350 results on '"Martino, Davide"'
Search Results
2. Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome
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Jain, Pritesh, Miller-Fleming, Tyne, Topaloudi, Apostolia, Yu, Dongmei, Drineas, Petros, Georgitsi, Marianthi, Yang, Zhiyu, Rizzo, Renata, Müller-Vahl, Kirsten R., Tumer, Zeynep, Mol Debes, Nanette, Hartmann, Andreas, Depienne, Christel, Worbe, Yulia, Mir, Pablo, Cath, Danielle C., Boomsma, Dorret I., Roessner, Veit, Wolanczyk, Tomasz, Janik, Piotr, Szejko, Natalia, Zekanowski, Cezary, Barta, Csaba, Nemoda, Zsofia, Tarnok, Zsanett, Buxbaum, Joseph D., Grice, Dorothy, Glennon, Jeffrey, Stefansson, Hreinn, Hengerer, Bastian, Benaroya-Milshtein, Noa, Cardona, Francesco, Hedderly, Tammy, Heyman, Isobel, Huyser, Chaim, Morer, Astrid, Mueller, Norbert, Munchau, Alexander, Plessen, Kerstin J., Porcelli, Cesare, Walitza, Susanne, Schrag, Anette, Martino, Davide, Dietrich, Andrea, Mathews, Carol A., Scharf, Jeremiah M., Hoekstra, Pieter J., Davis, Lea K., and Paschou, Peristera
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- 2023
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3. The effect of transcranial ultrasound pulse repetition frequency on sustained inhibition in the human primary motor cortex: A double-blind, sham-controlled study
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Zadeh, Ali K., Raghuram, Hrishikesh, Shrestha, Shirshak, Kibreab, Mekale, Kathol, Iris, Martino, Davide, Pike, G. Bruce, Pichardo, Samuel, and Monchi, Oury
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- 2024
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4. Advancing Parkinson's Disease Research in Canada: The Canadian Open Parkinson Network (C-OPN) Cohort.
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Cressatti, Marisa, Pinilla-Monsalve, Gabriel D., Blais, Mathieu, Normandeau, Catherine P., Degroot, Clotilde, Kathol, Iris, Bogard, Sarah, Bendas, Anna, Camicioli, Richard, Dupré, Nicolas, Gan-Or, Ziv, Grimes, David A., Kalia, Lorraine V., MacDonald, Penny A., McKeown, Martin J., Martino, Davide, Miyasaki, Janis M., Schlossmacher, Michael G., Stoessl, A. Jon, and Strafella, Antonio P.
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MONONUCLEAR leukocytes ,PARKINSON'S disease ,MEDICAL personnel ,SYMPTOMS ,DISEASE management - Abstract
Background: Enhancing the interactions between study participants, clinicians, and investigators is imperative for advancing Parkinson's disease (PD) research. The Canadian Open Parkinson Network (C-OPN) stands as a nationwide endeavor, connecting the PD community with ten accredited universities and movement disorders research centers spanning, at the time of this analysis, British Columbia, Alberta, Ontario, and Quebec. Objective: Our aim is to showcase C-OPN as a paradigm for bolstering national collaboration to accelerate PD research and to provide an initial overview of already collected data sets. Methods: The C-OPN database comprises de-identified data concerning demographics, symptoms and signs, treatment approaches, and standardized assessments. Additionally, it collects venous blood-derived biomaterials, such as for analyses of DNA, peripheral blood mononuclear cells (PBMC), and serum. Accessible to researchers, C-OPN resources are available through web-based data management systems for multi-center studies, including REDCap. Results: As of November 2023, the C-OPN had enrolled 1,505 PD participants. The male-to-female ratio was 1.77:1, with 83% (n = 1098) residing in urban areas and 82% (n = 1084) having pursued post-secondary education. The average age at diagnosis was 60.2±10.3 years. Herein, our analysis of the C-OPN PD cohort encompasses environmental factors, motor and non-motor symptoms, disease management, and regional differences among provinces. As of April 2024, 32 research projects have utilized C-OPN resources. Conclusions: C-OPN represents a national platform promoting multidisciplinary and multisite research that focuses on PD to promote innovation, exploration of care models, and collaboration among Canadian scientists. Plain Language Summary: Teamwork and communication between people living with Parkinson's disease (PD), physicians, health professionals, and research scientists is important for improving the lives of those living with this condition. The Canadian Open Parkinson Network (C-OPN) is a Canada-wide initiative, connecting the PD community with ten accredited universities and movement disorders research centers located in – at the time of this analysis–British Columbia, Alberta, Ontario, and Quebec. The aim of this paper is to showcase C-OPN as a useful resource for physician and research scientists studying PD in Canada and around the world, and to provide snapshot of already collected data. The C-OPN database comprises de-identified (meaning removal of any identifying information, such as name or date of birth) data concerning lifestyle, disease symptoms, treatments, and results from standardized tests. It also collects blood samples for further analysis. As of November 2023, C-OPN had enrolled 1,505 PD participants across Canada. Most of the participants were male (64%), living in urban areas (83%), and completed post-secondary education (82%). The average age at diagnosis was 60.2±10.3 years. In this paper, we look at environmental factors, motor and non-motor symptoms, different disease management strategies, and regional differences between provinces. In conclusion, C-OPN represents a national platform that encourages multidisciplinary and multisite research focusing on PD to promote innovation and collaboration among Canadian scientists. [ABSTRACT FROM AUTHOR]
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- 2024
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5. The effect of Transcranial Ultrasound Pulse Repetition Frequency on Sustained Inhibition in the Human Primary Motor Cortex: A Double-Blind, Sham-Controlled Study
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K.Zadeh, Ali, primary, Raghuram, Hrishikesh, additional, Shrestha, Shirshak, additional, Kibreab, Mekale, additional, Kathol, Iris, additional, Martino, Davide, additional, Pike, G. Bruce, additional, Pichardo, Samuel, additional, and Monchi, Oury, additional
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- 2024
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6. Testing the specificity of phenomenological criteria for functional tic‐like behaviours in youth with Tourette syndrome.
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Nilles, Christelle, Martino, Davide, and Pringsheim, Tamara
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TOURETTE syndrome , *TIC disorders , *MOVEMENT disorders , *SPEECH apraxia , *AGE of onset , *FOOTBALL techniques , *SPEECH - Abstract
Background and purpose: The aim was to test the specificity of phenomenological criteria for functional tic‐like behaviours (FTLBs). The European Society for the Study of Tourette Syndrome (ESSTS) criteria for the diagnosis of FTLBs include three major criteria: age at symptom onset ≥12 years, rapid evolution of symptoms and specific phenomenology. Methods: Children and adolescents with primary tic disorders have been included in a Registry in Calgary, Canada, since 2017. Using the Yale Global Tic Severity Scale, the proportion of youth with primary tic disorders who met specific phenomenological criteria for FTLBs at first visit was assessed: (1) having ≥1 specific complex motor tic commonly seen in FTLBs, including complex arm/hand movements, self‐injurious behaviour, blocking, copropraxia; (2) having ≥1 specific complex phonic tic commonly seen in FTLBs, including saying words, phrases, disinhibited speech, coprolalia; (3) having a greater number of complex tics than simple tics. Children seen for the first time between 2017 and 2019 and between 2021 and 2023 were analysed separately. Results: Of 156 participants included between 2017 and 2019, high specificity (94.2%) of the age at onset criterion (≥12 years) and of having at least two complex motor behaviours and one complex phonic behaviour at first visit (96.2%) was observed. Some of the complex motor tics had lower specificity. The specificity of the FTLB diagnostic criterion of having more complex tics than simple tics was 89.7%. There was no significant difference in specificity of the criteria for children seen for the first time between 2017 and 2019 and between 2021 and 2023 (n = 149). Conclusion: This information supports the use of the ESSTS criteria for FTLBs in clinical practice. [ABSTRACT FROM AUTHOR]
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- 2024
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7. Expediting telehealth use in clinical research studies: recommendations for overcoming barriers in North America
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Naito, Anna, Wills, Anne-Marie, Tropea, Thomas F., Ramirez-Zamora, Adolfo, Hauser, Robert A., Martino, Davide, Turner, Travis H., Rafferty, Miriam R., Afshari, Mitra, Williams, Karen L., Vaou, Okeanis, McKeown, Martin J., Ginsburg, Letty, Ezra, Adi, Iansek, Robert, Wallock, Kristin, Evers, Christiana, Schroeder, Karlin, DeLeon, Rebeca, Yarab, Nicole, Alcalay, Roy N., and Beck, James C.
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- 2021
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8. Investigating the relationship between the SNCA gene and cognitive abilities in idiopathic Parkinson’s disease using machine learning
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Ramezani, Mehrafarin, Mouches, Pauline, Yoon, Eunjin, Rajashekar, Deepthi, Ruskey, Jennifer A., Leveille, Etienne, Martens, Kristina, Kibreab, Mekale, Hammer, Tracy, Kathol, Iris, Maarouf, Nadia, Sarna, Justyna, Martino, Davide, Pfeffer, Gerald, Gan-Or, Ziv, Forkert, Nils D., and Monchi, Oury
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- 2021
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9. Developing a provincial patient support network for children and families affected by Tourette syndrome and/or obsessive–compulsive disorder: results of a stakeholder consultation
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Fletcher, Julian, Dimitropoulos, Gina, Martino, Davide, Wilcox, Gabrielle, MacMaster, Frank, Arnold, Paul, and Pringsheim, Tamara
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- 2021
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10. Non-motor symptoms in dystonia: from diagnosis to treatment
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Peall, Kathryn J., primary, Berman, Brian D., additional, Bruggemann, Norbert, additional, Defazio, Giovanni, additional, Gimeno, Hortensia, additional, Jinnah, H. A., additional, Perlmutter, Joel S., additional, Richardson, Sarah E. Pirio, additional, Roze, Emmanuel, additional, Schrag, Anette, additional, Tinazzi, Michele, additional, Vidailhet, Marie, additional, Wagle Shukla, Aparna, additional, Worbe, Yulia, additional, Teller, Jan K., additional, and Martino, Davide, additional
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- 2023
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11. The neural representation of actions in Tourette syndrome as window to decipher tics and their suppression
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Martino, Davide, primary and Ganos, Christos, additional
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- 2023
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12. Prospective follow‐up study of youth and adults with onset of functional tic‐like behaviours during the COVID‐19 pandemic.
