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Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study
Coronary artery disease (CAD) affects millions of individuals worldwide and results in a substantial burden to healthcare systems. Although it is established that CAD affects females differently than males, differences between the sexes are not routinely accounted for. Body mass index is a known ris...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470280/ https://www.ncbi.nlm.nih.gov/pubmed/37663544 http://dx.doi.org/10.1016/j.xhgg.2023.100230 |
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author | Ye, Qiang Gagliano Taliun, Sarah A. |
author_facet | Ye, Qiang Gagliano Taliun, Sarah A. |
author_sort | Ye, Qiang |
collection | PubMed |
description | Coronary artery disease (CAD) affects millions of individuals worldwide and results in a substantial burden to healthcare systems. Although it is established that CAD affects females differently than males, differences between the sexes are not routinely accounted for. Body mass index is a known risk factor for CAD. However, more accurate metrics of body fat, including waist-to-hip circumference ratio (WHR), could be more meaningful clinically. WHR exhibits sex differences due to sex hormones, differing effects at genetic risk loci, and other factors. It is unclear if WHR is a causal factor for CAD in one or both sexes, but this information will be crucial for improving heart health. Causal inference, however, can be challenging. Large-scale cohorts with genetic data allow for Mendelian randomization, which, given certain assumptions, tests whether there is a causal relationship between an exposure and the outcome using genetic variants. We conducted sex-specific, one-sample MR analyses using two-stage least-squares regression in the UK Biobank with genetic variants robustly associated with WHR. We found evidence of a causal relationship between WHR and CAD risk in females (OR [95% CI] = 1.16 [1.06–1.26]; p value = 7.5E-4), whereas in males, we did not find evidence of a causal relationship (OR [95% CI] = 1.40 [0.98–2.01]; p value = 0.063). Results were supported by two additional MR approaches (using a genetic risk score and two-sample MR using the inverse variance weighted approach). We encourage future work assessing sex-specific effects using causal inference techniques to better understand factors contributing to complex disease risk. |
format | Online Article Text |
id | pubmed-10470280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-104702802023-09-01 Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study Ye, Qiang Gagliano Taliun, Sarah A. HGG Adv Report Coronary artery disease (CAD) affects millions of individuals worldwide and results in a substantial burden to healthcare systems. Although it is established that CAD affects females differently than males, differences between the sexes are not routinely accounted for. Body mass index is a known risk factor for CAD. However, more accurate metrics of body fat, including waist-to-hip circumference ratio (WHR), could be more meaningful clinically. WHR exhibits sex differences due to sex hormones, differing effects at genetic risk loci, and other factors. It is unclear if WHR is a causal factor for CAD in one or both sexes, but this information will be crucial for improving heart health. Causal inference, however, can be challenging. Large-scale cohorts with genetic data allow for Mendelian randomization, which, given certain assumptions, tests whether there is a causal relationship between an exposure and the outcome using genetic variants. We conducted sex-specific, one-sample MR analyses using two-stage least-squares regression in the UK Biobank with genetic variants robustly associated with WHR. We found evidence of a causal relationship between WHR and CAD risk in females (OR [95% CI] = 1.16 [1.06–1.26]; p value = 7.5E-4), whereas in males, we did not find evidence of a causal relationship (OR [95% CI] = 1.40 [0.98–2.01]; p value = 0.063). Results were supported by two additional MR approaches (using a genetic risk score and two-sample MR using the inverse variance weighted approach). We encourage future work assessing sex-specific effects using causal inference techniques to better understand factors contributing to complex disease risk. Elsevier 2023-08-10 /pmc/articles/PMC10470280/ /pubmed/37663544 http://dx.doi.org/10.1016/j.xhgg.2023.100230 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Report Ye, Qiang Gagliano Taliun, Sarah A. Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study |
title | Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study |
title_full | Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study |
title_fullStr | Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study |
title_full_unstemmed | Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study |
title_short | Genetically predicted waist-to-hip circumference ratio and coronary artery disease: A sex-specific Mendelian randomization study |
title_sort | genetically predicted waist-to-hip circumference ratio and coronary artery disease: a sex-specific mendelian randomization study |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470280/ https://www.ncbi.nlm.nih.gov/pubmed/37663544 http://dx.doi.org/10.1016/j.xhgg.2023.100230 |
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