rs4680 (Val158Met) is a well studied SNP in the COMT gene. 23andMe blog summarizes them as
- rs4680(A) = Worrier. Met, more exploratory, lower COMT enzymatic activity, therefore higher dopamine levels; lower pain threshold, enhanced vulnerability to stress, yet also more efficient at processing information under most conditions
- rs4680(G) = Warrior. Val, less exploratory, higher COMT enzymatic activity, therefore lower dopamine levels; higher pain threshold, better stress resiliency, albeit with a modest reduction in executive cognition performance under most conditions
Roughly speaking, the predominant wisdom (known colloquially as the warrior/worrier hypothesis; summary at [PMID 17008817]) posits that people with Val alleles have increased COMT activity and lower prefrontal extracellular dopamine compared with those with the Met substitution. Val158 alleles may be associated with an advantage in the processing of aversive stimuli (warrior strategy), while Met158 alleles may be associated with an advantage in memory and attention tasks (worrier strategy). Under conditions of increased dopamine release (eg, stress), individuals with Val158 alleles may have improved dopaminergic transmission and better performance, while individuals with Met158 alleles may have less efficient neurotransmission and worse performance. Some evidence suggests that Val158 alleles are associated with schizophrenia, while Met158 alleles are associated with anxiety.
Specific studies include:
rs4680, a functional Val/Met polymorphism, showed modest association with Irish familial schizophrenia. Haplotype A-G-A for SNPs rs737865-rs4680-rs165599 was preferentially transmitted to the affected subjects.
A study of 400 individuals reported that an increase in plasma total homocysteine (tHcy) of 10.4% (CI: 0.01-0.21, p=0.03) for associated with rs4680(A;A) homozygotes compared with rs4680(G;G) subjects. The (A;A) genotype was also more common, but statistically not that significantly, in venous thrombosis patients (OR 1.61, CI: 0.97-2.65], p=0.06) compared to control subjects.[PMID 18064318]
And from [PMID 15866551]: "Adolescent cannabis use was associated with increased risk of schizophreniform disorder in adulthood among Val/Val (i.e. rs4680(G;G)) individuals (OR = 10.9, 95% CI: 2.2â€“54.1) and, to a lesser extent, among Met/Val individuals (rs4680(A;G)); OR = 2.5, 95% CI: .78 â€“ 8.2), but not among Met/Met (rs4680(A;A)) individuals (OR = 1.1, 95% CI: .21â€“5.4)."
Also potentially associated with schizophrenia
In a study of 2 populations of breast cancer patients (2,000+ patients), increased risk was associated with rs4680(G;G) genotypes in both the Ontario [odds ratio 2.22, CI: 1.49-3.28] and Finland [OR 1.73, CI: 1.08-2.78] populations.[PMID 18194538]
23andMe blog The A version of rs4680 appears to boost working memory and cognitive function compared to G â€” but it also hampers emotional control.
[PMID 18704099] A study of 330 cocaine-dependent individuals, all of African descent, concluded that there was a slight (odds ratio 1.44, CI: 1.12-1.86, p = 0.014) association between the rs4680(A) allele, in other words the Met encoding allele, and cocaine dependence.
[PMID 18989660] A study of the antidepressant paroxetine found better response in Met/Met homozygotes, worse effects in Val/Val homozygotes and intermediate effects in heterozygotes. The effect became significant at the third week of treatment. Paroxetine daily dose was proportional to baseline severity, but did not influence outcome.
g2b2mh (A;A) subjects deploy more attentional focus when they realize they have made an error.
A meta-analysis of neuroimaging studies found a significant association between the COMT genotype and prefrontal activation; strong and opposing effects were found for executive cognition paradigms (favoring Met allele carriers) and emotional paradigms (favoring Val).[PMID 19417742]
[PMID 19037200] rs4680(G;G) carriers deprived of sleep respond quite well to 2x 100mg modafinil in terms of improved vigor and well-being, and maintained baseline performance with respect to executive functioning, whereas rs4680(A;A) individuals barely responded to the drug at all.