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Nilles, Christelle, Szejko, Natalia, Martino, Davide, and Pringsheim, Tamara
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COVID-19 pandemic ,SEROTONIN uptake inhibitors ,SEROTONIN syndrome ,BEHAVIOR therapy ,TIC disorders - Abstract
Background and purpose: Very little is known about the long‐term prognosis of patients with functional tic‐like behaviours (FTLBs). We sought to characterize the trajectory of symptom severity over a 12‐month period. Methods: Patients with FTLBs were included in our prospective longitudinal child and adult clinical tic disorder registries at the University of Calgary. Patients were prospectively evaluated 6 and 12 months after their first clinical visit. Tic inventories and severity were measured with the Yale Global Tic Severity Scale (YGTSS). Results: Eighty‐three youths and adults with FTLBs were evaluated prospectively until April 2023. Mean YGTSS total tic severity scores were high at baseline, with a mean score of 29.8 points (95% confidence interval [CI] = 27.6–32.1). Fifty‐eight participants were reevaluated at 6 months, and 32 participants were reevaluated at 12 months. The YGTSS total tic severity score decreased significantly from the first clinical visit to 6 months (raw mean difference = 8.9 points, 95% CI = 5.1–12.7, p < 0.0001), and from 6 to 12 months (raw mean difference = 6.4 points, 95% CI = 0.8–12.0, p = 0.01). Multivariable linear regression demonstrated that tic severity at initial presentation and the presence of other functional neurological symptoms were associated with higher YGTSS total tic scores at 6 months, whereas younger age at baseline, receiving cognitive behavioural therapy for anxiety and/or depression, and prescription of selective serotonin reuptake inhibitors were associated with lower YGTSS total tic scores at 6 months. Conclusions: We observed a meaningful improvement in tic severity scores in youth and adults with FTLBs over a period of 6–12 months. [ABSTRACT FROM AUTHOR]
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- 2024
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13. Have We Forgotten What Tics Are? A Re‐Exploration of Tic Phenomenology in Youth with Primary Tics
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Nilles, Christelle, primary, Martino, Davide, additional, Fletcher, Julian, additional, and Pringsheim, Tamara, additional
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- 2023
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14. Clinical features of idiopathic normal pressure hydrocephalus : critical review of objective findings
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Bluett, Brent, Ash, Elissa, Farheen, Amtul, Fasano, Alfonso, Krauss, Joachim K., Maranzano, Alessio, Passaretti, Massimiliano, Tang-Wai, David F., Van Gerpen, Jay, Alonso-Canovas, Araceli, Youn, Jinyoung, Malm, Jan, Martino, Davide, Bluett, Brent, Ash, Elissa, Farheen, Amtul, Fasano, Alfonso, Krauss, Joachim K., Maranzano, Alessio, Passaretti, Massimiliano, Tang-Wai, David F., Van Gerpen, Jay, Alonso-Canovas, Araceli, Youn, Jinyoung, Malm, Jan, and Martino, Davide
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Background: Idiopathic normal pressure hydrocephalus (iNPH) is characterized by the classic clinical triad of gait, cognitive, and urinary dysfunction, albeit incomplete in a relevant proportion of patients. The clinical findings and evolution of these symptoms have been variably defined in the literature. Objectives: To evaluate how the phenomenology has been defined, assessed, and reported, we performed a critical review of the existing literature discussing the phenomenology of iNPH. The review also identified the instrumental tests most frequently used and the evolution of clinical and radiologic findings. Methods: The review was divided into 3 sections based on gait, cognitive, and urinary dysfunction. Each section performed a literature search using the terms “idiopathic normal pressure hydrocephalus” (iNPH), with additional search terms used by each section separately. The number of articles screened, duplicates, those meeting the inclusion criteria, and the number of articles excluded were recorded. Findings were subsequently tallied and analyzed. Results: A total of 1716 articles with the aforementioned search criteria were identified by the 3 groups. A total of 81 full-text articles were reviewed after the elimination of duplicates, articles that did not discuss phenomenological findings or instrumental testing of participants with iNPH prior to surgery, and articles with fewer than 10 participants. Conclusions: “Wide-based gait” was the most common gait dysfunction identified. Cognitive testing varied significantly across articles, and ultimately a specific cognitive profile was not identified. Urodynamic testing found detrusor overactivity and “overactive bladder” as the most common symptom of urinary dysfunction.
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- 2023
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15. European Society for the Study of Tourette Syndrome 2022 criteria for clinical diagnosis of functional tic-like behaviours:International consensus from experts in tic disorders
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Pringsheim, Tamara, Ganos, Christos, Nilles, Christelle, Cavanna, Andrea E., Gilbert, Donald L., Greenberg, Erica, Hartmann, Andreas, Hedderly, Tammy, Heyman, Isobel, Liang, Holan, Malaty, Irene, Malik, Osman, Debes, Nanette Mol, Vahl, Kirsten Muller, Munchau, Alexander, Murphy, Tara, Nagy, Peter, Owen, Tamsin, Rizzo, Renata, Skov, Liselotte, Stern, Jeremy, Szejko, Natalia, Worbe, Yulia, Martino, Davide, Pringsheim, Tamara, Ganos, Christos, Nilles, Christelle, Cavanna, Andrea E., Gilbert, Donald L., Greenberg, Erica, Hartmann, Andreas, Hedderly, Tammy, Heyman, Isobel, Liang, Holan, Malaty, Irene, Malik, Osman, Debes, Nanette Mol, Vahl, Kirsten Muller, Munchau, Alexander, Murphy, Tara, Nagy, Peter, Owen, Tamsin, Rizzo, Renata, Skov, Liselotte, Stern, Jeremy, Szejko, Natalia, Worbe, Yulia, and Martino, Davide
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Background and purpose: In 2020, health professionals witnessed a dramatic increase in referrals of young people with rapid onset of severe tic-like behaviours. We assembled a working group to develop criteria for the clinical diagnosis of functional tic-like behaviours (FTLBs) to help neurologists, pediatricians, psychiatrists, and psychologists recognize and diagnose this condition. Methods: We used a formal consensus development process, using a multiround, web-based Delphi survey. The survey was based on an in-person discussion at the European Society for the Study of Tourette Syndrome (ESSTS) meeting in Lausanne in June 2022. Members of an invited group with extensive clinical experience working with patients with Tourette syndrome and FTLBs discussed potential clinical criteria for diagnosis of FTLBs. An initial set of criteria were developed based on common clinical experiences and review of the literature on FTLBs and revised through iterative discussions, resulting in the survey items for voting. Results: In total, 24 members of the working group were invited to participate in the Delphi process. We propose that there are three major criteria and two minor criteria to support the clinical diagnosis of FTLBs. A clinically definite diagnosis of FTLBs can be confirmed by the presence of all three major criteria. A clinically probable diagnosis of FTLBs can be confirmed by the presence of two major criteria and one minor criterion. Conclusions: Distinguishing FTLBs from primary tics is important due to the distinct treatment paths required for these two conditions. A limitation of the ESSTS 2022 criteria is that they lack prospective testing of their sensitivity and specificity.
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- 2023
16. Study protocol: A cross-sectional survey of clinicians to identify barriers to clinical practice guideline implementation in the assessment and treatment of persistent tic disorders
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Martindale, Jaclyn M., Sarva, Harini, Martino, Davide, Gilbert, Donald L., Ganos, Christos, Pringsheim, Tamara, Black, Kevin, Malaty, Irene A., Movement Disorder Society Tic and Tourette Study Group, Mir, Pablo, Martindale, Jaclyn M., Sarva, Harini, Martino, Davide, Gilbert, Donald L., Ganos, Christos, Pringsheim, Tamara, Black, Kevin, Malaty, Irene A., Movement Disorder Society Tic and Tourette Study Group, and Mir, Pablo
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[Introduction] Eight members of the International Parkinson’s Disease and Movement Disorders Society Tic and Tourette Syndrome Study Group formed a subcommittee to discuss further barriers to practice guideline implementation. Based on expert opinion and literature review, the consensus was that practice variations continue to be quite broad and that many barriers in different clinical settings might negatively influence the adoption of the American Academy of Neurology and the European Society for the Study of Tourette Syndrome published guidelines., [Objectives] 1) To identify how clinical practices diverge from the existing American Academy of Neurology and European Society for the Study of Tourette Syndrome guidelines, and 2) to identify categories of barriers leading to these clinical care gaps., [Methods and analysis] This article presents the methodology of a planned cross-sectional survey amongst healthcare professionals routinely involved in the clinical care of patients with persistent tic disorders, aimed at 1) identifying how practices diverge from the published guidelines; and 2) identifying categories of barriers leading to these clinical care gaps. Purposeful sampling methods are used to identify and recruit critical persistent tic disorders stakeholders. The analysis will use descriptive statistics.
