. Abbott, O. Abdinov, B. Abeloos, S. H. Abidi, O. S. AbouZeid, N. L. Abraham, H. Abramowicz, H. Abreu, R. Abreu, Y. Abulaiti, B. S. Acharya, S. Adachi, L. Adamczyk, J. Adelman, M. Adersberger, T. Adye, A. A. Affolder, Y. Afik, T. Agatonovic-Jovin, C. Agheorghiesei, J. A. Aguilar-Saavedra, S. P. Ahlen, F. Ahmadov, G. Aielli, S. Akatsuka, H. Akerstedt, T. P. A. Åkesson, E. Akilli, A. V. Akimov, G. L. Alberghi, J. Albert, P. Albicocco, M. J. Alconada Verzini, S. C. Alderweireldt, M. Aleksa, I. N. Aleksandrov, C. Alexa, G. Alexander, T. Alexopoulos, M. Alhroob, B. Ali, M. Aliev, G. Alimonti, J. Alison, S. P. Alkire, B. M. M. Allbrooke, B. W. Allen, P. P. Allport, A. Aloisio, A. Alonso, F. Alonso, C. Alpigiani, A. A. Alshehri, M. I. Alstaty, B. Alvarez Gonzalez, D. Álvarez Piqueras, M. G. Alviggi, B. T. Amadio, Y. Amaral Coutinho, C. Amelung, D. Amidei, S. P. Amor Dos Santos, S. Amoroso, G. Amundsen, C. Anastopoulos, L. S. Ancu, N. Andari, T. Andeen, C. F. Anders, J. K. Anders, K. J. Anderson, A. Andreazza, V. Andrei, S. Angelidakis, I. Angelozzi, A. Angerami, A. V. Anisenkov, N. Anjos, A. Annovi, C. Antel, M. Antonelli, A. Antonov, D. J. Antrim, F. Anulli, M. Aoki, L. Aperio Bella, G. Arabidze, Y. Arai, J. P. Araque, V. Araujo Ferraz, A. T. H. Arce, R. E. Ardell, F. A. Arduh, J-F. Arguin, S. Argyropoulos, M. Arik, A. J. Armbruster, L. J. Armitage, O. Arnaez, H. Arnold, M. Arratia, O. Arslan, A. Artamonov, G. Artoni, S. Artz, S. Asai, N. Asbah, A. Ashkenazi, L. Asquith, K. Assamagan, R. Astalos, M. Atkinson, N. B. Atlay, K. Augsten, G. Avolio, B. Axen, M. K. Ayoub, G. Azuelos, A. E. Baas, M. J. Baca, H. Bachacou, K. Bachas, M. Backes, P. Bagnaia, M. Bahmani, H. Bahrasemani, J. T. Baines, M. Bajic, O. K. Baker, P. J. Bakker, E. M. Baldin, P. Balek, F. Balli, W. K. Balunas, E. Banas, A. Bandyopadhyay, Sw. Banerjee, A. A. E. Bannoura, L. Barak, E. L. Barberio, D. Barberis, M. Barbero, T. Barillari, M.-S. Barisits, J. T. Barkeloo, T. Barklow, N. Barlow, S. L. Barnes, B. M. Barnett, R. M. Barnett, Z. Barnovska-Blenessy, A. Baroncelli, G. Barone, A. J. Barr, L. Barranco Navarro, F. Barreiro, J. Barreiro Guimarães da Costa, R. Bartoldus, A. E. Barton, P. Bartos, A. Basalaev, A. Bassalat, R. L. Bates, S. J. Batista, J. R. Batley, M. Battaglia, M. Bauce, F. Bauer, H. S. Bawa, J. B. Beacham, M. D. Beattie, T. Beau, P. H. Beauchemin, P. Bechtle, H. P. Beck, H. C. Beck, K. Becker, M. Becker, C. Becot, A. J. Beddall, A. Beddall, V. A. Bednyakov, M. Bedognetti, C. P. Bee, T. A. Beermann, M. Begalli, M. Begel, J. K. Behr, A. S. Bell, G. Bella, L. Bellagamba, A. Bellerive, M. Bellomo, K. Belotskiy, O. Beltramello, N. L. Belyaev, O. Benary, D. Benchekroun, M. Bender, N. Benekos, Y. Benhammou, E. Benhar Noccioli, J. Benitez, D. P. Benjamin, M. Benoit, J. R. Bensinger, S. Bentvelsen, L. Beresford, M. Beretta, D. Berge, E. Bergeaas Kuutmann, N. Berger, L. J. Bergsten, J. Beringer, S. Berlendis, N. R. Bernard, G. Bernardi, C. Bernius, F. U. Bernlochner, T. Berry, P. Berta, C. Bertella, G. Bertoli, I. A. Bertram, C. Bertsche, G. J. Besjes, O. Bessidskaia Bylund, M. Bessner, N. Besson, A. Bethani, S. Bethke, A. Betti, A. J. Bevan, J. Beyer, R. M. Bianchi, O. Biebel, D. Biedermann, R. Bielski, K. Bierwagen, N. V. Biesuz, M. Biglietti, T. R. V. Billoud, H. Bilokon, M. Bindi, A. Bingul, C. Bini, S. Biondi, T. Bisanz, C. Bittrich, D. M. Bjergaard, J. E. Black, K. M. Black, R. E. Blair, T. Blazek, I. Bloch, C. Blocker, A. Blue, U. Blumenschein, Dr. Blunier, G. J. Bobbink, V. S. Bobrovnikov, S. S. Bocchetta, A. Bocci, C. Bock, M. Boehler, D. Boerner, D. Bogavac, A. G. Bogdanchikov, C. Bohm, V. Boisvert, P. Bokan, T. Bold, A. S. Boldyrev, A. E. Bolz, M. Bomben, M. Bona, M. Boonekamp, A. Borisov, G. Borissov, J. Bortfeldt, D. Bortoletto, V. Bortolotto, D. Boscherini, M. Bosman, J. D. Bossio Sola, J. Boudreau, E. V. Bouhova-Thacker, D. Boumediene, C. Bourdarios, S. K. Boutle, A. Boveia, J. Boyd, I. R. Boyko, A. J. Bozson, J. Bracinik, A. Brandt, G. Brandt, O. Brandt, F. Braren, U. Bratzler, B. Brau, J. E. Brau, W. D. Breaden Madden, K. Brendlinger, A. J. Brennan, L. Brenner, R. Brenner, S. Bressler, D. L. Briglin, T. M. Bristow, D. Britton, D. Britzger, F. M. Brochu, I. Brock, R. Brock, G. Brooijmans, T. Brooks, W. K. Brooks, J. Brosamer, E. Brost, J. H. Broughton, P. A. Bruckman de Renstrom, D. Bruncko, A. Bruni, G. Bruni, L. S. Bruni, S. Bruno, B. H. Brunt, M. Bruschi, N. Bruscino, P. Bryant, L. Bryngemark, T. Buanes, Q. Buat, P. Buchholz, A. G. Buckley, I. A. Budagov, F. Buehrer, M. K. Bugge, O. Bulekov, D. Bullock, T. J. Burch, S. Burdin, C. D. Burgard, A. M. Burger, B. Burghgrave, K. Burka, S. Burke, I. Burmeister, J. T. P. Burr, D. Büscher, V. Büscher, P. Bussey, J. M. Butler, C. M. Buttar, J. M. Butterworth, P. Butti, W. Buttinger, A. Buzatu, A. R. Buzykaev, S. Cabrera Urbán, D. Caforio, H. Cai, V. M. Cairo, O. Cakir, N. Calace, P. Calafiura, A. Calandri, G. Calderini, P. 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Taylor, P. T. E. Taylor, W. Taylor, P. Teixeira-Dias, D. Temple, H. Ten Kate, P. K. Teng, J. J. Teoh, F. Tepel, S. Terada, K. Terashi, J. Terron, S. Terzo, M. Testa, R. J. Teuscher, S. J. Thais, T. Theveneaux-Pelzer, F. Thiele, J. P. Thomas, J. Thomas-Wilsker, P. D. Thompson, A. S. Thompson, L. A. Thomsen, E. Thomson, Y. Tian, M. J. Tibbetts, R. E. Ticse Torres, V. O. Tikhomirov, Yu. A. Tikhonov, S. Timoshenko, P. Tipton, S. Tisserant, K. Todome, S. Todorova-Nova, S. Todt, J. Tojo, S. Tokár, K. Tokushuku, E. Tolley, L. Tomlinson, M. Tomoto, L. Tompkins, K. Toms, B. Tong, P. Tornambe, E. Torrence, H. Torres, E. Torró Pastor, J. Toth, F. Touchard, D. R. Tovey, C. J. Treado, T. Trefzger, F. Tresoldi, A. Tricoli, I. M. Trigger, S. Trincaz-Duvoid, M. F. Tripiana, W. Trischuk, B. Trocmé, A. Trofymov, C. Troncon, M. Trottier-McDonald, M. Trovatelli, L. Truong, M. Trzebinski, A. Trzupek, K. W. Tsang, J. C-L. Tseng, P. V. Tsiareshka, N. Tsirintanis, S. Tsiskaridze, V. Tsiskaridze, E. G. Tskhadadze, I. I. Tsukerman, V. Tsulaia, S. Tsuno, D. Tsybychev, Y. Tu, A. Tudorache, V. Tudorache, T. T. Tulbure, A. N. Tuna, S. Turchikhin, D. Turgeman, I. Turk Cakir, R. Turra, P. M. Tuts, G. Ucchielli, I. Ueda, M. Ughetto, F. Ukegawa, G. Unal, A. Undrus, G. Unel, F. C. Ungaro, Y. Unno, K. Uno, C. Unverdorben, J. Urban, P. Urquijo, P. Urrejola, G. Usai, J. Usui, L. Vacavant, V. Vacek, B. Vachon, K. O. H. Vadla, A. Vaidya, C. Valderanis, E. Valdes Santurio, M. Valente, S. Valentinetti, A. Valero, L. Valéry, S. Valkar, A. Vallier, J. A. Valls Ferrer, W. Van Den Wollenberg, H. van der Graaf, P. van Gemmeren, J. Van Nieuwkoop, I. van Vulpen, M. C. van Woerden, M. Vanadia, W. Vandelli, A. Vaniachine, P. Vankov, G. Vardanyan, R. Vari, E. W. Varnes, C. Varni, T. Varol, D. Varouchas, A. Vartapetian, K. E. Varvell, J. G. Vasquez, G. A. Vasquez, F. Vazeille, D. Vazquez Furelos, T. Vazquez Schroeder, J. Veatch, V. Veeraraghavan, L. M. Veloce, F. Veloso, S. Veneziano, A. Ventura, M. Venturi, N. Venturi, A. Venturini, V. Vercesi, M. Verducci, W. Verkerke, A. T. Vermeulen, J. C. Vermeulen, M. C. Vetterli, N. Viaux Maira, O. Viazlo, I. Vichou, T. Vickey, O. E. Vickey Boeriu, G. H. A. Viehhauser, S. Viel, L. Vigani, M. Villa, M. Villaplana Perez, E. Vilucchi, M. G. Vincter, V. B. Vinogradov, A. Vishwakarma, C. Vittori, I. Vivarelli, S. Vlachos, M. Vogel, P. Vokac, G. Volpi, H. von der Schmitt, E. von Toerne, V. Vorobel, K. Vorobev, M. Vos, R. Voss, J. H. Vossebeld, N. Vranjes, M. Vranjes Milosavljevic, V. Vrba, M. Vreeswijk, R. Vuillermet, I. Vukotic, P. Wagner, W. Wagner, J. Wagner-Kuhr, H. Wahlberg, S. Wahrmund, K. Wakamiya, J. Walder, R. Walker, W. Walkowiak, V. Wallangen, C. Wang, F. Wang, H. Wang, J. Wang, Q. Wang, R.-J. Wang, R. Wang, S. M. Wang, T. Wang, W. Wang, Z. Wang, C. Wanotayaroj, A. Warburton, C. P. Ward, D. R. Wardrope, A. Washbrook, P. M. Watkins, A. T. Watson, M. F. Watson, G. Watts, S. Watts, B. M. Waugh, A. F. Webb, S. Webb, M. S. Weber, S. M. Weber, S. W. Weber, S. A. Weber, J. S. Webster, A. R. Weidberg, B. Weinert, J. Weingarten, M. Weirich, C. Weiser, H. Weits, P. S. Wells, T. Wenaus, T. Wengler, S. Wenig, N. Wermes, M. D. Werner, P. Werner, M. Wessels, T. D. Weston, K. Whalen, N. L. Whallon, A. M. Wharton, A. S. White, A. White, M. J. White, R. White, D. Whiteson, B. W. Whitmore, F. J. Wickens, W. Wiedenmann, M. Wielers, C. Wiglesworth, L. A. M. Wiik-Fuchs, A. Wildauer, F. Wilk, H. G. Wilkens, H. H. Williams, S. Williams, C. Willis, S. Willocq, J. A. Wilson, I. Wingerter-Seez, E. Winkels, F. Winklmeier, O. J. Winston, B. T. Winter, M. Wittgen, M. Wobisch, A. Wolf, T. M. H. Wolf, R. Wolff, M. W. Wolter, H. Wolters, V. W. S. Wong, N. L. Woods, S. D. Worm, B. K. Wosiek, J. Wotschack, K. W. Wozniak, M. Wu, S. L. Wu, X. Wu, Y. Wu, T. R. Wyatt, B. M. Wynne, S. Xella, Z. Xi, L. Xia, D. Xu, L. Xu, T. Xu, W. Xu, B. Yabsley, S. Yacoob, D. Yamaguchi, Y. Yamaguchi, A. Yamamoto, S. Yamamoto, T. Yamanaka, F. Yamane, M. Yamatani, T. Yamazaki, Y. Yamazaki, Z. Yan, H. Yang, Y. Yang, Z. Yang, W-M. Yao, Y. C. Yap, Y. Yasu, E. Yatsenko, K. H. Yau Wong, J. Ye, S. Ye, I. Yeletskikh, E. Yigitbasi, E. Yildirim, K. Yorita, K. Yoshihara, C. Young, C. J. S. Young, J. Yu, S. P. Y. Yuen, I. Yusuff, B. Zabinski, G. Zacharis, R. Zaidan, A. M. Zaitsev, N. Zakharchuk, J. Zalieckas, A. Zaman, S. Zambito, D. Zanzi, C. Zeitnitz, G. Zemaityte, A. Zemla, J. C. Zeng, Q. Zeng, O. Zenin, T. Ženiš, D. Zerwas, D. Zhang, F. Zhang, G. Zhang, H. Zhang, J. Zhang, L. Zhang, M. Zhang, P. Zhang, R. Zhang, X. Zhang, Y. Zhang, Z. Zhang, X. Zhao, Y. Zhao, Z. Zhao, A. Zhemchugov, B. Zhou, C. Zhou, L. Zhou, M. Zhou, N. Zhou, Y. Zhou, C. G. Zhu, H. Zhu, J. Zhu, Y. Zhu, X. Zhuang, K. Zhukov, A. Zibell, D. Zieminska, N. I. Zimine, C. Zimmermann, S. Zimmermann, Z. Zinonos, M. Zinser, M. Ziolkowski, L. Živković, G. Zobernig, A. Zoccoli, R. Zou, M. zur Nedden, and L. Zwalinski

