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Association between the serotonin transporter gene polymorphism and verbal learning in older adults is moderated by gender

The S allele of the functional 5-HTTLPR polymorphism has previously been associated with reductions in memory function. Given the change in function of the serotonergic system in older adults, and the functional consequences of memory decline in this age group, further investigation into the impact...

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Autores principales: Imlach, A-R, Ward, D D, Vickers, J C, Summers, M J, Felmingham, K L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537635/
https://www.ncbi.nlm.nih.gov/pubmed/28585929
http://dx.doi.org/10.1038/tp.2017.107
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author Imlach, A-R
Ward, D D
Vickers, J C
Summers, M J
Felmingham, K L
author_facet Imlach, A-R
Ward, D D
Vickers, J C
Summers, M J
Felmingham, K L
author_sort Imlach, A-R
collection PubMed
description The S allele of the functional 5-HTTLPR polymorphism has previously been associated with reductions in memory function. Given the change in function of the serotonergic system in older adults, and the functional consequences of memory decline in this age group, further investigation into the impact of 5-HTTLPR in healthy older adults is required. This investigation examined the effect of 5-HTTLPR variants (S carriers versus L/L homozygotes) on verbal and visual episodic memory in 438 healthy older adults participating in the Tasmanian Healthy Brain Project (age range 50–79 years, M=60.35, s.d.=6.75). Direct effects of 5-HTTLPR on memory processes, in addition to indirect effects through interaction with age and gender, were assessed. Although no direct effects of 5-HTTLPR on memory processes were identified, our results indicated that gender significantly moderated the impact that 5-HTTLPR variants exerted on the relationship between age and verbal episodic memory function as assessed by the Rey Auditory Verbal Learning Test. No significant direct or indirect effects were identified in relation to visual memory performance. Overall, this investigation found evidence to suggest that 5-HTTLPR genotype affects the association of age and verbal episodic memory for males and females differently, with the predicted negative effect of S carriage present in males but not females. Such findings indicate a gender-dependent role for 5-HTTLPR in the verbal episodic memory system of healthy older adults.
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spelling pubmed-55376352017-08-02 Association between the serotonin transporter gene polymorphism and verbal learning in older adults is moderated by gender Imlach, A-R Ward, D D Vickers, J C Summers, M J Felmingham, K L Transl Psychiatry Original Article The S allele of the functional 5-HTTLPR polymorphism has previously been associated with reductions in memory function. Given the change in function of the serotonergic system in older adults, and the functional consequences of memory decline in this age group, further investigation into the impact of 5-HTTLPR in healthy older adults is required. This investigation examined the effect of 5-HTTLPR variants (S carriers versus L/L homozygotes) on verbal and visual episodic memory in 438 healthy older adults participating in the Tasmanian Healthy Brain Project (age range 50–79 years, M=60.35, s.d.=6.75). Direct effects of 5-HTTLPR on memory processes, in addition to indirect effects through interaction with age and gender, were assessed. Although no direct effects of 5-HTTLPR on memory processes were identified, our results indicated that gender significantly moderated the impact that 5-HTTLPR variants exerted on the relationship between age and verbal episodic memory function as assessed by the Rey Auditory Verbal Learning Test. No significant direct or indirect effects were identified in relation to visual memory performance. Overall, this investigation found evidence to suggest that 5-HTTLPR genotype affects the association of age and verbal episodic memory for males and females differently, with the predicted negative effect of S carriage present in males but not females. Such findings indicate a gender-dependent role for 5-HTTLPR in the verbal episodic memory system of healthy older adults. Nature Publishing Group 2017-06 2017-06-06 /pmc/articles/PMC5537635/ /pubmed/28585929 http://dx.doi.org/10.1038/tp.2017.107 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Imlach, A-R
Ward, D D
Vickers, J C
Summers, M J
Felmingham, K L
Association between the serotonin transporter gene polymorphism and verbal learning in older adults is moderated by gender
title Association between the serotonin transporter gene polymorphism and verbal learning in older adults is moderated by gender
title_full Association between the serotonin transporter gene polymorphism and verbal learning in older adults is moderated by gender
title_fullStr Association between the serotonin transporter gene polymorphism and verbal learning in older adults is moderated by gender
title_full_unstemmed Association between the serotonin transporter gene polymorphism and verbal learning in older adults is moderated by gender
title_short Association between the serotonin transporter gene polymorphism and verbal learning in older adults is moderated by gender
title_sort association between the serotonin transporter gene polymorphism and verbal learning in older adults is moderated by gender
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537635/
https://www.ncbi.nlm.nih.gov/pubmed/28585929
http://dx.doi.org/10.1038/tp.2017.107
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