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- 2023
17. Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome
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National Institutes of Health (US), Lundbeck Foundation, German Research Foundation, Royal Netherlands Academy of Arts and Sciences, National Science Centre (Poland), National Institute for Health and Care Research (US), NIHR Biomedical Research Centre (UK), Jain, Pritesh, Miller-Fleming, Tyne, Topaloudi, Apostolia, Yu, Dongmei, Drineas, Petros, Georgitsi, Marianthi, Yang, Zhiyu, Rizzo, Renata, Müller-Vahl, Kirsten R., Tumer, Zeynep, Mol Debes, Nanette, Hartmann, Andreas, Depienne, Christel, Worbe, Yulia, Mir, Pablo, Cath, Danielle, Boomsma, Dorret I., Roessner, Veit, Wolańczyk, Tomasz, Janik, Piotr, Szejko, Natalia, Zekanowski, Cezary, Barta, Csaba, Nemoda, Zsofia, Tarnok, Zsanett, Buxbaum, Joseph D., Grice, Dorothy, Glennon, Jeffrey, Stefansson, Hreinn, Hengerer, Bastian, Benaroya‑Milshtein, Noa, Cardona, Francesco, Hedderly, Tammy, Heyman, Isobel, Huyser, Chaim, Morer, Astrid, Mueller, Norbert, Münchau, Alexander, Plessen, Kerstin J., Porcelli, Cesare, Walitza, Susanne, Schrag, Anette, Martino, Davide, The Psychiatric Genomics Consortium Tourette Syndrome Working Group (PGC-TS), The EMTICS collaborative group, Dietrich, Andrea, The TS-EUROTRAIN Network, Mathews, Carol A., Scharf, Jeremiah M., Hoekstra, Pieter J., Davis, Lea K., Paschou, Peristera, National Institutes of Health (US), Lundbeck Foundation, German Research Foundation, Royal Netherlands Academy of Arts and Sciences, National Science Centre (Poland), National Institute for Health and Care Research (US), NIHR Biomedical Research Centre (UK), Jain, Pritesh, Miller-Fleming, Tyne, Topaloudi, Apostolia, Yu, Dongmei, Drineas, Petros, Georgitsi, Marianthi, Yang, Zhiyu, Rizzo, Renata, Müller-Vahl, Kirsten R., Tumer, Zeynep, Mol Debes, Nanette, Hartmann, Andreas, Depienne, Christel, Worbe, Yulia, Mir, Pablo, Cath, Danielle, Boomsma, Dorret I., Roessner, Veit, Wolańczyk, Tomasz, Janik, Piotr, Szejko, Natalia, Zekanowski, Cezary, Barta, Csaba, Nemoda, Zsofia, Tarnok, Zsanett, Buxbaum, Joseph D., Grice, Dorothy, Glennon, Jeffrey, Stefansson, Hreinn, Hengerer, Bastian, Benaroya‑Milshtein, Noa, Cardona, Francesco, Hedderly, Tammy, Heyman, Isobel, Huyser, Chaim, Morer, Astrid, Mueller, Norbert, Münchau, Alexander, Plessen, Kerstin J., Porcelli, Cesare, Walitza, Susanne, Schrag, Anette, Martino, Davide, The Psychiatric Genomics Consortium Tourette Syndrome Working Group (PGC-TS), The EMTICS collaborative group, Dietrich, Andrea, The TS-EUROTRAIN Network, Mathews, Carol A., Scharf, Jeremiah M., Hoekstra, Pieter J., Davis, Lea K., and Paschou, Peristera
- Abstract
Tourette Syndrome (TS) is a complex neurodevelopmental disorder characterized by vocal and motor tics lasting more than a year. It is highly polygenic in nature with both rare and common previously associated variants. Epidemiological studies have shown TS to be correlated with other phenotypes, but large-scale phenome wide analyses in biobank level data have not been performed to date. In this study, we used the summary statistics from the latest meta-analysis of TS to calculate the polygenic risk score (PRS) of individuals in the UK Biobank data and applied a Phenome Wide Association Study (PheWAS) approach to determine the association of disease risk with a wide range of phenotypes. A total of 57 traits were found to be significantly associated with TS polygenic risk, including multiple psychosocial factors and mental health conditions such as anxiety disorder and depression. Additional associations were observed with complex non-psychiatric disorders such as Type 2 diabetes, heart palpitations, and respiratory conditions. Cross-disorder comparisons of phenotypic associations with genetic risk for other childhood-onset disorders (e.g.: attention deficit hyperactivity disorder [ADHD], autism spectrum disorder [ASD], and obsessive-compulsive disorder [OCD]) indicated an overlap in associations between TS and these disorders. ADHD and ASD had a similar direction of effect with TS while OCD had an opposite direction of effect for all traits except mental health factors. Sex-specific PheWAS analysis identified differences in the associations with TS genetic risk between males and females. Type 2 diabetes and heart palpitations were significantly associated with TS risk in males but not in females, whereas diseases of the respiratory system were associated with TS risk in females but not in males. This analysis provides further evidence of shared genetic and phenotypic architecture of different complex disorders.
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- 2023
18. Development of a New Care Pathway for Depression and Anxiety in Adult‐Onset Isolated Dystonia
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Martino, Davide, primary, Nosratmirshekarlou, Elaheh, additional, Cothros, Nicholas, additional, Medina Escobar, Alex, additional, and Goodarzi, Zahra, additional
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- 2023
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19. Role of cortical cholinergic mechanisms in pallidal-DBS for dystonia
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Arantes, Ana, primary, Zalasky, Nicole, additional, Borges, Ludymila, additional, Sondergaard, Rachel, additional, Martino, Davide, additional, and Kiss, Zelma HT., additional
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- 2023
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20. Relevance of transcranial modeling in the planning of neurostimulation with low intensity focused ultrasound for deep targets
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Pichardo, Samuel, primary, Nankoo, Jean-Francois, additional, Zadeh, Ali K., additional, Darmani, Ghazaleh, additional, Martino, Davide, additional, Monchi, Oury, additional, Chen, Robert, additional, and Pike, G. Bruce, additional
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- 2023
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21. Characterization of a novel variant in the HR1 domain of MFN2 in a patient with ataxia, optic atrophy and sensorineural hearing loss
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Sharma, Govinda, primary, Zaman, Mashiat, additional, Sabouny, Rasha, additional, Joel, Matthew, additional, Martens, Kristina, additional, Martino, Davide, additional, de Koning, A.P. Jason, additional, Pfeffer, Gerald, additional, and Shutt, Timothy E., additional
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- 2022
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22. Temporal Expectation in Focal Hand Dystonia
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Avanzino, Laura, Martino, Davide, and Martino, Isadora
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Patients with writer's cramp present sensory and representational abnormalities relevant to motor control, such as impairment in the temporal discrimination between tactile stimuli and in pure motor imagery tasks, like the mental rotation of corporeal and inanimate objects. However, only limited information is available on the ability of patients with dystonia to process the time-dependent features (e.g. speed) of movement in real time. The processing of time-dependent features of movement has a crucial role in predicting whether the outcome of a complex motor sequence, such as handwriting or playing a musical passage, will be consistent with its ultimate goal, or results instead in an execution error. In this study, we sought to evaluate the implicit ability to perceive the temporal outcome of different movements in a group of patients with writer's cramp. Fourteen patients affected by writer's cramp in the right hand and 17 age- and gender-matched healthy subjects were recruited for the study. Subjects were asked to perform a temporal expectation task by predicting the end of visually perceived human body motion (handwriting, i.e. the action performed by the human body segment specifically affected by writer's cramp) or inanimate object motion (a moving circle reaching a spatial target). Videos representing movements were shown in full before experimental trials; the actual tasks consisted of watching the same videos, but interrupted after a variable interval ("pre-dark") from its onset by a dark interval of variable duration. During the "dark" interval, subjects were asked to indicate when the movement represented in the video reached its end by clicking on the space bar of the keyboard. We also included a visual working memory task. Performance on the timing task was analysed measuring the absolute value of timing error, the coefficient of variability and the percentage of anticipation responses. Patients with writer's cramp exhibited greater absolute timing error compared with control subjects in the human body motion task (whereas no difference was observed in the inanimate object motion task). No effect of group was documented on the visual working memory tasks. Absolute timing error on the human body motion task did not significantly correlate with symptom severity, disease duration or writing speed. Our findings suggest an alteration of the writing movement representation at a central level and are consistent with the view that dystonia is not a purely motor disorder, but it also involves non-motor (sensory, cognitive) aspects related to movement processing and planning.
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- 2013
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23. Vitamin D levels in children and adolescents with chronic tic disorders: a multicentre study
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Molly, Bond, Natalie, Moll, Alicia, Rosello, Rod, Bond, Jaana, Schnell, Bianka, Burger, Pieter, J Hoekstra, Andrea, Dietrich, Anette, Schrag, Eva, Kocovska, Martino, Davide, Norbert, Mueller, Markus, Schwarz, Ute-Christiane, Meier, EMTICS Collaborative Group: Alan Apter, Baglioni, Valentina, Juliane, Ball, Noa, Benaroya-Milshtein, Benjamin, Bodmer, Emese, Bognar, Judith, Buse, Cardona, Francesco Carmelo Giovanni, Marta Correa Vela, Nanette, M Debes, Maria Cristina Ferro, Carolin, Fremer, Blanca, Garcia-Delgar, Mariangela, Gulisano, Annelieke, Hagen, Julie, Hagstrøm, Tammy, J Hedderly, Isobel, Heyman, Chaim, Huyser, Marcos, Madruga-Garrido, Anna, Marotta, Pablo, Mir, Astrid, Morer, Norbert, Müller, Kirsten, R Müller-Vahl, Alexander, Münchau, Peter, Nagy, Neri, Valeria, Thaïra Jc Openneer, Pellico, Alessandra, Ángela Periañez Vasco, Kerstin, J Plessen, Cesare, Porcelli, Marina, Redondo, Rizzo, Renata, Veit, Roessner, Daphna, Ruhrman, Jaana Ml Schnell, Silvestri, PAOLA ROSARIA, Liselotte, Skov, Tamar, Steinberg, Friederike Tagwerker Gloor, Zsanett, Tarnok, Jennifer, Tübing, Victoria, L Turner, Susanne, Walitza, Elif, Weidinger, Clinical Cognitive Neuropsychiatry Research Program (CCNP), EMTICS Collaborative Group, Bruun, J.E., Grejsen, J., Ommundsen, C.L., Rubæk, M., Enghardt, S., Bokemeyer, S., Driedger-Garbe, C., Reichert, C., Schmalfeld, J., Duffield, T., Gergye, F., Kovacs, M., Vidomusz, R., Carmel, M., Fennig, S., Gev, E., Keller, N., Michaelovsky, E., Nahon, M., Regev, C., Simcha, T., Smollan, G., Weizman, A., Gagliardi, G., Tallon, M., Roazzi, P., van den Ban, E., de Bruijn, SFTM, Driessen, N., Lamerz, A., Messchendorp, M., Rath, JJG, Sival, NSD, Tromp, N., Visscher, F., de la Tourettes, S.G., Cáceres, M.T., Carrillo, F., Gómez-Garre, P., Vargas, L., Gariup, M., Stöber, S., Apter, A., Baglioni, V., Ball, J., Benaroya-Milshtein, N., Bodmer, B., Bond, M., Bognar, E., Burger, B., Buse, J., Cardona, F., Vela, M.C., Dietrich, A., Debes, N.M., Ferro, M.C., Fremer, C., Garcia-Delgar, B., Gulisano, M., Hagen, A., Hagstrøm, J., Hedderly, T.J., Heyman, I., Hoekstra, P.J., Huyser, C., Madruga-Garrido, M., Marotta, A., Martino, D., Meier, U.C., Mir, P., Moll, N., Morer, A., Mueller, N., Müller-Vahl, K., Münchau, A., Nagy, P., Neri, V., Openneer, TJC, Pellico, A., Vasco, Á.P., Plessen, K.J., Porcelli, C., Redondo, M., Rizzo, R., Roessner, V., Ruhrman, D., Schnell, JML, Schrag, A., Schwarz, M.J., Silvestri, P.R., Skov, L., Steinberg, T., Gloor, F.T., Tarnok, Z., Tübing, J., Turner, V.L., Walitza, S., Weidinger, E., and Woods, M.L.
