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Stroke and Alzheimer’s Disease: A Mendelian Randomization Study

Stroke and Alzheimer’s disease (AD) are common neurological diseases. Several exiting studies indicated that late onset-AD and ischemic stroke have shared genetic links. Different kinds of stroke have different mechanisms. However, it remains unclear whether there is a causal relationship between di...

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Autores principales: Wang, Tao, Ni, Qing-bin, Wang, Kun, Han, Zhifa, Sun, Bao-liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371994/
https://www.ncbi.nlm.nih.gov/pubmed/32760421
http://dx.doi.org/10.3389/fgene.2020.00581
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author Wang, Tao
Ni, Qing-bin
Wang, Kun
Han, Zhifa
Sun, Bao-liang
author_facet Wang, Tao
Ni, Qing-bin
Wang, Kun
Han, Zhifa
Sun, Bao-liang
author_sort Wang, Tao
collection PubMed
description Stroke and Alzheimer’s disease (AD) are common neurological diseases. Several exiting studies indicated that late onset-AD and ischemic stroke have shared genetic links. Different kinds of stroke have different mechanisms. However, it remains unclear whether there is a causal relationship between different types of strokes, including any stroke (AS), any ischemic stroke (AIS), large-artery atherosclerotic stroke (LAS), and cardio-embolic stroke (CES), and AD. Herein, we conducted several Mendelian randomization (MR) studies to explore genetically causal link of different kinds of strokes and AD. The results for inverse-variance weighted (IVW) meta-analysis (β = −0.039, OR = 0.9618, and P-value = 0.750) and weighted median regression (WMR) (β = −0.156, OR = 0.8556, and P-value = 0.274) demonstrated that AS is not causally associated with AD risk. The result of MR-Egger regression (β = −1.312, P-value = 0.098) and intercept term (P-value = 0.105) illustrated no pleiotropy in this MR study. According to the results for IVW (P-value = 0.305, β = −0.103, and OR = 0.9021) and WMR (P-value = 0.487, β = −0.092, and OR = 0.9121) in the MR study between AIS and AD, there is no causal association between AIS and AD risk. In addition, the MR-Egger regression (P-value = 0.290 and β = −0.512) and intercept term (P-value = 0.387) showed no potential pleiotropy. LAS is not causally associated with AD risk according to the MR results (IVW: P-value = 0.568, β = 0.037, and OR = 1.0377; WMR: P-value = 0.793, β = −0.022, and OR = 0.9782). Additionally, the results of MR-Egger regression (P-value = 0.122 and β = −1.220) and intercept term (P-value = 0.110) showed no potential pleiotropy. Our results [IVW: P-value = 0.245, β = −0.064, and OR = 0.938; WMR: P-value = 0.331, β = −0.057, and OR = 0.9446; MR-Egger: P-value = 0.673 and β = −0.062, and intercept term (P-value = 0.985)] further demonstrated there is no causal link between CES and AD and no pleiotropy in this MR study. In conclusion, different types of stroke, including AS, AIS, LAS, and CES, would not be causally associated with AD risk.
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spelling pubmed-73719942020-08-04 Stroke and Alzheimer’s Disease: A Mendelian Randomization Study Wang, Tao Ni, Qing-bin Wang, Kun Han, Zhifa Sun, Bao-liang Front Genet Genetics Stroke and Alzheimer’s disease (AD) are common neurological diseases. Several exiting studies indicated that late onset-AD and ischemic stroke have shared genetic links. Different kinds of stroke have different mechanisms. However, it remains unclear whether there is a causal relationship between different types of strokes, including any stroke (AS), any ischemic stroke (AIS), large-artery atherosclerotic stroke (LAS), and cardio-embolic stroke (CES), and AD. Herein, we conducted several Mendelian randomization (MR) studies to explore genetically causal link of different kinds of strokes and AD. The results for inverse-variance weighted (IVW) meta-analysis (β = −0.039, OR = 0.9618, and P-value = 0.750) and weighted median regression (WMR) (β = −0.156, OR = 0.8556, and P-value = 0.274) demonstrated that AS is not causally associated with AD risk. The result of MR-Egger regression (β = −1.312, P-value = 0.098) and intercept term (P-value = 0.105) illustrated no pleiotropy in this MR study. According to the results for IVW (P-value = 0.305, β = −0.103, and OR = 0.9021) and WMR (P-value = 0.487, β = −0.092, and OR = 0.9121) in the MR study between AIS and AD, there is no causal association between AIS and AD risk. In addition, the MR-Egger regression (P-value = 0.290 and β = −0.512) and intercept term (P-value = 0.387) showed no potential pleiotropy. LAS is not causally associated with AD risk according to the MR results (IVW: P-value = 0.568, β = 0.037, and OR = 1.0377; WMR: P-value = 0.793, β = −0.022, and OR = 0.9782). Additionally, the results of MR-Egger regression (P-value = 0.122 and β = −1.220) and intercept term (P-value = 0.110) showed no potential pleiotropy. Our results [IVW: P-value = 0.245, β = −0.064, and OR = 0.938; WMR: P-value = 0.331, β = −0.057, and OR = 0.9446; MR-Egger: P-value = 0.673 and β = −0.062, and intercept term (P-value = 0.985)] further demonstrated there is no causal link between CES and AD and no pleiotropy in this MR study. In conclusion, different types of stroke, including AS, AIS, LAS, and CES, would not be causally associated with AD risk. Frontiers Media S.A. 2020-07-14 /pmc/articles/PMC7371994/ /pubmed/32760421 http://dx.doi.org/10.3389/fgene.2020.00581 Text en Copyright © 2020 Wang, Ni, Wang, Han and Sun. 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(s) 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
Wang, Tao
Ni, Qing-bin
Wang, Kun
Han, Zhifa
Sun, Bao-liang
Stroke and Alzheimer’s Disease: A Mendelian Randomization Study
title Stroke and Alzheimer’s Disease: A Mendelian Randomization Study
title_full Stroke and Alzheimer’s Disease: A Mendelian Randomization Study
title_fullStr Stroke and Alzheimer’s Disease: A Mendelian Randomization Study
title_full_unstemmed Stroke and Alzheimer’s Disease: A Mendelian Randomization Study
title_short Stroke and Alzheimer’s Disease: A Mendelian Randomization Study
title_sort stroke and alzheimer’s disease: a mendelian randomization study
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371994/
https://www.ncbi.nlm.nih.gov/pubmed/32760421
http://dx.doi.org/10.3389/fgene.2020.00581
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