Body Mass Index and Polycystic Ovary Syndrome: A 2-Sample Bidirectional Mendelian Randomization Study

Abstract Background Observational studies have shown a link between elevated body mass index (BMI) and the risk of polycystic ovary syndrome (PCOS). While Mendelian randomization (MR) studies in Europeans have suggested a causal role of increased BMI in PCOS, whether the same role is suggested in As...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2020-06, Vol.105 (6), p.1778-1784
Hauptverfasser: Zhao, Yalin, Xu, Yuping, Wang, Xiaomeng, Xu, Lin, Chen, Jianhua, Gao, Chengwen, Wu, Chuanhong, Pan, Dun, Zhang, Qian, Zhou, Juan, Chen, Ruirui, Wang, Zhuo, Zhao, Han, You, Li, Cao, Yunxia, Li, Zhiqiang, Shi, Yongyong
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container_end_page 1784
container_issue 6
container_start_page 1778
container_title The journal of clinical endocrinology and metabolism
container_volume 105
creator Zhao, Yalin
Xu, Yuping
Wang, Xiaomeng
Xu, Lin
Chen, Jianhua
Gao, Chengwen
Wu, Chuanhong
Pan, Dun
Zhang, Qian
Zhou, Juan
Chen, Ruirui
Wang, Zhuo
Zhao, Han
You, Li
Cao, Yunxia
Li, Zhiqiang
Shi, Yongyong
description Abstract Background Observational studies have shown a link between elevated body mass index (BMI) and the risk of polycystic ovary syndrome (PCOS). While Mendelian randomization (MR) studies in Europeans have suggested a causal role of increased BMI in PCOS, whether the same role is suggested in Asians has yet to be investigated. We used MR studies to infer causal effects using genetic data from East Asian populations. Methods and Findings We performed a 2-sample bidirectional MR analysis using summary statistics from genome-wide association studies (GWAS) of BMI (with up to 173 430 individuals) and PCOS (4386 cases and 8017 controls) in East Asian populations. Seventy-eight single nucleotide polymorphisms (SNPs) correlated with BMI were selected as genetic instrumental variables to estimate the causal effect of BMI on PCOS using the inverse-variance weighted (IVW) method. To test the reliability of the results, further sensitivity analyses included MR–Egger regression, weighted median estimates, and leave-one-out analysis. The IVW analysis indicated a significant association between high BMI and the risk of PCOS (odds ratio per standard deviation higher BMI, 2.208; 95% confidence interval 1.537 to 3.168, P = 1.77 × 10–5). In contrast, the genetic risk of PCOS had no significant effect on BMI. Conclusions The results of our bidirectional MR study showed that an increase in BMI causes PCOS, while PCOS does not cause an increased BMI. This study provides further genetic support for a link between BMI and PCOS. Further research is needed to interpret the potential mechanisms of this association.
doi_str_mv 10.1210/clinem/dgaa125
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While Mendelian randomization (MR) studies in Europeans have suggested a causal role of increased BMI in PCOS, whether the same role is suggested in Asians has yet to be investigated. We used MR studies to infer causal effects using genetic data from East Asian populations. Methods and Findings We performed a 2-sample bidirectional MR analysis using summary statistics from genome-wide association studies (GWAS) of BMI (with up to 173 430 individuals) and PCOS (4386 cases and 8017 controls) in East Asian populations. Seventy-eight single nucleotide polymorphisms (SNPs) correlated with BMI were selected as genetic instrumental variables to estimate the causal effect of BMI on PCOS using the inverse-variance weighted (IVW) method. To test the reliability of the results, further sensitivity analyses included MR–Egger regression, weighted median estimates, and leave-one-out analysis. The IVW analysis indicated a significant association between high BMI and the risk of PCOS (odds ratio per standard deviation higher BMI, 2.208; 95% confidence interval 1.537 to 3.168, P = 1.77 × 10–5). In contrast, the genetic risk of PCOS had no significant effect on BMI. Conclusions The results of our bidirectional MR study showed that an increase in BMI causes PCOS, while PCOS does not cause an increased BMI. This study provides further genetic support for a link between BMI and PCOS. Further research is needed to interpret the potential mechanisms of this association.