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Obsessive-Compulsive Disorder ,Tic disorder ,medicine.medical_specialty ,Adolescent ,Tics ,Comorbidity ,Severity of Illness Index ,Pediatrics ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,mental disorders ,Developmental and Educational Psychology ,medicine ,Child and adolescent psychiatry ,Vitamin D and neurology ,Humans ,ADHD ,Vitamin D ,Child ,OCD ,business.industry ,Tourette ,Symptom severity ,General Medicine ,Attention Deficit Disorder with Hyperactivity/psychology ,Cross-Sectional Studies ,Obsessive-Compulsive Disorder/epidemiology ,Obsessive-Compulsive Disorder/psychology ,Tic Disorders/metabolism ,Tic Disorders/psychology ,Tics/complications ,Tics/metabolism ,Tourette Syndrome/psychology ,Vitamin D/metabolism ,medicine.disease ,030227 psychiatry ,Psychiatry and Mental health ,Attention Deficit Disorder with Hyperactivity ,Tic Disorders ,Pediatrics, Perinatology and Child Health ,Cohort ,CTD ,business ,030217 neurology & neurosurgery ,Tourette Syndrome - Abstract
This study investigated whether vitamin D is associated with the presence or severity of chronic tic disorders and their psychiatric comorbidities. This cross-sectional study compared serum 25-hydroxyvitamin D [25(OH)D] (ng/ml) levels among three groups: children and adolescents (3–16 years) with CTD (n = 327); first-degree relatives (3–10 years) of individuals with CTD who were assessed for a period of up to 7 years for possible onset of tics and developed tics within this period (n = 31); and first-degree relatives who did not develop tics and were ≥ 10 years old at their last assessment (n = 93). The relationship between 25(OH)D and the presence and severity of tics, as well as comorbid obsessive–compulsive disorder (OCD) and attention-deficit/hyperactivity disorder (ADHD), were analysed controlling for age, sex, season, centre, latitude, family relatedness, and comorbidities. When comparing the CTD cohort to the unaffected cohort, the observed result was contrary to the one expected: a 10 ng/ml increase in 25(OH)D was associated with higher odds of having CTD (OR 2.08, 95% CI 1.27–3.42, p p = 0.01) and was inversely associated with ADHD symptom severity (β = − 2.52, 95% CI − 4.16–0.88, p
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- 2022
24. Vitamin D levels in children and adolescents with chronic tic disorders: a multicentre study
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Bond, Molly, Moll, Natalie, Rosello, Alicia, Bond, Rod, Schnell, Jaana, Burger, Bianka, Hoekstra, Pieter J, Dietrich, Andrea, Schrag, Anette, Kocovska, Eva, Martino, Davide, Mueller, Norbert, Schwarz, Markus, Meier, Ute-Christiane, EMTICS Collaborative Group, et al, Ball, Juliane, Tagwerker Gloor, Friederike, Walitza, Susanne, and University of Zurich
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OCD ,Tourette ,ADHD ,610 Medicine & health ,Tic disorder ,10058 Department of Child and Adolescent Psychiatry ,Vitamin D ,Pediatrics - Published
- 2022
25. Rapid Onset Functional Tic-Like Disorder Outbreak: A Challenging Differential Diagnosis in the COVID-19 Pandemic
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Amorelli, Gabriel, Martino, Davide, and Pringsheim, Tamara
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Invited Commentary - Abstract
During the COVID-19 pandemic, several countries have observed an unexpected increase in the number of adolescents and young adults presenting with rapid onset functional tic-like behaviours after being exposed to social media content of others displaying a similar pattern of functional tics. Many of these patients have been referred to Movement Disorders Clinics with misdiagnoses of late-onset refractory Tourette Syndrome after failing different pharmacological treatments for tics. Tourette Syndrome is a well-known condition with clear clinical diagnostic criteria and which presents with the insidious onset of simple motor and phonic tics in a rostro-caudal evolution starting in early childhood. Clinical and demographic aspects can differentiate rapid onset functional tic-like behaviours from Tourette Syndrome, including the former having abrupt and explosive presentation of severe symptoms, later age of onset, female gender predominance, lack of suppressibility, comorbid anxiety and depression, atypical premonitory urge and history of exposure to social media content displaying tic-like behaviours. This new presentation of a functional neurological disorder may be explained in part by the relationship between social media exposure to tic-like behaviours, and maladaptive response to anxiety caused by life stressors (e.g. COVID-19 pandemic), especially in young individuals. Rapid onset functional tic-like behaviours may be considered a spreading neuropsychiatric disorder that is potentially fostered by the psychosocial impact caused by the COVID-19 pandemic.Durant la pandémie de la COVID-19, plusieurs pays ont observé une hausse inattendue du nombre d’adolescents et de jeunes adultes présentant des comportements fonctionnels de type tic à apparition rapide après avoir été exposés au contenu des médias sociaux d’autres personnes affichant un modèle semblable de tics fonctionnels. Nombre de ces patients ont été adressés à des cliniques de trouble du mouvement avec des diagnostics fautifs de syndrome de Tourette réfractaire d’apparition tardive après avoir échoué à différents traitements pharmacologiques pour les tics. Le syndrome de Tourette est un trouble bin connu dont les critères diagnostiques cliniques sont clairs et qui présente le début insidieux de simples tics moteurs et phoniques dans une évolution rostro-caudale au début de l’enfance. Les aspects cliniques et démographiques peuvent différencier l’apparition rapide de comportements fonctionnels de type tic du syndrome de Tourette, notamment parce que les premiers ont une présentation abrupte et explosive de symptômes graves, apparaissent à un âge plus avancé, ont une prédominance chez le sexe féminin, manquent de suppressibilité, anxiété et dépression comorbides, envie prémonitoire atypique et antécédents d‘exposition au contenu des médias sociaux affichant des comportements de type tic. Cette nouvelle présentation d’un trouble neurologique fonctionnel peut s‘expliquer en partie par la relation entre l’exposition aux comportements de type tic dans les médias sociaux et la réponse inadaptée à l’anxiété causée par les stresseurs de la vie (p. ex., pandémie de la COVID-19), surtout chez les jeunes personnes. Les comportements fonctionnels de type tic à apparition rapide peuvent être considérés comme un trouble neuropsychiatrique qui se propage et qui est potentiellement favorisé par l’effet psychosocial causé par la pandémie de la COVID-19.
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- 2022
26. The Prevalence of Idiopathic or Inherited Isolated Dystonia: A Systematic Review and Meta‐Analysis
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Medina, Alex, primary, Nilles, Christelle, additional, Martino, Davide, additional, Pelletier, Catherine, additional, and Pringsheim, Tamara, additional
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- 2022
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27. Multispectral Brain Morphometry in Tourette Syndrome Persisting into Adulthood
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Draganski, Bogdan, Martino, Davide, and Cavanna, Andrea E.
- Abstract
Tourette syndrome is a childhood-onset neuropsychiatric disorder with a high prevalence of attention deficit hyperactivity and obsessive-compulsive disorder co-morbidities. Structural changes have been found in frontal cortex and striatum in children and adolescents. A limited number of morphometric studies in Tourette syndrome persisting into adulthood suggest ongoing structural alterations affecting frontostriatal circuits. Using cortical thickness estimation and voxel-based analysis of T1- and diffusion-weighted structural magnetic resonance images, we examined 40 adults with Tourette syndrome in comparison with 40 age- and gender-matched healthy controls. Patients with Tourette syndrome showed relative grey matter volume reduction in orbitofrontal, anterior cingulate and ventrolateral prefrontal cortices bilaterally. Cortical thinning extended into the limbic mesial temporal lobe. The grey matter changes were modulated additionally by the presence of co-morbidities and symptom severity. Prefrontal cortical thickness reduction correlated negatively with tic severity, while volume increase in primary somatosensory cortex depended on the intensity of premonitory sensations. Orbitofrontal cortex volume changes were further associated with abnormal water diffusivity within grey matter. White matter analysis revealed changes in fibre coherence in patients with Tourette syndrome within anterior parts of the corpus callosum. The severity of motor tics and premonitory urges had an impact on the integrity of tracts corresponding to cortico-cortical and cortico-subcortical connections. Our results provide empirical support for a patho-aetiological model of Tourette syndrome based on developmental abnormalities, with perturbation of compensatory systems marking persistence of symptoms into adulthood. We interpret the symptom severity related grey matter volume increase in distinct functional brain areas as evidence of ongoing structural plasticity. The convergence of evidence from volume and water diffusivity imaging strengthens the validity of our findings and attests to the value of a novel multimodal combination of volume and cortical thickness estimations that provides unique and complementary information by exploiting their differential sensitivity to structural change.
