MRC Integrative Epidemiology Unit at the University of Bristol, United Kingdom
Department of Population Health Sciences, Bristol Medical School, University of Bristol, United Kingdom.
J Am Heart Assoc. 2018 Feb 10;7(4):e007780. doi: 10.1161/JAHA.117.007780.
Previous studies of age at menarche and cardiometabolic health report conflicting findings, and only a few could account for childhood characteristics. We aimed to estimate the associations of age at menarche with cardiovascular risk factors in unrelated women and within sister groups, under the assumption that within-sibship estimates will be better adjusted for shared genetics and early life environment.
Our study included 7770 women, from 5984 sibships, participating in the GS:SFHS (Generation Scotland: Scottish Family Health Study). We used fixed- and between-effects linear regression to estimate the associations within sister groups and between unrelated individuals, respectively. Within sibships, the mean difference between sisters with early menarche (≤11 years) and sisters with menarche at 12 to 13 years was 1.73 mm Hg (95% confidence interval [CI], -0.41 to 3.86) for systolic blood pressure, 1.26 mm Hg (95% CI, -0.02 to 2.55) for diastolic blood pressure, -0.06 nmol/L (95% CI, -0.11 to -0.02) for high-density lipoprotein, 0.20 nmol/L (95% CI, 0.08-0.32) for non-high-density lipoprotein, -0.34% (95% CI, -1.98 to 1.30) for glucose, 1.60 kg/m (95% CI, 0.92-2.28) for body mass index, and 2.75 cm (95% CI, 1.06-4.44) for waist circumference. There was weak evidence of associations between later menarche (14-15 or ≥16 years) and lower body mass index, waist circumference, and blood pressure. We found no strong evidence that estimates from within- and between-sibship analyses differed (all values >0.1). The associations with other cardiovascular risk factors were attenuated after adjustment for adult body mass index.
Our results suggest that confounding by shared familial characteristics is unlikely to be a major driver of the association between early menarche and adverse cardiometabolic health but do not exclude confounding by individual-level characteristics.
之前关于初潮年龄与心血管代谢健康的研究结果相互矛盾,且仅有少数研究考虑了儿童时期的特征。我们旨在假设同卵双胞胎内的估计值将更好地调整遗传和早期生活环境的共享因素,以此来评估初潮年龄与非相关女性和同卵双胞胎女性心血管风险因素的关联。
我们的研究纳入了来自 5984 个同卵双胞胎的 7770 名女性,参加了 GS:SFHS(苏格兰家族健康研究中的苏格兰一代)。我们分别使用固定效应和组间效应线性回归来估计同卵双胞胎内和非相关个体间的关联。在同卵双胞胎中,初潮早(≤11 岁)的姐妹与 12-13 岁初潮的姐妹之间的平均差异为收缩压 1.73mmHg(95%置信区间[CI],-0.41 至 3.86),舒张压 1.26mmHg(95%CI,-0.02 至 2.55),高密度脂蛋白-0.06nmol/L(95%CI,-0.11 至 -0.02),非高密度脂蛋白 0.20nmol/L(95%CI,0.08-0.32),血糖-0.34%(95%CI,-1.98 至 1.30),体重指数 1.60kg/m(95%CI,0.92-2.28),腰围 2.75cm(95%CI,1.06-4.44)。晚初潮(14-15 岁或≥16 岁)与较低的体重指数、腰围和血压之间存在较弱的关联。我们没有发现强有力的证据表明同卵双胞胎内和组间分析的估计值存在差异(所有 P 值均>0.1)。在调整成年体重指数后,其他心血管风险因素的相关性减弱。
我们的结果表明,共同的家族特征混杂不太可能是初潮年龄与不良心血管代谢健康之间关联的主要驱动因素,但不能排除个体特征的混杂。