rs4680, COMT;MIR4761

N. diseases: 249
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE Sixty-four outpatients with BD in full or partial remission were stratified according to COMT Val158Met genotype (ValVal [n=13], ValMet [n=34], and MetMet [n=17]). 28544426 2017
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE The COMT Val158Met Polymorphism Is Associated With Response to Add-on Dextromethorphan Treatment in Bipolar Disorder. 27930497 2017
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE In support of this notion, rich evidence has documented that the severity of various BD and schizophrenia symptoms is moderated by rs4680, a single nucleotide polymorphism of the COMT gene featuring a valine (Val)-to-methionine (Met) substitution that results in lower catalytic activity. 27458023 2017
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE Catechol-O-methyltransferase (COMT) inactivates catecholamines, Val/Val genotype was associated to an increased amygdala (Amy) response to negative stimuli and can influence the symptoms severity and the outcome of bipolar disorder, probably mediated by the COMT polymorphism (rs4680) interaction between cortical and subcortical dopaminergic neurotransmission. 28049082 2017
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE This work first showed the association of combined Leu136Leu and Val158Met variants of COMT gene with MDD and BD. 25766270 2015
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE Allele G from COMT SNPs rs4680 and rs165599 may represent reliable state-dependent predictors of global CD during manic and mixed episodes in BD. 22713126 2012
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE 64 BD type I patients (39 in manic and 25 in depressive episodes) and 75 healthy controls were genotyped for COMT rs4680 and assessed for FER using the Ekman 60 Faces (EK60) and Emotion Hexagon (Hx) tests. 22222175 2012
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE The impact of the Val158Met catechol-O-methyltransferase genotype on neural correlates of sad facial affect processing in patients with bipolar disorder and their relatives. 20667170 2011
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE We suggest that rs4680 could be an inheritable aspect of the mechanisms of dopamine regulation that influence the individual susceptibility of patients with bipolar disorder to develop manic episodes of illness. 21397335 2011
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE The aim of this study is to examine the role of the COMT gene Val158Met polymorphism on the clinical aspects of bipolar disorder including symptomatology and therapeutic response. 20004480 2010
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE We suggest that rs4680 could be an inheritable aspect of the mechanisms of dopamine regulation that could influence the individual susceptibility of patients with bipolar disorder to develop psychotic symptoms. 20122740 2010
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE In conclusion, the low-activity allele (Met) of rs4680 in COMT gene possibly confers risk for bipolar disorder in the Han population, while it needs further evidence for concluding its association with BP in the Caucasian population. 19578924 2009
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE Findings support the COMT Val158Met polymorphism conferring vulnerability for different clinical phenotypes in schizophrenia and bipolar disorder. 18571901 2008
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE Here, we report the investigation of the differential activity of membrane-bound catechol-O-methyltransferase (MB-COMT) due to altered promoter methylation and the nature of the contribution of COMT Val158Met polymorphism as risk factors for schizophrenia and bipolar disorder by analyzing 115 post-mortem brain samples from the frontal lobe. 16984965 2006
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE Both the COMT Val158Met polymorphism and serological evidence of HSV-1 infection affect cognitive functioning in individuals with bipolar disorder. 16542182 2006
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.100 GeneticVariation BEFREE Because of its role in catecholamine metabolism and several lines of evidence pointing to a locus for psychosis near the COMT gene on chromosome 22q11, we have analysed the COMT Val158Met polymorphism as a candidate susceptibility factor for bipolar affective disorder. 9352569 1997