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- 2010
- Full Text
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28. Hair cortisol-a stress marker in children and adolescents with chronic tic disorders? A large European cross-sectional study
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Judith, Buse, Josefine, Rothe, Anne, Uhlmann, Benjamin, Bodmer, Clemens, Kirschbaum, Hoekstra, Pieter J., Andrea, Dietrich, Veit, Roessner, EMTICS collaborative group: Alan Apter, Baglioni, Valentina, Juliane, Ball, Noa, Benaroya-Milshtein, Emese, Bognar, Bianka, Burger, Cardona, Francesco Carmelo Giovanni, Marta Correa Vela, Maria Cristina Ferro, Blanca, Garcia-Delgar, Mariangela, Gulisano, Annelieke, Hagen, Julie, Hagstrøm, Hedderly, Tammy J., Isobel, Heyman, Chaim, Huyser, Marcos, Madruga-Garrido, Martino, Davide, Pablo, Mir, Astrid, Morer, Kirsten, Müller-Vahl, Alexander, Münchau, Peter, Nagy, Neri, Valeria, Openneer, Thaïra J. C., Pellico, Alessandra, Plessen, Kerstin J., Cesare, Porcelli, Rizzo, Renata, Daphna, Ruhrman, Schnell, Jaana M. L., Anette, Schrag, Silvestri, PAOLA ROSARIA, Liselotte, Skov, Tamar, Steinberg, Friederike Tagwerker Gloor, Zsanett Tarnok &, Elif, Weidinger, EMTICS collaborative group, Apter, A., Baglioni, V., Ball, J., Benaroya-Milshtein, N., Bodmer, B., Bognar, E., Burger, B., Buse, J., Cardona, F., Vela, M.C., Dietrich, A., Ferro, M.C., Garcia-Delgar, B., Gulisano, M., Hagen, A., Hagstrøm, J., Hedderly, T.J., Heyman, I., Hoekstra, P.J., Huyser, C., Madruga-Garrido, M., Martino, D., Mir, P., Morer, A., Müller-Vahl, K., Münchau, A., Nagy, P., Neri, V., Openneer, TJC, Pellico, A., Plessen, K.J., Porcelli, C., Rizzo, R., Roessner, V., Ruhrman, D., Schnell, JML, Schrag, A., Silvestri, P.R., Skov, L., Steinberg, T., Gloor, F.T., Tarnok, Z., Weidinger, E., and Clinical Cognitive Neuropsychiatry Research Program (CCNP)
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BIOMARKER ,medicine.medical_specialty ,Adolescent ,Hydrocortisone ,GENETICS ,Tics ,RESPONSIVITY ,Cross-sectional study ,Chronic tic disorders ,Emotional and behavioral problems ,Physiological stress marker ,Psychosocial stress ,Tourette ,Tourette syndrome ,03 medical and health sciences ,0302 clinical medicine ,Biomarkers ,Child ,Cross-Sectional Studies ,Hair ,Humans ,Tic Disorders/diagnosis ,Developmental and Educational Psychology ,Child and adolescent psychiatry ,Medicine ,ASSOCIATIONS ,business.industry ,TOURETTE-SYNDROME ,Stressor ,OBSESSIVE-COMPULSIVE DISORDER ,General Medicine ,medicine.disease ,PREVALENCE ,030227 psychiatry ,INDIVIDUALS ,Psychiatry and Mental health ,PSYCHOMETRIC PROPERTIES ,Tic Disorders ,Pediatrics, Perinatology and Child Health ,Cohort ,Biomarker (medicine) ,STRENGTHS ,business ,030217 neurology & neurosurgery ,Clinical psychology - Abstract
Background There is clear evidence that tic disorders (TDs) are associated with psychosocial stress as well as emotional and behavioral problems. Studies have shown that individuals with TDs have higher acute physiological stress responses to external, single stressors (as reflected by saliva cortisol). The aim of the present study was to examine a physiological marker of longer-term stress (as reflected by hair cortisol concentration) in children and adolescents with TDs and unaffected siblings of individuals with TDs. Methods Two samples of a European cohort were included in this study. In the COURSE sample, 412 children and adolescents aged 3–16 years with a chronic TD including Tourette syndrome according to DSM IV-TR criteria were included. The ONSET sample included 131 3–10 years old siblings of individuals with TDs, who themselves had no tics. Differences in hair cortisol concentration (HCC) between the two samples were examined. Within the COURSE sample, relations of HCC with tic severity and perceived psychosocial stress as well as potential effects and interaction effects of comorbid emotional and behavioral problems and psychotropic medication on HCC were investigated. Results There were no differences in HCC between the two samples. In participants with TDs, there were no associations between HCC and tic severity or perceived psychosocial stress. No main effects of sex, psychotropic medication status and comorbid emotional and behavioral problems on HCC were found in participants with TDs. Conclusion A link between HCC and TDs is not supported by the present results.
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- 2021
29. Observing the Diversity of Alleviating Manoeuvres in Cervical Dystonia
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Avanzino, Laura, Di Biasio, Francesca, Bonassi, Gaia, Pelosin, Elisa, Cothros, Nicholas, Marchese, Roberta, and Martino, Davide
- Abstract
The alleviating manoeuvres (AMs), classically referred to as “sensory tricks” are voluntary manoeuvres that temporarily improve dystonic postures. Although self-induced application of sensory stimuli is the most common AM, clinical experience suggests that the phenomenon is more diverse, possibly reflecting the complexity of the pathophysiological mechanisms provoking dystonia. We specifically explored five different categories of AMs in patients with cervical dystonia (CD): 1) pure sensory; sensorimotor manoeuvres in which sensory input is associated with a motor output component incorporating 2) active non-oppositional, 3) active oppositional or 4) passive motion; and 5) complex motor manoeuvres. Using an ad hoc structured clinical interview, we collected data on the frequency and efficacy of each subgroup and the possible correlation with some clinical features of CD. One-hundred patients were included in this study. Seventy-five percent of patients reported at least one AM. Half of those reporting AMs acknowledged the use of different phenomenological categories of AMs. Different categories of AMs showed noteworthy differences in prevalence of use amongst CD patients, and in the relationship of frequency of use and efficacy to patient demographic and clinical characteristics. Our observational study supports the existence of different AMs that are phenomenologically different and could be related to different degrees of sensorimotor integration dysfunction. Given that AMs are probably the most efficacious, non-invasive strategy to ameliorate CD and other dystonias, accurate phenotyping and physiological exploration of their diversity may produce relevant insight for new therapeutic strategies or appraisal of existing ones.
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- 2022
30. Lack of Association of Group A Streptococcal Infections and Onset of Tics: European Multicenter Tics in Children Study
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Schrag, Anette Eleonore, Martino, Davide, Wang, Hanyuying, et al, Walitza, Susanne, and University of Zurich
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Streptococcal ,Tics ,610 Medicine & health ,10058 Department of Child and Adolescent Psychiatry - Published
- 2022
31. Clinical features of idiopathic normal pressure Hydrocephalus : critical review of objective findings
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Bluett, Brent, Ash, Elissa, Farheen, Amtul, Fasano, Alfonso, Krauss, Joachim K., Maranzano, Alessio, Passaretti, Massimiliano, Tang‐Wai, David F., Van Gerpen, Jay, Alonso‐Canovas, Araceli, Youn, Jinyoung, Malm, Jan, Martino, Davide, Bluett, Brent, Ash, Elissa, Farheen, Amtul, Fasano, Alfonso, Krauss, Joachim K., Maranzano, Alessio, Passaretti, Massimiliano, Tang‐Wai, David F., Van Gerpen, Jay, Alonso‐Canovas, Araceli, Youn, Jinyoung, Malm, Jan, and Martino, Davide
- Abstract
Background: Idiopathic normal pressure hydrocephalus (iNPH) is characterized by the classic clinical triad of gait, cognitive, and urinary dysfunction, albeit incomplete in a relevant proportion of patients. The clinical findings and evolution of these symptoms have been variably defined in the literature. Objectives: To evaluate how the phenomenology has been defined, assessed, and reported, we performed a critical review of the existing literature discussing the phenomenology of iNPH. The review also identified the instrumental tests most frequently used and the evolution of clinical and radiologic findings. Methods: The review was divided into 3 sections based on gait, cognitive, and urinary dysfunction. Each section performed a literature search using the terms “idiopathic normal pressure hydrocephalus” (iNPH), with additional search terms used by each section separately. The number of articles screened, duplicates, those meeting the inclusion criteria, and the number of articles excluded were recorded. Findings were subsequently tallied and analyzed. Results: A total of 1716 articles with the aforementioned search criteria were identified by the 3 groups. A total of 81 full-text articles were reviewed after the elimination of duplicates, articles that did not discuss phenomenological findings or instrumental testing of participants with iNPH prior to surgery, and articles with fewer than 10 participants. Conclusions: “Wide-based gait” was the most common gait dysfunction identified. Cognitive testing varied significantly across articles, and ultimately a specific cognitive profile was not identified. Urodynamic testing found detrusor overactivity and “overactive bladder” as the most common symptom of urinary dysfunction.
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- 2022
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32. A neural network for tics: insights from causal brain lesions and deep brain stimulation
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Ganos, Christos, Al-Fatly, Bassam, Fischer, Jan-Frederik, Baldermann, Juan-Carlos, Hennen, Christina, Visser-Vandewalle, Veerle, Neudorfer, Clemens, Martino, Davide, Li, Jing, Bouwens, Tim, Ackermanns, Linda, Leentjens, Albert F G, Pyatigorskaya, Nadya, Worbe, Yulia, Fox, Michael D, Kühn, Andrea A, Horn, Andreas, Ganos, Christos, Al-Fatly, Bassam, Fischer, Jan-Frederik, Baldermann, Juan-Carlos, Hennen, Christina, Visser-Vandewalle, Veerle, Neudorfer, Clemens, Martino, Davide, Li, Jing, Bouwens, Tim, Ackermanns, Linda, Leentjens, Albert F G, Pyatigorskaya, Nadya, Worbe, Yulia, Fox, Michael D, Kühn, Andrea A, and Horn, Andreas
- Abstract
Brain lesions are a rare cause of tic disorders. However, they can provide unique insights into tic pathophysiology and can also inform on possible neuromodulatory therapeutic targets. Based on a systematic literature review, we identified 22 cases of tics causally attributed to brain lesions and employed 'lesion network mapping' to interrogate whether tic-inducing lesions would be associated with a common network in the average human brain. We probed this using a normative functional connectome acquired in 1,000 healthy participants. We then examined the specificity of the identified network by contrasting tic-lesion connectivity maps to those seeding from 717 lesions associated with a wide array of neurological and/or psychiatric symptoms within the Harvard Lesion Repository. Finally, we determined the predictive utility of the tic-inducing lesion network as a therapeutic target for neuromodulation. Specifically, we collected retrospective data of 30 individuals with Tourette disorder, who underwent either thalamic (n = 15; centromedian/ventrooralis internus) or pallidal (n = 15; anterior segment of globus pallidus internus) deep brain stimulation and calculated whether connectivity between deep brain stimulation sites and the lesion network map could predict clinical improvements. Despite spatial heterogeneity, tic-inducing lesions mapped to a common network map, which comprised the insular cortices, cingulate gyrus, striatum, globus pallidus internus, thalami, and the cerebellum. Connectivity to a region within the anterior striatum (putamen) was specific to tic-inducing lesions when compared with control lesions. Connectivity between deep brain stimulation electrodes and the lesion network map was predictive of tic improvement, regardless of the deep brain stimulation target. Taken together, our results reveal a common brain network involved in tic generation which shows potential as a therapeutic target for neuromodulation.
