Journal
PLOS MEDICINE
Volume 19, Issue 2, Pages -Publisher
PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pmed.1003679
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Funding
- Rhodes Scholarships at the University of Oxford
- Clarendon Fund at the University of Oxford
- Medical Sciences Doctoral Training Centre at the University of Oxford
- Li Ka Shing Foundation
- UK Medical Research Council
- British Heart Foundation Intermediate Clinical Research Fellowship [FS/18/23/33512]
- National Institute for Health Research Oxford Biomedical Research Centre
- NIHR Oxford Biomedical Research Centre, Oxford
- NIH [1P50HD10422401]
- Gates Foundation [INV-024200]
- Wellcome Trust Investigator Award [221782/Z/20/ Z]
- Wellcome Trust [221651/Z/20/Z]
- Wellcome Trust Core Award [203141/Z/16/Z]
- NIHR Oxford BRC
- Wellcome Trust [221782/Z/20/Z, 221651/Z/20/Z] Funding Source: Wellcome Trust
- Bill and Melinda Gates Foundation [INV-024200] Funding Source: Bill and Melinda Gates Foundation
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This study analyzed data on obesity and reproductive diseases in women of European ancestry and found that obesity is associated with increased risks of various reproductive disorders, including uterine fibroids, polycystic ovary syndrome, heavy menstrual bleeding, and pre-eclampsia. The study also identified associations between obesity, metabolic hormones, and reproductive diseases, and found that the relationship between obesity and reproductive disorders is influenced by genetic factors.
Background Obesity is observationally associated with altered risk of many female reproductive conditions. These include polycystic ovary syndrome (PCOS), abnormal uterine bleeding, endometriosis, infertility, and pregnancy-related disorders. However, the roles and mechanisms of obesity in the aetiology of reproductive disorders remain unclear. Thus, we aimed to estimate observational and genetically predicted causal associations between obesity, metabolic hormones, and female reproductive disorders. Methods and findings Logistic regression, generalised additive models, and Mendelian randomisation (MR) (2-sample, non-linear, and multivariable) were applied to obesity and reproductive disease data on up to 257,193 women of European ancestry in UK Biobank and publicly available genome-wide association studies (GWASs). Body mass index (BMI), waist-to-hip ratio (WHR), and WHR adjusted for BMI were observationally (odds ratios [ORs] = 1.02-1.87 per 1-SD increase in obesity trait) and genetically (ORs = 1.06-2.09) associated with uterine fibroids (UF), PCOS, heavy menstrual bleeding (HMB), and pre-eclampsia. Genetically predicted visceral adipose tissue (VAT) mass was associated with the development of HMB (OR [95% CI] per 1-kg increase in predicted VAT mass = 1.32 [1.06-1.64], P = 0.0130), PCOS (OR [95% CI] = 1.15 [1.08-1.23], P = 3.24 x 10(-05)), and pre-eclampsia (OR [95% CI] = 3.08 [1.98-4.79], P = 6.65 x 10(-07)). Increased waist circumference posed a higher genetic risk (ORs = 1.16-1.93) for the development of these disorders and UF than did increased hip circumference (ORs = 1.06-1.10). Leptin, fasting insulin, and insulin resistance each mediated between 20% and 50% of the total genetically predicted association of obesity with pre-eclampsia. Reproductive conditions clustered based on shared genetic components of their aetiological relationships with obesity. This study was limited in power by the low prevalence of female reproductive conditions among women in the UK Biobank, with little information on pre-diagnostic anthropometric traits, and by the susceptibility of MR estimates to genetic pleiotropy. Conclusions We found that common indices of overall and central obesity were associated with increased risks of reproductive disorders to heterogenous extents in a systematic, large-scale genetics-based analysis of the aetiological relationships between obesity and female reproductive conditions. Our results suggest the utility of exploring the mechanisms mediating the causal associations of overweight and obesity with gynaecological health to identify targets for disease prevention and treatment.
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