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Telomere length and the risk of cardiovascular diseases: A Mendelian randomization study

BACKGROUND: The causal direction and magnitude of the associations between telomere length (TL) and cardiovascular diseases (CVDs) remain uncertain due to susceptibility of reverse causation and confounding. This study aimed to investigate the associations between TL and CVDs using Mendelian randomi...

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Autores principales: Deng, Yingjian, Li, Qiang, Zhou, Faguang, Li, Guiyang, Liu, Jianghai, Lv, Jialan, Li, Linlin, Chang, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637552/
https://www.ncbi.nlm.nih.gov/pubmed/36352846
http://dx.doi.org/10.3389/fcvm.2022.1012615
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author Deng, Yingjian
Li, Qiang
Zhou, Faguang
Li, Guiyang
Liu, Jianghai
Lv, Jialan
Li, Linlin
Chang, Dong
author_facet Deng, Yingjian
Li, Qiang
Zhou, Faguang
Li, Guiyang
Liu, Jianghai
Lv, Jialan
Li, Linlin
Chang, Dong
author_sort Deng, Yingjian
collection PubMed
description BACKGROUND: The causal direction and magnitude of the associations between telomere length (TL) and cardiovascular diseases (CVDs) remain uncertain due to susceptibility of reverse causation and confounding. This study aimed to investigate the associations between TL and CVDs using Mendelian randomization (MR). MATERIALS AND METHODS: In this two-sample MR study, we identified 154 independent TL-associated genetic variants from a genome-wide association study (GWAS) consisting of 472,174 individuals (aged 40–69) in the UK Biobank. Summary level data of CVDs were obtained from different GWASs datasets. Methods of inverse variance weighted (IVW), Mendelian Randomization-Egger (MR-Egger), Mendelian Randomization robust adjusted profile score (MR-RAPS), maximum likelihood estimation, weighted mode, penalized weighted mode methods, and Mendelian randomization pleiotropy residual sum and outlier test (MR-PRESSO) were conducted to investigate the associations between TL and CVDs. RESULTS: Our findings indicated that longer TL was significantly associated with decreased risk of coronary atherosclerosis [odds ratio (OR), 0.85; 95% confidence interval (CI), 0.75–0.95; P = 4.36E-03], myocardial infarction (OR, 0.72; 95% CI, 0.63–0.83; P = 2.31E-06), ischemic heart disease (OR, 0.87; 95% CI, 0.78–0.97; P = 1.01E-02), stroke (OR, 0.87; 95% CI, 0.79–0.95; P = 1.60E-03), but an increased risk of hypertension (OR, 1.12; 95% CI, 1.02–1.23; P = 2.00E-02). However, there was no significant association between TL and heart failure (OR, 0.94; 95% CI, 0.87–1.01; P = 1.10E-01), atrial fibrillation (OR, 1.01; 95% CI, 0.93–1.11; P = 7.50E-01), or cardiac death (OR, 0.95; 95% CI, 0.82–1.10; P = 4.80E-01). Both raw and outlier corrected estimates from MR-PRESSO were consistent with those of IVW results. The sensitivity analyses showed no evidence of pleiotropy (MR-Egger intercept, P > 0.05), while Cochran’s Q test and MR-Egger suggested different degrees of heterogeneity. CONCLUSION: Our MR study suggested that longer telomeres were associated with decreased risk of several CVDs, including coronary atherosclerosis, myocardial infarction, ischemic heart disease, and stroke, as well as an increased risk of hypertension. Future studies are still warranted to validate the results and investigate the mechanisms underlying these associations.
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spelling pubmed-96375522022-11-08 Telomere length and the risk of cardiovascular diseases: A Mendelian randomization study Deng, Yingjian Li, Qiang Zhou, Faguang Li, Guiyang Liu, Jianghai Lv, Jialan Li, Linlin Chang, Dong Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: The causal direction and magnitude of the associations between telomere length (TL) and cardiovascular diseases (CVDs) remain uncertain due to susceptibility of reverse causation and confounding. This study aimed to investigate the associations between TL and CVDs using Mendelian randomization (MR). MATERIALS AND METHODS: In this two-sample MR study, we identified 154 independent TL-associated genetic variants from a genome-wide association study (GWAS) consisting of 472,174 individuals (aged 40–69) in the UK Biobank. Summary level data of CVDs were obtained from different GWASs datasets. Methods of inverse variance weighted (IVW), Mendelian Randomization-Egger (MR-Egger), Mendelian Randomization robust adjusted profile score (MR-RAPS), maximum likelihood estimation, weighted mode, penalized weighted mode methods, and Mendelian randomization pleiotropy residual sum and outlier test (MR-PRESSO) were conducted to investigate the associations between TL and CVDs. RESULTS: Our findings indicated that longer TL was significantly associated with decreased risk of coronary atherosclerosis [odds ratio (OR), 0.85; 95% confidence interval (CI), 0.75–0.95; P = 4.36E-03], myocardial infarction (OR, 0.72; 95% CI, 0.63–0.83; P = 2.31E-06), ischemic heart disease (OR, 0.87; 95% CI, 0.78–0.97; P = 1.01E-02), stroke (OR, 0.87; 95% CI, 0.79–0.95; P = 1.60E-03), but an increased risk of hypertension (OR, 1.12; 95% CI, 1.02–1.23; P = 2.00E-02). However, there was no significant association between TL and heart failure (OR, 0.94; 95% CI, 0.87–1.01; P = 1.10E-01), atrial fibrillation (OR, 1.01; 95% CI, 0.93–1.11; P = 7.50E-01), or cardiac death (OR, 0.95; 95% CI, 0.82–1.10; P = 4.80E-01). Both raw and outlier corrected estimates from MR-PRESSO were consistent with those of IVW results. The sensitivity analyses showed no evidence of pleiotropy (MR-Egger intercept, P > 0.05), while Cochran’s Q test and MR-Egger suggested different degrees of heterogeneity. CONCLUSION: Our MR study suggested that longer telomeres were associated with decreased risk of several CVDs, including coronary atherosclerosis, myocardial infarction, ischemic heart disease, and stroke, as well as an increased risk of hypertension. Future studies are still warranted to validate the results and investigate the mechanisms underlying these associations. Frontiers Media S.A. 2022-10-24 /pmc/articles/PMC9637552/ /pubmed/36352846 http://dx.doi.org/10.3389/fcvm.2022.1012615 Text en Copyright © 2022 Deng, Li, Zhou, Li, Liu, Lv, Li and Chang. https://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 Cardiovascular Medicine
Deng, Yingjian
Li, Qiang
Zhou, Faguang
Li, Guiyang
Liu, Jianghai
Lv, Jialan
Li, Linlin
Chang, Dong
Telomere length and the risk of cardiovascular diseases: A Mendelian randomization study
title Telomere length and the risk of cardiovascular diseases: A Mendelian randomization study
title_full Telomere length and the risk of cardiovascular diseases: A Mendelian randomization study
title_fullStr Telomere length and the risk of cardiovascular diseases: A Mendelian randomization study
title_full_unstemmed Telomere length and the risk of cardiovascular diseases: A Mendelian randomization study
title_short Telomere length and the risk of cardiovascular diseases: A Mendelian randomization study
title_sort telomere length and the risk of cardiovascular diseases: a mendelian randomization study
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637552/
https://www.ncbi.nlm.nih.gov/pubmed/36352846
http://dx.doi.org/10.3389/fcvm.2022.1012615
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