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- 2022
33. Tic disorders in children and adolescents:does the clinical presentation differ in males and females? A report by the EMTICS group
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Garcia-Delgar, Blanca, Servera, Mateu, Coffey, Barbara J, Lázaro, Luisa, Openneer, Thaïra J C, Benaroya-Milshtein, Noa, Steinberg, Tami, Hoekstra, Pieter J, Dietrich, Andrea, Morer, Astrid, Apter, Alan, Baglioni, Valentina, Ball, Juliane, Bognar, Emese, Burger, Bianka, Buse, Judith, Cardona, Francesco, Vela, Marta Correa, Debes, Nanette M., Ferro, Maria Cristina, Fremer, Carolin, Gulisano, Mariangela, Hagen, Annelieke, Hagstrøm, Julie, Hedderly, Tammy J., Heyman, Isobel, Huyser, Chaim, Madruga-Garrido, Marcos, Marotta, Anna, Martino, Davide, Mir, Pablo, Müller, Norbert, Müller-Vahl, Kirsten, Münchau, Alexander, Nagy, Peter, Neri, Valeria, Openneer, Thaïra J.C., Pellico, Alessandra, Plessen, Kerstin J., Porcelli, Cesare, Rizzo, Renata, Roessner, Veit, Ruhrman, Daphna, Schnell, Jaana M.L., Silvestri, Paola Rosaria, Skov, Liselotte, Steinberg, Tamar, Gloor, Friederike Tagwerker, Tarnok, Zsanett, Garcia-Delgar, Blanca, Servera, Mateu, Coffey, Barbara J, Lázaro, Luisa, Openneer, Thaïra J C, Benaroya-Milshtein, Noa, Steinberg, Tami, Hoekstra, Pieter J, Dietrich, Andrea, Morer, Astrid, Apter, Alan, Baglioni, Valentina, Ball, Juliane, Bognar, Emese, Burger, Bianka, Buse, Judith, Cardona, Francesco, Vela, Marta Correa, Debes, Nanette M., Ferro, Maria Cristina, Fremer, Carolin, Gulisano, Mariangela, Hagen, Annelieke, Hagstrøm, Julie, Hedderly, Tammy J., Heyman, Isobel, Huyser, Chaim, Madruga-Garrido, Marcos, Marotta, Anna, Martino, Davide, Mir, Pablo, Müller, Norbert, Müller-Vahl, Kirsten, Münchau, Alexander, Nagy, Peter, Neri, Valeria, Openneer, Thaïra J.C., Pellico, Alessandra, Plessen, Kerstin J., Porcelli, Cesare, Rizzo, Renata, Roessner, Veit, Ruhrman, Daphna, Schnell, Jaana M.L., Silvestri, Paola Rosaria, Skov, Liselotte, Steinberg, Tamar, Gloor, Friederike Tagwerker, and Tarnok, Zsanett
- Abstract
Tic disorders have a strong male predominance, with a male-to-female ratio of 4:1 in Tourette syndrome (TS) and 2:1 in persistent tic disorders. In other neurodevelopmental conditions, such as autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD), the disparity in sex distribution has been partially related to differences in symptom presentation between males and females. In tic disorders, however, little research has been conducted on this topic, probably due to the limited access to large samples with a significant proportion of females. The aim of this study was to describe sex differences in the clinical presentation of tic disorders in children and adolescents in one of the largest pediatric samples with TS/persistent tic disorders (n = 709, 23.3% females) recruited as part of the European Multicenter Tics in Children Study (EMTICS). Validated measures assessed the severity of tics and comorbid psychiatric symptoms. Using mixed-effect models, we found that sex had a significant influence on the severity of tics, ADHD symptoms, ASD symptoms, and emotional problems. Males had more severe symptoms than females, except for emotional problems. We also observed a statistically significant interaction between sex and age on the severity of tics and compulsions, with females showing higher symptom severity with increasing age than males. These findings indicate that the clinical presentation of TS/persistent tic disorders varies with sex. Males seem to exhibit a more noticeable pattern of clinical symptoms at a younger age that may contribute to their earlier detection in comparison to females.
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- 2022
34. Lack of Association of Group A Streptococcal Infections and Onset of Tics: European Multicenter Tics in Children Study
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European Commission, Schrag, Anette-Eleonore, Martino, Davide, Wang, Hanyuying, Ambler, Gareth, Benaroya-Milstein, Noa, Buttiglione, Maura, Cardona, Francesco, Creti, Roberta, Efstratiou, Androulla, Hedderly, Tammy, Heyman, Isobel, Huyser, Chaim, Mir, Pablo, Morer, Astrid, Moll, Natalie, Müller, Norbert, Müller-Vahl, Kirsten R., Plessen, Kerstin J., Porcelli, Cesare, Rizzo, Renata, Roessner, Veit, Schwarz, Markus, Tarnok, Zsanett, Walitza, Susanne, Dietrich, Andrea, Hoekstra, Pieter J., European Commission, Schrag, Anette-Eleonore, Martino, Davide, Wang, Hanyuying, Ambler, Gareth, Benaroya-Milstein, Noa, Buttiglione, Maura, Cardona, Francesco, Creti, Roberta, Efstratiou, Androulla, Hedderly, Tammy, Heyman, Isobel, Huyser, Chaim, Mir, Pablo, Morer, Astrid, Moll, Natalie, Müller, Norbert, Müller-Vahl, Kirsten R., Plessen, Kerstin J., Porcelli, Cesare, Rizzo, Renata, Roessner, Veit, Schwarz, Markus, Tarnok, Zsanett, Walitza, Susanne, Dietrich, Andrea, and Hoekstra, Pieter J.
- Abstract
[Background and Objectives] The goal of this work was to investigate the association between group A streptococcal (GAS) infections and tic incidence among unaffected children with a family history of chronic tic disorders (CTDs)., [Methods] In a prospective cohort study, children with no history for tics who were 3 to 10 years of age with a first-degree relative with a CTD were recruited from the European Multicentre Tics in Children Study (EMTICS) across 16 European centers. Presence of GAS infection was assessed with throat swabs, serum anti–streptolysin O titers, and anti-DNAse titers blinded to clinical status. GAS exposure was defined with 4 different definitions based on these parameters. Cox regression analyses with time-varying GAS exposure were conducted to examine the association of onset of tics and GAS exposure during follow-up. Sensitivity analyses were conducted with Cox regression and logistic regression analyses., [Results] A total of 259 children were recruited; 1 child was found to have tic onset before study entry and therefore was excluded. Sixty-one children (23.6%) developed tics over an average follow-up period of 1 (SD 0.7) year. There was a strong association of sex and onset of tics, with girls having an ≈60% lower risk of developing tics compared to boys (hazard ratio [HR] 0.4, 95% confidence interval [CI] 0.2–0.7). However, there was no statistical evidence to suggest an association of any of the 4 GAS exposure definitions with tic onset (GAS exposure definition 1: HR 0.310, 95% CI 0.037–2.590; definition 2: HR 0.561, 95% CI 0.219–1.436; definition 3: HR 0.853, 95% CI 0.466–1.561; definition 4: HR 0.725, 95% CI 0.384–1.370)., [Discussion] These results do not suggest an association between GAS exposure and development of tics.
- Published
- 2022
35. European clinical guidelines for Tourette syndrome and other tic disorders—version 2.0. Part I:assessment
- Author
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Szejko, Natalia, Robinson, Sally, Hartmann, Andreas, Ganos, Christos, Debes, Nanette M., Skov, Liselotte, Haas, Martina, Rizzo, Renata, Stern, Jeremy, Münchau, Alexander, Czernecki, Virginie, Dietrich, Andrea, Murphy, Tara L., Martino, Davide, Tarnok, Zsanett, Hedderly, Tammy, Müller-Vahl, Kirsten R., Cath, Danielle C., Szejko, Natalia, Robinson, Sally, Hartmann, Andreas, Ganos, Christos, Debes, Nanette M., Skov, Liselotte, Haas, Martina, Rizzo, Renata, Stern, Jeremy, Münchau, Alexander, Czernecki, Virginie, Dietrich, Andrea, Murphy, Tara L., Martino, Davide, Tarnok, Zsanett, Hedderly, Tammy, Müller-Vahl, Kirsten R., and Cath, Danielle C.
- Abstract
In 2011 a working group of the European Society for the Study of Tourette Syndrome (ESSTS) has developed the first European assessment guidelines for Tourette syndrome (TS). Now, we present an updated version 2.0 of these European clinical guidelines for Tourette syndrome and other tic disorders, part I: assessment. Therefore, the available literature has been thoroughly screened, supplemented with national guidelines across countries and discussions among ESSTS experts. Diagnostic changes between DSM-IV and DSM-5 classifications were taken into account and new information has been added regarding differential diagnoses, with an emphasis on functional movement disorders in both children and adults. Further, recommendations regarding rating scales to evaluate tics, comorbidities, and neuropsychological status are provided. Finally, results from a recently performed survey among ESSTS members on assessment in TS are described. We acknowledge that the Yale Global Tic Severity Scale (YGTSS) is still the gold standard for assessing tics. Recommendations are provided for scales for the assessment of tics and psychiatric comorbidities in patients with TS not only in routine clinical practice, but also in the context of clinical research. Furthermore, assessments supporting the differential diagnosis process are given as well as tests to analyse cognitive abilities, emotional functions and motor skills.