[PMID 16878403] Met158 allele carriers had "a more focused response...during a working memory task." "The met158 allele seems to be beneficial during the performance of working memory and attention-related tasks, whereas the val158 allele appears to be advantageous during the processing of aversive emotional stimuli."
[PMID 15673663] "Increased limbic and prefrontal activation elicited by unpleasant stimuli in subjects with more met158 alleles might contribute to the observed lower emotional resilience against negative mood states."
[PMID 12595695] In response to pain Met/Met allele carriers showed greater "sensory and affective ratings of pain and a more negative internal affective state. Opposite effects were observed in val158 homozygotes. The COMT val158met polymorphism thus influences the human experience of pain and may underlie interindividual differences in the adaptation and responses to pain and other stressful stimuli."
see gs226 for a report related to impulsiveness
[PMID 19367610] Gender-specific COMT Val158Met polymorphism association in Spanish schizophrenic patients
[PMID 19369177] Association of the 3' Region of COMT with Schizophrenia in Taiwan
[PMID 19417742] Neural substrates of pleiotropic action of genetic variation in COMT: a meta-analysis
[PMID 19290789] Association studies of catechol-O-methyltransferase (COMT) gene with schizophrenia and response to antipsychotic treatment
[PMID 19077118] Genetic variants in COMT and neurocognitive impairment in families of patients with schizophrenia
[PMID 19474754] Antidepressive-drug-induced bodyweight gain is associated with polymorphisms in genes coding for COMT and TPH1
http://www.jneurosci.org/cgi/content/abstract/30/1/64 and blog discussion of data about rs4680 thinking about nothing in an fmri.
[PMID 19915868] Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aborigines
[PMID 19946713] Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant
[PMID 20071037] Catechol-O-methyltransferase val108/158met genotype, major depressive disorder and response to selective serotonin reuptake inhibitors in major depressive disorder
[PMID 19690620] Polymorphisms of serotonin receptor 2A and 2C genes and COMT in relation to obesity and type 2 diabetes
[PMID 20150638] Association of COMT Haplotypes and Breast Cancer Risk in Caucasian Women
[PMID 20431430] The interaction between serotonin receptor 2A and catechol-O-methyltransferase gene polymorphisms is associated with the novelty-seeking subscale impulsiveness
[PMID 20488458] Heterozygosity at catechol-O-methyltransferase Val158Met and schizophrenia: New data and meta-analysis
[PMID 20934310] HapMap tag-SNP analysis confirms a role for COMT in schizophrenia risk and reveals a novel association
[PMID 20570835] No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain
[PMID 21084795] Acute Intravenous Synaptamine Complex Variant KB220™ "Normalizes" Neurological Dysregulation in Patients During Protracted Abstinence From Alcohol and Opiates as Observed Using Quantitative Electroencephalographic and Genetic Analysis for Reward Polymorphisms: Part 1, Pilot Study with 2 Case Reports
[PMID 21092186] Polymorphisms in genes involved in the estrogen pathway and mammographic density
[PMID 21120493] Influence of catechol-O-methyltransferase (COMT) gene polymorphisms in pain sensibility of Brazilian fibromialgia patients
[PMID 21191472] Genetic Association Between the COMT Genotype and Urinary Levels of Tea Polyphenols and Their Metabolites among Daily Green Tea Drinkers
[PMID 21300128] COMT Val158met variant and functional haplotypes associated with childhood ADHD history in women with bulimia nervosa
[PMID 10490706] Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype
[PMID 17949513] Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS
[PMID 21310591] Interaction between COMT haplotypes and cannabis in schizophrenia: A case-only study in two samples from Spain
[PMID 21449006] Role of COMT, 5-HT(1A) , and SERT genetic polymorphisms on antidepressant response to transcranial magnetic stimulation
[PMID 21567099] Estrogen metabolism genotypes, use of long-term hormone replacement therapy and risk of postmenopausal breast cancer
[PMID 21570824] Clinical and genetic factors associated with nausea and vomiting in cancer patients receiving opioids
[PMID 21595525] Sensory gating deficit is associated with catechol-O-methyltransferase polymorphisms in bipolar disorder
