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Associations between coronary heart disease and risk of cognitive impairment: A meta‐analysis

BACKGROUND: Several studies have demonstrated that coronary heart disease (CHD) is a high risk factor for cognitive impairment, whereas other studies showed that there was no association between cognitive impairment and CHD. The relationship between CHD and cognitive impairment is still unclear base...

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Autores principales: Liang, Xuan, Huang, Yilin, Han, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119850/
https://www.ncbi.nlm.nih.gov/pubmed/33742562
http://dx.doi.org/10.1002/brb3.2108
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author Liang, Xuan
Huang, Yilin
Han, Xu
author_facet Liang, Xuan
Huang, Yilin
Han, Xu
author_sort Liang, Xuan
collection PubMed
description BACKGROUND: Several studies have demonstrated that coronary heart disease (CHD) is a high risk factor for cognitive impairment, whereas other studies showed that there was no association between cognitive impairment and CHD. The relationship between CHD and cognitive impairment is still unclear based on these conflicting results. Thus, it is of importance to evaluate the association between CHD and cognitive impairment. The present study made a meta‐analysis to explore the association between CHD and risk of cognitive impairment. METHODS: Articles exploring the association between CHD and cognitive impairment and published before November 2020 were searched in the following databases: PubMed, Web of Science, Medline, EMBASE, and Google Scholar. We used STATA 12.0 software to compute the relative risks (RRs), odds ratios (ORs), or hazard ratios (HRs) and 95% confidence intervals (CIs). RESULTS: The meta‐analysis showed a positive association between CHD and risk of all‐cause cognitive impairment with a random effects model (RR = 1.27, 95% CI 1.18 to 1.36, I(2) = 82.8%, p < .001). Additionally, the study showed a positive association between myocardial infraction (MI) and risk of all‐cause cognitive impairment with a random effects model (RR = 1.49, 95% CI 1.20 to 1.84, I(2) = 76.0%, p < .001). However, no significant association was detected between angina pectoris (AP) and risk of all‐cause cognitive impairment with a random effects model (RR = 1.23, 95% CI 0.95 to 1.58, I(2) = 79.1%, p < .001). Subgroup studies also showed that CHD patients are at higher risk for vascular dementia (VD), but not Alzheimer's disease (AD) (VD: RR = 1.34, 95% CI: 1.28–1.39; AD: RR = 0.99, 95% CI: 0.92–1.07). CONCLUSION: In a word, CHD was significantly associated with an increased risk of developing cognitive impairment.
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spelling pubmed-81198502021-05-20 Associations between coronary heart disease and risk of cognitive impairment: A meta‐analysis Liang, Xuan Huang, Yilin Han, Xu Brain Behav Original Research BACKGROUND: Several studies have demonstrated that coronary heart disease (CHD) is a high risk factor for cognitive impairment, whereas other studies showed that there was no association between cognitive impairment and CHD. The relationship between CHD and cognitive impairment is still unclear based on these conflicting results. Thus, it is of importance to evaluate the association between CHD and cognitive impairment. The present study made a meta‐analysis to explore the association between CHD and risk of cognitive impairment. METHODS: Articles exploring the association between CHD and cognitive impairment and published before November 2020 were searched in the following databases: PubMed, Web of Science, Medline, EMBASE, and Google Scholar. We used STATA 12.0 software to compute the relative risks (RRs), odds ratios (ORs), or hazard ratios (HRs) and 95% confidence intervals (CIs). RESULTS: The meta‐analysis showed a positive association between CHD and risk of all‐cause cognitive impairment with a random effects model (RR = 1.27, 95% CI 1.18 to 1.36, I(2) = 82.8%, p < .001). Additionally, the study showed a positive association between myocardial infraction (MI) and risk of all‐cause cognitive impairment with a random effects model (RR = 1.49, 95% CI 1.20 to 1.84, I(2) = 76.0%, p < .001). However, no significant association was detected between angina pectoris (AP) and risk of all‐cause cognitive impairment with a random effects model (RR = 1.23, 95% CI 0.95 to 1.58, I(2) = 79.1%, p < .001). Subgroup studies also showed that CHD patients are at higher risk for vascular dementia (VD), but not Alzheimer's disease (AD) (VD: RR = 1.34, 95% CI: 1.28–1.39; AD: RR = 0.99, 95% CI: 0.92–1.07). CONCLUSION: In a word, CHD was significantly associated with an increased risk of developing cognitive impairment. John Wiley and Sons Inc. 2021-03-20 /pmc/articles/PMC8119850/ /pubmed/33742562 http://dx.doi.org/10.1002/brb3.2108 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Liang, Xuan
Huang, Yilin
Han, Xu
Associations between coronary heart disease and risk of cognitive impairment: A meta‐analysis
title Associations between coronary heart disease and risk of cognitive impairment: A meta‐analysis
title_full Associations between coronary heart disease and risk of cognitive impairment: A meta‐analysis
title_fullStr Associations between coronary heart disease and risk of cognitive impairment: A meta‐analysis
title_full_unstemmed Associations between coronary heart disease and risk of cognitive impairment: A meta‐analysis
title_short Associations between coronary heart disease and risk of cognitive impairment: A meta‐analysis
title_sort associations between coronary heart disease and risk of cognitive impairment: a meta‐analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119850/
https://www.ncbi.nlm.nih.gov/pubmed/33742562
http://dx.doi.org/10.1002/brb3.2108
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