- Published
- 2022
36. Multi-robot Routing and Scheduling with Temporal Logic and Synchronization Constraints
- Author
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Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology. Laboratory for Information and Decision Systems, Mosca, Alessio, Vasile, Cristian-Ioan, Belta, Calin, Martino, Davide, Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology. Laboratory for Information and Decision Systems, Mosca, Alessio, Vasile, Cristian-Ioan, Belta, Calin, and Martino, Davide
- Published
- 2022
37. Prognosis of rapid onset functional tic‐like behaviors: Prospective follow‐up over 6 months
- Author
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Howlett, Megan, primary, Martino, Davide, additional, Nilles, Christelle, additional, and Pringsheim, Tamara, additional
- Published
- 2022
- Full Text
- View/download PDF
38. Lack of Association of Group A Streptococcal Infections and Onset of Tics: European Multicenter Tics in Children Study
- Author
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Schrag, Anette-Eleonore, Martino, Davide, Wang, Hanyuying, Ambler, Gareth, Benaroya-Milstein, Noa, Buttiglione, Maura, Cardona, Francesco, Creti, Roberta, Efstratiou, Androulla, Hedderly, Tammy, Heyman, Isobel, Huyser, Chaim, Mir, Pablo, Morer, Astrid, Moll, Natalie, Müller, Norbert E, Müller-Vahl, Kirsten R, Plessen, Kerstin J, Porcelli, Cesare, Rizzo, Renata, Roessner, Veit, Schwarz, Markus, Tarnok, Zsanett, Walitza, Susanne, Dietrich, Andrea, Hoekstra, Pieter J, European Multicentre Tics in Children Study (EMTICS), Clinical Cognitive Neuropsychiatry Research Program (CCNP), and European Commission
- Subjects
Male ,Incidence ,Streptococcal Infections ,Tic Disorders ,Tics ,Humans ,Female ,Neurology (clinical) ,Prospective Studies ,Child - Abstract
[Background and Objectives] The goal of this work was to investigate the association between group A streptococcal (GAS) infections and tic incidence among unaffected children with a family history of chronic tic disorders (CTDs)., [Methods] In a prospective cohort study, children with no history for tics who were 3 to 10 years of age with a first-degree relative with a CTD were recruited from the European Multicentre Tics in Children Study (EMTICS) across 16 European centers. Presence of GAS infection was assessed with throat swabs, serum anti–streptolysin O titers, and anti-DNAse titers blinded to clinical status. GAS exposure was defined with 4 different definitions based on these parameters. Cox regression analyses with time-varying GAS exposure were conducted to examine the association of onset of tics and GAS exposure during follow-up. Sensitivity analyses were conducted with Cox regression and logistic regression analyses., [Results] A total of 259 children were recruited; 1 child was found to have tic onset before study entry and therefore was excluded. Sixty-one children (23.6%) developed tics over an average follow-up period of 1 (SD 0.7) year. There was a strong association of sex and onset of tics, with girls having an ≈60% lower risk of developing tics compared to boys (hazard ratio [HR] 0.4, 95% confidence interval [CI] 0.2–0.7). However, there was no statistical evidence to suggest an association of any of the 4 GAS exposure definitions with tic onset (GAS exposure definition 1: HR 0.310, 95% CI 0.037–2.590; definition 2: HR 0.561, 95% CI 0.219–1.436; definition 3: HR 0.853, 95% CI 0.466–1.561; definition 4: HR 0.725, 95% CI 0.384–1.370)., [Discussion] These results do not suggest an association between GAS exposure and development of tics., This project has received funding from the European Union’s Seventh Framework Program for research and technological development under grant agreement No. 278367.
- Published
- 2022
39. Tic disorders in children and adolescents: does the clinical presentation differ in males and females? A report by the EMTICS group
- Author
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Blanca, Garcia‐delgar, Mateu, Servera, Coffey, Barbara J., Luisa, Lázaro, Thaïra, Openneer, Noa, Benaroya‐milshtein, Tami, Steinberg, Hoekstra, Pieter J., Andrea, Dietrich, Astrid Morer EMTICS collaborative group Alan Apter, Baglioni, Valentina, Juliane, Ball, Noa, Benaroya-Milshtein, Emese, Bognar, Bianka, Burger, Judith, Buse, Cardona, Francesco Carmelo Giovanni, Marta Correa Vela, Debes, Nanette M., Maria Cristina Ferro, Carolin, Fremer, Blanca, Garcia-Delgar, Mariangela, Gulisano, Annelieke, Hagen, Julie, Hagstrøm, Hedderly, Tammy J., Isobel, Heyman, Chaim, Huyser, Marcos, Madruga-Garrido, Anna, Marotta, Martino, Davide, Pablo, Mir, Astrid, Morer, Norbert, Müller, Kirsten, Müller-Vahl, Alexander, Münchau, Peter, Nagy, Neri, Valeria, Openneer, Thaïra J. C., Pellico, Alessandra, Plessen, Kerstin J., Cesare, Porcelli, Rizzo, Renata, Veit, Roessner, Daphna, Ruhrman, Schnell, Jaana M. L., Silvestri, PAOLA ROSARIA, Liselotte, Skov, Tamar, Steinberg, Friederike Tagwerker Gloor, Zsanett, Tarnok, Susanne Walitza &, Elif, Weidinger, Clinical Cognitive Neuropsychiatry Research Program (CCNP), Child Psychiatry, Child and Adolescent Psychiatry & Psychosocial Care, and ANS - Cellular & Molecular Mechanisms
- Subjects
Male ,Pediatrics ,medicine.medical_specialty ,congenital, hereditary, and neonatal diseases and abnormalities ,Younger age ,Tics ,Adolescent ,Autism Spectrum Disorder ,Comorbidity ,Adolescents ,Tourette syndrome ,Severity of Illness Index ,Limited access ,03 medical and health sciences ,0302 clinical medicine ,mental disorders ,Sex differences ,Developmental and Educational Psychology ,Child and adolescent psychiatry ,Medicine ,Humans ,0501 psychology and cognitive sciences ,10. No inequality ,Child ,Children ,business.industry ,05 social sciences ,General Medicine ,medicine.disease ,030227 psychiatry ,body regions ,Psychiatry and Mental health ,Autism spectrum disorder ,Attention Deficit Disorder with Hyperactivity ,Tic Disorders ,Pediatrics, Perinatology and Child Health ,Female ,Presentation (obstetrics) ,business ,human activities ,050104 developmental & child psychology ,Male predominance - Abstract
Tic disorders have a strong male predominance, with a male-to-female ratio of 4:1 in Tourette syndrome (TS) and 2:1 in persistent tic disorders. In other neurodevelopmental conditions, such as autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD), the disparity in sex distribution has been partially related to differences in symptom presentation between males and females. In tic disorders, however, little research has been conducted on this topic, probably due to the limited access to large samples with a significant proportion of females. The aim of this study was to describe sex differences in the clinical presentation of tic disorders in children and adolescents in one of the largest pediatric samples with TS/persistent tic disorders (n = 709, 23.3% females) recruited as part of the European Multicenter Tics in Children Study (EMTICS). Validated measures assessed the severity of tics and comorbid psychiatric symptoms. Using mixed-effect models, we found that sex had a significant influence on the severity of tics, ADHD symptoms, ASD symptoms, and emotional problems. Males had more severe symptoms than females, except for emotional problems. We also observed a statistically significant interaction between sex and age on the severity of tics and compulsions, with females showing higher symptom severity with increasing age than males. These findings indicate that the clinical presentation of TS/persistent tic disorders varies with sex. Males seem to exhibit a more noticeable pattern of clinical symptoms at a younger age that may contribute to their earlier detection in comparison to females.
- Published
- 2022
40. Lack of Association of Group A Streptococcal Infections and Onset of Tics: European Multicenter Tics in Children Study
- Author
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Anette-Eleonore, Schrag, Martino, Davide, Hanyuying, Wang, Gareth, Ambler, Noa, Benaroya-Milstein, Maura, Buttiglione, Cardona, Francesco Carmelo Giovanni, Roberta, Creti, Androulla, Efstratiou, Tammy, Hedderly, Isobel, Heyman, Chaim, Huyser, Pablo, Mir, Astrid, Morer, Natalie, Moll, Norbert, E Müller, Kirsten, R Müller-Vahl, Kerstin, J Plessen, Cesare, Porcelli, Rizzo, Renata, Veit, Roessner, Markus, Schwarz, Zsanett, Tarnok, Susanne, Walitza, Andrea, Dietrich, Pieter, J Hoekstra Alan Apter, Baglioni, Valentina, Juliane, Ball, Noa, Benaroya-Milshtein, Benjamin, Bodmer, Emese, Bognar, Bianka, Burger, Judith, Buse, Marta Correa Vela, Nanette, M Debes, Maria Cristina Ferro, Carolin, Fremer, Blanca, Garcia-Delgar, Mariangela, Gulisano, Annelieke, Hagen, Julie, Hagstrøm, Tammy, J Hedderly, Pieter, J Hoekstra, Marcos, Madruga-Garrido, Anna, Marotta, Norbert, Müller, Alexander, Münchau, Peter, Nagy, Neri, Valeria, Thaïra Jc Openneer, Pellico, Alessandra, Ángela Periañez Vasco, Marina, Redondo, Daphna, Ruhrman, Jaana Ml Schnell, Anette, Schrag, Silvestri, PAOLA ROSARIA, Liselotte, Skov, Tamar, Steinberg, Friederike Tagwerker Gloor, Jennifer, Tübing, Victoria, L Turner, and Elif, Weidinger
- Subjects
Neuroimmunity ,Neuroinflammation ,Tic Disorders ,Streptococcal infections - Published