Subjects
Nuclear and particle physics. Atomic energy. Radioactivity, QC770-798
Published
2023
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19. The Mediterranean Forecasting System – Part 1: Evolution and performance

Author

G. Coppini, E. Clementi, G. Cossarini, S. Salon, G. Korres, M. Ravdas, R. Lecci, J. Pistoia, A. C. Goglio, M. Drudi, A. Grandi, A. Aydogdu, R. Escudier, A. Cipollone, V. Lyubartsev, A. Mariani, S. Cretì, F. Palermo, M. Scuro, S. Masina, N. Pinardi, A. Navarra, D. Delrosso, A. Teruzzi, V. Di Biagio, G. Bolzon, L. Feudale, G. Coidessa, C. Amadio, A. Brosich, A. Miró, E. Alvarez, P. Lazzari, C. Solidoro, C. Oikonomou, and A. Zacharioudaki

Subjects
Geography. Anthropology. Recreation, Environmental sciences, GE1-350
Abstract

The Mediterranean Forecasting System produces operational analyses and reanalyses and 10 d forecasts for many essential ocean variables (EOVs), from currents, temperature, salinity, and sea level to wind waves and pelagic biogeochemistry. The products are available at a horizontal resolution of 1/24∘ (approximately 4 km) and with 141 unevenly spaced vertical levels. The core of the Mediterranean Forecasting System is constituted by the physical (PHY), the biogeochemical (BIO), and the wave (WAV) components, consisting of both numerical models and data assimilation modules. The three components together constitute the so-called Mediterranean Monitoring and Forecasting Center (Med-MFC) of the Copernicus Marine Service. Daily 10 d forecasts and analyses are produced by the PHY, BIO, and WAV operational systems, while reanalyses are produced every ∼ 3 years for the past 30 years and are extended (yearly). The modelling systems, their coupling strategy, and their evolutions are illustrated in detail. For the first time, the quality of the products is documented in terms of skill metrics evaluated over a common 3-year period (2018–2020), giving the first complete assessment of uncertainties for all the Mediterranean environmental variable analyses.

Published
2023
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23. Viability of 2D Swimming Kinematical Analysis Using a Single Moving Camera

Author

Bruno Mezêncio, Aléxia Fernandes, Gustavo Soares Pereira, Alberto Carlos Amadio, Júlio Cerca Serrão, Susana Soares, Ricardo J. Fernandes, and João Paulo Vilas-Boas

Subjects
kinematic analysis, camera calibration, swimming, Technology, Engineering (General). Civil engineering (General), TA1-2040, Biology (General), QH301-705.5, Physics, QC1-999, Chemistry, QD1-999
Abstract

Despite its limitations, 2D kinematical analysis remains a simple and valid alternative for swimming analysis. This analysis is limited by the length of the field of view, and the reconstruction errors are proportional to the calibrated area. A possible solution for these problems is the usage of moving cameras that allow for tracking an object across a larger area without the concerns of the calibration area. The purpose of this study was to verify the viability of the utilization of moving cameras for underwater 2D kinematical analysis. Two calibration processes were evaluated: (i) obtaining the extrinsic parameters for every frame based on pool markers (M1) and; (ii) constraining the degrees of freedom of the camera’s movements and tracking translation based on the principal point (M2). M1 obtained better accuracy in reconstructing the coordinates of static markers (mean error: 12.1 against 14.2 mm from a static camera) and in the estimation of the rod length (−2.6 vs. 12.6 mm). M2 obtained better accuracy when evaluating the distance between the points (−0.3 mm) than that for position estimation (58.6 mm). The results indicate that moving cameras are a viable alternative for 2D underwater kinematic analysis, but M2 had limitations about real position extraction.

Published
2024
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24. Cdk12 maintains the integrity of adult axons by suppressing actin remodeling

Author

L. N. Townsend, H. Clarke, D. Maddison, K. M. Jones, L. Amadio, A. Jefferson, U. Chughtai, D. M. Bis, S. Züchner, N. D. Allen, W. Van der Goes van Naters, O. M. Peters, and G. A. Smith

Subjects
Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Cytology, QH573-671
Abstract

Abstract The role of cyclin-dependent kinases (CDKs) that are ubiquitously expressed in the adult nervous system remains unclear. Cdk12 is enriched in terminally differentiated neurons where its conical role in the cell cycle progression is redundant. We find that in adult neurons Cdk12 acts a negative regulator of actin formation, mitochondrial dynamics and neuronal physiology. Cdk12 maintains the size of the axon at sites proximal to the cell body through the transcription of homeostatic enzymes in the 1-carbon by folate pathway which utilize the amino acid homocysteine. Loss of Cdk12 leads to elevated homocysteine and in turn leads to uncontrolled F-actin formation and axonal swelling. Actin remodeling further induces Drp1-dependent fission of mitochondria and the breakdown of axon-soma filtration barrier allowing soma restricted cargos to enter the axon. We demonstrate that Cdk12 is also an essential gene for long-term neuronal survival and loss of this gene causes age-dependent neurodegeneration. Hyperhomocysteinemia, actin changes, and mitochondrial fragmentation are associated with several neurodegenerative conditions such as Alzheimer’s disease and we provide a candidate molecular pathway to link together such pathological events.

