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Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers

Introduction: SuperAgers are adults age 80+ with episodic memory performance that is at least as good as that of average middle-aged adults. Understanding the biological determinants of SuperAging may have relevance to preventing age-related cognitive decline and dementia. This study aimed to identi...

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Autores principales: Huentelman, Matthew J., Piras, Ignazio S., Siniard, Ashley L., De Both, Matthew D., Richholt, Ryan F., Balak, Chris D., Jamshidi, Pouya, Bigio, Eileen H., Weintraub, Sandra, Loyer, Emmaleigh T., Mesulam, M.-Marsel, Geula, Changiz, Rogalski, Emily J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987172/
https://www.ncbi.nlm.nih.gov/pubmed/29896098
http://dx.doi.org/10.3389/fnagi.2018.00155
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author Huentelman, Matthew J.
Piras, Ignazio S.
Siniard, Ashley L.
De Both, Matthew D.
Richholt, Ryan F.
Balak, Chris D.
Jamshidi, Pouya
Bigio, Eileen H.
Weintraub, Sandra
Loyer, Emmaleigh T.
Mesulam, M.-Marsel
Geula, Changiz
Rogalski, Emily J.
author_facet Huentelman, Matthew J.
Piras, Ignazio S.
Siniard, Ashley L.
De Both, Matthew D.
Richholt, Ryan F.
Balak, Chris D.
Jamshidi, Pouya
Bigio, Eileen H.
Weintraub, Sandra
Loyer, Emmaleigh T.
Mesulam, M.-Marsel
Geula, Changiz
Rogalski, Emily J.
author_sort Huentelman, Matthew J.
collection PubMed
description Introduction: SuperAgers are adults age 80+ with episodic memory performance that is at least as good as that of average middle-aged adults. Understanding the biological determinants of SuperAging may have relevance to preventing age-related cognitive decline and dementia. This study aimed to identify associations between genetic variations and the SuperAging phenotype using Whole Exome Sequencing (WES). Methods: Sequence Kernel Association Combined (SKAT-C) test was conducted at the gene level including both rare and common variants in 56 SuperAgers and 22 cognitively-average controls from the Alzheimer’s disease Neuroimaging Initiative (ADNI). Results: The SuperAging phenotype was associated with variants in the Mitogen-Activated Protein Kinase Kinase 3 (MAP2K3) gene. Three single nucleotide polymorphisms (SNPs) contributed to the significance (rs2363221 [intron 1], rs2230435 [exon 5], rs736103 [intron 7]). Conclusions: MAP2K3 resides in a biological pathway linked to memory. It is in a signaling cascade associated with beta-amyloid mediated apoptosis and has enriched expression in microglia. This preliminary work suggests MAP2K3 may represent a novel therapeutic target for age-related memory decline and perhaps Alzheimer’s disease (AD).
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spelling pubmed-59871722018-06-12 Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers Huentelman, Matthew J. Piras, Ignazio S. Siniard, Ashley L. De Both, Matthew D. Richholt, Ryan F. Balak, Chris D. Jamshidi, Pouya Bigio, Eileen H. Weintraub, Sandra Loyer, Emmaleigh T. Mesulam, M.-Marsel Geula, Changiz Rogalski, Emily J. Front Aging Neurosci Neuroscience Introduction: SuperAgers are adults age 80+ with episodic memory performance that is at least as good as that of average middle-aged adults. Understanding the biological determinants of SuperAging may have relevance to preventing age-related cognitive decline and dementia. This study aimed to identify associations between genetic variations and the SuperAging phenotype using Whole Exome Sequencing (WES). Methods: Sequence Kernel Association Combined (SKAT-C) test was conducted at the gene level including both rare and common variants in 56 SuperAgers and 22 cognitively-average controls from the Alzheimer’s disease Neuroimaging Initiative (ADNI). Results: The SuperAging phenotype was associated with variants in the Mitogen-Activated Protein Kinase Kinase 3 (MAP2K3) gene. Three single nucleotide polymorphisms (SNPs) contributed to the significance (rs2363221 [intron 1], rs2230435 [exon 5], rs736103 [intron 7]). Conclusions: MAP2K3 resides in a biological pathway linked to memory. It is in a signaling cascade associated with beta-amyloid mediated apoptosis and has enriched expression in microglia. This preliminary work suggests MAP2K3 may represent a novel therapeutic target for age-related memory decline and perhaps Alzheimer’s disease (AD). Frontiers Media S.A. 2018-05-29 /pmc/articles/PMC5987172/ /pubmed/29896098 http://dx.doi.org/10.3389/fnagi.2018.00155 Text en Copyright © 2018 Huentelman, Piras, Siniard, De Both, Richholt, Balak, Jamshidi, Bigio, Weintraub, Loyer, Mesulam, Geula and Rogalski for The Alzheimer’s Disease Neuroimaging Initiative. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Huentelman, Matthew J.
Piras, Ignazio S.
Siniard, Ashley L.
De Both, Matthew D.
Richholt, Ryan F.
Balak, Chris D.
Jamshidi, Pouya
Bigio, Eileen H.
Weintraub, Sandra
Loyer, Emmaleigh T.
Mesulam, M.-Marsel
Geula, Changiz
Rogalski, Emily J.
Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers
title Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers
title_full Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers
title_fullStr Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers
title_full_unstemmed Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers
title_short Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers
title_sort associations of map2k3 gene variants with superior memory in superagers
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987172/
https://www.ncbi.nlm.nih.gov/pubmed/29896098
http://dx.doi.org/10.3389/fnagi.2018.00155
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