IL-16 Mediates the Effect of Circulating Metabolites on Postmenopausal Osteoporosis: A Two-Step, Multivariable Mendelian Randomization Study

被引:2
|
作者
Chen, Yi [1 ,2 ,3 ]
Xiao, Hefang [1 ,2 ,3 ]
Teng, Fei [1 ,2 ,3 ]
Yang, Ao [1 ,2 ,3 ]
Yang, Fei [1 ,2 ,3 ]
Chen, Changshun [1 ,2 ,3 ]
Chen, Rongjin [1 ,2 ,3 ]
Geng, Bin [1 ,2 ,3 ]
Xia, Yayi [1 ,2 ,3 ]
机构
[1] Lanzhou Univ, Dept Orthopaed, Hosp 2, 82,Cuiyingmen, Lanzhou 730030, Peoples R China
[2] Gansu Prov Orthopaed Clin Med Res Ctr, Lanzhou, Peoples R China
[3] Gansu Prov Intelligent Orthoped Ind Technol Ctr, Lanzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
inflammatory factors; postmenopausal osteoporosis; circulating metabolites; Mendelian randomization; mediation; LIPID PROFILES; ASSOCIATION; RISK;
D O I
10.1177/10998004241279934
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
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.
引用
收藏
页码:91 / 100
页数:10
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