Published
2023
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25. KINEMATIC ANALYSIS OF CROSS ON TRAINING AND COMPETITION RINGS: COMPARISON BETWEEN ELITE AND INTERNATIONAL LEVEL GYMNASTS

Author

Paulo Daniel Sabino Carrara, Gareth Irwin, Timothy Exell, Julio Cerca Serrão, Alberto Carlos Amadio, and Luis Mochizuki

Subjects
artistic gymnastics, shoulder angle, video analysis, symmetry analysis, strength exercise, Sports, GV557-1198.995
Abstract

Auxiliary devices are used to train gymnastics skills. Based on the principles of training specificity, this study aimed to investigate the effectiveness of a training device for the static cross posture on Men’s Artistic Gymnastics rings through kinematic analysis. Twelve national team gymnasts were divided into two groups, based on their competitive results: the elite group (age: 21.8±3.2 years) and the international group (age: 19.3±3.3 years) performed the cross three times under both conditions: standard competition rings, and training rings with an auxiliary device. The videos were digitised and analysed with shoulder angles as trunk and arm segments. The variables included the right and the left shoulder angles in the frontal plane, as well as any asymmetry of those angles. Two-way ANOVA (conditions versus groups) and individual t-test statistics were conducted. Both groups performed the cross on training rings with increased abduction at both right (p

Published
2024
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26. Plasma Exosomes Refl Ect Myocardial Injury Detected by Cardiac Magnetic Resonance in STEMI Patients

Author

Andrea Baggiano, MD, Marta Zarà, PhD, Cristina Banfi, PhD, Jeness Campodonico, MD, Calogero Tedesco, PhD, Patrizia Amadio, PhD, Sebastiano Gili, MD, Gianluca De Dona, PhD, Leonardo Sandrini, PhD, Riccardo Maragna, MD, Daniele Junod, MD, Laura Fusini, MD, MSc, Saima Mushtaq, MD, Fabio Fazzari, MD, Giancarlo Marenzi, MD, Gianluca Pontone, MD, PhD, and Silvia Barbieri, PhD

Subjects
Diseases of the circulatory (Cardiovascular) system, RC666-701
Published
2024
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27. Erratum to: Search for exclusive Higgs and Z boson decays to ϕγ and ργ with the ATLAS detector

Author

Aaboud, M., Aad, G., Abbott, B., Abdinov, O., Abeloos, B., Abidi, S. H., AbouZeid, O. S., Abraham, N. L., Abramowicz, H., Abreu, H., Abreu, R., Abulaiti, Y., Acharya, B. S., Adachi, S., Adamczyk, L., Adelman, J., Adersberger, M., Adye, T., Affolder, A. A., Afik, Y., Agatonovic-Jovin, T., Agheorghiesei, C., Aguilar-Saavedra, J. A., Ahlen, S. P., Ahmadov, F., Aielli, G., Akatsuka, S., Akerstedt, H., Åkesson, T. P. A., Akilli, E., Akimov, A. V., Alberghi, G. L., Albert, J., Albicocco, P., Alconada Verzini, M. J., Alderweireldt, S. C., Aleksa, M., Aleksandrov, I. N., Alexa, C., Alexander, G., Alexopoulos, T., Alhroob, M., Ali, B., Aliev, M., Alimonti, G., Alison, J., Alkire, S. P., Allbrooke, B. M. M., Allen, B. W., Allport, P. P., Aloisio, A., Alonso, A., Alonso, F., Alpigiani, C., Alshehri, A. A., Alstaty, M. I., Alvarez Gonzalez, B., Álvarez Piqueras, D., Alviggi, M. G., Amadio, B. T., Amaral Coutinho, Y., Amelung, C., Amidei, D., Amor Dos Santos, S. P., Amoroso, S., Amundsen, G., Anastopoulos, C., Ancu, L. S., Andari, N., Andeen, T., Anders, C. F., Anders, J. K., Anderson, K. J., Andreazza, A., Andrei, V., Angelidakis, S., Angelozzi, I., Angerami, A., Anisenkov, A. V., Anjos, N., Annovi, A., Antel, C., Antonelli, M., Antonov, A., Antrim, D. J., Anulli, F., Aoki, M., Aperio Bella, L., Arabidze, G., Arai, Y., Araque, J. P., Araujo Ferraz, V., Arce, A. T. H., Ardell, R. E., Arduh, F. A., Arguin, J-F., Argyropoulos, S., Arik, M., Armbruster, A. J., Armitage, L. J., Arnaez, O., Arnold, H., Arratia, M., Arslan, O., Artamonov, A., Artoni, G., Artz, S., Asai, S., Asbah, N., Ashkenazi, A., Asquith, L., Assamagan, K., Astalos, R., Atkinson, M., Atlay, N. B., Augsten, K., Avolio, G., Axen, B., Ayoub, M. K., Azuelos, G., Baas, A. E., Baca, M. J., Bachacou, H., Bachas, K., Backes, M., Bagnaia, P., Bahmani, M., Bahrasemani, H., Baines, J. T., Bajic, M., Baker, O. K., Bakker, P. J., Baldin, E. M., Balek, P., Balli, F., Balunas, W. K., Banas, E., Bandyopadhyay, A., Banerjee, Sw., Bannoura, A. A. E., Barak, L., Barberio, E. L., Barberis, D., Barbero, M., Barillari, T., Barisits, M.-S., Barkeloo, J. T., Barklow, T., Barlow, N., Barnes, S. L., Barnett, B. M., Barnett, R. M., Barnovska-Blenessy, Z., Baroncelli, A., Barone, G., Barr, A. J., Barranco Navarro, L., Barreiro, F., Barreiro Guimarães da Costa, J., Bartoldus, R., Barton, A. E., Bartos, P., Basalaev, A., Bassalat, A., Bates, R. L., Batista, S. J., Batley, J. R., Battaglia, M., Bauce, M., Bauer, F., Bawa, H. S., Beacham, J. B., Beattie, M. D., Beau, T., Beauchemin, P. H., Bechtle, P., Beck, H. P., Beck, H. C., Becker, K., Becker, M., Becot, C., Beddall, A. J., Beddall, A., Bednyakov, V. A., Bedognetti, M., Bee, C. P., Beermann, T. A., Begalli, M., Begel, M., Behr, J. K., Bell, A. S., Bella, G., Bellagamba, L., Bellerive, A., Bellomo, M., Belotskiy, K., Beltramello, O., Belyaev, N. L., Benary, O., Benchekroun, D., Bender, M., Benekos, N., Benhammou, Y., Benhar Noccioli, E., Benitez, J., Benjamin, D. P., Benoit, M., Bensinger, J. R., Bentvelsen, S., Beresford, L., Beretta, M., Berge, D., Bergeaas Kuutmann, E., Berger, N., Bergsten, L. J., Beringer, J., Berlendis, S., Bernard, N. R., Bernardi, G., Bernius, C., Bernlochner, F. U., Berry, T., Berta, P., Bertella, C., Bertoli, G., Bertram, I. A., Bertsche, C., Besjes, G. J., Bessidskaia Bylund, O., Bessner, M., Besson, N., Bethani, A., Bethke, S., Betti, A., Bevan, A. J., Beyer, J., Bianchi, R. M., Biebel, O., Biedermann, D., Bielski, R., Bierwagen, K., Biesuz, N. V., Biglietti, M., Billoud, T. R. V., Bilokon, H., Bindi, M., Bingul, A., Bini, C., Biondi, S., Bisanz, T., Bittrich, C., Bjergaard, D. M., Black, J. E., Black, K. M., Blair, R. E., Blazek, T., Bloch, I., Blocker, C., Blue, A., Blumenschein, U., Blunier, Dr., Bobbink, G. J., Bobrovnikov, V. S., Bocchetta, S. S., Bocci, A., Bock, C., Boehler, M., Boerner, D., Bogavac, D., Bogdanchikov, A. G., Bohm, C., Boisvert, V., Bokan, P., Bold, T., Boldyrev, A. S., Bolz, A. E., Bomben, M., Bona, M., Boonekamp, M., Borisov, A., Borissov, G., Bortfeldt, J., Bortoletto, D., Bortolotto, V., Boscherini, D., Bosman, M., Bossio Sola, J. D., Boudreau, J., Bouhova-Thacker, E. V., Boumediene, D., Bourdarios, C., Boutle, S. K., Boveia, A., Boyd, J., Boyko, I. R., Bozson, A. J., Bracinik, J., Brandt, A., Brandt, G., Brandt, O., Braren, F., Bratzler, U., Brau, B., Brau, J. E., Breaden Madden, W. D., Brendlinger, K., Brennan, A. J., Brenner, L., Brenner, R., Bressler, S., Briglin, D. L., Bristow, T. M., Britton, D., Britzger, D., Brochu, F. M., Brock, I., Brock, R., Brooijmans, G., Brooks, T., Brooks, W. K., Brosamer, J., Brost, E., Broughton, J. H., Bruckman de Renstrom, P. A., Bruncko, D., Bruni, A., Bruni, G., Bruni, L. S., Bruno, S., Brunt, B. H., Bruschi, M., Bruscino, N., Bryant, P., Bryngemark, L., Buanes, T., Buat, Q., Buchholz, P., Buckley, A. G., Budagov, I. A., Buehrer, F., Bugge, M. K., Bulekov, O., Bullock, D., Burch, T. J., Burdin, S., Burgard, C. D., Burger, A. M., Burghgrave, B., Burka, K., Burke, S., Burmeister, I., Burr, J. T. P., Büscher, D., Büscher, V., Bussey, P., Butler, J. M., Buttar, C. M., Butterworth, J. M., Butti, P., Buttinger, W., Buzatu, A., Buzykaev, A. R., Cabrera Urbán, S., Caforio, D., Cai, H., Cairo, V. M., Cakir, O., Calace, N., Calafiura, P., Calandri, A., Calderini, G., Calfayan, P., Callea, G., Caloba, L. P., Calvente Lopez, S., Calvet, D., Calvet, S., Calvet, T. P., Camacho Toro, R., Camarda, S., Camarri, P., Cameron, D., Caminal Armadans, R., Camincher, C., Campana, S., Campanelli, M., Camplani, A., Campoverde, A., Canale, V., Cano Bret, M., Cantero, J., Cao, T., Capeans Garrido, M. D. M., Caprini, I., Caprini, M., Capua, M., Carbone, R. M., Cardarelli, R., Cardillo, F., Carli, I., Carli, T., Carlino, G., Carlson, B. T., Carminati, L., Carney, R. M. D., Caron, S., Carquin, E., Carrá, S., Carrillo-Montoya, G. D., Casadei, D., Casado, M. P., Casha, A. F., Casolino, M., Casper, D. W., Castelijn, R., Castillo Gimenez, V., Castro, N. F., Catinaccio, A., Catmore, J. R., Cattai, A., Caudron, J., Cavaliere, V., Cavallaro, E., Cavalli, D., Cavalli-Sforza, M., Cavasinni, V., Celebi, E., Ceradini, F., Cerda Alberich, L., Cerqueira, A. S., Cerri, A., Cerrito, L., Cerutti, F., Cervelli, A., Cetin, S. A., Chafaq, A., Chakraborty, D., Chan, S. K., Chan, W. S., Chan, Y. L., Chang, P., Chapman, J. D., Charlton, D. G., Chau, C. C., Chavez Barajas, C. A., Che, S., Cheatham, S., Chegwidden, A., Chekanov, S., Chekulaev, S. V., Chelkov, G. A., Chelstowska, M. A., Chen, C., Chen, C., Chen, H., Chen, J., Chen, S., Chen, S., Chen, X., Chen, Y., Cheng, H. C., Cheng, H. J., Cheplakov, A., Cheremushkina, E., Cherkaoui El Moursli, R., Cheu, E., Cheung, K., Chevalier, L., Chiarella, V., Chiarelli, G., Chiodini, G., Chisholm, A. S., Chitan, A., Chiu, Y. H., Chizhov, M. V., Choi, K., Chomont, A. R., Chouridou, S., Chow, Y. S., Christodoulou, V., Chu, M. C., Chudoba, J., Chuinard, A. J., Chwastowski, J. J., Chytka, L., Ciftci, A. K., Cinca, D., Cindro, V., Cioară, I. A., Ciocio, A., Cirotto, F., Citron, Z. H., Citterio, M., Ciubancan, M., Clark, A., Clark, B. L., Clark, M. R., Clark, P. J., Clarke, R. N., Clement, C., Coadou, Y., Cobal, M., Coccaro, A., Cochran, J., Colasurdo, L., Cole, B., Colijn, A. P., Collot, J., Colombo, T., Conde Muiño, P., Coniavitis, E., Connell, S. H., Connelly, I. A., Constantinescu, S., Conti, G., Conventi, F., Cooke, M., Cooper-Sarkar, A. M., Cormier, F., Cormier, K. J. R., Corradi, M., Corriveau, F., Cortes-Gonzalez, A., Costa, G., Costa, M. J., Costanzo, D., Cottin, G., Cowan, G., Cox, B. E., Cranmer, K., Crawley, S. J., Creager, R. A., Cree, G., Crépé-Renaudin, S., Crescioli, F., Cribbs, W. A., Cristinziani, M., Croft, V., Crosetti, G., Cueto, A., Cuhadar Donszelmann, T., Cukierman, A. R., Cummings, J., Curatolo, M., Cúth, J., Czekierda, S., Czodrowski, P., D’amen, G., D’Auria, S., D’eramo, L., D’Onofrio, M., Da Cunha Sargedas De Sousa, M. J., Da Via, C., Dabrowski, W., Dado, T., Dai, T., Dale, O., Dallaire, F., Dallapiccola, C., Dam, M., Dandoy, J. R., Daneri, M. F., Dang, N. P., Daniells, A. C., Dann, N. S., Danninger, M., Dano Hoffmann, M., Dao, V., Darbo, G., Darmora, S., Dassoulas, J., Dattagupta, A., Daubney, T., Davey, W., David, C., Davidek, T., Davis, D. R., Davison, P., Dawe, E., Dawson, I., De, K., de Asmundis, R., De Benedetti, A., De Castro, S., De Cecco, S., De Groot, N., de Jong, P., De la Torre, H., De Lorenzi, F., De Maria, A., De Pedis, D., De Salvo, A., De Sanctis, U., De Santo, A., De Vasconcelos Corga, K., De Vivie De Regie, J. B., Debbe, R., Debenedetti, C., Dedovich, D. 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2023
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29. Relevance of Spike/Estrogen Receptor-α interaction for endothelial-based coagulopathy induced by SARS-CoV-2

