7 results on '"Moser, D"'
Search Results
2. No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder.
- Author
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Hummel E, Elgizouli M, Sicorello M, Leitão E, Beygo J, Schröder C, Zeschnigk M, Müller S, Herpertz S, Moser D, Kessler H, Horsthemke B, and Kumsta R
- Subjects
- Bayes Theorem, Epigenesis, Genetic, Female, Humans, Monocytes, Serotonin Plasma Membrane Transport Proteins genetics, DNA Methylation, Stress Disorders, Post-Traumatic genetics, Stress Disorders, Post-Traumatic psychology
- Abstract
DNA methylation patterns can be responsive to environmental influences. This observation has sparked interest in the potential for psychological interventions to influence epigenetic processes. Recent studies have observed correlations between DNA methylation changes and therapy outcome. However, most did not control for changes in cell composition. This study had two aims: first, we sought to replicate therapy-associated changes in DNA methylation of commonly assessed candidate genes in isolated monocytes from 60 female patients with post-traumatic stress disorder (PTSD). Our second, exploratory goal was to identify novel genomic regions with substantial pre-to-post intervention DNA methylation changes by performing whole-genome bisulfite sequencing (WGBS) in two patients with PTSD. Equivalence testing and Bayesian analyses provided evidence against physiologically meaningful intervention-associated DNA methylation changes in monocytes of PTSD patients in commonly investigated target genes (NR3C1, FKBP5, SLC6A4, OXTR). Furthermore, WGBS yielded only a limited set of candidate regions with suggestive evidence of differential DNA methylation pre- to post-therapy. These differential DNA methylation patterns did not prove replicable when investigated in the entire cohort. We conclude that there is no evidence for major, recurrent intervention-associated DNA methylation changes in the investigated genes in monocytes of patients with PTSD., (© 2022. The Author(s).)
- Published
- 2022
- Full Text
- View/download PDF
3. SARS-CoV-2 pneumonia and bacterial pneumonia patients differ in a second hit immune response model.
- Author
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Moser D, Feuerecker M, Biere K, Han B, Hoerl M, Schelling G, Kaufmann I, Choukér A, and Woehrle T
- Subjects
- Cytokines, Humans, Immunity, Interleukin-2, Pokeweed Mitogens, SARS-CoV-2, COVID-19, Pneumonia, Bacterial, Sepsis
- Abstract
Secondary infections have been shown to complicate the clinical course and worsen the outcome of critically ill patients. Severe Coronavirus Disease 2019 (COVID-19) may be accompanied by a pronounced cytokine release, and immune competence of these patients towards most pathogenic antigens remains uncompromised early in the disease. Patients with bacterial sepsis also exhibit excessive cytokine release with systemic hyper-inflammation, however, typically followed by an anti-inflammatory phase, causing immune paralysis. In a second hit immune response model, leukocyte activation capacity of severely ill patients with pneumonia caused by SARS-CoV-2 or by bacteria were compared upon ICU admission and at days 4 and 7 of the ICU stay. Blood cell count and release of the pro-inflammatory cytokines IL-2, IFNγ and TNF were assessed after whole-blood incubation with the potent immune stimulus pokeweed mitogen (PWM). For comparison, patients with bacterial sepsis not originating from pneumonia, and healthy volunteers were included. Lymphopenia and granulocytosis were less pronounced in COVID-19 patients compared to bacterial sepsis patients. After PWM stimulation, COVID-19 patients showed a reduced release of IFNγ, while IL-2 levels were found similar and TNF levels were increased compared to healthy controls. Interestingly, concentrations of all three cytokines were significantly higher in samples from COVID-19 patients compared to samples from patients with bacterial infection. This fundamental difference in immune competence during a second hit between COVID-19 and sepsis patients may have implications for the selection of immune suppressive or enhancing therapies in personalized medicine., (© 2022. The Author(s).)
- Published
- 2022
- Full Text
- View/download PDF
4. DNA methylation of dopamine-related gene promoters is associated with line bisection deviation in healthy adults.
- Author
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Schmitz J, Kumsta R, Moser D, Güntürkün O, and Ocklenburg S
- Subjects
- Adult, Brain physiopathology, Brain Mapping, Female, Humans, Male, Psychomotor Performance, Space Perception, Young Adult, Attention, DNA Methylation, Dopamine Plasma Membrane Transport Proteins genetics, Functional Laterality genetics, Language, Perceptual Disorders genetics, Promoter Regions, Genetic
- Abstract
Handedness and language lateralization are the most investigated phenotypes among functional hemispheric asymmetries, i.e. differences in function between the left and the right half of the human brain. Both phenotypes are left hemisphere-dominant, while investigations of the molecular factors underlying right hemisphere-dominant phenotypes are less prominent. In the classical line bisection task, healthy subjects typically show a leftward attentional bias due to a relative dominance of the right hemisphere for visuospatial attention. Based on findings of variations in dopamine-related genes affecting performance in the line bisection task, we first tested whether DNA methylation in non-neuronal tissue in the promoter regions of DBH, SLC6A3, and DRD2 are associated with line bisection deviation. We replicated the typical behavioral pattern and found an effect of DNA methylation in the DBH promoter region on line bisection deviation in right-aligned trials. A second exploratory analysis indicated that an overall DNA methylation profile of genes involved in dopamine function predicts line bisection performance in right-aligned trials. Genetic variation in dopamine-related genes has been linked to attention deficit hyperactivity disorder (ADHD), a neurodevelopmental trait associated with rightward attentional bias. Overall, our findings point towards epigenetic markers for functional hemispheric asymmetries in non-neuronal tissue not only for left hemisphere-dominant, but also for right hemisphere-dominant phenotypes.