[PMID 21884617] Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults
[PMID 21934638] A COMT gene haplotype associated with methamphetamine abuse
[PMID 21940152] The impact of COMT gene polymorphisms on suicidality in treatment resistant major depressive disorder - A European Multicenter Study
[PMID 22067551] When control fails: Influence of the prefrontal but not striatal dopaminergic system on behavioural flexibility in a change detection task
[PMID 21947654] Cannabis, COMT and psychotic experiences
[PMID 22222175] COMT Met (158) modulates facial emotion recognition in bipolar I disorder mood episodes
[PMID 22337560] The COMT rs4680 Met allele contributes to long-lasting low back pain, sciatica and disability after lumbar disc herniation
[PMID 22417933] Variation in the catechol-O-methyltransferase (COMT) gene and treatment response to venlafaxine XR in generalized anxiety disorder
[PMID 22451510] Catechol-O-Methyltransferase Gene and Executive Function in Children With ADHD
[PMID 22479488] No Association of COMT (Val158Met) Genotype with Brain Structure Differences between Men and Women
[PMID 22475780] Association Between Val158Met Functional Polymorphism in the COMT Gene and Risk of Preeclampsia in a Chinese Population
[PMID 22528689] Pain sensitivity in fibromyalgia is associated with catechol-O-methyltransferase (COMT) gene
[PMID 22208661] A novel SNP in COMT is associated with alcohol dependence but not opiate or nicotine dependence : a case control study
[PMID 22178088] Catechol-O-methyltransferase (COMT) single nucleotide polymorphisms and haplotypes are not major risk factors for polycystic ovary syndrome
[PMID 22658813] Association Between Polymorphisms in COMT, PLCH1, and CYP17A1, and Non-Small-Cell Lung Cancer Risk in Chinese Nonsmokers
|CLNSRC||OMIM Allelic Variant|
[PMID 12802784] A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain.
[PMID 15098000] COMT haplotypes suggest P2 promoter region relevance for schizophrenia.
[PMID 15124004] Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families.
[PMID 15290009] Differential expression of human COMT alleles in brain and lymphoblasts detected by RT-coupled 5' nuclease assay.
[PMID 15457404] Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.
[PMID 15505638] Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia.
[PMID 15931594] An entropy-based statistic for genomewide association studies.
[PMID 15956988] COMT polymorphisms and anxiety-related personality traits.
[PMID 16027741] Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease.
[PMID 16232322] COMT genetic variation confers risk for psychotic and affective disorders: a case control study.
[PMID 16380905] Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios.
[PMID 16380908] Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder.
[PMID 16395295] Significant association of catechol-O-methyltransferase (COMT) haplotypes with nicotine dependence in male and female smokers of two ethnic populations.
[PMID 16412218] Multilocus analysis of SNP and metabolic data within a given pathway.
[PMID 16453988] Daytime sleepiness and the COMT val158met polymorphism in patients with Parkinson disease.
[PMID 16483362] The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression.
[PMID 16574089] PCR screening for 22q11.2 microdeletion: development of a new cost-effective diagnostic tool.
[PMID 16786032] Impact of complex genetic variation in COMT on human brain function.
[PMID 16816420] Nonlinear tests for genomewide association studies.
[PMID 16816940] Direct molecular haplotyping of multiple polymorphisms within exon 4 of the human catechol-O-methyltransferase gene by liquid chromatography-electrospray ionization time-of-flight mass spectrometry.
[PMID 16837108] Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease.
[PMID 16848906] Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.
[PMID 17006672] Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia.
[PMID 17116718] Dietary phytoestrogen intake is associated with reduced colorectal cancer risk.
[PMID 17299513] Gender-dependent association of the functional catechol-O-methyltransferase Val158Met genotype with sensation seeking personality trait.
[PMID 17363961] Clinical involvement of catechol-O-methyltransferase polymorphisms in schizophrenia spectrum disorders: influence on the severity of psychotic symptoms and on the response to neuroleptic treatment.
