نتایج جستجو برای: comt 158valmet polymorphism

تعداد نتایج: 108502  

Journal: :American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010
Richard Delorme Catalina Betancur Pauline Chaste Solen Kernéis Astrid Stopin Marie-Christine Mouren Corinne Collet Thomas Bourgeron Marion Leboyer Jean-Marie Launay

The catechol-O-methyltransferase (COMT) gene is considered as a candidate gene in obsessive-compulsive disorder (OCD). Specifically, the COMT low-activity M158 allele has been suggested to be associated with OCD. However, there is no study reporting that COMT activity is decreased in OCD patients and that the decrease is mediated by the V158M polymorphism. Therefore, the purpose of our study wa...

Journal: :Frontiers in Human Neuroscience 2008
Kirk I. Erickson Jennifer S. Kim Barbara L. Suever Michelle W. Voss B. Magnus Francis Arthur F. Kramer

Genetic variability in the dopaminergic and neurotrophic systems could contribute to age-related impairments in executive control and memory function. In this study we examined whether genetic polymorphisms for catechol-O-methyltransferase (COMT) and brain-derived neurotrophic factor (BDNF) were related to the trajectory of cognitive decline occurring over a 10-year period in older adults. A si...

Journal: :The American journal of psychiatry 2002
Jong-Min Woo Kyung-Sik Yoon Bum-Hee Yu

OBJECTIVE The authors examined the distribution of catechol O-methyltransferase (COMT) genotypes in patients with panic disorder as well as the relationship between a COMT polymorphism and the clinical characteristics of these patients. METHOD Fifty-one patients with panic disorder and 45 healthy comparison subjects were tested for a genetic polymorphism of COMT. Clinical variables were asses...

Journal: :Genetics and molecular research : GMR 2011
S F Tee P Y Tang H C Loh

Molecular components of the dopamine D3 receptor (DRD3) may play an important role in the pathophysiology of schizophrenia. Previous studies have demonstrated an association between DRD3 Ser9Gly and cathechol-o-methyltransferase (COMT, SNP = rs165656) polymorphisms and schizophrenia but the results were inconclusive. We investigated this apparent association between Ser9Gly (A/G) polymorph...

2006
Katie A Ashton Cliff J Meldrum Mary L McPhillips Janina Suchy Grzegorz Kurzawski Jan Lubinski Rodney J Scott

Catechol-O-methyltransferase (COMT) is vital for the conjugation of catechol estrogens that are produced during oestrogen metabolism. The efficiency of this process varies due to a polymorphism in COMT, which changes valine to methionine (V158M). The Met genotypes slow the metabolism of catechol oestrogens, which are agents that are capable of causing DNA damage through the formation of DNA add...

Journal: :The American journal of psychiatry 2006
Bronwyn Glaser Martin Debbane Christine Hinard Michael A Morris Sophie P Dahoun Stylianos E Antonarakis Stephan Eliez

OBJECTIVE Previous studies linking the catechol O-methyltransferase (COMT) functional polymorphism to the specific phenotype in 22q11.2 deletion syndrome (22q11.2DS) have yielded inconsistent results. The goal of the present study was to replicate a recent finding that executive function is higher in individuals hemizygous for the Met allele. METHOD Thirty-four children and young adults with ...

