After a transgression, people often either tend to avoid the transgressor or seek revenge. These tendencies can be investigated via a trait approach and surprisingly little is known about their biological underpinnings. One promising candidate gene polymorphism, which may influence individual differences in avoidance of a transgressor and vengefulness, is the COMT Val158Met (rs4680) polymorphism known to affect dopaminergic signaling and among others brain activity in situations in which people punish others for their behavior. We therefore investigated the molecular genetics of individual differences in Avoidance Motivation and vengefulness with a focus on this polymorphism. Possible genetic associations were first investigated in a sample of = 730 Chinese participants ( = 196 females) using buccal cells to extract the DNA for genotyping. To replicate the findings we carried out a parallelized investigation in a sample of = 585 German participants ( = 399 females). Chinese and German versions of the TRIM-12 and the Vengeance Scale were implemented to assess individual differences in tendencies to react to a transgression. Results show that Met allele carriers of the COMT Val158Met polymorphism (Val/Met and Met/Met) score significantly higher on the tendency to avoid a transgressor in the Chinese male and female samples, with an especially pronounced effect in the female subgroup. The same effect could be found in the German sample, again especially in females. Additionally, carrying a Met allele was associated with higher vengefulness in the Chinese sample only, especially in males. The present findings indicate that the COMT Val158Met polymorphism might influence individual differences in the motivation to avoid transgressors across cultures, especially in females. However, its association with vengefulness seems to be more complex and may exhibit some cultural and gender specific effects.
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http://dx.doi.org/10.3389/fnbeh.2018.00148 | DOI Listing |
Eur J Neurosci
December 2024
Post-Graduated Program in Health and Behavior, Catholic University of Pelotas, Pelotas, Rio Grande do Sul, Brazil.
Neurobiol Aging
February 2025
Department of Psychology, School of Behavioral and Brain Sciences, Center for Vital Longevity, The University of Texas at Dallas, 1600 Viceroy Dr, Ste 800, Dallas, TX 75235 USA, United States. Electronic address:
Dopamine (DA) signaling is critical for optimal cognitive aging, especially in prefrontal-parietal and fronto-striatal networks. Single nucleotide polymorphisms associated with dopamine regulation, COMTVal158Met and DRD2C957T, stand to exert influence on executive function performance via neural properties. The current study investigated whether longitudinal thinning of mesocortical regions is related to COMT and DRD2 genetic predisposition and associated with decline in executive function over four-years.
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Department of Sports Medicine, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki 216-8511, Japan.
The balance of mental, physical, and technical aspects is essential in improving ballet performance. Ballet dancers' emotional and behavioral characteristics vary, even under identical stress conditions. This study aimed to investigate the association between the pain candidate genes 5-HTTLPR and COMT and anxiety in Japanese ballet dancers.
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Faculty of Physical Education, Gdansk University of Physical Education and Sport, 80-336 Gdańsk, Poland.
This narrative review examines the relationship between dopamine-related genetic polymorphisms, personality traits, and athletic success. Advances in sports genetics have identified specific single nucleotide polymorphisms (SNPs) in dopamine-related genes linked to personality traits crucial for athletic performance, such as motivation, cognitive function, and emotional resilience. This review clarifies how genetic variations can influence athletic predisposition through dopaminergic pathways and environmental interactions.
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October 2024
Discipline of Medical Genetics, Department of Microscopic Morphology, Center of Genomic Medicine, "Victor Babes" University of Medicine and Pharmacy, Eftimie Murgu Square 2, 300041 Timisoara, Romania.
Research on the interaction between antipsychotic treatment and cognitive dysfunction in schizophrenia spectrum disorders (SSDs) is extensive, yet the role of genetic polymorphisms in catechol-O-methyltransferase (COMT) and neuregulin 1 (NRG1) remains underexplored. : This study evaluates the impact of COMT (rs4680) and NRG1 (rs3924999 and rs35753505) polymorphisms on cognitive functions in SSD patients. A cross-sectional study was conducted with fifty-four patients, assessed using the Positive and Negative Syndrome Scale (PANSS) and the CNS Vital Signs battery.
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