IL-16 介导循环代谢物对绝经后骨质疏松症的影响:一项两步多变量孟德尔随机研究

Biological research for nursing Pub Date : 2025-01-01 Epub Date: 2024-08-30 DOI:10.1177/10998004241279934
Yi Chen, Hefang Xiao, Fei Teng, Ao Yang, Fei Yang, Changshun Chen, Rongjin Chen, Bin Geng, Yayi Xia
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引用次数: 0

摘要

研究目的本研究旨在探讨循环代谢物与绝经后骨质疏松症(PMOP)之间的关系,并评估炎症因素的中介作用。研究方法:利用基因组学分析的汇总数据,对绝经后骨质疏松症患者的循环代谢物进行分析:利用全基因组关联研究(GWAS)的汇总级数据,并采用孟德尔随机化方法,进行双样本 MR 分析,以评估循环代谢物与 PMOP 之间的关系。此外,还采用了两步 MR 来量化炎症因素对循环代谢物对 PMOP 影响的中介作用。结果显示结果显示,某些代谢物与罹患 PMOP 的风险之间存在明显关联,尤其是超大 VLDL 颗粒中游离胆固醇与总血脂的比率(OR:1.399,95% CI:1.002-1.954,p = 0.048)和 IL-16(OR:0.773,95% CI:0.608-0.983,p = 0.036)。研究发现,IL-16 可部分调解循环代谢物对 PMOP 的影响,调解效应为 10.4%。结论本研究强调了循环代谢物和炎症因子在 PMOP 发病机制中的关键作用。研究确定了循环代谢物与 PMOP 之间的因果关系,IL-16 对某些影响具有中介作用。这些发现有望应用于早期检测、个性化医疗和确定 PMOP 的治疗靶点等临床领域。
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IL-16 Mediates the Effect of Circulating Metabolites on Postmenopausal Osteoporosis: A Two-Step, Multivariable Mendelian Randomization Study.

Objectives: This study aimed to explore the relationship between circulating metabolites and postmenopausal osteoporosis (PMOP) and to assess the mediating role of inflammatory factors. Methods: Utilizing summary-level data from genome-wide association studies (GWAS) and employing a Mendelian Randomization approach, a two-sample MR analysis was conducted to assess the relationship between circulating metabolites and PMOP. Additionally, a two-step MR was used to quantify the mediating impact of inflammatory factors on the effect of circulating metabolites on PMOP. Results: The results revealed a significant association between certain metabolites and the risk of PMOP, notably the ratio of free cholesterol to total lipids in very large VLDL particles (OR: 1.399, 95% CI: 1.002-1.954, p = 0.048) and IL-16 (OR: 0.773, 95% CI: 0.608-0.983, p = 0.036). IL-16 was found to partially mediate the impact of circulating metabolites on PMOP, with a mediation effect of 10.4%. Conclusion: This study underscores the crucial role of circulating metabolites and inflammatory factors in PMOP pathogenesis. A causal relationship between circulating metabolites and PMOP was established, with IL-16 mediating some effects. These findings hold promise for clinical applications in early detection, personalized medicine, and the identification of therapeutic targets for PMOP.

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