Association between executive functions and COMT Val108/158Met polymorphism among healthy younger and older adults: A preliminary study

PLoS One. 2024 May 13;19(5):e0303343. doi: 10.1371/journal.pone.0303343. eCollection 2024.

Abstract

Background and objectives: Genetic variability in the dopaminergic system could contribute to age-related impairments in executive control. In this study, we examined whether genetic polymorphism for catechol-O-methyltransferase (COMT Val158Met) is related to performance on updating, shifting and inhibition tasks.

Methods: We administered a battery of executive tasks assessing updating, shifting and inhibition functions to 45 older and 55 younger healthy participants, and created composite z-scores associated to each function. Six groups were created based on genetic alleles (Val/Val, Val/Met, Met/Met) derived from the COMT gene and age (younger, older). Age and genotype effects were assessed with t-test and ANOVA (p<0.05).

Results: A lower performance was observed in the older group for the three executive processes, and more particularly for inhibition. Moreover, older participants homozygous for the Val allele have a lower performance on the inhibition composite in comparison to younger Val/Val.

Conclusions: These results confirm presence of executive performance decrease in healthy aging. With regard to genetic effect, older participants seem particularly disadvantaged when they have a lower baseline dopamine level (i.e., Val/Val homozygous) that is magnified by aging, and when the executive measure emphasize the need of stable representations (as in inhibition task requiring to maintain active the instruction to not perform an automated process).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aging / genetics
  • Aging / physiology
  • Alleles
  • Catechol O-Methyltransferase* / genetics
  • Executive Function* / physiology
  • Female
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Young Adult

Substances

  • Catechol O-Methyltransferase
  • COMT protein, human

Grants and funding

This work was supported by the University of Liège and grant EOS 30446199 from the Belgian National Fund for Scientific Research F.R.S-FNRS. JG and ZA are research fellows (FNRS and University of Liège, respectively) and FC is Research Director at the F.R.S-FNRS.