Cargando…

Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy

Electroconvulsive therapy (ECT) is the treatment of choice for severe and treatment‐resistant depression; disorder severity and unfavorable treatment outcomes are shown to be influenced by an increased genetic burden for major depression (MD). Here, we tested whether ECT assignment and response/nonr...

Descripción completa

Detalles Bibliográficos
Autores principales:	Foo, Jerome C., Streit, Fabian, Frank, Josef, Witt, Stephanie H., Treutlein, Jens, Baune, Bernhard T., Moebus, Susanne, Jöckel, Karl‐Heinz, Forstner, Andreas J., Nöthen, Markus M., Rietschel, Marcella, Sartorius, Alexander, Kranaster, Laura
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2018
Materias:	Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368636/ https://www.ncbi.nlm.nih.gov/pubmed/30507021 http://dx.doi.org/10.1002/ajmg.b.32700

Ejemplares similares

Methylome-wide change associated with response to electroconvulsive therapy in depressed patients
por: Sirignano, Lea, et al.
Publicado: (2021)

Response to therapeutic sleep deprivation: a naturalistic study of clinical and genetic factors and post-treatment depressive symptom trajectory
por: Trautmann, Nina, et al.
Publicado: (2018)

Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist
por: Martin, Jessica, et al.
Publicado: (2017)

Depression and bipolar disorder subtypes differ in their genetic correlations with biological rhythms
por: Sirignano, Lea, et al.
Publicado: (2022)

Glutamate concentration in the anterior cingulate cortex in alcohol dependence: association with alcohol withdrawal and exploration of contribution from glutamatergic candidate genes
por: Streit, Fabian, et al.
Publicado: (2018)

Dexmedetomidine for the management of postictal agitation after electroconvulsive therapy with S-ketamine anesthesia
por: Aksay, Suna Su, et al.
Publicado: (2017)

A genetic sum score of risk alleles associated with body mass index interacts with socioeconomic position in the Heinz Nixdorf Recall Study
por: Frank, Mirjam, et al.
Publicado: (2019)

DNA methylation in cocaine use disorder–An epigenome-wide approach in the human prefrontal cortex
por: Poisel, Eric, et al.
Publicado: (2023)

Longitudinal transcriptome-wide gene expression analysis of sleep deprivation treatment shows involvement of circadian genes and immune pathways
por: Foo, Jerome C., et al.
Publicado: (2019)

Baseline levels of miR-223-3p correlate with the effectiveness of electroconvulsive therapy in patients with major depression
por: Kaurani, Lalit, et al.
Publicado: (2023)

Empirical ratio of the combined use of S-ketamine and propofol in electroconvulsive therapy and its impact on seizure quality
por: Sartorius, Alexander, et al.
Publicado: (2020)

Epigenetic Signatures of Smoking in Five Brain Regions
por: Zillich, Lea, et al.
Publicado: (2022)

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis
por: Treutlein, Jens, et al.
Publicado: (2017)

Epigenome-wide association study of alcohol use disorder in five brain regions
por: Zillich, Lea, et al.
Publicado: (2021)

Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study
por: Pechlivanis, Sonali, et al.
Publicado: (2020)

Shared genetic etiology between alcohol dependence and major depressive disorder
por: Foo, Jerome C., et al.
Publicado: (2018)

Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation
por: Witt, Stephanie H., et al.
Publicado: (2018)

Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum
por: Zillich, Lea, et al.
Publicado: (2022)

Attitudes toward the right to autonomous decision‐making in psychiatric genetic testing: Controversial and context‐dependent
por: Strohmaier, Jana, et al.
Publicado: (2019)

Exploring genetic variants predisposing to diabetes mellitus and their association with indicators of socioeconomic status
por: Schmidt, Börge, et al.
Publicado: (2014)

An analysis of sickness absence in chronically ill patients receiving Complementary and Alternative Medicine: A longterm prospective intermittent study
por: Moebus, Susanne, et al.
Publicado: (2006)

Impact of time since last caloric intake on blood glucose levels
por: Moebus, Susanne, et al.
Publicado: (2011)

Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
por: Pechlivanis, Sonali, et al.
Publicado: (2019)

Genetic risk scores for coronary artery disease and its traditional risk factors: Their role in the progression of coronary artery calcification—Results of the Heinz Nixdorf Recall study
por: Pechlivanis, Sonali, et al.
Publicado: (2020)

Neurocognitive Endophenotypes of Schizophrenia and Bipolar Disorder and Possible Associations with FKBP Variant rs3800373
por: Memic, Amra, et al.
Publicado: (2018)

Impact of 4 different definitions used for the assessment of the prevalence of the Metabolic Syndrome in primary healthcare:The German Metabolic and Cardiovascular Risk Project (GEMCAS)
por: Moebus, Susanne, et al.
Publicado: (2007)

Assessing the prevalence of the Metabolic Syndrome according to NCEP ATP III in Germany: feasibility and quality aspects of a two step approach in 1550 randomly selected primary health care practices
por: Moebus, Susanne, et al.
Publicado: (2006)

Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects
por: Jansen, Andreas, et al.
Publicado: (2009)

Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcification
por: Pechlivanis, Sonali, et al.
Publicado: (2020)

Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4
por: Degenhardt, Franziska, et al.
Publicado: (2016)

Molecular Biomarkers of Electroconvulsive Therapy Effects and Clinical Response: Understanding the Present to Shape the Future
por: Maffioletti, Elisabetta, et al.
Publicado: (2021)

Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study
por: Pechlivanis, Sonali, et al.
Publicado: (2013)

Neighbourhood socio-economic status and positive affectivity among older residents in Germany: a cross-sectional analysis with data from the Heinz Nixdorf Recall Study
por: Hartig, Christina, et al.
Publicado: (2022)

Association of polygenic risk for schizophrenia with fast sleep spindle density depends on pro-cognitive variants
por: Schilling, Claudia, et al.
Publicado: (2022)

Association of Locomotor Activity During Sleep Deprivation Treatment With Response
por: Foo, Jerome Clifford, et al.
Publicado: (2020)

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders
por: Andlauer, Till F. M., et al.
Publicado: (2019)

Childhood maltreatment and cognitive functioning: the role of depression, parental education, and polygenic predisposition
por: Goltermann, Janik, et al.
Publicado: (2020)

Safety of concomitant tranylcypromine treatment during electroconvulsive therapy (ECT) series
por: Kavakbasi, E., et al.
Publicado: (2022)

New-born females show higher stress- and genotype-independent methylation of SLC6A4 than males
por: Dukal, Helene, et al.
Publicado: (2015)

New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?
por: Nieratschker, Vanessa, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_juu5dcuc4r28cksagb07ii3md3