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/clinem/dgaa125</identifier><identifier>PMID: 32163573</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Biomarkers - analysis ; Body Mass Index ; Care and treatment ; Development and progression ; Female ; Genetic aspects ; Genome-Wide Association Study ; Genomes ; Health aspects ; Humans ; Mendelian Randomization Analysis - statistics &amp; numerical data ; Polycystic ovary syndrome ; Polycystic Ovary Syndrome - genetics ; Polycystic Ovary Syndrome - pathology ; Polymorphism, Single Nucleotide ; Prognosis ; Sensitivity analysis ; Single nucleotide polymorphisms ; Single-nucleotide polymorphism ; Statistical analysis ; Stein-Leventhal syndrome</subject><ispartof>The journal of clinical endocrinology and metabolism, 2020-06, Vol.105 (6), p.1778-1784</ispartof><rights>Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2020</rights><rights>Copyright © Oxford University Press 2015</rights><rights>Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>COPYRIGHT 2020 Oxford University Press</rights><rights>Endocrine Society 2020. All rights reserved. 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While Mendelian randomization (MR) studies in Europeans have suggested a causal role of increased BMI in PCOS, whether the same role is suggested in Asians has yet to be investigated. We used MR studies to infer causal effects using genetic data from East Asian populations. Methods and Findings We performed a 2-sample bidirectional MR analysis using summary statistics from genome-wide association studies (GWAS) of BMI (with up to 173 430 individuals) and PCOS (4386 cases and 8017 controls) in East Asian populations. Seventy-eight single nucleotide polymorphisms (SNPs) correlated with BMI were selected as genetic instrumental variables to estimate the causal effect of BMI on PCOS using the inverse-variance weighted (IVW) method. To test the reliability of the results, further sensitivity analyses included MR–Egger regression, weighted median estimates, and leave-one-out analysis. The IVW analysis indicated a significant association between high BMI and the risk of PCOS (odds ratio per standard deviation higher BMI, 2.208; 95% confidence interval 1.537 to 3.168, P = 1.77 × 10–5). In contrast, the genetic risk of PCOS had no significant effect on BMI. Conclusions The results of our bidirectional MR study showed that an increase in BMI causes PCOS, while PCOS does not cause an increased BMI. This study provides further genetic support for a link between BMI and PCOS. 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While Mendelian randomization (MR) studies in Europeans have suggested a causal role of increased BMI in PCOS, whether the same role is suggested in Asians has yet to be investigated. We used MR studies to infer causal effects using genetic data from East Asian populations. Methods and Findings We performed a 2-sample bidirectional MR analysis using summary statistics from genome-wide association studies (GWAS) of BMI (with up to 173 430 individuals) and PCOS (4386 cases and 8017 controls) in East Asian populations. Seventy-eight single nucleotide polymorphisms (SNPs) correlated with BMI were selected as genetic instrumental variables to estimate the causal effect of BMI on PCOS using the inverse-variance weighted (IVW) method. To test the reliability of the results, further sensitivity analyses included MR–Egger regression, weighted median estimates, and leave-one-out analysis. The IVW analysis indicated a significant association between high BMI and the risk of PCOS (odds ratio per standard deviation higher BMI, 2.208; 95% confidence interval 1.537 to 3.168, P = 1.77 × 10–5). In contrast, the genetic risk of PCOS had no significant effect on BMI. Conclusions The results of our bidirectional MR study showed that an increase in BMI causes PCOS, while PCOS does not cause an increased BMI. This study provides further genetic support for a link between BMI and PCOS. Further research is needed to interpret the potential mechanisms of this association.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>32163573</pmid><doi>10.1210/clinem/dgaa125</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-6485-0221</orcidid><oa>free_for_read</oa></addata></record>
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subjects Biomarkers - analysis
Body Mass Index
Care and treatment
Development and progression
Female
Genetic aspects
Genome-Wide Association Study
Genomes
Health aspects
Humans
Mendelian Randomization Analysis - statistics & numerical data
Polycystic ovary syndrome
Polycystic Ovary Syndrome - genetics
Polycystic Ovary Syndrome - pathology
Polymorphism, Single Nucleotide
Prognosis
Sensitivity analysis
Single nucleotide polymorphisms
Single-nucleotide polymorphism
Statistical analysis
Stein-Leventhal syndrome
title Body Mass Index and Polycystic Ovary Syndrome: A 2-Sample Bidirectional Mendelian Randomization Study
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