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Barbieri, Silvia Stella, Cattani, Franca, Sandrini, Leonardo, Grillo, Magda Maria, Amendola, Alessandra, Valente, Carmen, Talarico, Carmine, Iaconis, Daniela, Turacchio, Gabriele, Lucariello, Miriam, Lione, Lucia, Salvatori, Erika, Amadio, Patrizia, Garoffolo, Gloria, Maffei, Mariano, Galli, Francesca, Beccari, Andrea Rosario, Sberna, Giuseppe, Marra, Emanuele, Zoppi, Marica, Michaelides, Michael, Roscilli, Giuseppe, Aurisicchio, Luigi, Bertini, Riccardo, Allegretti, Marcello, and Pesce, Maurizio

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2023
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30. DOCUMENTATION OF ARCHAEOLOGICAL STRATIGRAPHIC UNITS. NEW DIGITAL TECHNOLOGIES APPLIED TO THE BURIALS IN SANT’ANDREA IN MOMBASIGLIO

Author

G. Bruschi and D. Amadio

Subjects
Technology, Engineering (General). Civil engineering (General), TA1-2040, Applied optics. Photonics, TA1501-1820
Abstract

Archaeological site activities are extremely destructive. To understand how civilizations have developed, archaeologists have to remove layers and layers of land to find evidences of their theories. An important task for researchers is to accurately document every single detail of the site before the definitive removal of precious information. Position, orientation and the context where findings are located could represent important data to be stored and compared many months after excavation process. Survey operations during site activities has to be considered extremely important, since they have to immortalize a particular moment of past human activities before its destruction. Despite this, most of the time archaeological records consist of two-dimensional representation of three-dimensional subjects. In recent years, the spreading of techniques to digitally document heritage assets have allowed to tested new approaches also in archaeological fields. Using digital cameras, drones and laser scanners it is possible to collect a multitude of details, such as textures, materials, decay phenomena, and to collect all these data inside 3D models. Digital techniques for documenting archaeological site has been tested during excavation campaigns in Sant’Andrea in Mombasiglio church, in the northern of Italy. The site has been documented along many years and in different excavation progresses, to be able to digitally recreate multiple stages of site evolution. 4D stored information can be used by archaeologist for scientific purpose, as in the museums through VR and AR applications.

Published
2023
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31. Relevance of Spike/Estrogen Receptor-α interaction for endothelial-based coagulopathy induced by SARS-CoV-2

Author

Silvia Stella Barbieri, Franca Cattani, Leonardo Sandrini, Magda Maria Grillo, Alessandra Amendola, Carmen Valente, Carmine Talarico, Daniela Iaconis, Gabriele Turacchio, Miriam Lucariello, Lucia Lione, Erika Salvatori, Patrizia Amadio, Gloria Garoffolo, Mariano Maffei, Francesca Galli, Andrea Rosario Beccari, Giuseppe Sberna, Emanuele Marra, Marica Zoppi, Michael Michaelides, Giuseppe Roscilli, Luigi Aurisicchio, Riccardo Bertini, Marcello Allegretti, and Maurizio Pesce

Subjects
Medicine, Biology (General), QH301-705.5
Published
2023
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32. Survey of Surgeon-reported Postoperative Protocols for Deep Inferior Epigastric Perforator Flap in Breast Reconstruction

Author

Sthefano Araya, MD, Madison Hackley, BS, Grace M. Amadio, BS, Mengying Deng, MS, Civanni Moss, BSN, RN, Eliann Reinhardt, BA, BM, Adam Walchak, MD, Michael G. Tecce, MD, and Sameer A. Patel, MD, FACS

Subjects
Surgery, RD1-811
Abstract

Background:. The use of deep inferior epigastric perforator (DIEP) flaps is a well-established breast reconstruction technique. Methods:. A 29-question survey was e-mailed to 3186 active American Society of Plastic Surgeons members, aiming to describe postoperative monitoring practice patterns among surgeons performing DIEP flaps. Results:. From 255 responses (8%), 79% performing DIEP surgery were analyzed. Among them, 34.8% practiced for more than 20 years, 34.3% for 10–20 years, and 30.9% for less than 10 years. Initial 24-hour post-DIEP monitoring: intensive care unit (39%) and floor (36%). Flap monitoring: external Doppler (71%), tissue oximetry (41%), and implantable Doppler (32%). Postoperative analgesia: acetaminophen (74%), non-steroidal anti-inflammatory drugs (69%), neuromodulators (52%), and opioids (4.4%) were administered on a scheduled basis. On postoperative day 1, 61% halt intravenous fluids, 67% allow ambulation, 70% remove Foley catheter, and 71% start diet. Most surgeons discharged patients from the hospital on postoperative day 3+. Regardless of experience, patients were commonly discharged on day 3. Half of the surgeons are in academic/nonacademic settings and discharge on/after day 3. Conclusions:. This study reveals significant heterogeneity among the practice patterns of DIEP surgeons. In light of these findings, it is recommended that a task force be convened to establish standardized monitoring protocols for DIEP flaps. Such protocols have the potential to reduce both the length of hospital stays and overall care costs all while ensuring optimal pain management and vigilant flap monitoring.