[PMID 17427186] Association analysis of COMT polymorphisms and schizophrenia in a Chinese Han population: a case-control study.
[PMID 17429315] Genetic polymorphisms in estrogen-metabolizing genes and breast cancer survival.
[PMID 17442488] An association study between cathechol-O-methyltransferase gene and mental retardation in the Chinese Han population.
[PMID 17466074] Genetic polymorphisms in dopamine-related genes and smoking cessation in women: a prospective cohort study.
[PMID 17482701] No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population.
[PMID 17483451] Gene-gene interaction associated with neural reward sensitivity.
[PMID 17504246] Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.
[PMID 17604122] A quantitative association study between schizotypal traits and COMT, PRODH and BDNF genes in a healthy Chinese population.
[PMID 17630406] Dopamine genes and schizophrenia: case closed or evidence pending?
[PMID 17636223] Val153Met polymorphism of catechol-O-methyltransferase and prevalence of uterine leiomyomata.
[PMID 17707347] Genetic variation in catechol-O-methyltransferase: effects on working memory in schizophrenic patients, their siblings, and healthy controls.
[PMID 17961261] Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia.
[PMID 17994190] Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults.
[PMID 18081002] Association of catechol-O-methyltransferase variants with loudness dependence of auditory evoked potentials.
[PMID 18180394] Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans.
[PMID 18196244] Polymorphisms of the serotonin-2A receptor and catechol-O-methyltransferase genes: a study on fibromyalgia susceptibility.
[PMID 18213617] Putative role of the COMT gene polymorphism (Val158Met) on verbal working memory functioning in a healthy population.
[PMID 18235427] Catechol-O-methyltransferase (COMT) val158met genotype is associated with BOLD response as a function of task characteristic.
[PMID 18324659] COMT polymorphisms affecting protein expression are risk factors for endometrial cancer.
[PMID 18340529] A prospective study of genetic polymorphism in MPO, antioxidant status, and breast cancer risk.
[PMID 18351593] DRD3, but not COMT or DRD2, genotype affects executive functions in healthy and first-episode psychosis adolescents.
[PMID 18384078] Association study of candidate variants of COMT with neuroticism, anxiety and depression.
[PMID 18389087] Rarity of Somatic Mutation and Frequency of Normal Sequence Variation Detected in Sporadic Colon Adenocarcinoma Using High-Throughput cDNA Sequencing.
[PMID 18408230] Structural cerebral variations as useful endophenotypes in schizophrenia: do they help construct "extended endophenotypes"?
[PMID 18436194] Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes.
[PMID 18444252] Neurotransmission and bipolar disorder: a systematic family-based association study.
[PMID 18466599] Linkage studies of catechol-O-methyltransferase (COMT) and dopamine-beta-hydroxylase (DBH) cDNA expression levels.
[PMID 18466879] Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample.
[PMID 18486967] A community-based study of cigarette smoking behavior in relation to variation in three genes involved in dopamine metabolism: Catechol-O-methyltransferase (COMT), dopamine beta-hydroxylase (DBH) and monoamine oxidase-A (MAO-A).
[PMID 18562342] Catechol-O-methyltransferase Val 158 Met polymorphism and antisaccade eye movements in schizophrenia.
[PMID 18574484] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
[PMID 18592033] Sex steroid-related candidate genes in psychiatric disorders.
[PMID 18628428] Polymorphisms in genes involved in sex hormone metabolism, estrogen plus progestin hormone therapy use, and risk of postmenopausal breast cancer.
[PMID 18698234] The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications.
[PMID 18715757] Genetic associations with schizophrenia: meta-analyses of 12 candidate genes.
[PMID 18755576] Effect of COMT val158met genotype on cognition and personality.
[PMID 18787887] Genetic variation in candidate osteoporosis genes, bone mineral density, and fracture risk: the study of osteoporotic fractures.
[PMID 18802928] Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults.
[PMID 18805939] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.