- Published
- 2019
- Full Text
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5. Risk of Infection and Sepsis in Pediatric Patients with Traumatic Brain Injury Admitted to Hospital Following Major Trauma.
- Author
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Pandya A, Chaput KH, Schertzer A, Moser D, Guilfoyle J, MacGillivray S, Blackwood J, Joffe AR, and Thompson GC
- Subjects
- Brain Injuries, Traumatic mortality, Child, Female, Humans, Logistic Models, Male, Risk Factors, Treatment Outcome, Brain Injuries, Traumatic complications, Communicable Diseases epidemiology, Hospitalization, Sepsis epidemiology
- Abstract
Head injury accounts for 29% of all traumatic deaths in children. Sepsis is significantly associated with an increased risk of mortality in adult traumatic brain injury patients. In the pediatric population, this relationship is not well understood. The objective of this study was to compare the proportion of pediatric traumatic brain injury (TBI) patients and trauma patients without brain injury (NTBI) who developed sepsis or any infection during their index hospital admission. We performed a retrospective study of all trauma patients <18 years of age, admitted to trauma centres in Alberta, Canada from January 1, 2003 to December 31, 2012. Patients who died within 24 hrs of trauma (n = 147) and those with burns as the primary mechanism of injury (n = 53) were excluded. Hospital admission data for the remaining 2556 patients was analyzed. 1727 TBI patients and 829 NTBI patients were included. TBI was associated with lower odds of developing sepsis (OR 0.32 95% CI 0.14-0.77 p = 0.011). TBI was not found to be independently associated with developing any infectious complication after adjusting for confounding by Injury Severity Score (OR 1.25 95% CI 0.90-1.74 p = 0.180). These relationships warrant further study.
- Published
- 2018
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6. Small cell lung cancer: model of circulating tumor cell tumorospheres in chemoresistance.
- Author
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Klameth L, Rath B, Hochmaier M, Moser D, Redl M, Mungenast F, Gelles K, Ulsperger E, Zeillinger R, and Hamilton G
- Subjects
- Carbonic Anhydrase IX analysis, Cell Line, Tumor, Humans, Ki-67 Antigen analysis, Models, Biological, Antineoplastic Agents pharmacology, Cell Aggregation, Drug Resistance, Neoplastic Cells, Circulating drug effects, Small Cell Lung Carcinoma pathology
- Abstract
Small cell lung cancer (SCLC) represents 15% of lung cancers and is characterized by early dissemination, development of chemoresistance and a poor prognosis. A host of diverse drugs failed invariably and its mechanisms of global chemoresistance have not been characterized so far. SCLC represents the prototype of an aggressive and highly metastatic tumor which is ultimately refractory to any treatment. High numbers of circulating tumor cells (CTCs) allowed us to establish 5 CTC cell lines (BHGc7, 10, 16, 26 and UHGc5) from patients with recurrent SCLC. These cell lines exhibit the typical SCLC markers and CTCs of all patients developed spontaneously large multicellular aggregates, termed tumorospheres. Ki67 and carbonic anhydrase 9 (CAIX) staining of tumorosphere sections revealed quiescent and hypoxic cells, respectively. Accordingly, comparison of the chemosensitivity of CTC single cell suspensions with tumorospheres demonstrated increased resistance of the clusters against chemotherapeutics commonly used for treatment of SCLC. Therefore, global chemoresistance of relapsing SCLC seems to rely on formation of large tumorospheres which reveal limited accessibility, lower growth fraction and hypoxic conditions. Since similar tumor spheroids were found in other tumor types, SCLC seems to represent a unique tumor model to study the association of CTCs, metastasis and drug resistance.
- Published
- 2017
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7. Insights into functional bacterial diversity and its effects on Alpine bog ecosystem functioning.
- Author
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Bragina A, Berg C, Müller H, Moser D, and Berg G
- Subjects
- Austria, Bacteria classification, Bacteria genetics, Biodiversity, Cluster Analysis, Computational Biology, Genes, Bacterial, High-Throughput Nucleotide Sequencing, Methane metabolism, Nitrogen Fixation, Oxidation-Reduction, Oxygenases metabolism, Phylogeny, Bacteria metabolism, Ecosystem, Microbiota, Sphagnopsida microbiology
- Abstract
Plant-associated bacteria are important for the growth and health of their host, but little is known about its functional diversity and impact on ecosystem functioning. We studied bacterial nitrogen fixation and methane oxidation from indicator Sphagnum mosses in Alpine bogs to test a hypothesis that the plant microbiome contained different functional patterns depending on their functions within the ecosystem. A high abundance and diversity of nitrogenase genes were detected, mostly specific for each Sphagnum. In contrast, methanotrophs formed highly similar patterns despite a high abundance and diversity of methane monooxygenase genes. Our hypothesis was supported by these contrasting functional patterns together with the result that the Sphagnum sporophyte contained a high proportion of specific diazotrophs (45.5%) but no potential methanotrophs. While essential for plant growth under nutrient-limited conditions, nitrogen-fixing bacteria were highly specific and transferred with the sporophyte unlike the ubiquitous methanotrophs which are important for the climate-relevant ecosystem itself.
- Published
- 2013
- Full Text
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