Published
2023
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34. How much does a liter of donor human milk cost? Cost analysis of operating a human milk bank in Italy

Author

Guglielmo Salvatori, Domenico Umberto De Rose, Maria Clemente, Cristina Gentili, Giovanni Paride Verardi, Patrizia Amadio, Maria Paola Reposi, Pietro Bagolan, and Andrea Dotta

Subjects
Newborn, Human milk bank, Donor human milk, Pediatrics, RJ1-570, Public aspects of medicine, RA1-1270
Abstract

Abstract Background To date, 40 Human Milk Banks (HMB) have been established in Italy; however, recent cost analysis data for operating an HMB in Italy are not available in the literature. Methods This study was a cross-sectional study performed at “Bambino Gesù” Children’s Hospital in Rome, Italy in 2019. We assessed the one-year operational costs and, the per liter unit costs at our HMB. Results During the 2019 year we collected 771 l of human milk supplied by 128 donors. The total cost was € 178,287.00 and the average cost was € 231.00 per liter. € 188,716.00 would have been spent had the maximum capacity for 904 l been reached. We found a significant difference (€ 231.00 vs € 209.00 per liter, p = 0.016) comparing the cost for collected liters in the year 2019 and the cost for the maximum capacity of the bank for that year of activity. Analyzing each cost item that determines the charge of donor human milk (DHM), the highest costs are the salaries of medical and paramedical staff, and then the costs related to transporting. If the HMB works at maximum capacity and manages a greater number of liters of milk, this can represent an important saving. Conversely, the price of consumables is modest (i.e., the price of a single-use kit for breast pumps was € 0.22 per unit). Conclusion The costs for a liter of DHM are quite high, but they must be related to the benefits, especially for preterm infants. Comparing the cost for collected liters in 2019 and the costs for the 2019 maximum capacity of the HMB, we calculated how much fixed costs of collection and distribution of DHM can be reduced, by increasing the volume of milk collected. To the best of our knowledge, this is the first complete cost analysis for an Italian Milk Bank. A thorough analysis could help to abate fixed costs and reduce the cost of a liter of DHM. The centralization of DHM can allow savings, rather than creating small HMBs scattered throughout the territory that would operate with lower milk volumes.

Published
2022
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35. Novel potential pharmacological applications of dimethyl fumarate—an overview and update

Author

Giorgia Bresciani, Federico Manai, Sergio Davinelli, Paolo Tucci, Luciano Saso, and Marialaura Amadio

Subjects
Nrf2 pathway, drug repurposing, dimethyl fumarate, inflammation, oxidative stress, antioxidant, Therapeutics. Pharmacology, RM1-950
Abstract

Dimethyl fumarate (DMF) is an FDA-approved drug for the treatment of psoriasis and multiple sclerosis. DMF is known to stabilize the transcription factor Nrf2, which in turn induces the expression of antioxidant response element genes. It has also been shown that DMF influences autophagy and participates in the transcriptional control of inflammatory factors by inhibiting NF-κB and its downstream targets. DMF is receiving increasing attention for its potential to be repurposed for several diseases. This versatile molecule is indeed able to exert beneficial effects on different medical conditions through a pleiotropic mechanism, in virtue of its antioxidant, immunomodulatory, neuroprotective, anti-inflammatory, and anti-proliferative effects. A growing number of preclinical and clinical studies show that DMF may have important therapeutic implications for chronic diseases, such as cardiovascular and respiratory pathologies, cancer, eye disorders, neurodegenerative conditions, and systemic or organ specific inflammatory and immune-mediated diseases. This comprehensive review summarizes and highlights the plethora of DMF’s beneficial effects and underlines its repurposing opportunities in a variety of clinical conditions.

Published
2023
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36. COPI-regulated mitochondria-ER contact site formation maintains axonal integrity

Author

Daniel C. Maddison, Bilal Malik, Leonardo Amadio, Dana M. Bis-Brewer, Stephan Züchner, Owen M. Peters, and Gaynor A. Smith

Subjects
CP: Cell biology, Biology (General), QH301-705.5
Abstract

Summary: Coat protein complex I (COPI) is best known for its role in Golgi-endoplasmic reticulum (ER) trafficking, responsible for the retrograde transport of ER-resident proteins. The ER is crucial to neuronal function, regulating Ca2+ homeostasis and the distribution and function of other organelles such as endosomes, peroxisomes, and mitochondria via functional contact sites. Here we demonstrate that disruption of COPI results in mitochondrial dysfunction in Drosophila axons and human cells. The ER network is also disrupted, and the neurons undergo rapid degeneration. We demonstrate that mitochondria-ER contact sites (MERCS) are decreased in COPI-deficient axons, leading to Ca2+ dysregulation, heightened mitophagy, and a decrease in respiratory capacity. Reintroducing MERCS is sufficient to rescue not only mitochondrial distribution and Ca2+ uptake but also ER morphology, dramatically delaying neurodegeneration. This work demonstrates an important role for COPI-mediated trafficking in MERC formation, which is an essential process for maintaining axonal integrity.

Published
2023
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37. Operation of the CERN disk storage infrastructure during LHC Run-3

Author

Caffy Cedric, Amadio Guilherme, Arsuaga Rios Maria, Batalha Reis Manuel, Capitoni Niccolo, Contescu Cristian, Guenther Jaroslav, Mascetti Luca, Peters Andreas, Sindrilaru Elvin, Vrachnaki Ioanna, and Lekshmanan Abhishek

Subjects
Physics, QC1-999
Abstract

The CERN IT Storage group operates multiple distributed storage systems to support all CERN data storage requirements. The storage and distribution of physics data generated by LHC and non-LHC experiments is one of the biggest challenges the group has to take on during LHC Run-3.EOS [1], the CERN distributed disk storage system is playing a key role in LHC data-taking. During the first ten months of 2022, more than 440PB have been written by the experiments and 2.9EB have been read out. The data storage requirements of LHC Run-3 are higher than what was previously delivered. The storage operations team has started investigating multiple areas to upgrade and optimize the current storage resources. A new, dedicated and redundant EOS infrastructure based on 100Gbit servers was installed, commissioned and deployed for the ALICE Online and Offline (O2) project. This cluster can sustain high-throughput data transfer between the ALICE Event Processing Nodes (EPN) and the CERN’s data center.This paper will present the architecture, techniques and workflows in place allowing EOS to deliver fast, reliable and scalable data storage to meet experiment needs during LHC Run-3 and beyond.

Published
2024
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38. XRootD Client: A robust technology for LHC Run-3 and beyond

Author

Amadio Guilherme, Caffy Cedric, Hanushevsky Andrew Bohdan, Simon Michał Kamil, and Smith David

Subjects
Physics, QC1-999
Abstract

During the LHC era the XRootD framework has proven to be a critical component of numerous data management and software defined storage solutions (most importantly EOS, the CERN storage technology used for the LHC experiments), and as such grew into one of the most strategic storage technologies in the High Energy Physics (HEP) community. Over the last year significant developments in the area of the XRootD client have been introduced, making it even more reliable and robust, as well as easier to debug. Here, we present an overview of the new XRootD client and its main features, namely, support for erasure coding, in-flight data integrity checks, and the new record plug-in and replay tool that allow to record an I/O pattern and then replay it for debugging or benchmarking purposes.

Published
2024
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39. EOS software evolution enabling LHC Run 3

Author

Caffy Cedric, Amadio Guilherme, Guenther Jaroslav, Lekshmanan Abhishek, Mascetti Luca, Peters Andreas, Reis Manuel, Simon Michal Kamil, Sindrilaru Elvin, and Smith David

Subjects
Physics, QC1-999
Abstract

EOS has been the main storage system at CERN for more than a decade, continuously improving in order to meet the ever evolving requirements of the LHC experiments and the whole physics user community. In order to satisfy the demands of LHC Run-3, in terms of storage performance and tradeoff between cost and capacity, EOS was enhanced with a set of new functionalities and features that we will detail in this paper. First of all, we describe the use of erasure coded layouts in a large-scale deployment which enables an efficient use of available storage capacity, while at the same time providing end-users with better throughput when accessing their data. This new operating model implies more coupling between the machines in a cluster, which in turn leads to the next set of EOS improvements that we discuss, targeting I/O traffic shaping, better I/O scheduling policies and tagged traffic prioritization. Increasing the size of the EOS clusters to cope with experiment demands, means stringent constraints on the data integrity and durability that we addressed by a re-designed consistency check engine. Another focus area of EOS development was to minimize the operational load by making the internal operational procedures (draining, balancing or conversions) more robust and efficient, to allow managing easily multiple clusters and avoid possible scaling issues. All these improvements available in the EOS 5 release series, are coupled with the new XRootD 5 framework which brings additional security features like TLS support and optimizations for large data transfers like page read and page write functionalities. Last but not least, the area of authentication/authorization methods has seen important developments by adding support for different types of bearer tokens that we will describe along with EOS specific token extensions. We conclude by highlighting potential areas of the EOS architecture that might require further developments or re-design in order to cope with the ever-increasing demands of our end-users.

