نتایج جستجو برای: comt 158valmet polymorphism

تعداد نتایج: 108502  

2013
Esther M. Opmeer Rudie Kortekaas Marie-José van Tol Nic J. A. van der Wee Saskia Woudstra Mark A. van Buchem Brenda W. Penninx Dick J. Veltman André Aleman

Major depressive disorder (MDD) has been associated with abnormal prefrontal-limbic interactions and altered catecholaminergic neurotransmission. The val158met polymorphism on the catechol-O-methyltransferase (COMT) gene has been shown to influence prefrontal cortex (PFC) activation during both emotional processing and working memory (WM). Although COMT-genotype is not directly associated with ...

Journal: :Schizophrenia bulletin 2010
Haraldur Magnus Haraldsson Ulrich Ettinger Brynja B Magnusdottir Thordur Sigmundsson Engilbert Sigurdsson Andres Ingason Hannes Petursson

The catechol-O-methyltransferase (COMT) enzyme catabolizes dopamine. The val(158)met single nucleotide polymorphism (rs4680) in the COMT gene has received considerable attention as a candidate gene for schizophrenia as well as for frontally mediated cognitive functions. Antisaccade performance is a good measure of frontal lobe integrity. Deficits on the task are considered a trait marker for sc...

2014
Emerson Barchi Cordts Monise Castro Santos Carla Peluso Erika Azuma Kayaki Bianca Bianco Caio Parente Barbosa Denise Maria Christofolini

BACKGROUND Estrogens are important factors in the female reproductive functions and are processed by a number of enzymes along their metabolic pathway. The COMT gene constitutes a crucial element in estrogen metabolism and is assumed to be involved in the development of Premature Ovarian Insufficiency (POI). This study aimed to determine whether the presence of the COMT Val/Met polymorphism (rs...

Journal: :Comprehensive psychiatry 2010
Zsolt Demetrovics Gabor Varga Anna Szekely Andrea Vereczkei Jozsef Csorba Hedvig Balazs Katalin Hoffman Maria Sasvari-Szekely Csaba Barta

BACKGROUND Candidate genes of the dopaminergic system have been reported as key elements in shaping human temperament. Catechol-O-methyltransferase (COMT) plays a vital role in dopamine inactivation, and the Val(158)Met single nucleotide polymorphism (rs4680) in its gene has been recently associated with the Novelty Seeking (NS) temperament scale of the Temperament and Character Inventory in st...

Journal: :Schizophrenia bulletin 2010
Boris B Quednow Michael Wagner Rainald Mössner Wolfgang Maier Kai-Uwe Kühn

It has been recently shown that Catechol O-methyltransferase (COMT) Val(158)Met polymorphism strongly influences prepulse inhibition (PPI) of the acoustic startle response (ASR) in healthy human volunteers. Given that schizophrenia patients exhibit impairment in PPI and that COMT is a putative susceptibility gene for schizophrenia, we investigated the impact of the COMT Val(158)Met polymorphism...

Journal: :Journal of child and adolescent psychopharmacology 2009
Christian E Waugh Karen F Dearing Jutta Joormann Ian H Gotlib

Low perceived social acceptance is a significant risk factor for emotional difficulties in children. No studies, however, have examined genetic factors that may underlie individual differences in perceived social acceptance. In the present study we examined the relation between polymorphisms on the catechol-O-methyltransferase (COMT) Val158Met and serotonin transporter promoter (5-HTTLPR) genes...

Journal: :The international journal of neuropsychopharmacology 2014
Jackob Moskovitz Consuelo Walss-Bass Dianne A Cruz Peter M Thompson Marco Bortolato

Catechol-O-methyl transferase (COMT) plays a key role in the degradation of brain dopamine (DA). Specifically, low COMT activity results in higher DA levels in the prefrontal cortex (PFC), thereby reducing the vulnerability for attentional and cognitive deficits in both psychotic and healthy individuals. COMT activity is markedly reduced by a non-synonymous single-nucleotide polymorphism (SNP) ...

Journal: :Folia neuropathologica 2012
Anahita Torkaman-Boutorabi Gholam Ali Shahidi Samira Choopani Mohammad Reza Zarrindast

Genetic polymorphisms have been shown to be involved in dopaminergic neurotransmission. This may influence susceptibility to Parkinson's disease (PD). We performed a case-control study of the association between PD susceptibility and a genetic polymorphism of MAOB and COMT, both separately and in combination, in Iranians. The study enrolled 103 Iranian patients with PD and 70 healthy individual...

2012
Lorena R. R. Gianotti Bernd Figner Richard P. Ebstein Daria Knoch

Individuals differ widely in how steeply they discount future rewards. The sources of these stable individual differences in delay discounting (DD) are largely unknown. One candidate is the COMT Val158Met polymorphism, known to modulate prefrontal dopamine levels and affect DD. To identify possible neural mechanisms by which this polymorphism may contribute to stable individual DD differences, ...

2016
Tijana Krnjeta Ljiljana Mirković Svetlana Ignjatović Dragana Tomašević Jelena Lukić Drina Topalov Ivan Soldatović Nada Majkić-Singh

BACKGROUND Up until now there have been contradictory data about the association between p.Val158Met catechol-O-methyltransferase (COMT) polymorphism and risk of preeclampsia (PE). The goal of this study was to assess the potential correlation between p.Val158Met COMT polymorphism and risk of early-onset PE, risk of a severe form of early-onset PE, as well as risk of small-for-gestational-age (...

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