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COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention

A common single nucleotide polymorphism (SNP) in the gene encoding catechol-O-methyltransferase (COMT), Val158Met, is thought to influence cognitive performance due to differences in prefrontal dopaminergic neurotransmission. Previous studies lend support for the hypothesis that the “at risk” genoty...

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Autores principales: Witte, Anja Veronica, Jansen, Stefanie, Schirmacher, Anja, Young, Peter, Flöel, Agnes
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990456/
https://www.ncbi.nlm.nih.gov/pubmed/21119769
http://dx.doi.org/10.3389/fnagi.2010.00146
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author Witte, Anja Veronica
Jansen, Stefanie
Schirmacher, Anja
Young, Peter
Flöel, Agnes
author_facet Witte, Anja Veronica
Jansen, Stefanie
Schirmacher, Anja
Young, Peter
Flöel, Agnes
author_sort Witte, Anja Veronica
collection PubMed
description A common single nucleotide polymorphism (SNP) in the gene encoding catechol-O-methyltransferase (COMT), Val158Met, is thought to influence cognitive performance due to differences in prefrontal dopaminergic neurotransmission. Previous studies lend support for the hypothesis that the “at risk” genotype comprising two Val-alleles (low dopamine) might benefit more from plasticity-enhancing interventions than carriers of one or two Met-alleles. This study aimed to determine whether the response to dietary interventions, known to modulate cognition, is dependent on COMT genotype. Blood samples of 35 healthy elderly subjects (61.3 years ±8 SD; 19 women, 16 men, BMI: 28.2 kg/m(2) ±4 SD) were genotyped for COMT Val158Met by standard procedures (Val/Val = 6; Val/Met = 20; Met/Met = 9). Subjects had previously completed a randomized controlled trial investigating the effects of caloric restriction (CR) or enhancement of unsaturated fatty acids (UFA) on immediate and delayed verbal recognition memory. Homozygous Val/Val-carriers had significantly lower memory scores than Met-carriers at baseline (p < 0.001). Significant interactions of genotype and dietary intervention with regard to cognition were found: CR- and UFA enhancement-induced memory improvements of Val/Val-carriers were considerably greater than those of Met-carriers (ANOVA p's < 0.02). The current study shows for the first time that cognitive effects of dietary interventions are dependent on COMT Val158Met genotype. Our findings lend further support to the hypothesis that an “at risk” genotype might benefit more from plasticity-enhancing interventions than the “not at risk” genotype. This might help to develop individualized therapies in future research based on genetic background.
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spelling pubmed-29904562010-11-30 COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention Witte, Anja Veronica Jansen, Stefanie Schirmacher, Anja Young, Peter Flöel, Agnes Front Aging Neurosci Neuroscience A common single nucleotide polymorphism (SNP) in the gene encoding catechol-O-methyltransferase (COMT), Val158Met, is thought to influence cognitive performance due to differences in prefrontal dopaminergic neurotransmission. Previous studies lend support for the hypothesis that the “at risk” genotype comprising two Val-alleles (low dopamine) might benefit more from plasticity-enhancing interventions than carriers of one or two Met-alleles. This study aimed to determine whether the response to dietary interventions, known to modulate cognition, is dependent on COMT genotype. Blood samples of 35 healthy elderly subjects (61.3 years ±8 SD; 19 women, 16 men, BMI: 28.2 kg/m(2) ±4 SD) were genotyped for COMT Val158Met by standard procedures (Val/Val = 6; Val/Met = 20; Met/Met = 9). Subjects had previously completed a randomized controlled trial investigating the effects of caloric restriction (CR) or enhancement of unsaturated fatty acids (UFA) on immediate and delayed verbal recognition memory. Homozygous Val/Val-carriers had significantly lower memory scores than Met-carriers at baseline (p < 0.001). Significant interactions of genotype and dietary intervention with regard to cognition were found: CR- and UFA enhancement-induced memory improvements of Val/Val-carriers were considerably greater than those of Met-carriers (ANOVA p's < 0.02). The current study shows for the first time that cognitive effects of dietary interventions are dependent on COMT Val158Met genotype. Our findings lend further support to the hypothesis that an “at risk” genotype might benefit more from plasticity-enhancing interventions than the “not at risk” genotype. This might help to develop individualized therapies in future research based on genetic background. Frontiers Research Foundation 2010-11-05 /pmc/articles/PMC2990456/ /pubmed/21119769 http://dx.doi.org/10.3389/fnagi.2010.00146 Text en Copyright © 2010 Witte, Jansen, Schirmacher, Young and Flöel. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Witte, Anja Veronica
Jansen, Stefanie
Schirmacher, Anja
Young, Peter
Flöel, Agnes
COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention
title COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention
title_full COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention
title_fullStr COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention
title_full_unstemmed COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention
title_short COMT Val158Met Polymorphism Modulates Cognitive Effects of Dietary Intervention
title_sort comt val158met polymorphism modulates cognitive effects of dietary intervention
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990456/
https://www.ncbi.nlm.nih.gov/pubmed/21119769
http://dx.doi.org/10.3389/fnagi.2010.00146
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