Published
2024
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40. Protective Role of Limosilactobacillus fermentum Lf2 and Its Exopolysaccharides (EPS) in a TNBS-Induced Chronic Colitis Mouse Model

Author

Elisa C. Ale, José M. Irazoqui, Analía Ale, Guillermo H. Peralta, Melisa Puntillo, Patricia Burns, Gabriela Correa Olivar, Jimena Cazenave, Carina V. Bergamini, Ariel F. Amadio, and Ana G. Binetti

Subjects
exopolysaccharides, lactobacilli, chronic colitis, intestinal microbiota, antioxidant enzymes, immunomodulation, Fermentation industries. Beverages. Alcohol, TP500-660
Abstract

Limosilactobacillus fermentum Lf2 (Lf2) is an autochthonous strain that produces high levels of exopolysaccharides (EPS). The objective of this work was to evaluate the probiotic potential of Lf2 and its relationship with these metabolites in a mouse model of TNBS (trinitrobenzene sulfonic acid)-induced chronic colitis. Mice were treated intrarectally with increasing doses of TNBS resuspended in 50% ethanol for 14 days. In parallel, they received different treatments by gavage (lactose 10% as the matrix): freeze-dried Lf2 (L); purified EPS (E); and lactose 10% (T). A healthy control group (H) was treated with 50% alcohol without TNBS (intrarectally) and 10% lactose (by gavage). In the small intestine, there was a significant increase in IgA levels for the group that received EPS and a decrease in IFN-γ for mice treated with the strain compared to the other groups. In the large intestine, IL-2 and IFN-γ presented the lowest levels in the groups treated with EPS and the strain. The concentrations of acetic and propionic acids in mice that received Lf2 were the highest, while the levels of butyric acid were comparable to the healthy control group. An increase in the abundance of SCFA-producing bacteria was observed for mice treated with EPS and the strain in comparison with the colitis control group. The enzyme activity of catalase was higher in all the treatments compared to the TNBS-induced colitis control mice. To summarize the results obtained, a principal component analysis (PCA) was performed, clearly grouping the treatments in different clusters according to the variables studied. This is one of the first studies to address the role of a potential probiotic strain in a chronic colitis mouse model, trying to elucidate the relationship between its properties and the EPS synthesized.

Published
2024
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42. Safety and efficacy of substance-based medical devices: Design of an in vitro barrier effect test

Author

Rebecca Bassetto, Stefano Perin, Emanuele Amadio, Samuele Zanatta, Davide Nenzioni, and Walter Bertin

Subjects
medical devices, franz cell, biomimetic membrane, permeability, barrier effect, nutraceuticals, Therapeutics. Pharmacology, RM1-950
Abstract

This study aims to develop an in vitro barrier effect test over biomimetic membrane, which is useful to establish the film forming ability of a substance-based medical device (SB-MD). The method contemplates a multiparametric approach including: i) the measurement of the transmembrane passage of a molecular-like marker over a lipid-impregnated biomimetic membrane (simulating the skin and gastro-intestinal and buccal tissues) by using a static diffusion cell apparatus (Franz cell); and ii) the evaluation of the integrity of the membrane (colorimetric test). In the first step, a series of lipid-impregnated biomimetic membranes (simulating gastro-intestinal, buccal, and skin tissues) were implemented and their permeability performance validated using model drugs (caffeine and acyclovir) by referring to literature data. As a result, the apparent permeability (Papp) of caffeine over the biomimetic gastro-intestinal membrane (Papp = 30.5E-6 cm/s) was roughly comparable to the literature values obtained with Caco-2 cell line membrane (Papp = 30.8E-6 cm/s) and with the Franz cell method (Papp = 36.2E-6 cm/s). Acyclovir was shown to be a poorly permeable substance both in the literature and experimental data. Following this step, the permeability study was extended to both biomimetic buccal and skin (STRAT-M®) membranes: for caffeine, biomimetic gastro-intestinal membrane was the most permeable (Papp = 30.5E-6 cm/s), followed by the buccal (Papp = 18.2E-6 cm/s) then the skin (Papp = 0.5E-6 cm/s) biomimetic membranes. In a second part of the work, the barrier effect test was developed following a similar permeability-like approach. The protocol was designed with the idea of assessing the capacity of a certain product to prevent the passage of caffeine across the biomimetic membrane with respect to a negative and positive control. The untreated membrane was the negative control, while membrane covered with a Vaseline film was the positive. As a last step, the developed barrier effect protocol was applied to an experimental gel-like SB-MD under development for the treatment of aphthae (Aphthae gel, an invented trade name), herein used as a case study. Regarding the results, Aphthae gel reduced the caffeine passage by 60.3%, thus highlighting its effectiveness to form a protective film. Overall, these results provide important knowledge and may pave the way for the use—including for industrial applications—of these simple but effective biomimetic membranes for carrying out high throughput screening necessary to design safe and effective SB-MDs before proceeding further with clinical trials, as requested by the regulations.

Published
2023
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43. Sparing the Prod: Providing an Alternative to Endomyocardial Biopsies With Noninvasive Surveillance After Heart Transplantation During COVID-19

Author

Jennifer M. Amadio, MD, MEHP, Eduard Rodenas-Alesina, MD, Stefan Superina, MHSc, Stella Kozuszko, NP, RN, Katherine Tsang, RN, MN, Anne Simard, MHSc, Natasha Aleksova, MD, Jeremy Kobulnik, MD, MHSc, Chun-Po Steve Fan, PhD, Harindra C. Wijeysundera, MD, PhD, Heather J. Ross, MD, MHSc, Michael A. McDonald, MD, Juan G. Duero Posada, MD, MSc, and Yasbanoo Moayedi, MD MHSc

Subjects
Diseases of the circulatory (Cardiovascular) system, RC666-701
Abstract

Background: The COVID-19 pandemic has reduced access to endomyocardial biopsy (EMB) rejection surveillance in heart transplant (HT) recipients. This study is the first in Canada to assess the role for noninvasive rejection surveillance in personalizing titration of immunosuppression and patient satisfaction post-HT. Methods: In this mixed-methods prospective cohort study, adult HT recipients more than 6 months from HT had their routine EMBs replaced by noninvasive rejection surveillance with gene expression profiling (GEP) and donor-derived cell-free DNA (dd-cfDNA) testing. Demographics, outcomes of noninvasive surveillance score, hospital admissions, patient satisfaction, and health status on the medical outcomes study 12-item short-form health survey (SF-12) were collected and analyzed, using t tests and χ2 tests. Thematic qualitative analysis was performed for open-ended responses. Results: Among 90 patients, 31 (33%) were enrolled. A total of 36 combined GEP/dd-cfDNA tests were performed; 22 (61%) had negative results for both, 10 (27%) had positive GEP/negative dd-cfDNA results, 4 (11%) had negative GEP/positive dd-cfDNA results, and 0 were positive on both. All patients with a positive dd-cfDNA result (range: 0.19%-0.81%) underwent EMB with no significant cellular or antibody-mediated rejection. A total of 15 cases (42%) had immunosuppression reduction, and this increased to 55% in patients with negative concordant testing. Overall, patients’ reported satisfaction was 90%, and on thematic analysis they were more satisfied, with less anxiety, during the noninvasive testing experience. Conclusions: Noninvasive rejection surveillance was associated with the ability to lower immunosuppression, increase satisfaction, and reduce anxiety in HT recipients, minimizing exposure for patients and providers during a global pandemic. Résumé: Contexte: La pandémie de COVID-19 a réduit l’accès à la biopsie endomyocardique pour surveiller le risque de rejet après une greffe du cœur. Cette étude est la première à être menée au Canada pour évaluer le rôle de la surveillance non invasive du risque de rejet en personnalisant le titrage de l’immunosuppression et la satisfaction du patient après la greffe cardiaque. Méthodologie: Dans le cadre de cette étude de cohorte prospective à méthodes mixtes, des adultes ayant reçu une greffe cardiaque depuis plus de six mois ont vu leurs biopsies endomyocardiques régulières remplacées par une surveillance non invasive du risque de rejet qui consiste à établir le profil de l’expression génique et à analyser l’ADN acellulaire dérivé du donneur. Les données démographiques, les résultats du score de surveillance non invasive, les admissions à l’hôpital, la satisfaction des patients et l’état de santé tirés du questionnaire SF-12 (questionnaire abrégé sur la santé comprenant 12 items) de l’étude sur les issues médicales ont été colligés et analysés au moyen des tests T et des tests χ2. Les réponses ouvertes ont fait l’objet d’une analyse qualitative thématique. Résultats: Parmi 90 patients, 31 (33 %) ont été recrutés. Au total, 36 tests combinés de profilages de l’expression génique et d’ADN acellulaire dérivé du donneur ont été réalisés; les résultats ont été négatifs pour les deux tests dans 22 cas (61 %), positifs pour le profilage de l’expression génique et négatifs pour l’ADN acellulaire dans 10 cas (27 %), négatifs pour le profilage de l’expression génique et positifs pour l’ADN acellulaire dans quatre cas (11 %) et aucun cas n’a donné de résultats positifs pour les deux types de tests. Tous les patients qui ont donné des résultats positifs à l’analyse de l’ADN acellulaire dérivé du donneur (fourchette : 0,19 % à 0,81 %) ont subi une biopsie endomyocardique n’ayant révélé aucun rejet cellulaire ou à médiation par anticorps important. Au total, 15 cas (42 %) affichaient une immunosuppression réduite, proportion qui a grimpé à 55 % chez les patients dont les tests de concordance ont donné des résultats négatifs. Dans l’ensemble, le niveau de satisfaction rapporté par les patients était de 90 % et, à l’analyse thématique, ils étaient plus satisfaits et moins anxieux pendant les tests non invasifs. Conclusions: La surveillance non invasive du risque de rejet a été associée à la capacité de diminuer l’immunosuppression, d’augmenter la satisfaction et de réduire l’anxiété chez les patients qui ont reçu une greffe cardiaque, en plus de réduire l’exposition des patients et du personnel médical dans le contexte d’une pandémie.

Published
2022
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44. Análise do scout do campeonato brasileiro de futebol 2013

Author

Rafael Soncin, Wilson Pereira Lima, Rhuan Lopes, Reuder Diniz, Alberto Carlos Amadio, Júlio Cerca Serrão, and Bruno Mezêncio

Subjects
scout, modelagem de jogo, futebol, Sports, GV557-1198.995
Abstract

O objetivo foi identificar modelos que explicam as relações entre as diferentes variáveis do Scout e comparar as variáveis entre turnos e mandos de campo do Campeonato Brasileiro 2013. Foram analisados 380 jogos. Os modelos de regressão múltipla indicaram que finalizações, finalizações no gol, gols feitos, saldo de gols, passes certos e posse de bola foram significativos como variáveis dependentes; para o 1º turno, total de finalizações, gols feitos, posse de bola, saldo de gols e passes certos; no 2º turno total de finalizações, gols feitos, posse de bola e finalizações no gol. Identificar modelos e suas variáveis independentes pode contribuir para realização de um trabalho técnico-tático que melhor atende a complexidade do jogo.

