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Causal relationship between Alzheimer’s disease and cardiovascular disease: a bidirectional Mendelian randomization analysis

Observational studies suggest that cardiovascular disease (CVD) increases the risk of developing Alzheimer’s disease (AD). However, the causal relationship between the two is not clear. This study applied a two-sample bidirectional Mendelian randomization method to explore the causal relationship be...

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Autores principales: Zhang, Fengjun, Xian, Dexian, Feng, Junchen, Ning, Luning, Jiang, Tianshou, Xu, Wenchang, Liu, Yuan, Zhao, Qiong, Peng, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522384/
https://www.ncbi.nlm.nih.gov/pubmed/37665672
http://dx.doi.org/10.18632/aging.205013
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author Zhang, Fengjun
Xian, Dexian
Feng, Junchen
Ning, Luning
Jiang, Tianshou
Xu, Wenchang
Liu, Yuan
Zhao, Qiong
Peng, Min
author_facet Zhang, Fengjun
Xian, Dexian
Feng, Junchen
Ning, Luning
Jiang, Tianshou
Xu, Wenchang
Liu, Yuan
Zhao, Qiong
Peng, Min
author_sort Zhang, Fengjun
collection PubMed
description Observational studies suggest that cardiovascular disease (CVD) increases the risk of developing Alzheimer’s disease (AD). However, the causal relationship between the two is not clear. This study applied a two-sample bidirectional Mendelian randomization method to explore the causal relationship between CVD and AD. Genome-wide association study (GWAS) data from 46 datasets of European populations (21,982 cases of AD and 41,944 controls) were utilized to obtain genetic instrumental variables for AD. In addition, genetic instrumental variables for atrial fibrillation (AF), heart failure (HF), myocardial infarction (MI), coronary heart disease (CHD), angina pectoris (AP), and ischemic stroke (IS) (including large-artery atherosclerotic stroke [LAS] and cardioembolic stroke [CES]) were selected from GWAS data of European populations (P < 5E-8). The inverse variance weighting method was employed as the major Mendelian randomization analysis method. Genetically predicted AD odds ratios (OR) (1.06) (95% CI: 1.02–1.10, P = 0.003) were linked to higher AP analysis. A higher genetically predicted OR for CES (0.9) (95% CI 0.82–0.99, P = 0.02) was linked to a decreased AD risk. This Mendelian randomized study identified AD as a risk factor for AP. In addition, CES was related to a reduced incidence of AD. Therefore, these modifiable risk factors are crucial targets for preventing and treating AD.
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spelling pubmed-105223842023-09-27 Causal relationship between Alzheimer’s disease and cardiovascular disease: a bidirectional Mendelian randomization analysis Zhang, Fengjun Xian, Dexian Feng, Junchen Ning, Luning Jiang, Tianshou Xu, Wenchang Liu, Yuan Zhao, Qiong Peng, Min Aging (Albany NY) Research Paper Observational studies suggest that cardiovascular disease (CVD) increases the risk of developing Alzheimer’s disease (AD). However, the causal relationship between the two is not clear. This study applied a two-sample bidirectional Mendelian randomization method to explore the causal relationship between CVD and AD. Genome-wide association study (GWAS) data from 46 datasets of European populations (21,982 cases of AD and 41,944 controls) were utilized to obtain genetic instrumental variables for AD. In addition, genetic instrumental variables for atrial fibrillation (AF), heart failure (HF), myocardial infarction (MI), coronary heart disease (CHD), angina pectoris (AP), and ischemic stroke (IS) (including large-artery atherosclerotic stroke [LAS] and cardioembolic stroke [CES]) were selected from GWAS data of European populations (P < 5E-8). The inverse variance weighting method was employed as the major Mendelian randomization analysis method. Genetically predicted AD odds ratios (OR) (1.06) (95% CI: 1.02–1.10, P = 0.003) were linked to higher AP analysis. A higher genetically predicted OR for CES (0.9) (95% CI 0.82–0.99, P = 0.02) was linked to a decreased AD risk. This Mendelian randomized study identified AD as a risk factor for AP. In addition, CES was related to a reduced incidence of AD. Therefore, these modifiable risk factors are crucial targets for preventing and treating AD. Impact Journals 2023-09-02 /pmc/articles/PMC10522384/ /pubmed/37665672 http://dx.doi.org/10.18632/aging.205013 Text en Copyright: © 2023 Zhang et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhang, Fengjun
Xian, Dexian
Feng, Junchen
Ning, Luning
Jiang, Tianshou
Xu, Wenchang
Liu, Yuan
Zhao, Qiong
Peng, Min
Causal relationship between Alzheimer’s disease and cardiovascular disease: a bidirectional Mendelian randomization analysis
title Causal relationship between Alzheimer’s disease and cardiovascular disease: a bidirectional Mendelian randomization analysis
title_full Causal relationship between Alzheimer’s disease and cardiovascular disease: a bidirectional Mendelian randomization analysis
title_fullStr Causal relationship between Alzheimer’s disease and cardiovascular disease: a bidirectional Mendelian randomization analysis
title_full_unstemmed Causal relationship between Alzheimer’s disease and cardiovascular disease: a bidirectional Mendelian randomization analysis
title_short Causal relationship between Alzheimer’s disease and cardiovascular disease: a bidirectional Mendelian randomization analysis
title_sort causal relationship between alzheimer’s disease and cardiovascular disease: a bidirectional mendelian randomization analysis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522384/
https://www.ncbi.nlm.nih.gov/pubmed/37665672
http://dx.doi.org/10.18632/aging.205013
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