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一项关于血浆脂质组、循环炎症蛋白与勃起功能障碍之间关联的孟德尔随机化研究。

A Mendelian randomization study on associations between plasma lipidome, circulating inflammatory proteins, and erectile dysfunction.

作者信息

Yu Jiacheng, Liang Peihe

机构信息

Department of Urology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.

出版信息

Transl Androl Urol. 2024 Dec 31;13(12):2724-2734. doi: 10.21037/tau-24-378. Epub 2024 Dec 28.

Abstract

BACKGROUND

Some studies suggest a potential association between plasma lipidome and erectile dysfunction (ED), but the underlying mechanism and whether circulating inflammatory proteins act as mediators remain unclear. The purpose of this study was to investigate the potential causal relationships between plasma lipidome, inflammatory proteins, and ED.

METHODS

Plasma lipidome, circulating inflammatory proteins, and ED cases were identified based on the summary data from several large-scale genome-wide association studies (GWAS). The causal relationships of plasma lipidome and circulating inflammatory proteins with ED were explored by a bidirectional two-sample, two-sample Mendelian randomization (MR) method. The inverse variance weighted (IVW) method was used as the primary analytical method. MR-Egger and the weighted median (IVW) methods were utilized as supplementary analytical techniques. Sensitivity analyses including MR-Pleiotropy RESidual Sum and Outlier method (PRESSO), Cochran's Q test, and MR-Egger intercept test were conducted to address heterogeneity and horizontal pleiotropy.

RESULTS

Ceramide (d42:2) and triacylglycerol (56:3) were found to be associated with an increased risk of ED, while phosphatidylethanolamine (O-18:1_18:2) and phosphatidylinositol (18:1_18:1) were linked to a decreased risk of ED. Interleukin-1α (IL-1α), IL-7, IL-17C, and the tumor necrosis factor (TNF) receptor superfamily member 9 (TNFRSF9) positively affected ED. Conversely, leukemia inhibitory factor and urokinase-type plasminogen activator (uPA) showed a negative impact. Mediation analysis indicated that the uPA mediated between Triacylglycerol (56:3) and ED, accounting for a mediation proportion of -14.71%.

CONCLUSIONS

There was a causal relationship between plasma lipidome and circulating inflammatory proteins with ED. Circulating inflammatory proteins appeared to mediate between triacylglycerol (56:3) levels and ED.

摘要

背景

一些研究表明血浆脂质组与勃起功能障碍(ED)之间可能存在关联,但潜在机制以及循环炎症蛋白是否作为中介尚不清楚。本研究的目的是探讨血浆脂质组、炎症蛋白与ED之间的潜在因果关系。

方法

基于几项大规模全基因组关联研究(GWAS)的汇总数据确定血浆脂质组、循环炎症蛋白和ED病例。采用双向双样本孟德尔随机化(MR)方法探讨血浆脂质组和循环炎症蛋白与ED的因果关系。采用逆方差加权(IVW)方法作为主要分析方法。MR-Egger和加权中位数(IVW)方法用作补充分析技术。进行了敏感性分析,包括MR-多效性残差和异常值方法(PRESSO)、 Cochr an's Q检验和MR-Egger截距检验,以解决异质性和水平多效性问题。

结果

发现神经酰胺(d42:2)和三酰甘油(56:3)与ED风险增加相关,而磷脂酰乙醇胺(O-18:1_18:2)和磷脂酰肌醇(18:1_18:1)与ED风险降低相关。白细胞介素-1α(IL-1α)、IL-7、IL-17C和肿瘤坏死因子(TNF)受体超家族成员9(TNFRSF9)对ED有正向影响。相反,白血病抑制因子和尿激酶型纤溶酶原激活剂(uPA)显示出负面影响。中介分析表明,uPA在三酰甘油(56:3)和ED之间起中介作用,中介比例为-14.71%。

结论

血浆脂质组和循环炎症蛋白与ED之间存在因果关系。循环炎症蛋白似乎在三酰甘油(56:3)水平和ED之间起中介作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ac6/11732301/b8d58a2e9864/tau-13-12-2724-f1.jpg

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