COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 Biomarker disease HPO
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE Catechol-O-methyltransferase Val(108/158)Met polymorphism affects fronto-limbic connectivity during emotional processing in bipolar disorder. 28049082 2017
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 Biomarker disease PSYGENET A gene coexpression network was developed based on a mutual information approach including four candidate genes (NRG1, DISC1, BDNF and COMT) along with other coexpressing genes in unipolar disorder, bipolar disorder and schizophrenia. 22777684 2012
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE A significant association between bipolar disorder and COMT polymorphisms was found. 15211633 2004
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease LHGDN A significant association between bipolar disorder and COMT polymorphisms was found. 15211633 2004
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease 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
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE Association between catechol-O-methyltransferase Val(108/158)Met polymorphism and psychotic features of bipolar disorder. 20122740 2010
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE Associations with the COMT polymorphism were absent in relatives of patients with bipolar disorder and control participants. 19025226 2008
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 Biomarker disease PSYGENET Because dopaminergic disturbance is thought to be involved in the development of bipolar disorder (BPD), it seems essential to investigate dopamine-related genes like the catechol-O-methyltransferase (COMT) gene, which are involved in dopamine metabolism, and the methylenetetrahydrofolate reductase (MTHFR) gene, which may affect COMT methylation and COMT function. 25744938 2015
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE Cognitive manic symptoms in bipolar disorder associated with polymorphisms in the DAOA and COMT genes. 23861766 2013
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 Biomarker disease PSYGENET Cognitive manic symptoms in bipolar disorder associated with polymorphisms in the DAOA and COMT genes. 23861766 2013
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE Findings support the COMT Val158Met polymorphism conferring vulnerability for different clinical phenotypes in schizophrenia and bipolar disorder. 18571901 2008
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease LHGDN Findings support the COMT Val158Met polymorphism conferring vulnerability for different clinical phenotypes in schizophrenia and bipolar disorder. 18571901 2008
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE Genetic variation at the catechol-O-methyltransferase (COMT) gene has been significantly associated with risk for various neuropsychiatric conditions such as schizophrenia, panic disorder, bipolar disorders, anorexia nervosa and others. 18574484 2010
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 Biomarker disease PSYGENET Genotyping for COMT polymorphisms was carried out by DNA direct sequencing in 112 patients (54 MDD and 58 BD) and 58 healthy subjects. 25766270 2015
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease 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
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE In conclusion, we partially replicated our previous findings confirming a possible influence of COMT variants in MD and BD, particularly in early onset subjects, though not with the same risk genotypes. 21600957 2011
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 Biomarker disease BEFREE In this paper, we review extant studies involving neurocognitive-genetic and neuroimaging-genetic perspectives and particularly related to catechol-O-methyltransferase (COMT), brain-derived neurotrophic factor (BDNF) and neuregulin-1 (NRG1) genes in SZ and BD. 21688113 2011
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE In this study, we first investigate the possible association between the Val/Met polymorphism in COMT and bipolar disorder in the Han population, which has never been done before. 19578924 2009
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE Influence of the catechol-O-methyltransferase Val108/158Met polymorphism on the plasma concentration of catecholamine metabolites and on clinical features in type I bipolar disorder--a preliminary report. 16542735 2006
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 AlteredExpression disease BEFREE It has been suggested that a common functional genetic polymorphism in the COMT gene, which results in 3 to 4-fold difference in COMT enzyme activity, may contribute to the etiology of mental disorders such as bipolar disorder and alcoholism. 10395222 1999
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 GeneticVariation disease BEFREE Lack of association of catechol-O-methyltransferase (COMT) functional polymorphism in bipolar affective disorder. 9264133 1997
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 Biomarker disease BEFREE Monoaminergic dysfunction has been implicated in the pathogenesis of BP, it may be important to investigate genes such as the catechol-O-methyltransferase (COMT), involved in monoamine metabolism and brain-derived neurotrophic factor (BDNF) genes, modulating the monoamine system. 23026378 2013
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 Biomarker disease BEFREE Moreover, COMT was risk factor for onset of both major depression and bipolar disorder, in conjunction with adversities. 16756688 2007
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 AlteredExpression disease BEFREE Nevertheless, the specific relevance of COMT enzymatic activity in the pathophysiology of BD and schizophrenia dimensions remains elusive. 27458023 2017