The role of metabolic factors in the association between obesity and cholelithiasis: A two-step, two-sample multivariable mendelian randomization study.

IF 2.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Clinics Pub Date : 2024-10-19 eCollection Date: 2024-01-01 DOI:10.1016/j.clinsp.2024.100520
Xiangrong Xu, Jiawei Gao, Jun Sun, Ruiwen Liu, Wei Chen
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Abstract

Background and purpose: The extent to which the effects of BMI on cholelithiasis are mediated by metabolic factors (including blood pressure, blood lipids, body mass, and fasting blood glucose) is unclear. Therefore, in this study, the authors used genetic evidence to test the effects of these characteristics.

Methods: Summary-level data for exposures and main outcomes were extracted from GWAS consortia. The authors used a two-step, two-sample Multivariable Mendelian Randomization (MVMR) analysis to illustrate the effect of BMI on cholelithiasis and a stepwise test method to quantify the possible mediating effects of cardiometabolic factors on cholelithiasis.

Results: For each one-unit logarithmic increase in body mass index, the risk of cholelithiasis increased by 98 % (Odds Ratio [OR = 1.98], 95 % CI: 1.73 %‒2.28 %). After mediation analysis, the authors found that high-density lipoprotein and triglycerides were the main mediating factors, while the mediating effects of other metabolic factors were not significant. The total effect ratios of HDL and TG on cholelithiasis were 7.3 % (95 % CI: 8.51 %‒12.85 %) and 3.5 % (95 % CI: 3.59 %‒6.50 %), respectively. HDL and TG played a significant role in regulating cholelithiasis, but there was no evidence to show the regulatory effect of LDL on cholelithiasis. The total effects of BMI and triglycerides on cholelithiasis were 10.7 % and 5.0 %, respectively.

Conclusion: The authors found that among the metabolic factors evaluated, the decrease of HDL and the increase of TG mediated a high proportion of the effect of BMI on cholelithiasis. Therefore, intervention with these factors may reduce the increased risk of cholelithiasis in patients with high BMI.

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代谢因素在肥胖与胆石症关系中的作用:两步骤、两样本多变量孟德尔随机研究。
背景和目的:BMI 对胆石症的影响在多大程度上受代谢因素(包括血压、血脂、体重和空腹血糖)的介导尚不清楚。因此,在本研究中,作者利用遗传证据来检验这些特征的影响:方法:从全球基因组研究联盟(GWAS consortia)中提取了暴露和主要结果的摘要级数据。作者采用两步双样本多变量孟德尔随机化(MVMR)分析法来说明体重指数对胆石症的影响,并采用逐步检验法来量化心脏代谢因素对胆石症可能产生的中介效应:结果:体重指数每增加一个对数单位,胆石症的发病风险就会增加 98 %(Odds Ratio [OR = 1.98],95 % CI:1.73 %-2.28 %)。经过中介分析,作者发现高密度脂蛋白和甘油三酯是主要的中介因素,而其他代谢因素的中介效应并不显著。高密度脂蛋白和甘油三酯对胆石症的总效应比分别为 7.3 %(95 % CI:8.51 %-12.85 %)和 3.5 %(95 % CI:3.59 %-6.50 %)。高密度脂蛋白和总胆固醇在调节胆石症方面发挥了重要作用,但没有证据显示低密度脂蛋白对胆石症有调节作用。体重指数和甘油三酯对胆石症的总影响分别为10.7%和5.0%:作者发现,在评估的代谢因素中,高密度脂蛋白的降低和甘油三酯的升高在 BMI 对胆石症的影响中占很大比例。因此,对这些因素进行干预可降低高体重指数患者胆石症风险的增加。
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来源期刊
Clinics
Clinics 医学-医学:内科
CiteScore
4.10
自引率
3.70%
发文量
129
审稿时长
52 days
期刊介绍: CLINICS is an electronic journal that publishes peer-reviewed articles in continuous flow, of interest to clinicians and researchers in the medical sciences. CLINICS complies with the policies of funding agencies which request or require deposition of the published articles that they fund into publicly available databases. CLINICS supports the position of the International Committee of Medical Journal Editors (ICMJE) on trial registration.
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