نتایج جستجو برای: comt 158valmet polymorphism

تعداد نتایج: 108502  

Journal: :International journal of geriatric psychiatry 2009
G G Potter W D Taylor D R McQuoid D C Steffens K A Welsh-Bohmer K R R Krishnan

OBJECTIVE The objective of the current study was to examine the relationship between the COMT Val(158)Met polymorphism and neuropsychological performance in depressed and nondepressed older adults. METHODS One hundred and twenty-six clinically depressed older adults and 105 nondepressed comparison participants were compared on neuropsychological performance and COMT Val(158)Met (Val/Val, Val/...

Journal: :Brain : a journal of neurology 2006
Takashi Ohnishi Ryota Hashimoto Takeyuki Mori Kiyotaka Nemoto Yoshiya Moriguchi Hidehiro Iida Hiroko Noguchi Tetsuo Nakabayashi Hiroaki Hori Mayu Ohmori Ryoutaro Tsukue Kimitaka Anami Naotugu Hirabayashi Seiichi Harada Kunimasa Arima Osamu Saitoh Hiroshi Kunugi

The catechol-O-methyl transferase (COMT) gene is considered to be a promising schizophrenia susceptibility gene. A common functional polymorphism (Val158Met) in the COMT gene affects dopamine regulation in the prefrontal cortex (PFC). Recent studies suggest that this polymorphism contributes to poor prefrontal functions, particularly working memory, in both normal individuals and patients with ...

2014
Xiang Tan Mingwu Chen

BACKGROUND The association between the Val158Met polymorphism in the catechol-O-methyltransferase (COMT) gene and lung cancer risk remains controversial and inconclusive. Therefore, the meta-analysis was performed to provide a quality reevaluation of the association between the COMT Val158Met polymorphism and the risk of lung cancer. METHODS Two major public databases (Pubmed and Embase) and ...

2016
Ruth de Diego-Balaguer Catherine Schramm Isabelle Rebeix Emmanuel Dupoux Alexandra Durr Alexis Brice Perrine Charles Laurent Cleret de Langavant Katia Youssov Christophe Verny Vincent Damotte Jean-Philippe Azulay Cyril Goizet Clémence Simonin Christine Tranchant Patrick Maison Amandine Rialland David Schmitz Charlotte Jacquemot Bertrand Fontaine Anne-Catherine Bachoud-Lévi

Little is known about the genetic factors modulating the progression of Huntington's disease (HD). Dopamine levels are affected in HD and modulate executive functions, the main cognitive disorder of HD. We investigated whether the Val158Met polymorphism of the catechol-O-methyltransferase (COMT) gene, which influences dopamine (DA) degradation, affects clinical progression in HD. We carried out...

Journal: :Journal of Clinical Neurology (Seoul, Korea) 2007
Jeong Wook Park Kwang Soo Lee Joong Seok Kim Yeong In Kim Hae Eun Shin

BACKGROUND Recent genetic association studies have investigated the possible genetic role of the dopaminergic system in migraine. Catechol-O-methyltransferase (COMT) is an enzyme that plays a crucial role in the metabolism of dopamine and its genetic polymorphism is associated with three- to fourfold variation of enzymatic activity. OBJECTIVES The objective of this study was to elucidate the ...

2014
Esma Ozturk Deveci Adnan Incebiyik Salih Selek Aysun Camuzcuoglu Nese Gul Hilali Hakan Camuzcuoglu Mehmet Emin Erdal Mehmet Vural

OBJECTIVE The objective of this study was to investigate whether there was a correlation between catechol-o-methyltransferase (COMT) gene polymorphism, which is believed to play a role in the etiology of psychotic disorders, and premenstrual syndrome (PMS). METHODS Fifty-three women with regular menstrual cycles, aged between 18 and 46 years and diagnosed with PMS according to the American Co...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2008
Francesco Papaleo Jacqueline N Crawley Jian Song Barbara K Lipska Jim Pickel Daniel R Weinberger Jingshan Chen

The COMT (catechol-O-methyltransferase) gene has been linked to a spectrum of human phenotypes, including cognition, anxiety, pain sensitivity and psychosis. Doubts about its clinical impact exist, however, because of the complexity of human COMT polymorphism and clinical variability. We generated transgenic mice overexpressing a human COMT-Val polymorphism (Val-tg), and compared them with mice...

Journal: :Schizophrenia research 2007
Haiyan Xu Christoph B Kellendonk Eleanor H Simpson John G Keilp Gerard E Bruder H Jonathan Polan Eric R Kandel T Conrad Gilliam

The C957T polymorphism in the dopamine D2 receptor (DRD2) gene and the Val158Met polymorphism in the Catechol-O-Methyl-Transferase (COMT) gene affect dopamine transmission and have been found to be associated with schizophrenia. Since DRD2 in mice and the COMT gene in humans modulate working memory, we examined the relationship and possible interaction of both polymorphisms to working memory pe...

Journal: :BMC Musculoskeletal Disorders 2006
Knut Hagen Elin Pettersen Lars Jacob Stovner Frank Skorpen John-Anker Zwart

BACKGROUND The Catechol-O-methyltransferase (COMT) gene contains a functional polymorphism, Val158Met, that has been found to influence human pain perception. In one study fibromyalgia was less likely among those with Val/Val genotype. METHODS In the 1995-97 Nord-Trøndelag Health Study (HUNT), the association between Val/Met polymorphism at the COMT gene and chronic musculoskeletal complaints...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2000
J E Goodman J A Lavigne J G Hengstler B Tanner K J Helzlsouer J D Yager

A valine-108-methionine polymorphism in exon 4 of the catechol-O-methyltransferase (COMT) gene causes a 3- to 4-fold reduction in enzyme activity and has been associated with an increased risk of breast cancer. This increased risk may be attributable to a decreased ability of the protein encoded by the low-activity allele (COMT(L)) to methylate and inactivate catechol estrogens, which have been...

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