[PMID 18820009] Possible difference in frequencies of genetic polymorphisms of estrogen receptor alpha, estrogen metabolism and P53 genes between estrogen receptor-positive and -negative breast cancers.
[PMID 18929622] Dopamine 2 receptor C957T and catechol-o-methyltransferase Val158Met polymorphisms are associated with treatment response in electroconvulsive therapy.
[PMID 18937309] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.
[PMID 18988738] MTHFR 677C --> T genotype disrupts prefrontal function in schizophrenia through an interaction with COMT 158Val --> Met.
[PMID 19074205] Drinking green tea modestly reduces breast cancer risk.
[PMID 19094200] Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.
[PMID 19094875] [Effect of polymorphisms of the cathecol-O-methyltransferase on schizophrenia risk in a Spanish population].
[PMID 19127255] Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium.
[PMID 19174490] Tobacco and estrogen metabolic polymorphisms and risk of non-small cell lung cancer in women.
[PMID 19197363] A genome-wide investigation of SNPs and CNVs in schizophrenia.
[PMID 19258022] Now or Later? An fMRI study of the effects of endogenous opioid blockade on a decision-making network.
[PMID 19287484] Clique-finding for heterogeneity and multidimensionality in biomarker epidemiology research: the CHAMBER algorithm.
[PMID 19329282] Meta-analysis of association between genetic variants in COMT and schizophrenia: an update.
[PMID 19359258] Cohort profile: risk patterns and processes for psychopathology emerging during adolescence: the ROOTS project.
[PMID 19379518] Development of a fingerprinting panel using medically relevant polymorphisms.
[PMID 19520435] Acute antidepressant response to sleep deprivation combined with light therapy is influenced by the catechol-O-methyltransferase Val(108/158)Met polymorphism.
[PMID 19545856] Sensorimotor gating depends on polymorphisms of the serotonin-2A receptor and catechol-O-methyltransferase, but not on neuregulin-1 Arg38Gln genotype: a replication study.
[PMID 19578924] The Val/Met functional polymorphism in COMT confers susceptibility to bipolar disorder: evidence from an association study and a meta-analysis.
[PMID 19582565] Association of COMT (Val158Met) and BDNF (Val66Met) gene polymorphisms with anxiety, ADHD and tics in children with autism spectrum disorder.
[PMID 19584770] Variants in COMT and spontaneous smoking cessation: retrospective cohort analysis of 925 cessation events.
[PMID 19647329] COMT val(158)met genotype and smooth pursuit eye movements in schizophrenia.
[PMID 19664744] A genome-wide in vitro bacterial-infection screen reveals human variation in the host response associated with inflammatory disease.
[PMID 19693005] Executive function, neural circuitry, and genetic mechanisms in schizophrenia.
[PMID 19693267] Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene.
[PMID 19721400] Association between COMT gene and Chinese male schizophrenic patients with violent behavior.
[PMID 19852950] The association of catechol-O-methyltransferase genotype with the phenotype of women with eating disorders.
[PMID 19911060] Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.
[PMID 19940176] Functional variation of the dopamine D2 receptor gene is associated with emotional control as well as brain activity and connectivity during emotion processing in humans.
[PMID 20122740] Association between catechol-O-methyltransferase Val(108/158)Met polymorphism and psychotic features of bipolar disorder.
[PMID 20148275] Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.
[PMID 20179754] Genetically determined measures of striatal D2 signaling predict prefrontal activity during working memory performance.
[PMID 20191112] The Genetics of Anorexia Nervosa: Current Findings and Future Perspectives.
[PMID 20205808] Association between dopaminergic polymorphisms and borderline personality traits among at-risk young adults and psychiatric inpatients.
[PMID 20483479] Analysis of association between the catechol-O-methyltransferase (COMT) gene and negative symptoms in chronic schizophrenia.
[PMID 20531207] The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.
[PMID 20565774] Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project.
[PMID 20627703] The association of single nucleotide polymorphisms in the catechol-O-methyltransferase gene and pain scores in female patients with major depressive disorder.
[PMID 20667552] Catechol-o-methyltransferase gene modulation on suicidal behavior and personality traits: review, meta-analysis and association study.
