Association of the Age at Menarche with Site-Specific Cancer Risks in Pooled Data from Nine Cohorts.
Association of the Age at Menarche with Site-Specific Cancer Risks in Pooled Data from Nine Cohorts.
复制标题
DOI:
10.1158/0008-5472.can-19-3093
复制
发表时间:
2021-04-15
期刊:
影响因子:
11.2
通讯作者:
Hoover RN
中科院分区:
文献类型:
--
作者:
Fuhrman BJ;Moore SC;Byrne C;Makhoul I;Kitahara CM;Berrington de González A;Linet MS;Weiderpass E;Adami HO;Freedman ND;Liao LM;Matthews CE;Stolzenberg-Solomon RZ;Gaudet MM;Patel AV;Lee IM;Buring JE;Wolk A;Larsson SC;Prizment AE;Robien K;Spriggs M;Check DP;Murphy N;Gunter MJ;Van Dusen HL Jr;Ziegler RG;Hoover RN
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, 31-9 years]) in nine prospective US and European cohorts that enrolled participants from 1981 through 1998. Cox regression estimated multivariable-adjusted hazard ratios (HR) 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, CI:0.89-0.94), liver cancer (HR:0.92, CI:0.85-0.99), melanoma (HR:0.95, CI:0.93-0.98), bladder cancer (HR:0.96, CI:0.93-0.99), and cancers of the colon (HR:0.97, CI:0.96-0.99), lung (HR:0.98, 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 (BMI). 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.
影响因子:
8.8
作者:
Gallagher RP;Elwood JM;Hill GB;Coldman AJ;Threlfall WJ;Spinelli JJ
通讯作者:
Spinelli JJ