Published
2022

45. Cost–benefit analysis of coastal flood defence measures in the North Adriatic Sea

Author

M. Amadio, A. H. Essenfelder, S. Bagli, S. Marzi, P. Mazzoli, J. Mysiak, and S. Roberts

Subjects
Environmental technology. Sanitary engineering, TD1-1066, Geography. Anthropology. Recreation, Environmental sciences, GE1-350, Geology, QE1-996.5
Abstract

The combined effect of global sea level rise and land subsidence phenomena poses a major threat to coastal settlements. Coastal flooding events are expected to grow in frequency and magnitude, increasing the potential economic losses and costs of adaptation. In Italy, a large share of the population and economic activities are located along the low-lying coastal plain of the North Adriatic coast, one of the most sensitive areas to relative sea level changes. Over the last half a century, this stretch of coast has experienced a significant rise in relative sea level, the main component of which was land subsidence; in the forthcoming decades, climate-induced sea level rise is expected to become the first driver of coastal inundation hazard. We propose an assessment of flood hazard and risk linked with extreme sea level scenarios, under both historical conditions and sea level rise projections in 2050 and 2100. We run a hydrodynamic inundation model on two pilot sites located along the North Adriatic coast of Emilia-Romagna: Rimini and Cesenatico. Here, we compare alternative extreme sea level scenarios accounting for the effect of planned and hypothetical seaside renovation projects against the historical baseline. We apply a flood damage model to estimate the potential economic damage linked to flood scenarios, and we calculate the change in expected annual damage according to changes in the relative sea level. Finally, damage reduction benefits are evaluated by means of cost–benefit analysis. Results suggest an overall profitability of the investigated projects over time, with increasing benefits due to increased probability of intense flooding in the near future.

Published
2022
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46. Erratum to: Search for single top-quark production via flavour-changing neutral currents at 8 TeV with the ATLAS detector

Author

G. Aad, B. Abbott, J. Abdallah, O. Abdinov, R. Aben, M. Abolins, O. S. AbouZeid, H. Abramowicz, H. Abreu, R. Abreu, Y. Abulaiti, B. S. Acharya, L. Adamczyk, D. L. Adams, J. Adelman, S. Adomeit, T. Adye, A. A. Affolder, T. Agatonovic-Jovin, J. Agricola, J. A. Aguilar-Saavedra, S. P. Ahlen, F. Ahmadov, G. Aielli, H. Akerstedt, T. P. A. Åkesson, A. V. Akimov, G. L. Alberghi, J. Albert, S. Albrand, M. J. Alconada Verzini, M. Aleksa, I. N. Aleksandrov, C. Alexa, G. Alexander, T. Alexopoulos, M. Alhroob, G. Alimonti, L. Alio, J. Alison, S. P. Alkire, B. M. M. Allbrooke, P. P. Allport, A. Aloisio, A. Alonso, F. Alonso, C. Alpigiani, A. Altheimer, B. Alvarez Gonzalez, D. Álvarez Piqueras, M. G. Alviggi, B. T. Amadio, K. Amako, Y. Amaral Coutinho, C. Amelung, D. Amidei, S. P. Amor Dos Santos, A. Amorim, S. Amoroso, N. Amram, G. Amundsen, C. Anastopoulos, L. S. Ancu, N. Andari, T. Andeen, C. F. Anders, G. Anders, J. K. Anders, K. J. Anderson, A. Andreazza, V. Andrei, S. Angelidakis, I. Angelozzi, P. Anger, A. Angerami, F. Anghinolfi, A. V. Anisenkov, N. Anjos, A. Annovi, M. Antonelli, A. Antonov, J. Antos, F. Anulli, M. Aoki, L. Aperio Bella, G. Arabidze, Y. Arai, J. P. Araque, A. T. H. Arce, F. A. Arduh, J-F. Arguin, S. Argyropoulos, M. Arik, A. J. Armbruster, O. Arnaez, V. Arnal, H. Arnold, M. Arratia, O. Arslan, A. Artamonov, G. Artoni, S. Asai, N. Asbah, A. Ashkenazi, B. Åsman, L. Asquith, K. Assamagan, R. Astalos, M. Atkinson, N. B. Atlay, K. Augsten, M. Aurousseau, G. Avolio, B. Axen, M. K. Ayoub, G. Azuelos, M. A. Baak, A. E. Baas, M. J. Baca, C. Bacci, H. Bachacou, K. Bachas, M. Backes, M. Backhaus, P. Bagiacchi, P. Bagnaia, Y. Bai, T. Bain, J. T. Baines, O. K. Baker, E. M. Baldin, P. Balek, T. Balestri, F. Balli, E. Banas, Sw. Banerjee, A. A. E. Bannoura, H. S. Bansil, L. Barak, E. L. Barberio, D. Barberis, M. Barbero, T. Barillari, M. Barisonzi, T. Barklow, N. Barlow, S. L. Barnes, B. M. Barnett, R. M. Barnett, Z. Barnovska, A. Baroncelli, G. Barone, A. J. 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Tackmann, J. Taenzer, A. Taffard, R. Tafirout, N. Taiblum, H. Takai, R. Takashima, H. Takeda, T. Takeshita, Y. Takubo, M. Talby, A. A. Talyshev, J. Y. C. Tam, K. G. Tan, J. Tanaka, R. Tanaka, S. Tanaka, B. B. Tannenwald, N. Tannoury, S. Tapprogge, S. Tarem, F. Tarrade, G. F. Tartarelli, P. Tas, M. Tasevsky, T. Tashiro, E. Tassi, A. Tavares Delgado, Y. Tayalati, F. E. Taylor, G. N. Taylor, W. Taylor, F. A. Teischinger, M. Teixeira Dias Castanheira, P. Teixeira-Dias, K. K. Temming, D. Temple, H. Ten Kate, P. K. Teng, J. J. Teoh, F. Tepel, S. Terada, K. Terashi, J. Terron, S. Terzo, M. Testa, R. J. Teuscher, T. Theveneaux-Pelzer, J. P. Thomas, J. Thomas-Wilsker, E. N. Thompson, P. D. Thompson, R. J. Thompson, A. S. Thompson, L. A. Thomsen, E. Thomson, M. Thomson, R. P. Thun, M. J. Tibbetts, R. E. Ticse Torres, V. O. Tikhomirov, Yu. A. Tikhonov, S. Timoshenko, E. Tiouchichine, P. Tipton, S. Tisserant, K. Todome, T. Todorov, S. Todorova-Nova, J. Tojo, S. Tokár, K. Tokushuku, K. Tollefson, E. Tolley, L. Tomlinson, M. Tomoto, L. Tompkins, K. Toms, E. Torrence, H. Torres, E. Torró Pastor, J. Toth, F. Touchard, D. R. Tovey, T. Trefzger, L. Tremblet, A. Tricoli, I. M. Trigger, S. Trincaz-Duvoid, M. F. Tripiana, W. Trischuk, B. Trocmé, C. Troncon, M. Trottier-McDonald, M. Trovatelli, P. True, L. Truong, M. Trzebinski, A. Trzupek, C. Tsarouchas, J. C-L. Tseng, P. V. Tsiareshka, D. Tsionou, G. Tsipolitis, N. Tsirintanis, S. Tsiskaridze, V. Tsiskaridze, E. G. Tskhadadze, I. I. Tsukerman, V. Tsulaia, S. Tsuno, D. Tsybychev, A. Tudorache, V. Tudorache, A. N. Tuna, S. A. Tupputi, S. Turchikhin, D. Turecek, R. Turra, A. J. Turvey, P. M. Tuts, A. Tykhonov, M. Tylmad, M. Tyndel, I. Ueda, R. Ueno, M. Ughetto, M. Ugland, F. Ukegawa, G. Unal, A. Undrus, G. Unel, F. C. Ungaro, Y. Unno, C. Unverdorben, J. Urban, P. Urquijo, P. Urrejola, G. Usai, A. Usanova, L. Vacavant, V. Vacek, B. Vachon, C. Valderanis, N. Valencic, S. Valentinetti, A. Valero, L. Valery, S. Valkar, E. Valladolid Gallego, S. Vallecorsa, J. A. Valls Ferrer, W. Van Den Wollenberg, P. C. Van Der Deijl, R. van der Geer, H. van der Graaf, N. van Eldik, P. van Gemmeren, J. Van Nieuwkoop, I. van Vulpen, M. C. van Woerden, M. Vanadia, W. Vandelli, R. Vanguri, A. Vaniachine, F. Vannucci, G. Vardanyan, R. Vari, E. W. Varnes, T. Varol, D. Varouchas, A. Vartapetian, K. E. Varvell, F. Vazeille, T. Vazquez Schroeder, J. Veatch, L. M. Veloce, F. Veloso, T. Velz, S. Veneziano, A. Ventura, D. Ventura, M. Venturi, N. Venturi, A. Venturini, V. Vercesi, M. Verducci, W. Verkerke, J. C. Vermeulen, A. Vest, M. C. Vetterli, O. Viazlo, I. Vichou, T. Vickey, O. E. Vickey Boeriu, G. H. A. Viehhauser, S. Viel, R. Vigne, M. Villa, M. Villaplana Perez, E. Vilucchi, M. G. Vincter, V. B. Vinogradov, I. Vivarelli, F. Vives Vaque, S. Vlachos, D. Vladoiu, M. Vlasak, M. Vogel, P. Vokac, G. Volpi, M. Volpi, H. von der Schmitt, H. von Radziewski, E. von Toerne, V. Vorobel, K. Vorobev, M. Vos, R. Voss, J. H. Vossebeld, N. Vranjes, M. Vranjes Milosavljevic, V. Vrba, M. Vreeswijk, R. Vuillermet, I. Vukotic, Z. Vykydal, P. Wagner, W. Wagner, H. Wahlberg, S. Wahrmund, J. Wakabayashi, J. Walder, R. Walker, W. Walkowiak, C. Wang, F. Wang, H. Wang, J. Wang, K. Wang, R. Wang, S. M. Wang, T. Wang, X. Wang, C. Wanotayaroj, A. Warburton, C. P. Ward, D. R. Wardrope, A. Washbrook, C. Wasicki, P. M. Watkins, A. T. Watson, I. J. Watson, M. F. Watson, G. Watts, S. Watts, B. M. Waugh, S. Webb, M. S. Weber, S. W. Weber, J. S. Webster, A. R. Weidberg, B. Weinert, J. Weingarten, C. Weiser, H. Weits, P. S. Wells, T. Wenaus, T. Wengler, S. Wenig, N. Wermes, M. Werner, P. Werner, M. Wessels, J. Wetter, K. Whalen, A. M. Wharton, A. White, M. J. White, R. White, S. White, D. Whiteson, F. J. Wickens, W. Wiedenmann, M. Wielers, P. Wienemann, C. Wiglesworth, L. A. M. Wiik-Fuchs, A. Wildauer, H. G. Wilkens, H. H. Williams, S. Williams, C. Willis, S. Willocq, A. Wilson, J. A. Wilson, I. Wingerter-Seez, F. Winklmeier, B. T. Winter, M. Wittgen, J. Wittkowski, S. J. Wollstadt, M. W. Wolter, H. Wolters, B. K. Wosiek, J. Wotschack, M. J. Woudstra, K. W. Wozniak, M. Wu, S. L. Wu, X. Wu, Y. Wu, T. R. Wyatt, B. M. Wynne, S. Xella, D. Xu, L. Xu, B. Yabsley, S. Yacoob, R. Yakabe, M. Yamada, D. Yamaguchi, Y. Yamaguchi, A. Yamamoto, S. Yamamoto, T. Yamanaka, K. Yamauchi, Y. Yamazaki, Z. Yan, H. Yang, Y. Yang, W-M. Yao, Y. Yasu, E. Yatsenko, K. H. Yau Wong, J. Ye, S. Ye, I. Yeletskikh, A. L. Yen, E. Yildirim, K. Yorita, R. Yoshida, K. Yoshihara, C. Young, C. J. S. Young, S. Youssef, D. R. Yu, J. Yu, J. M. Yu, L. Yuan, S. P. Y. Yuen, A. Yurkewicz, I. Yusuff, B. Zabinski, R. Zaidan, A. M. Zaitsev, J. Zalieckas, A. Zaman, S. Zambito, L. Zanello, D. Zanzi, C. Zeitnitz, M. Zeman, A. Zemla, Q. Zeng, K. Zengel, O. Zenin, T. Ženiš, D. Zerwas, D. Zhang, F. Zhang, H. Zhang, J. Zhang, L. Zhang, R. Zhang, X. Zhang, Z. Zhang, X. Zhao, Y. Zhao, Z. Zhao, A. Zhemchugov, J. Zhong, B. Zhou, C. Zhou, L. Zhou, M. Zhou, N. Zhou, C. G. Zhu, H. Zhu, J. Zhu, Y. Zhu, X. Zhuang, K. Zhukov, A. Zibell, D. Zieminska, N. I. Zimine, C. Zimmermann, S. Zimmermann, Z. Zinonos, M. Zinser, M. Ziolkowski, L. Živković, G. Zobernig, A. Zoccoli, M. zur Nedden, G. Zurzolo, L. Zwalinski, and ATLAS Collaboration

