ApoB与骨密度的因果关系研究:孟德尔随机化研究
首发时间:2020-03-10
摘要:【目的】载脂蛋白B(ApoB)是低密度脂蛋白(LDL)的主要载脂蛋白,在细胞识别和摄取LDL中起重要作用。先前的研究已经建立了ApoB和BMD之间的统计关联,但尚未进行因果推断。【方法】基于下载的ApoB和BMD的全基因组关联研究(GWAS)数据,采用两个样本的孟德尔随机方法推断其因果关系。【结果】逆方差加权法(IVW)估计ApoB和BMD的β值为0.016(95%CI:0.003?0.029,P <0.05),表明对于ApoB的每个标准偏差,BMD增加1.6%。 MR-Egger回归结果表明,遗传多效性未能改变结果(截距= 0.001,P = 0.601)。敏感性分析表明,β稳定在0.016。这些结果表明,BMD上ApoB之间存在因果关系。【结论】我们的结果为预测骨质疏松风险和ApoB对BMD变化的临床意义提供了有用的信息。
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Causal Link between ApoB and Osteoporosis: a Mendelian Randomized Study
Abstract:Objective: Apolipoprotein B (ApoB) as the main apolipoprotein of low density lipoproteins (LDL), plays important role in cell recognition and uptake of LDL. Previous studies have established the statistical associations between ApoB and BMD, but have not made causal inference. Methods: Based on the downloaded genome wide association study (GWAS) data for ApoB and BMD, two-sample Mendelian randomization method was used to infer their causal link. Results: The inverse-variance weighting (IVW) method estimated that the β value of ApoB and BMD is 0.016 (95% CI: 0.003 ~ 0.029, P <0.05), suggesting that for each standard deviation of ApoB, BMD increases by 1.6%. MR-Egger regression results showed that genetic pleiotropy failed to shift the results (intercept = 0.001, P = 0.601). The sensitivity analyses showed that that the β is stable at 0.016. Conclusion: These results showed there exists a causal link between ApoB on BMD. Our result provided useful information in the prediction of osteoporosis risk and the clinical relevance of ApoB on BMD variation.
Keywords: Mendelian randomization ApoB Bone mineral density Causal effect
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