Life course and Intergenerational Health Research Group, Robinson Institute, The University of Adelaide, Adelaide South Australia 5005, Australia.
BMC Public Health. 2010 Jun 15;10:341. doi: 10.1186/1471-2458-10-341.
While menarche indicates the beginning of a woman's reproductive life, relatively little is known about the association between age at menarche and subsequent morbidity and mortality. We aimed to examine the effect of lower age at menarche on all-cause mortality in older Australian women over 15 years of follow-up.
Data were drawn from the Australian Longitudinal Study of Ageing (n = 1,031 women aged 65-103 years). We estimated the hazard ratio (HR) associated with lower age at menarche using Cox proportional hazards models, and adjusted for a broad range of reproductive, demographic, health and lifestyle covariates.
During the follow-up period, 673 women (65%) died (average 7.3 years (SD 4.1) of follow-up for decedents). Women with menses onset < 12 years of age (10.7%; n = 106) had an increased hazard of death over the follow-up period (adjusted HR 1.28; 95%CI 0.99-1.65) compared with women who began menstruating aged >or= 12 years (89.3%; n = 883). However, when age at menarche was considered as a continuous variable, the adjusted HRs associated with the linear and quadratic terms for age at menarche were not statistically significant at a 5% level of significance (linear HR 0.76; 95%CI 0.56 - 1.04; quadratic HR 1.01; 95%CI 1.00-1.02).
Women with lower age at menarche may have reduced survival into old age. These results lend support to the known associations between earlier menarche and risk of metabolic disease in early adulthood. Strategies to minimise earlier menarche, such as promoting healthy weights and minimising family dysfunction during childhood, may also have positive longer-term effects on survival in later life.
月经初潮标志着女性生殖生命的开始,但人们对初潮年龄与随后的发病率和死亡率之间的关系知之甚少。我们旨在研究初潮年龄较低与 15 年以上随访期间老年澳大利亚女性的全因死亡率之间的关系。
数据来自澳大利亚老龄化纵向研究(n=1031 名 65-103 岁的女性)。我们使用 Cox 比例风险模型估计与初潮年龄较低相关的风险比(HR),并调整了广泛的生殖、人口统计学、健康和生活方式协变量。
在随访期间,有 673 名女性(65%)死亡(死亡者的平均随访时间为 7.3 年(SD 4.1))。与 12 岁以上开始月经的女性(89.3%,n=883)相比,12 岁以下月经初潮的女性(10.7%,n=106)在随访期间死亡的风险更高(调整后的 HR 1.28;95%CI 0.99-1.65)。然而,当将初潮年龄视为连续变量时,初潮年龄线性和二次项的调整 HR 在 5%的显著性水平上没有统计学意义(线性 HR 0.76;95%CI 0.56-1.04;二次 HR 1.01;95%CI 1.00-1.02)。
初潮年龄较低的女性可能在老年时的生存机会降低。这些结果支持了较早的初潮与成年早期代谢疾病风险之间的已知关联。为了尽量减少较早的初潮,例如在儿童期促进健康体重和减少家庭功能障碍,可能对晚年的生存也有积极的长期影响。