血浆代谢物和代谢途径对谵妄因果效应的遗传评估

Xin He, XinYu Shi, YiNi Wang, Shuang Han, JiaYan Liu, Fei Yang, Kun Ma, Bai-Xiang Li
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引用次数: 0

摘要

目的谵妄对全球数百万人产生了重大影响,并与并发症的不良预后密切相关。观察性研究表明,血浆代谢物可能作为谵妄的标记物和效应物发挥重要作用,但其因果关系尚未阐明。基于最新的全基因组关联研究(GWAS)数据,我们的研究旨在对谵妄与血浆代谢物之间的遗传关系提出新的见解。方法我们进行了全面的孟德尔随机化(MR)分析,研究了血浆中1091种代谢物和309种代谢物比率与谵妄之间的因果关系。主要估算方法为反方差加权法(IVW),同时采用 MR-Egger 和权重中值法评估结果的稳健性。还进行了敏感性分析,包括 MR 多熵RESidual Sum and Outlier(MR-PRESSO)检验、Cochran Q 检验、leave-one-out 分析和 MR Egger 截距分析。此外,还进行了 MR Steiger 检验,以探讨代谢物对谵妄的潜在反向因果效应。结果 使用 IVW 方法共检测出 63 种与谵妄相关的血浆代谢物(p < 0.05)。在已知的代谢物中,我们的分析表明,两种特定代谢物(1-棕榈酰-2-棕榈酰-gpc (16:0/16:1)和高香草酸酯)和一种代谢物比值(磷酸盐与油酰-亚油酰-甘油(18:1 至 18:2))在所有分析方法中都与谵妄具有一致且显著的因果关系。结论我们的研究揭示了血液代谢物与谵妄风险之间的因果关系。众所周知,高甘油三酯与免疫和氧化还原有关,1-棕榈酰-2-棕榈酰-甘油三酯(16:0/16:1)和代谢物比率(磷酸盐与油酰-亚油酰-甘油(18:1 至 18:2))可能在脂质调节中发挥作用。这些发现可能会为确定合适的诊断标志物和针对谵妄患者特定血浆代谢物的潜在治疗策略提供新的见解。然而,要全面了解相关的生物机制,还需要进一步的实验。
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Genetic assessment of the causal effect of plasma metabolites and metabolic pathways on delirium

Purpose

Delirium has a significant impact on millions of people globally and is closely linked to an unfavorable prognosis for complications. Observational studies suggest that plasma metabolites may play significant roles as markers and effectors of delirium, but causal relationships have not yet been elucidated. Based on the most recent genome-wide association study (GWAS) data, our study aims to present novel insights into the genetic relationship between delirium and plasma metabolites. This investigation offers potential clues for utilizing plasma metabolites as predictors of delirium development.

Methods

We performed a thorough Mendelian randomization (MR) analysis to investigate the causal relationship between 1,091 individual metabolites and 309 metabolite ratios in plasma with respect to delirium. Inverse-variance weighting (IVW) was employed as the primary estimation method, while MR-Egger and weighed median methods were utilized to assess the robustness of the results. Sensitivity analyses encompassing the MR Pleiotropy RESidual Sum and Outlier (MR-PRESSO) test, Cochran Q test, leave-one-out analysis and MR Egger intercept analysis were also undertaken. Additionally, the MR Steiger test was performed to explore any potential reverse causal effect of metabolites on delirium.

Results

A total of 63 types of plasma metabolites associated with delirium were detected using the IVW method (p < 0.05). Among the known metabolites, our analysis revealed that two specific metabolites (1-palmitoyl-2-palmitoleoyl-gpc (16:0/16:1) and homovanillate) and a metabolite ratio (phosphate to oleoyl-linoleoyl-glycerol (18:1 to 18:2)) demonstrated a consistent and significant causal relationship with delirium across all analysis methods. Finally, no evidence of pleiotropy was detected in our analysis.

Conclusions

Our study has revealed a causal association between blood metabolites and the risk of delirium. homovanillate is known to be associated with immunity and redox, 1-palmitoyl-2-palmitoleoyl-gpc (16:0/16:1) and metabolite ratio (phosphate to oleoyl-linoleoyl-glycerol (18:1 to 18:2)) may play a role in lipid regulation. These findings may provide fresh insights into the identification of suitable diagnostic markers and potential treatment strategies focused on specific plasma metabolites in patients with delirium. However, further experiments are required to gain a comprehensive understanding of the underlying biological mechanisms involved.

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