骨质疏松症和骨密度与胃食管反流病的孟德尔随机化研究
Mendelian randomization study about osteoporosis and bone mineral density on gastroesophageal reflux disease
投稿时间:2023-11-12  修订日期:2024-02-27
DOI:
中文关键词:  骨质疏松,骨密度,胃食管反流病,孟德尔随机化
英文关键词:osteoporosis  bone mineral density  gastroesophageal reflux disease  mendelian randomization analysis.
基金项目:陕西省自然科学基础研究计划(编号:2022JM-456);国家自然科学基金(编号:81900489); 国家自然科学基金(编号:82303169)
作者单位邮编
陈雯雯 西安交通大学第一附属医院消化内科中国 西安 710061
周元植 西安交通大学第一附属医院消化内科中国 西安 
张旭 西安交通大学第一附属医院消化内科中国 西安 
马佳昕 西安交通大学第一附属医院消化内科中国 西安 
赵雅涵 西安交通大学第一附属医院消化内科中国 西安 
李雅睿 西安交通大学第一附属医院消化内科中国 西安 
赵艳 西安交通大学第一附属医院消化内科中国 西安 
和水祥 西安交通大学第一附属医院消化内科中国 西安 
任牡丹* 西安交通大学第一附属医院消化内科中国 西安 710061
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中文摘要:
      目的:用两样本孟德尔随机化法评估骨质疏松与骨密度和胃食管反流病(GERD)的因果关系。方法: 暴露包括骨质疏松、全身骨密度、腰椎骨密度、股骨颈骨密度、足跟骨密度、前臂骨密度,结局为GERD。筛选与暴露强相关的单核苷酸多态性位点为工具变量进行两样本孟德尔随机化(MR)分析。采用逆方差加权(IVW)法作为主要方法、加权中位数法、MR-Egger法作为补充,评估暴露与结局的因果关系。敏感性分析验证结果的稳定性与可靠性。结果:IVW法表明遗传预测的骨质疏松是GERD的危险因素(P = 0.005, OR = 35.687, 95%CI: 3.009-423.194),全身骨密度(P = 1.57×10-5, OR = 0.910, 95%CI: 0.872-0.950)和腰椎骨密度(P = 0.005,OR = 0.917,95%CI: 0.863-0.974)的增加是GERD的保护因素,而股骨颈骨密度、前臂骨密度、足跟骨密度与GERD不存在因果关系。异质性检验表明足跟骨密度与GERD之间存在异质性,但不影响随机效应IVW法得出的因果关系的结论,其余暴露与GERD不存在异质性。MR-Egger-intercept表明无水平多效性。留一法表明分析结果稳健。结论:骨质疏松是GERD的危险因素,全身骨密度和腰椎骨密度的增加是GERD的保护因素。这提示骨质疏松患者应进行GERD的早期筛查及诊治,这为临床医生提供了新的诊疗思路。
英文摘要:
      Objective: To evaluate the causal relationship between osteoporosis and bone mineral density (BMD) on gastroesophageal reflux disease (GERD) through two-sample mendelian randomization analysis. Method: The exposure factors include osteoporosis, total body BMD, lumbar spine BMD, femoral neck BMD, heel BMD, and forearm BMD. The outcome factor is GERD. The single nucleotide polymorphisms (SNPs) associated with exposure factors were screened as instrumental variables for two-sample Mendelian randomization analysis. The inverse variance-weighted (IVW) method was used as main method to assess causal relationship between exposure and outcome factors, meanwhile weighted median and MR-Egger regression were supplemented. The stability and reliability of the results were verified by several sensitivity analysis methods. Result: The inverse variance-weighted analysis indicated that osteoporosis was a risk factor for GERD(P = 0.005, OR = 35.687,95%CI: 3.009-423.194), increased total body BMD(P = 1.57×10-5,OR = 0.910,95%CI: 0.872- 0.950) and increased lumbar spine BMD(P = 0.005,OR = 0.917,95%CI: 0.863- 0.974) were protective factors for GERD. However, there was no causal relationship between femoral neck BMD, heel BMD, and forearm BMD and GERD. Heterogeneity was found between heel BMD and GERD, but the casual relationship through random effects IVW method was not be influenced. Heterogeneity was not demonstrated between GERD and other exposure factors. No pleiotropy was found by using MR-Egger-intercept. The “leave one out method" analysis showed that the MR analysis results were robust. Conclusion: Osteoporosis is a risk factor for GERD, while increased total body bone density and increased lumbar bone density are protective factors for GERD. This implied that osteoporosis patients should screen GERD earlier for further diagnosis and treatment, which provide a new diagnosis and treatment idea for clinicians.
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