2013
Stephan Klebe Jean-Louis Golmard Michael A Nalls Mohamad Saad Andrew B Singleton Jose M Bras John Hardy Javier Simon-Sanchez Peter Heutink Gregor Kuhlenbäumer Rim Charfi Christine Klein Johann Hagenah Thomas Gasser Isabel Wurster Suzanne Lesage Delia Lorenz Günther Deuschl Franck Durif Pierre Pollak Philippe Damier François Tison Alexandra Durr Philippe Amouyel Jean-Charles Lambert Christophe Tzourio Cécilia Maubaret Fanny Charbonnier-Beaupel Khadija Tahiri Marie Vidailhet Maria Martinez Alexis Brice Jean-Christophe Corvol Y Agid M Anheim A-M Bonnet M Borg A. Brice E Broussolle J-C Corvol Ph. Damier A. Destée A Durr F Durif S Klebe E Lohmann M Martinez C Penet P Pollak P Krack O Rascol F Tison C Tranchant M Vérin F Viallet Vincent Plagnol Jose M Bras Dena G Hernandez Manu Sharma Una-Marie Sheerin Mohamad Saad Javier Simón-Sánchez Claudia Schulte Suzanne Lesage Sigurlaug Sveinbjörnsdóttir Philippe Amouyel Sampath Arepalli Gavin Band Roger A Barker Céline Bellinguez Yoav Ben-Shlomo Henk W Berendse Daniela Berg Kailash Bhatia Rob MA de Bie Alessandro Biffi Bas Bloem Zoltan Bochdanovits Michael Bonin Kathrin Brockmann Janet Brooks David J Burn Gavin Charlesworth Honglei Chen Patrick F Chinnery Sean Chong Carl E Clarke Mark R Cookson J Mark Cooper Jean Christophe Corvol Carl Counsell Philippe Damier Jean-François Dartigues Panos Deloukas David T Dexter Karin D van Dijk Allissa Dillman Frank Durif Sarah Edkins Jonathan R Evans Thomas Foltynie Colin Freeman Jianjun Gao Michelle Gardner Raphael Gibbs Alison Goate Emma Gray Rita Guerreiro Ómar Gústafsson Clare Harris Garrett Hellenthal Jacobus J van Hilten Albert Hofman Albert Hollenbeck Janice Holton Michele Hu Xuemei Huang Heiko Huber Gavin Hudson Sarah E Hunt Johanna Huttenlocher Thomas Illig Pálmi V Jónsson Cordelia Langford Andrew Lees Peter Lichtner Patricia Limousin Grisel Lopez Delia Lorenz Alisdair McNeill Catriona Moorby Huw Morris Karen E Morrison Ese Mudanohwo Sean S O'Sullivan Justin Pearson Richard Pearson Joel S Perlmutter Hjörvar Pétursson Matti Pirinen Pierre Pollak Bart Post Simon Potter Bernard Ravina Tamas Revesz Olaf Riess Fernando Rivadeneira Patrizia Rizzu Mina Ryten Stephen Sawcer Anthony Schapira Hans Scheffer Karen Shaw Ira Shoulson Ellen Sidransky Rohan de Silva Colin Smith Chris CA Spencer Hreinn Stefánsson Stacy Steinberg Joanna D Stockton Amy Strange Zhan Su Kevin Talbot Carlie M Tanner Avazeh Tashakkori-Ghanbaria François Tison Daniah Trabzuni Bryan J Traynor G Uitterlinden Jana Vandrovcova Daan Velseboer Marie Vidailhet Damjan Vukcevic Robert Walker Bart van de Warrenburg Michael E Weale Mirdhu Wickremaratchi Nigel Williams Caroline H Williams-Gray Sophie Winder-Rhodes Maria Martinez Peter Donnelly John Hardy Peter Heutink Alexis Brice Thomas Gasser Nicholas W Wood Andrew B Singleton

The catechol-O-methyltranferase (COMT) is one of the main enzymes that metabolise dopamine in the brain. The Val158Met polymorphism in the COMT gene (rs4680) causes a trimodal distribution of high (Val/Val), intermediate (Val/Met) and low (Met/Met) enzyme activity. We tested whether the Val158Met polymorphism is a modifier of the age at onset (AAO) in Parkinson's disease (PD). The rs4680 was ge...

Journal: :Schizophrenia Research 2013
Christiaan H. Vinkers Willemijn A. Van Gastel Christian D. Schubart Kristel R. Van Eijk Jurjen J. Luykx Ruud Van Winkel Marian Joëls Roel A. Ophoff Marco P.M. Boks

BACKGROUND Cannabis use and childhood maltreatment are independent risk factors for the development of psychotic symptoms. These factors have been found to interact in some but not all studies. One of the reasons may be that childhood maltreatment and cannabis primarily induce psychotic symptoms in genetically susceptible individuals. In this context, an extensively studied psychosis vulnerabil...

Journal: :Schizophrenia research 2008
Vina M Goghari Scott R Sponheim

Schizophrenia and bipolar disorder, although diagnostically separate, likely share elements of their genetic etiology. This study assessed whether the COMT Val158Met polymorphism has shared or specific associations with clinical phenotypes evident in schizophrenia and bipolar disorder. Schizophrenia and bipolar patients completed a clinical assessment encompassing premorbid functioning and curr...

2017
Vandana Rai Upendra Yadav Pradeep Kumar

Background: Catechol-O-methyltransferase (COMT) is an important estrogen-metabolizing enzyme. Numerous case-control studies have evaluated the role COMT Val 158Met (rs4680;472G->A) polymorphism in the risk of breast cancer and provided inconclusive results, hence present meta-analysis was designed to get a more reliable assessment in Asian population. Methods: A total of 26 articles were identi...

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