通过抗缪勒氏管激素水平和女性生殖因素对骨质疏松症进行遗传预测:孟德尔随机化研究》。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-07-01 Epub Date: 2024-05-14 DOI:10.1007/s00223-024-01220-5
Yuan Li, Jinquan Lai, Wenbo Wu, Shuyi Ling, Yuqing Dai, Zhisheng Zhong, Xiaodong Chen, Yuehui Zheng
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引用次数: 0

摘要

以往的观察性研究表明,抗缪勒氏管激素(AMH)和生殖因素与女性骨质密度(BMD)降低和骨质疏松症(OP)风险增加有关。然而,相关研究十分有限,而且这些传统的观察性研究可能会受到残留混杂因素和反向因果关系的影响,同时也缺乏对各种生殖因素的更全面观察。研究采用随机效应逆方差加权法进行了单变量和多变量双样本孟德尔随机分析,以确定 AMH 水平和六个生殖因素与 BMD 和 OP 的因果关系。使用 Cochran 的 Q 统计量评估异质性,并进行敏感性分析以确定因果相关性。初潮年龄(AAM)与 45-60 岁和 60 岁以上女性的全身 BMD(TB-BMD)以及足跟骨矿物质密度(eBMD)呈负相关。相反,自然绝经年龄(ANM)与相同年龄段的 TB-BMD 以及 eBMD 呈正相关。自然绝经年龄只与自我报告的 OP 有因果关系,与确诊的 OP 没有显著相关性。AMH 水平或其他生殖因素均与任何年龄段的 BMD 遗传易感性和 OP 无明显关联。AAM较晚和ANM较早与BMD下降有明显的遗传因果关系,但与OP无关。就遗传背景而言,AMH 水平、月经周期长度、初产妇年龄、末产妇年龄和活产数与 BMD 或 OP 没有因果关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Genetic Prediction of Osteoporosis by Anti-Müllerian Hormone Levels and Reproductive Factors in Women: A Mendelian Randomization Study.

Previous observational studies have suggested that anti-Müllerian hormone (AMH) and reproductive factors are linked to reduced bone mineral density (BMD) and an increased risk of osteoporosis (OP) in women. However, related studies are limited, and these traditional observational studies may be subject to residual confounders and reverse causation, while also lacking a more comprehensive observation of various reproductive factors. Univariate and multivariate two-sample Mendelian randomization analyses were conducted to determine the causal associations of AMH levels and six reproductive factors with BMD and OP, using the random-effects inverse-variance weighted method. Heterogeneity was assessed using Cochran's Q-statistic, and sensitivity analyses were performed to identify causal correlations. Age at menarche (AAM) was negatively associated with total body BMD (TB-BMD) in females aged 45-60 and over 60 years, as well as with heel bone mineral density (eBMD). Conversely, age at natural menopause (ANM) was positively associated with TB-BMD in the same age ranges and with eBMD. ANM was only causally associated with self-reported OP and showed no significant correlation with definitively diagnosed OP. Neither AMH level nor other reproductive factors were significantly associated with a genetic predisposition to BMD at any age and OP. Later AAM and earlier ANM are significantly genetically causally associated with decreased BMD but not with OP. AMH levels, length of menstrual cycle, age at first birth, age at last birth, and number of live births, in terms of genetic backgrounds, are not causally related to BMD or OP.

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