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


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 07 08 2023
accepted: 21 04 2024
medline: 13 5 2024
pubmed: 13 5 2024
entrez: 13 5 2024
Statut: epublish

Résumé

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. 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). 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. 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).

Sections du résumé

BACKGROUND AND OBJECTIVES OBJECTIVE
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 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 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 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).

Identifiants

pubmed: 38739620
doi: 10.1371/journal.pone.0303343
pii: PONE-D-23-21633
doi:

Substances chimiques

Catechol O-Methyltransferase EC 2.1.1.6
COMT protein, human EC 2.1.1.6

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0303343

Informations de copyright

Copyright: © 2024 Apa et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Zoltan Apa (Z)

GIGA-CRC In Vivo Imaging, Université de Liège, Liège, Belgique.
Psychology and Neuroscience of Cognition Research Unit, Université de Liège, Liège, Belgique.

Jessica Gilsoul (J)

GIGA-CRC In Vivo Imaging, Université de Liège, Liège, Belgique.
Psychology and Neuroscience of Cognition Research Unit, Université de Liège, Liège, Belgique.

Vinciane Dideberg (V)

Department of Medical Genetics, University Hospital, Liège, Belgium.

Fabienne Collette (F)

GIGA-CRC In Vivo Imaging, Université de Liège, Liège, Belgique.
Psychology and Neuroscience of Cognition Research Unit, Université de Liège, Liège, Belgique.

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Classifications MeSH