[PMID 20728009] Association between Novelty Seeking of opiate-dependent patients and the catechol-O-methyltransferase Val(158)Met polymorphism.
[PMID 20863768] Association of catechol-O-methyltransferase genetic variants with outcome in patients undergoing surgical treatment for lumbar degenerative disc disease.
[PMID 20878621] Impact of CYP1A1 and COMT genotypes on breast cancer risk in Mexican women: a pilot study.
[PMID 20979431] Polymorphisms of COMT and XPD and risk of esophageal squamous cell carcinoma in a population of Yili Prefecture, in Xinjiang, China.
[PMID 21059181] Polymorphisms of adrenergic cardiovascular control genes are associated with adolescent chronic fatigue syndrome.
[PMID 21106664] Association of COMT Val(108/158)Met genotype and cigarette smoking in pregnant women.
[PMID 21144097] The impact of the catechol-O-methyltransferase genotype on the acute responsiveness of vascular reactivity to a green tea extract.
[PMID 21162693] Pharmacogenetics and antipsychotics: therapeutic efficacy and side effects prediction.
[PMID 21172166] Pharmacogenetics of antidepressant response.
[PMID 21215384] Interactive effects of DAOA (G72) and catechol-O-methyltransferase on neurophysiology in prefrontal cortex.
[PMID 21216270] Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands.
[PMID 21300759] EGFR L858R mutation and polymorphisms of genes related to estrogen biosynthesis and metabolism in never-smoking female lung adenocarcinoma patients.
[PMID 21304959] Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia.
[PMID 21330274] Pharmacogenetics of smoking cessation in general practice: results from the patch II and patch in practice trials.
[PMID 21355050] A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2).
[PMID 21356266] Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes.
[PMID 21423693] Effect sizes in experimental pain produced by gender, genetic variants and sensitization procedures.
[PMID 21445667] Variation in genes involved in dopamine clearance influence the startle response in older adults.
[PMID 21462137] [An association study of COMT gene polymorphisms with schizophrenia].
[PMID 21486391] The association between catechol-O-methyl-transferase Val108/158Met polymorphism and suicide.
[PMID 21495799] COMT polymorphism and the risk of endometriosis-related infertility.
[PMID 21508242] Dopaminergic genes predict individual differences in susceptibility to confirmation bias.
[PMID 21600957] COMT and age at onset in mood disorders: a replication and extension study.
[PMID 21609749] Role of functional dopaminergic gene polymorphisms in the etiology of idiopathic intellectual disability.
[PMID 21656904] Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations.
[PMID 21776034] Association of the catechol-O-methyl transferase gene Val158Met polymorphism with blood pressure and prevalence of hypertension: interaction with dietary energy intake.
[PMID 21895373] Psychological distress in fibromyalgia patients: a role for catechol-O-methyl-transferase Val158met polymorphism.
[PMID 21999147] Diverse facets of COMT: from a plausible predictive marker to a potential drug target for schizophrenia.
[PMID 22024485] Genetic associations with performance on a behavioral measure of distress intolerance.
[PMID 22259185] Additive effects of serotonergic and dopaminergic polymorphisms on trait impulsivity.
[PMID 22293393] Association between the catechol-O-methyltransferase (rs4680: Val158Met) polymorphism and serum alanine aminotransferase activity.
[PMID 22349272] Age modulates the effect of COMT genotype on delay discounting behavior.
[PMID 22366815] Anorexia nervosa and the Val158Met polymorphism of the COMT gene: meta-analysis and new data.
[PMID 22466345] Joint effects of smoking and gene variants involved in sex steroid metabolism on hot flashes in late reproductive-age women.
[PMID 22487365] C957T polymorphism of the dopamine D2 receptor gene is associated with motor learning and heart rate.
[PMID 22530780] Impact of five SNPs in dopamine-related genes on executive function.