- 2022
41. The neural representation of actions in Tourette syndrome as a window to decipher tics and their suppression.
- Author
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Martino, Davide and Ganos, Christos
- Published
- 2023
- Full Text
- View/download PDF
42. A neural network for tics: insights from causal brain lesions and deep brain stimulation
- Author
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Ganos, Christos, primary, Al-Fatly, Bassam, additional, Fischer, Jan-Frederik, additional, Baldermann, Juan-Carlos, additional, Hennen, Christina, additional, Visser-Vandewalle, Veerle, additional, Neudorfer, Clemens, additional, Martino, Davide, additional, Li, Jing, additional, Bouwens, Tim, additional, Ackermanns, Linda, additional, Leentjens, Albert F G, additional, Pyatigorskaya, Nadya, additional, Worbe, Yulia, additional, Fox, Michael D, additional, Kühn, Andrea A, additional, and Horn, Andreas, additional
- Published
- 2022
- Full Text
- View/download PDF
43. Clinical Practice Patterns in Tic Disorders Among Movement Disorder Society Members
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Ganos, Christos, Sarva, Harini, Kurvits, Lille, Gilbert, Donald L., Hartmann, Andreas, Worbe, Yulia, Mir Rivera, Pablo, Martino, Davide, and Universidad de Sevilla. Departamento de Medicina
- Subjects
Tic disorders ,Tic Disorders and Tourette Syndrome Study Group ,Movement Disorder Society ,Survey ,Tourette disorder - Abstract
Background: Tic disorders belong to the broad spectrum of pediatric and adult movement disorders. The wide variability in clinical presentations, applied assessment tools, and treatments are poorly understood. Objectives: To map practices and knowledge base of movement disorder clinicians concerning clinical features, pathophysiology, and treatment approaches in tic disorders. Methods: A 33-item survey was developed by the Tic Disorders and Tourette syndrome Study Group members of the Movement Disorder Society. The survey was distributed to the complete society membership and included responses from 346 members, 314 of whom reported treating tic disorders. Results: Approximately one third of survey respondents (35%) frequently evaluated patients with tics. The data revealed widespread use of existing guidelines (about 70%) and screening for comorbid disorders (>90%). The most common investigations used to rule out secondary causes of tics were imaging (92%), laboratory tests (66%) and neurophysiology (38%). Functional tics were the second most common tic etiology following primary tics. Only 27% of respondents reported confidence in knowledge about tic pathogenesis. Top rated interventions to treat tics were psychoeducation, cognitive behavioral intervention for tics (CBIT) and treatment for neuropsychiatric comorbidities. Antipsychotics were ranked as the most effective pharmacologic tic intervention. Conclusions: The majority of movement disorders specialists do not frequently encounter tics. There was sparse knowledge about tic pathophysiology. Psychoeducation, CBIT, the treatment of neuropsychiatric comorbidities and use of antipsychotics emerged as the most common interventions to treat tics. These results provide insight into what will be needed to improve the diagnosis and treatment of tic disorders.
- Published
- 2021
44. neural network for tics: insights from causal brain lesions and deep brain stimulation.
- Author
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Ganos, Christos, Al-Fatly, Bassam, Fischer, Jan-Frederik, Baldermann, Juan-Carlos, Hennen, Christina, Visser-Vandewalle, Veerle, Neudorfer, Clemens, Martino, Davide, Li, Jing, Bouwens, Tim, Ackermanns, Linda, Leentjens, Albert F G, Pyatigorskaya, Nadya, Worbe, Yulia, Fox, Michael D, Kühn, Andrea A, and Horn, Andreas
- Subjects
DEEP brain stimulation ,BRAIN damage ,MOVEMENT disorders ,TOURETTE syndrome ,LARGE-scale brain networks ,TIC disorders - Abstract
Brain lesions are a rare cause of tic disorders. However, they can provide uniquely causal insights into tic pathophysiology and can also inform on possible neuromodulatory therapeutic targets. Based on a systematic literature review, we identified 22 cases of tics causally attributed to brain lesions and employed 'lesion network mapping' to interrogate whether tic-inducing lesions would be associated with a common network in the average human brain. We probed this using a normative functional connectome acquired in 1000 healthy participants. We then examined the specificity of the identified network by contrasting tic-lesion connectivity maps to those seeding from 717 lesions associated with a wide array of neurological and/or psychiatric symptoms within the Harvard Lesion Repository. Finally, we determined the predictive utility of the tic-inducing lesion network as a therapeutic target for neuromodulation. Specifically, we collected retrospective data of 30 individuals with Tourette disorder, who underwent either thalamic (n = 15; centromedian/ventrooralis internus) or pallidal (n = 15; anterior segment of globus pallidus internus) deep brain stimulation and calculated whether connectivity between deep brain stimulation sites and the lesion network map could predict clinical improvements. Despite spatial heterogeneity, tic-inducing lesions mapped to a common network map, which comprised the insular cortices, cingulate gyrus, striatum, globus pallidus internus, thalami and cerebellum. Connectivity to a region within the anterior striatum (putamen) was specific to tic-inducing lesions when compared with control lesions. Connectivity between deep brain stimulation electrodes and the lesion network map was predictive of tic improvement, regardless of the deep brain stimulation target. Taken together, our results reveal a common brain network involved in tic generation, which shows potential as a therapeutic target for neuromodulation. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
45. Response to Thalamic Ventralis Intermedius Nucleus Deep Brain Stimulation in Essential Tremor vs. Essential Tremor-Plus
- Author
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Gilmour, Gabriela S., primary, Martino, Davide, additional, Hunka, Karen, additional, Lawrence, Pia, additional, Kiss, Zelma H. T., additional, and Bruno, Veronica, additional
- Published
- 2021
- Full Text
- View/download PDF
46. Clinical Practice Patterns in Tic Disorders Among Movement Disorder Society Members
- Author
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Ganos, Christos, primary, Sarva, Harini, additional, Kurvits, Lille, additional, Gilbert, Donald L., additional, Hartmann, Andreas, additional, Worbe, Yulia, additional, Mir, Pablo, additional, Müller-Vahl, Kirsten R., additional, Münchau, Alexander, additional, Shprecher, David, additional, Singer, Harvey S., additional, Deeb, Wissam, additional, Okun, Michael S., additional, Malaty, Irene A., additional, Hallett, Mark, additional, Tijssen, Marina AJ, additional, Pringsheim, Tamara, additional, and Martino, Davide, additional
- Published
- 2021
- Full Text
- View/download PDF
47. Influence of sex on tic severity and psychiatric comorbidity profile in patients with pediatric tic disorder
- Author
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Girgis, Joseph, primary, Martino, Davide, additional, and Pringsheim, Tamara, additional
- Published
- 2021
- Full Text
- View/download PDF
48. Prescriptions for Alpha Agonists and Antipsychotics in Children and Youth with Tic Disorders: A Pharmacoepidemiologic Study
- Author
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Cothros, Nicholas, Martino, Davide, McMorris, Carly, Stewart, David, Tehrani, Ali, and Pringsheim, Tamara
- Subjects
Male ,pharmacoepidemiology ,lcsh:Diseases of the musculoskeletal system ,Adolescent ,Tic disorders ,Tourette syndrome ,Phenylpropanolamine ,Aripiprazole ,Infant ,Articles ,Risperidone ,lcsh:RC346-429 ,Guanfacine ,antipsychotics ,Prescriptions ,Child, Preschool ,Humans ,Female ,Antipsychotic drugs ,alpha agonists ,lcsh:RC925-935 ,Child ,lcsh:Neurology. Diseases of the nervous system ,Antipsychotic Agents ,Tourette syndrome in children - Abstract
Background: Trends in the use of antipsychotics and alpha agonists for the treatment of tic disorders in Canadian children, and how closely these trends align with evidence-based guidelines on the pharmacotherapy of tic disorders, have not been explored. Methods: IQVIA’s Canadian Disease and Therapeutic Index, a survey-based data set, was used to identify prescription patterns by physicians. Respondents recorded all patient visits during a 48-hour period in each quarter of the year, including patient age, gender, drug recommendation and therapeutic indication. Recommendations for alpha agonists and antipsychotics from 2012 to 2016 were analysed for children and adolescents with tic disorders. Results: Risperidone and clonidine were the most commonly recommended medications for tic disorders over the study period, with 36,868 and 35,500 recommendations in 2016, respectively. Recommendations for clonidine increased over the study period, whereas those for risperidone decreased. Guanfacine (approved in Canada in 2013) was used less frequently than clonidine. Clonidine was more frequently recommended than antipsychotics in children younger than 6, in whom antipsychotic recommendations were uncommon. Aripiprazole was the second most commonly recommended antipsychotic for tic disorders, with 22,892 recommendations in 2016. Of the first-generation antipsychotics, pimozide was most commonly recommended (11,334 recommendations in 2016); haloperidol was infrequently recommended. Discussion: The trends observed are in line with guideline recommendations reflected in the decreasing use of risperidone, and the growing use of clonidine and guanfacine. The growing use of aripiprazole is likely due to emerging evidence from clinical trials supporting its efficacy for tics. Recommendations for pimozide and haloperidol were limited, likely due to the greater adverse effects associated with these medications. Keywords: Tic disorders, Tourette syndrome, pharmacoepidemiology, antipsychotics, alpha agonists Citation: Cothros et al. Prescriptions for alpha agonists and antipsychotics in children and youth with tic disorders: a pharmacoepidemiologic study. Tremor Other Hyperkinet Mov. 2019; 9. doi: 10.7916/tohm.v0.645, Tremor and Other Hyperkinetic Movements, Tremor and Other Hyperkinetic Movements
- Published
- 2019
49. TMS Motor Mapping Methodology and Reliability: A Structured Review
- Author
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Sondergaard, Rachel E., primary, Martino, Davide, additional, Kiss, Zelma H. T., additional, and Condliffe, Elizabeth G., additional
- Published
- 2021
- Full Text
- View/download PDF
50. Inhibitory Control Deficits in Children with Tic Disorders Revealed by Object-Hit-and-Avoid Task
- Author
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Cothros, Nicholas, primary, Medina, Alex, additional, Martino, Davide, additional, Dukelow, Sean P., additional, Hawe, Rachel L., additional, Kirton, Adam, additional, Ganos, Christos, additional, Nosratmirshekarlou, Elaheh, additional, and Pringsheim, Tamara, additional
- Published
- 2021
- Full Text
- View/download PDF
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