Age at menarche and lung function: a Mendelian randomization study

被引:0
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作者
Dipender Gill
Nuala A. Sheehan
Matthias Wielscher
Nick Shrine
Andre F. S. Amaral
John R. Thompson
Raquel Granell
Bénédicte Leynaert
Francisco Gómez Real
Ian P. Hall
Martin D. Tobin
Juha Auvinen
Susan M. Ring
Marjo-Riitta Jarvelin
Louise V. Wain
John Henderson
Deborah Jarvis
Cosetta Minelli
机构
[1] Hammersmith Hospital,Department of Clinical Pharmacology and Therapeutics, Imperial College London
[2] Imperial College Healthcare NHS Trust,St. Mary’s Hospital
[3] University of Leicester,Department of Health Sciences
[4] Imperial College London,Department of Epidemiology and Biostatistics, School of Public Health
[5] Imperial College London,Population Health and Occupational Disease, NHLI
[6] MRC-PHE Centre for Environment and Health,School of Social and Community Medicine
[7] University of Bristol,UMR 1152, Pathophysiology and Epidemiology of Respiratory Diseases, Epidemiology Team
[8] Inserm,UMR 1152
[9] Univ Paris Diderot - Paris 7,Department of Gynecology and Obstetrics
[10] Haukeland University Hospital,Department of Clinical Science
[11] University of Bergen,Division of Respiratory Medicine, Queen’s Medical Centre
[12] University of Nottingham,National Institute for Health Research, Leicester Respiratory Biomedical Research Unit
[13] Glenfield Hospital,Institute of Health Sciences
[14] University of Oulu,Biocenter Oulu
[15] University of Oulu,Center for Life Course Epidemiology, Faculty of Medicine
[16] University of Oulu,Unit of Primary Care
[17] Oulu University Hospital,undefined
来源
关键词
Mendelian randomization; Menarche; Puberty; Lung function; FVC; FEV1/FVC;
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摘要
A trend towards earlier menarche in women has been associated with childhood factors (e.g. obesity) and hypothesised environmental exposures (e.g. endocrine disruptors present in household products). Observational evidence has shown detrimental effects of early menarche on various health outcomes including adult lung function, but these might represent spurious associations due to confounding. To address this we used Mendelian randomization where genetic variants are used as proxies for age at menarche, since genetic associations are not affected by classical confounding. We estimated the effects of age at menarche on forced vital capacity (FVC), a proxy for restrictive lung impairment, and ratio of forced expiratory volume in one second to FVC (FEV1/FVC), a measure of airway obstruction, in both adulthood and adolescence. We derived SNP-age at menarche association estimates for 122 variants from a published genome-wide meta-analysis (N = 182,416), with SNP-lung function estimates obtained by meta-analysing three studies of adult women (N = 46,944) and two of adolescent girls (N = 3025). We investigated the impact of departures from the assumption of no pleiotropy through sensitivity analyses. In adult women, in line with previous evidence, we found an effect on restrictive lung impairment with a 24.8 mL increase in FVC per year increase in age at menarche (95% CI 1.8–47.9; p = 0.035); evidence was stronger after excluding potential pleiotropic variants (43.6 mL; 17.2–69.9; p = 0.001). In adolescent girls we found an opposite effect (−56.5 mL; −108.3 to −4.7; p = 0.033), suggesting that the detrimental effect in adulthood may be preceded by a short-term post-pubertal benefit. Our secondary analyses showing results in the same direction in men and boys, in whom age at menarche SNPs have also shown association with sexual development, suggest a role for pubertal timing in general rather than menarche specifically. We found no effect on airway obstruction (FEV1/FVC).
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页码:701 / 710
页数:9
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