| Literature DB >> 33820799 |
Barbara J Fuhrman1,2, Steven C Moore3, Celia Byrne4, Issam Makhoul2, Cari M Kitahara3, Amy Berrington de González3, Martha S Linet3, Elisabete Weiderpass5, Hans-Olov Adami6,7, Neal D Freedman3, Linda M Liao3, Charles E Matthews3, Rachael Z Stolzenberg-Solomon3, Mia M Gaudet3,8, Alpa V Patel8, I-Min Lee9, Julie E Buring9, Alicja Wolk10, Susanna C Larsson10, Anna E Prizment11, Kim Robien12, Michael Spriggs13, David P Check3, Neil Murphy14, Marc J Gunter14, Harold L Van Dusen13, Regina G Ziegler3, Robert N Hoover3.
Abstract
The average age at menarche declined in European and U.S. populations during the 19th and 20th centuries. The timing of pubertal events may have broad implications for chronic disease risks in aging women. Here we tested for associations of recalled menarcheal age with risks of 19 cancers in 536,450 women [median age, 60 years (range, 31-39 years)] in nine prospective U.S. and European cohorts that enrolled participants from 1981 to 1998. Cox regression estimated multivariable-adjusted HRs and 95% confidence intervals (CI) for associations of the age at menarche with risk of each cancer in each cohort and random-effects meta-analysis was used to generate summary estimates for each cancer. Over a median 10 years of follow-up, 60,968 women were diagnosed with a first primary incident cancer. Inverse linear associations were observed for seven of 19 cancers studied. Each additional year in the age at menarche was associated with reduced risks of endometrial cancer (HR = 0.91; 95% CI, 0.89-0.94), liver cancer (HR = 0.92; 95% CI, 0.85-0.99), melanoma (HR = 0.95; 95% CI, 0.93-0.98), bladder cancer (HR = 0.96; 95% CI, 0.93-0.99), and cancers of the colon (HR = 0.97; 95% CI, 0.96-0.99), lung (HR = 0.98; 95% CI, 0.96-0.99), and breast (HR = 0.98; 95% CI, 0.93-0.99). All but one of these associations remained statistically significant following adjustment for baseline body mass index. Similarities in the observed associations between menarche and seven cancers suggest shared underlying causes rooted early in life. We propose as a testable hypothesis that early exposure to sex hormones increases mid-life cancer risks by altering functional capacities of stem cells with roles in systemic energy balance and tissue homeostasis. SIGNIFICANCE: Age at menarche is associated with risk for seven cancers in middle-aged women, and understanding the shared underlying causal pathways across these cancers may suggest new avenues for cancer prevention. ©2021 American Association for Cancer Research.Entities:
Mesh:
Year: 2021 PMID: 33820799 PMCID: PMC8137527 DOI: 10.1158/0008-5472.CAN-19-3093
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 13.312