Timing of menarche and menopause and epigenetic aging among U.S. adults: results from the National Health and Nutrition Examination Survey 1999-2002.

IF 4.4 2区 医学 Q1 GENETICS & HEREDITY Clinical Epigenetics Pub Date : 2025-02-21 DOI:10.1186/s13148-025-01827-x
Saher Daredia, Dennis Khodasevich, Nicole Gladish, Hanyang Shen, Jamaji C Nwanaji-Enwerem, Anne K Bozack, Belinda L Needham, David H Rehkopf, Julianna Deardorff, Andres Cardenas
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Abstract

Reproductive aging, including timing of menarche and menopause, influences long-term morbidity and mortality in women, yet underlying biological mechanisms remain poorly understood. Using DNA methylation-based biomarkers, we assessed associations of age at menarche (N = 1,033) and menopause (N = 658) with epigenetic aging in a nationally representative sample of women ≥ 50 years. Later age at menopause was associated with lower GrimAge epigenetic age deviation ( B = - 0.10 years, 95% CI: - 0.19, - 0.02). No associations were observed for menarche timing. This suggests a connection between earlier menopause and biological aging, with potential clinical implications for identifying those at high risk for age-related disease.

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美国成年人月经初潮和更年期的时间与表观遗传衰老:1999-2002年全国健康和营养检查调查的结果。
生殖老化,包括月经初潮和更年期的时间,影响妇女的长期发病率和死亡率,但潜在的生物学机制仍然知之甚少。使用基于DNA甲基化的生物标志物,我们评估了初潮年龄(N = 1033)和更年期年龄(N = 658)与表观遗传衰老的关系,这些研究对象为≥50岁的全国代表性女性样本。绝经年龄越晚,GrimAge表观遗传年龄偏差越小(B = - 0.10年,95% CI: - 0.19, - 0.02)。未观察到与月经初潮时间有关。这表明更年期提前与生物衰老之间存在联系,对于识别年龄相关疾病的高风险人群具有潜在的临床意义。
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来源期刊
自引率
5.30%
发文量
150
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
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