Cargando…
Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease
As the most common type of dementia, Alzheimer's disease (AD) is a neurodegenerative disorder initially manifested by impaired memory performances. While the diagnosis information indicates a dichotomous status of a patient, memory scores have the potential to capture the continuous nature of t...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374536/ https://www.ncbi.nlm.nih.gov/pubmed/25859259 http://dx.doi.org/10.3389/fgene.2015.00117 |
_version_ | 1782363506057674752 |
---|---|
author | Yan, Jingwen Kim, Sungeun Nho, Kwangsik Chen, Rui Risacher, Shannon L. Moore, Jason H. Saykin, Andrew J. Shen, Li |
author_facet | Yan, Jingwen Kim, Sungeun Nho, Kwangsik Chen, Rui Risacher, Shannon L. Moore, Jason H. Saykin, Andrew J. Shen, Li |
author_sort | Yan, Jingwen |
collection | PubMed |
description | As the most common type of dementia, Alzheimer's disease (AD) is a neurodegenerative disorder initially manifested by impaired memory performances. While the diagnosis information indicates a dichotomous status of a patient, memory scores have the potential to capture the continuous nature of the disease progression and may provide more insights into the underlying mechanism. In this work, we performed a targeted genetic study of memory scores on an AD cohort to identify the associations between a set of genes highly expressed in the hippocampal region and seven cognitive scores related to episodic memory. Both main effects and interaction effects of the targeted genetic markers on these correlated memory scores were examined. In addition to well-known AD genetic markers APOE and TOMM40, our analysis identified a new risk gene NAV2 through the gene-level main effect analysis. NAV2 was found to be significantly and consistently associated with all seven episodic memory scores. Genetic interaction analysis also yielded a few promising hits warranting further investigation, especially for the RAVLT list B Score. |
format | Online Article Text |
id | pubmed-4374536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43745362015-04-09 Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease Yan, Jingwen Kim, Sungeun Nho, Kwangsik Chen, Rui Risacher, Shannon L. Moore, Jason H. Saykin, Andrew J. Shen, Li Front Genet Genetics As the most common type of dementia, Alzheimer's disease (AD) is a neurodegenerative disorder initially manifested by impaired memory performances. While the diagnosis information indicates a dichotomous status of a patient, memory scores have the potential to capture the continuous nature of the disease progression and may provide more insights into the underlying mechanism. In this work, we performed a targeted genetic study of memory scores on an AD cohort to identify the associations between a set of genes highly expressed in the hippocampal region and seven cognitive scores related to episodic memory. Both main effects and interaction effects of the targeted genetic markers on these correlated memory scores were examined. In addition to well-known AD genetic markers APOE and TOMM40, our analysis identified a new risk gene NAV2 through the gene-level main effect analysis. NAV2 was found to be significantly and consistently associated with all seven episodic memory scores. Genetic interaction analysis also yielded a few promising hits warranting further investigation, especially for the RAVLT list B Score. Frontiers Media S.A. 2015-03-26 /pmc/articles/PMC4374536/ /pubmed/25859259 http://dx.doi.org/10.3389/fgene.2015.00117 Text en Copyright © 2015 Yan, Kim, Nho, Chen, Risacher, Moore, Saykin and Shen. 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) or licensor 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 | Genetics Yan, Jingwen Kim, Sungeun Nho, Kwangsik Chen, Rui Risacher, Shannon L. Moore, Jason H. Saykin, Andrew J. Shen, Li Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease |
title | Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease |
title_full | Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease |
title_fullStr | Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease |
title_full_unstemmed | Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease |
title_short | Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease |
title_sort | hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in alzheimer's disease |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374536/ https://www.ncbi.nlm.nih.gov/pubmed/25859259 http://dx.doi.org/10.3389/fgene.2015.00117 |
work_keys_str_mv | AT yanjingwen hippocampaltranscriptomeguidedgeneticanalysisofcorrelatedepisodicmemoryphenotypesinalzheimersdisease AT kimsungeun hippocampaltranscriptomeguidedgeneticanalysisofcorrelatedepisodicmemoryphenotypesinalzheimersdisease AT nhokwangsik hippocampaltranscriptomeguidedgeneticanalysisofcorrelatedepisodicmemoryphenotypesinalzheimersdisease AT chenrui hippocampaltranscriptomeguidedgeneticanalysisofcorrelatedepisodicmemoryphenotypesinalzheimersdisease AT risachershannonl hippocampaltranscriptomeguidedgeneticanalysisofcorrelatedepisodicmemoryphenotypesinalzheimersdisease AT moorejasonh hippocampaltranscriptomeguidedgeneticanalysisofcorrelatedepisodicmemoryphenotypesinalzheimersdisease AT saykinandrewj hippocampaltranscriptomeguidedgeneticanalysisofcorrelatedepisodicmemoryphenotypesinalzheimersdisease AT shenli hippocampaltranscriptomeguidedgeneticanalysisofcorrelatedepisodicmemoryphenotypesinalzheimersdisease AT hippocampaltranscriptomeguidedgeneticanalysisofcorrelatedepisodicmemoryphenotypesinalzheimersdisease |