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Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization study

BACKGROUND: Growing evidence suggests that various reproductive factors, including early menarche, early menopause, and age at first birth, may increase the risk of developing cardiovascular disease (CVD) later in life. However, the associations between reproductive factors and CVDs are inconsistent...

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Autores principales: Chen, Miao, Wang, Zhen, Xu, Hongfei, Chen, Xiaofang, Teng, Peng, Ma, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080931/
https://www.ncbi.nlm.nih.gov/pubmed/37024926
http://dx.doi.org/10.1186/s12920-023-01496-w
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author Chen, Miao
Wang, Zhen
Xu, Hongfei
Chen, Xiaofang
Teng, Peng
Ma, Liang
author_facet Chen, Miao
Wang, Zhen
Xu, Hongfei
Chen, Xiaofang
Teng, Peng
Ma, Liang
author_sort Chen, Miao
collection PubMed
description BACKGROUND: Growing evidence suggests that various reproductive factors, including early menarche, early menopause, and age at first birth, may increase the risk of developing cardiovascular disease (CVD) later in life. However, the associations between reproductive factors and CVDs are inconsistent and controversial. Therefore, we conducted a two-sample Mendelian randomization (MR) analysis to explore the potential links between age at first sex (AFS) and age at first birth (AFB) and several CVDs. METHODS: We obtained summary statistics for exposure from the largest genome-wide association studies of AFS and AFB. To serve as instrumental variables, we selected 259 SNPs associated with AFS and 81 SNPs associated with AFB at the genome-wide significance level. We employed a random-effects inverse-variance weighted method to pool estimates, and conducted multivariable MR analysis to determine the direct association between AFS and AFB with CVDs, while accounting for the effects of confounders. RESULTS: The genetic liability to later AFS was associated with decreased risks of heart failure (odd ratio [OR] 0.700; 95% confidence interval [CI] 0.639–0.767; p = 2.23 × 10(−14)), coronary artery disease (OR 0.728; 95% CI 0.657–0.808; p = 1.82 × 10(−9)), myocardial infarction (OR 0.731; 95% CI 0.657–0.813; p = 8.33 × 10(−9)), stroke (OR 0.747; 95% CI 0.684–0.816; p = 6.89 × 10(−11)), and atrial fibrillation (OR 0.871; 95% CI 0.806–0.941; p = 4.48 × 10(−4)). The genetic liability to later AFB was also associated with decreased risks of CVDs, including myocardial infarction (OR 0.895; 95% CI 0.852–0.940; p = 8.66 × 10(−6)), coronary heart disease (OR 0.901; 95% CI 0.860–0.943; p = 9.02 × 10(−6)), heart failure (OR 0.925; 95% CI 0.891–0.961; p = 5.32 × 10(−5)), and atrial fibrillation (OR 0.944; 95% CI 0.911–0.978; p = 0.001). However, no association was found between AFB and stroke. The associations remained independent from the effects of AFS and AFB on potential confounders, including smoking, alcohol intake, body mass index, and depression. Mediation analysis suggested that education attainment partly mediates the link from AFS and AFB to CVD outcomes. CONCLUSION: Our results observed a causal relationship between later AFS, AFB and lower CVDs risk; it emphasizes the importance of providing sex education since early sex and birth may have undesirable effects. Cardiovascular risk stratification that considers reproductive factors may help address CVD risk. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01496-w.
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spelling pubmed-100809312023-04-08 Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization study Chen, Miao Wang, Zhen Xu, Hongfei Chen, Xiaofang Teng, Peng Ma, Liang BMC Med Genomics Research BACKGROUND: Growing evidence suggests that various reproductive factors, including early menarche, early menopause, and age at first birth, may increase the risk of developing cardiovascular disease (CVD) later in life. However, the associations between reproductive factors and CVDs are inconsistent and controversial. Therefore, we conducted a two-sample Mendelian randomization (MR) analysis to explore the potential links between age at first sex (AFS) and age at first birth (AFB) and several CVDs. METHODS: We obtained summary statistics for exposure from the largest genome-wide association studies of AFS and AFB. To serve as instrumental variables, we selected 259 SNPs associated with AFS and 81 SNPs associated with AFB at the genome-wide significance level. We employed a random-effects inverse-variance weighted method to pool estimates, and conducted multivariable MR analysis to determine the direct association between AFS and AFB with CVDs, while accounting for the effects of confounders. RESULTS: The genetic liability to later AFS was associated with decreased risks of heart failure (odd ratio [OR] 0.700; 95% confidence interval [CI] 0.639–0.767; p = 2.23 × 10(−14)), coronary artery disease (OR 0.728; 95% CI 0.657–0.808; p = 1.82 × 10(−9)), myocardial infarction (OR 0.731; 95% CI 0.657–0.813; p = 8.33 × 10(−9)), stroke (OR 0.747; 95% CI 0.684–0.816; p = 6.89 × 10(−11)), and atrial fibrillation (OR 0.871; 95% CI 0.806–0.941; p = 4.48 × 10(−4)). The genetic liability to later AFB was also associated with decreased risks of CVDs, including myocardial infarction (OR 0.895; 95% CI 0.852–0.940; p = 8.66 × 10(−6)), coronary heart disease (OR 0.901; 95% CI 0.860–0.943; p = 9.02 × 10(−6)), heart failure (OR 0.925; 95% CI 0.891–0.961; p = 5.32 × 10(−5)), and atrial fibrillation (OR 0.944; 95% CI 0.911–0.978; p = 0.001). However, no association was found between AFB and stroke. The associations remained independent from the effects of AFS and AFB on potential confounders, including smoking, alcohol intake, body mass index, and depression. Mediation analysis suggested that education attainment partly mediates the link from AFS and AFB to CVD outcomes. CONCLUSION: Our results observed a causal relationship between later AFS, AFB and lower CVDs risk; it emphasizes the importance of providing sex education since early sex and birth may have undesirable effects. Cardiovascular risk stratification that considers reproductive factors may help address CVD risk. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01496-w. BioMed Central 2023-04-06 /pmc/articles/PMC10080931/ /pubmed/37024926 http://dx.doi.org/10.1186/s12920-023-01496-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Miao
Wang, Zhen
Xu, Hongfei
Chen, Xiaofang
Teng, Peng
Ma, Liang
Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization study
title Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization study
title_full Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization study
title_fullStr Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization study
title_full_unstemmed Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization study
title_short Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization study
title_sort genetic liability to age at first sex and birth in relation to cardiovascular diseases: a mendelian randomization study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080931/
https://www.ncbi.nlm.nih.gov/pubmed/37024926
http://dx.doi.org/10.1186/s12920-023-01496-w
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