Yale School of Medicine, New Haven, Connecticut, USA.
Department of Anthropology, Yale University, New Haven, Connecticut, USA.
Am J Hum Biol. 2024 Jan;36(1):e23982. doi: 10.1002/ajhb.23982. Epub 2023 Sep 5.
Recent studies suggest that early menarche may increase cardiometabolic morbidity and mortality. Yet few studies have examined this association in the Pacific Islands, where obesity prevalence is among the highest globally. We sought to examine associations between age at menarche and cardiometabolic risk in Samoa.
Participants were from the Soifua Manuia study (n = 285, age 32-72 years) conducted in Samoa from 2017 to 2019. Logistic regressions were conducted to estimate odds of obesity, hypertension, diabetes, dyslipidemia, and metabolic syndrome per one-year increase in age at menarche. Linear regressions were conducted to examine associations between age at menarche and continuous measures of adiposity, blood pressure, insulin resistance, and serum lipids.
Median age at menarche was 14 years (IQR = 2). After controlling for relevant covariates, each one-year increase in age at menarche was associated with a 15% decrease (OR = 0.85, 95% CI: 0.72-1.01, p = .067) in odds of hypertension, but a 21% increase (OR = 1.21, 95% CI: 1.01-1.45, p = .044) in odds of diabetes and 18% increase (OR = 1.18, 95% CI: 0.98-1.42, p = .081) in odds of high total cholesterol. Each additional year in age at menarche was associated with a 1.60 ± 0.52 kg (p = .002) decrease in lean mass and 1.56 ± 0.51 kg (p = .003) decrease in fat-free mass.
Associations between age at menarche and cardiometabolic risk may be population-specific and are likely influenced by both current and historical nutritional and epidemiological contexts. Prospective studies are needed to clarify the role of childhood adiposity and other early life exposures on age at menarche and subsequent cardiometabolic risk.
最近的研究表明,初潮较早可能会增加心血管代谢疾病的发病率和死亡率。然而,在肥胖率位居全球前列的太平洋岛屿地区,很少有研究对此进行过调查。我们试图研究萨摩亚初潮年龄与心血管代谢风险之间的关系。
本研究参与者来自于 2017 年至 2019 年在萨摩亚进行的 Soifua Manuia 研究(n=285,年龄 32-72 岁)。采用 logistic 回归分析估计初潮年龄每增加一年,肥胖、高血压、糖尿病、血脂异常和代谢综合征的发病风险比。采用线性回归分析初潮年龄与体脂、血压、胰岛素抵抗和血清脂质等连续指标之间的关系。
初潮年龄中位数为 14 岁(IQR=2)。在校正了相关协变量后,初潮年龄每增加一年,高血压的发病风险比降低 15%(OR=0.85,95%CI:0.72-1.01,p=0.067),而糖尿病的发病风险比增加 21%(OR=1.21,95%CI:1.01-1.45,p=0.044),总胆固醇水平较高的发病风险比增加 18%(OR=1.18,95%CI:0.98-1.42,p=0.081)。初潮年龄每增加一年,瘦体重减少 1.60±0.52kg(p=0.002),去脂体重减少 1.56±0.51kg(p=0.003)。
初潮年龄与心血管代谢风险之间的关联可能具有人群特异性,并且可能受到当前和历史营养和流行病学背景的影响。需要进行前瞻性研究,以阐明儿童期肥胖和其他早期生活暴露对初潮年龄和随后的心血管代谢风险的作用。