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基于两样本 Mendelian 随机化设计的骨质疏松症与脓毒症因果关系的遗传预测:证据。

GENETIC PREDICTION OF CAUSAL RELATIONSHIPS BETWEEN OSTEOPOROSIS AND SEPSIS: EVIDENCE FROM MENDELIAN RANDOMIZATION WITH TWO-SAMPLE DESIGNS.

机构信息

Intensive Care Unit, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

出版信息

Shock. 2024 Nov 1;62(5):628-632. doi: 10.1097/SHK.0000000000002383. Epub 2024 May 23.

Abstract

Background: Recent observational studies have suggested that osteoporosis may be a risk factor for sepsis. To mitigate confounding factors and establish the causal relationship between sepsis and osteoporosis, we conducted a two-sample Mendelian randomization analysis using publicly available summary statistics. Methods: Utilizing summary data from FinnGen Biobank, we employed a two-sample Mendelian randomization (MR) analysis to predict the causal relationship between osteoporosis and sepsis. The MR analysis primarily utilized the inverse variance weighted (IVW) method, supplemented by MR-Egger, weighted median, weighted mode, and simple mode analyses, with Bayesian weighted MR (BWMR) analysis employed for result validation. Sensitivity analyses included MR-PRESSO, "leave-one-out" analysis, MR-Egger regression, and Cochran Q test. Results: In the European population, an increase of one standard deviation in osteoporosis was associated with an 11% increased risk of sepsis, with an odds ratio (OR) of 1.11 (95% CI, 1.06-1.16; P = 3.75E-06). BWMR yielded an OR of 1.11 (95% CI, 1.06-1.67; P = 1.21E-05), suggesting osteoporosis as a risk factor for sepsis. Conversely, an increase of one standard deviation in sepsis was associated with a 26% increased risk of osteoporosis, with an OR of 1.26 (95% CI, 1.11-1.16; P = 0.45E-03). BWMR yielded an OR of 1.26 (95% CI, 1.09-1.45; P = 1.45E-03), supporting sepsis as a risk factor for osteoporosis. Conclusion: There is an association between osteoporosis and sepsis, with osteoporosis serving as a risk factor for the development of sepsis, while sepsis may also promote the progression of osteoporosis.

摘要

背景

最近的观察性研究表明,骨质疏松症可能是脓毒症的一个危险因素。为了减轻混杂因素的影响,并确定脓毒症和骨质疏松症之间的因果关系,我们利用公开的汇总统计数据进行了两样本孟德尔随机化分析。

方法

我们利用芬兰基因生物库的汇总数据,采用两样本孟德尔随机化(MR)分析来预测骨质疏松症与脓毒症之间的因果关系。MR 分析主要采用逆方差加权(IVW)法,辅之以 MR-Egger、加权中位数、加权众数和简单众数分析,贝叶斯加权 MR(BWMR)分析用于结果验证。敏感性分析包括 MR-PRESSO、“逐个剔除”分析、MR-Egger 回归和 Cochran Q 检验。

结果

在欧洲人群中,骨质疏松症每增加一个标准差,患脓毒症的风险增加 11%,比值比(OR)为 1.11(95%置信区间,1.06-1.16;P=3.75E-06)。BWMR 得出的 OR 为 1.11(95%置信区间,1.06-1.67;P=1.21E-05),提示骨质疏松症是脓毒症的一个危险因素。相反,脓毒症每增加一个标准差,患骨质疏松症的风险增加 26%,OR 为 1.26(95%置信区间,1.11-1.16;P=0.45E-03)。BWMR 得出的 OR 为 1.26(95%置信区间,1.09-1.45;P=1.45E-03),支持脓毒症是骨质疏松症的一个危险因素。

结论

骨质疏松症与脓毒症之间存在关联,骨质疏松症是脓毒症发展的一个危险因素,而脓毒症也可能促进骨质疏松症的进展。

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