Your browser doesn't support javascript.
loading
Age at menarche and lung function: a Mendelian randomization study.
Gill, Dipender; Sheehan, Nuala A; Wielscher, Matthias; Shrine, Nick; Amaral, Andre F S; Thompson, John R; Granell, Raquel; Leynaert, Bénédicte; Real, Francisco Gómez; Hall, Ian P; Tobin, Martin D; Auvinen, Juha; Ring, Susan M; Jarvelin, Marjo-Riitta; Wain, Louise V; Henderson, John; Jarvis, Deborah; Minelli, Cosetta.
Affiliation
  • Gill D; Department of Clinical Pharmacology and Therapeutics, Imperial College London, Hammersmith Hospital, London, UK.
  • Sheehan NA; St. Mary's Hospital, Imperial College Healthcare NHS Trust, London, UK.
  • Wielscher M; Department of Health Sciences, University of Leicester, Leicester, UK.
  • Shrine N; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
  • Amaral AFS; Department of Health Sciences, University of Leicester, Leicester, UK.
  • Thompson JR; Population Health and Occupational Disease, NHLI, Imperial College London, Emmanuel Kaye Building, 1B Manresa Road, SW3 6LR, London, UK.
  • Granell R; MRC-PHE Centre for Environment and Health, London, UK.
  • Leynaert B; Department of Health Sciences, University of Leicester, Leicester, UK.
  • Real FG; School of Social and Community Medicine, University of Bristol, Bristol, UK.
  • Hall IP; UMR 1152, Pathophysiology and Epidemiology of Respiratory Diseases, Epidemiology Team, Inserm, Paris, France.
  • Tobin MD; UMR 1152, Univ Paris Diderot - Paris 7, Paris, France.
  • Auvinen J; Department of Gynecology and Obstetrics, Haukeland University Hospital, Bergen, Norway.
  • Ring SM; Department of Clinical Science, University of Bergen, Bergen, Norway.
  • Jarvelin MR; Division of Respiratory Medicine, Queen's Medical Centre, University of Nottingham, Nottingham, UK.
  • Wain LV; Department of Health Sciences, University of Leicester, Leicester, UK.
  • Henderson J; National Institute for Health Research, Leicester Respiratory Biomedical Research Unit, Glenfield Hospital, Leicester, UK.
  • Jarvis D; Institute of Health Sciences, University of Oulu, Oulu, Finland.
  • Minelli C; School of Social and Community Medicine, University of Bristol, Bristol, UK.
Eur J Epidemiol ; 32(8): 701-710, 2017 08.
Article de En | MEDLINE | ID: mdl-28624884
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).
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Ménarche / Capacité vitale / Volume expiratoire maximal par seconde / Poumon Type d'étude: Clinical_trials / Diagnostic_studies / Prognostic_studies / Systematic_reviews Limites: Adolescent / Adult / Female / Humans Langue: En Journal: Eur J Epidemiol Sujet du journal: EPIDEMIOLOGIA Année: 2017 Type de document: Article Pays de publication: Pays-Bas

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Ménarche / Capacité vitale / Volume expiratoire maximal par seconde / Poumon Type d'étude: Clinical_trials / Diagnostic_studies / Prognostic_studies / Systematic_reviews Limites: Adolescent / Adult / Female / Humans Langue: En Journal: Eur J Epidemiol Sujet du journal: EPIDEMIOLOGIA Année: 2017 Type de document: Article Pays de publication: Pays-Bas