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Associations between the COMT Val/Met polymorphism, early life stress, and personality among healthy adults
Journal article   Peer reviewed

Associations between the COMT Val/Met polymorphism, early life stress, and personality among healthy adults

Karin F Hoth, Robert H Paul, Leanne M Williams, Carol Dobson-Stone, Elizabeth Todd, Peter R Schofield, John Gunstad, Ronald A Cohen and Evian Gordon
Neuropsychiatric disease and treatment, Vol.2(2), pp.219-225
06/2006
DOI: 10.2147/nedt.2006.2.2.219
PMID: 19412467
url
https://www.ncbi.nlm.nih.gov/pmc/articles/2671786View
Open Access

Abstract

Efforts to identify genetic factors that confer an increased risk for the expression of psychiatric symptoms have focused on polymorphisms in variety of candidate genes, including the catechol-O-methyltransferase (\nCOMT\n) gene. Results from previous studies that have examined associations between the functional\nCOMT\npolymorphism (\nVal158Met\n) and mental health have been mixed. In the present study, we examined the relationships between\nCOMT\n, early life stress, and personality in a healthy adult sample. Consistent with previous studies, we hypothesized that individuals with the low-activity genotype would have higher neuroticism and lower extraversion and that this effect would be more pronounced in females. In addition, we extended the previous literature by investigating the potential influence of early life stress. A total of 486 healthy adults underwent genetic testing and personality assessment. Results revealed that individuals homozygous for the\nCOMT\nlow enzyme activity allele had lower extraversion on the NEO-FFI and demonstrated a trend toward greater neuroticism. These relationships were not influenced by sex or the presence of reported early life stress. The finding that\nCOMT\ngenotype was associated with extraversion, and more weakly with neuroticism, is consistent with previous studies. Future research to clarify the influence of sex and gene–environmental interactions is warranted.
anxiety depression Original Research early life stress gene-environment interaction

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