Subjects
Astrophysics, QB460-466, Nuclear and particle physics. Atomic energy. Radioactivity, QC770-798
Published
2022
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47. Deficiency of the RNA-binding protein ELAVL1/HuR leads to the failure of endogenous and exogenous neuroprotection of retinal ganglion cells

Author

Anna Pacwa, Joanna Machowicz, Saeed Akhtar, Piotr Rodak, Xiaonan Liu, Marita Pietrucha-Dutczak, Joanna Lewin-Kowalik, Marialaura Amadio, and Adrian Smedowski

Subjects
glaucoma, retinal ganglion cells (RGC), RNA-binding protein, HuR (ELAVL1), neuroprotection, AAV (adeno-associated virus), Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
Abstract

IntroductionELAVL1/HuR is a keystone regulator of gene expression at the posttranscriptional level, including stress response and homeostasis maintenance. The aim of this study was to evaluate the impact of hur silencing on the age-related degeneration of retinal ganglion cells (RGC), which potentially describes the efficiency of endogenous neuroprotection mechanisms, as well as to assess the exogenous neuroprotection capacity of hur-silenced RGC in the rat glaucoma model.MethodsThe study consisted of in vitro and in vivo approaches. In vitro, we used rat B-35 cells to investigate, whether AAV-shRNA-HuR delivery affects survival and oxidative stress markers under temperature and excitotoxic insults. In vivo approach consisted of two different settings. In first one, 35 eight-week-old rats received intravitreal injection of AAV-shRNA-HuR or AAV-shRNA scramble control. Animals underwent electroretinography tests and were sacrificed 2, 4 or 6 months after injection. Retinas and optic nerves were collected and processed for immunostainings, electron microscopy and stereology. For the second approach, animals received similar gene constructs. To induce chronic glaucoma, 8 weeks after AAV injection, unilateral episcleral vein cauterization was performed. Animals from each group received intravitreal injection of metallothionein II. Animals underwent electroretinography tests and were sacrificed 8 weeks later. Retinas and optic nerves were collected and processed for immunostainings, electron microscopy and stereology.ResultsSilencing of hur induced apoptosis and increased oxidative stress markers in B-35 cells. Additionally, shRNA treatment impaired the cellular stress response to temperature and excitotoxic insults. In vivo, RGC count was decreased by 39% in shRNA-HuR group 6 months after injection, when compared to shRNA scramble control group. In neuroprotection study, the average loss of RGCs was 35% in animals with glaucoma treated with metallothionein and shRNA-HuR and 11.4% in animals with glaucoma treated with metallothionein and the scramble control shRNA. An alteration in HuR cellular content resulted in diminished photopic negative responses in the electroretinogram.ConclusionsBased on our findings, we conclude that HuR is essential for the survival and efficient neuroprotection of RGC and that the induced alteration in HuR content accelerates both the age-related and glaucoma-induced decline in RGC number and function, further confirming HuR’s key role in maintaining cell homeostasis and its possible involvement in the pathogenesis of glaucoma.

Published
2023
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48. Should Sickle Cell Trait Be a Contraindication to Breast Reconstruction?—A Case Series Analysis

Author

Theresa K. Webster, Sthefano Araya, Joseph Bartolacci, Grace M. Amadio, Juliet C. Panichella, Joseph Costa, and Sameer A. Patel

Subjects
deep inferior epigastric perforator free flap, latissimus dorsi flap, diep, sickle cell trait, breast reconstruction, autologous breast reconstruction, Surgery, RD1-811
Abstract

Background While sickle cell disease has long been considered a contraindication to breast free flap reconstruction, there have been less definitive decisions about the impact of sickle cell trait on these procedures. We sought to analyze the patients with sickle cell trait who underwent free deep inferior epigastric perforator (DIEP) flap and pedicled latissimus dorsi (LD) flap at a single institution to determine the reconstructive outcomes. Methods Patients with sickle cell trait who underwent breast free DIEP and pedicled LD reconstruction from 2007 to 2021 at a single institution by the lead surgeon were analyzed for demographics and surgical outcomes. Results Four patients were identified as having sickle cell trait and having undergone a breast flap reconstruction. The average age of the patients was 54 years, median body mass index was 25, and past medical history was notable for one patient being a current smoker, and one patient having hypertension. Two patients received a unilateral free DIEP flap, one received a bilateral free DIEP flap, and one received a unilateral pedicled LD flap for a total of five flaps in four patients. Three of the patients received prior hormone therapy, one received prior radiation therapy, and one received prior chemotherapy. There were no instances of flap failure, vessel thrombosis, pulmonary embolism, or deep venous thrombosis. One patient experienced wound dehiscence. Conclusion In this case series we present four patients with sickle cell trait who successfully underwent breast flap reconstruction without any instances of flap or systemic thrombosis. More work is needed to determine how to pre- and postoperatively optimize patients with sickle cell trait for favorable breast flap reconstruction outcomes.

Published
2023
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50. Bloodstream infections in the COVID-19 era: results from an Italian multi-centre study

Author

Zeno Pasquini, Iacopo Barocci, Lucia Brescini, Bianca Candelaresi, Sefora Castelletti, Valentina Iencinella, Sara Mazzanti, Gaia Procaccini, Elena Orsetti, Francesco Pallotta, Giorgio Amadio, Andrea Giacometti, Marcello Tavio, and Francesco Barchiesi

Subjects
bloodstream infections, COVID-19, SARS-CoV-2 pandemic, Hospital acquired infection, Multi drug resistant, Infectious and parasitic diseases, RC109-216
Abstract

ABSTRACT: Background: Correlation between coronavirus disease 2019 (COVID-19) and superinfections has been investigated, but remains to be fully assessed. This multi-centre study reports the impact of the pandemic on bloodstream infections (BSIs). Methods: This study included all patients with BSIs admitted to four Italian hospitals between 1 January and 30 June 2020. Clinical, demographic and microbiologic data were compared with data for patients hospitalized during the same period in 2019. Results: Among 26,012 patients admitted between 1 January and 30 June 2020, 1182 had COVID-19. Among the patients with COVID-19, 107 BSIs were observed, with an incidence rate of 8.19 episodes per 1000 patient-days. The incidence of BSI was significantly higher in these patients compared with patients without COVID-19 (2.72/1000 patient-days) and patients admitted in 2019 (2.76/1000 patient-days). In comparison with patients without COVID-19, BSI onset in patients with COVID-19 was delayed during the course of hospitalization (16.0 vs 5 days, respectively). Thirty-day mortality among patients with COVID-19 was 40.2%, which was significantly higher compared with patients without COVID-19 (23.7%). BSIs in patients with COVID-19 were frequently caused by multi-drug-resistant pathogens, which were often centre-dependent. Conclusions: BSIs are a common secondary infection in patients with COVID-19, characterized by increased risk during hospitalization and potentially burdened with high mortality.

Published
2021
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