[PMID 22963606] No association of catechol-o-methyltransferase polymorphisms with schizophrenia in the han chinese population
[PMID 22615781] Candidate gene-based association study of antipsychotic-induced movement disorders in long-stay psychiatric patients: a prospective study
[PMID 22978509] Convergence of Genome-Wide Association and Candidate Gene Studies for Alcoholism
[PMID 22707271] The impact of the catechol-O-methyltransferase genotype on vascular function and blood pressure after acute green tea ingestion
|qualified_impact||Insufficiently evaluated benign|
|summary||A codominant allele affecting COMT enzyme activity, considered a benign functional polymorphism.|
[PMID 23141115] The effects of the catechol-O-methyltransferase val158met polymorphism on white matter connectivity in patients with panic disorder
[PMID 22790479] Association of COMT gene polymorphisms with systemic atherosclerosis in elderly Japanese
[PMID 22612913] Genetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study
[PMID 23269216] Association between the COMT gene and rumination in a Hungarian sample
[PMID 23278923] The COMT Val/Met polymorphism is associated with reading-related skills and consistent patterns of functional neural activation
[PMID 23288874] Lack of Association of a Functional Catechol-O-Methyltransferase Gene Polymorphism With Risk of Tobacco Smoking: Results From a Multicenter Case-Control Study
[PMID 23370603] Catechol-O-Methyltransferase and Cytochrome P-450 1B1 Polymorphisms and Endometrial Cancer Risk: A Meta-analysis
[PMID 23369671] Genetic moderation of the association between regulatory focus and reward responsiveness: a proof-of-concept study
[PMID 23440431] Association of the COMT Met158 allele with trait impulsivity in healthy young adults
[PMID 23515273] Playing nice: a multi-methodological study on the effects of social conformity on memory
[PMID 23715639] The association between the catechol-O-methyltransferase Val108/158Met polymorphism and hyperactive-impulsive and inattentive symptoms in youth
[PMID 23728717] Common functional polymorphisms in SLC6A4 and COMT genes are associated with circadian phenotypes in a South American sample
[PMID 23785672] Genetic polymorphisms in CYP1A1, CYP1B1 and COMT genes in Greenlandic Inuit and Europeans
[PMID 23798967] No Effect of Serotoninergic Gene Variants on Response to Interpersonal Counseling and Antidepressants in Major Depression
[PMID 23353103] COMT and MTHFR polymorphisms interaction on cognition in schizophrenia: an exploratory study
[PMID 23840506] Multivariate analysis of dopaminergic gene variants as risk factors of heroin dependence
[PMID 23880798] No association between germline variation in catechol-O-methyltransferase and colorectal cancer survival in postmenopausal women
[PMID 23928748] Impact of COMT genotype on serotonin-1A receptor binding investigated with PET
[PMID 23941313] Influence of a Dopamine Pathway Additive Genetic Efficacy Score on Smoking Cessation: Results from Two Randomized Clinical Trials of Bupropion
[PMID 24167357] COMT-Val158Met-Polymorphism Is Not a Risk Factor for Acute Kidney Injury after Cardiac Surgery
[PMID 24320736] Role of single nucleotide polymorphisms in estrogen-metabolizing enzymes and susceptibility to uterine leiomyoma in Han Chinese: A case-control study
[PMID 24382678] Association between maternal COMT gene polymorphisms and fetal neural tube defects risk in a Chinese population
[PMID 24399714] BDNF rs 6265 polymorphism and COMT rs 4680 polymorphism in deficit schizophrenia in Polish sample
[PMID 24407958] Risky alcohol consumption in young people is associated with the fatty acid amide hydrolase gene polymorphism C385A and affective rating of drug pictures
[PMID 24448899] Metabolic syndrome in patients taking clozapine: prevalence and influence of catechol-O-methyltransferase genotype
[PMID 24499375] Association of Oxidative Stress Related Genes with Idiopathic Recurrent Miscarriage
[PMID 23706899] Catechol-O-methyltransferase genotype as modifier of superior responses to venlafaxine treatment in major depressive disorder
[PMID 24575113] Association between the COMTVal158Met Genotype and Alzheimer's Disease in the Han Chinese Population