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孟德尔随机化研究:通过白细胞介素-20受体α亚基表达探索磷脂酰肌醇水平与肥厚型心肌病风险之间的关系。

Mendelian randomization investigation: Exploring the relationship between phosphatidylinositol levels and hypertrophic cardiomyopathy risk through interleukin-20 receptor subunit alpha expression.

作者信息

Huang Luofei, Shi Jian, Li Han, Lin Quanzhi

机构信息

Liuzhou Municipal Liutie Central Hospital, Liuzhou, Guangxi, China.

Department of Internal Medicine, The People's Hospital of Laibin, Laibin, Guangxi, China.

出版信息

Medicine (Baltimore). 2025 Aug 8;104(32):e43432. doi: 10.1097/MD.0000000000043432.

Abstract

This Mendelian randomization study investigated the causal relationship between phosphatidylinositol (PI) levels and hypertrophic cardiomyopathy (HCM) risk, while evaluating the potential mediating role of interleukin-20 receptor subunit alpha (IL-20RA). Leveraging genome-wide association study data from Finnish and European populations, our 2-sample Mendelian randomization analysis revealed a significant inverse association between PI levels and HCM risk (odds ratio [OR] = 0.686, 95% confidence interval [CI]: 0.512-0.921; P = .012), with no evidence of reverse causation. The analysis further demonstrated a positive correlation between PI and IL-20RA levels (OR = 1.090, 95% CI: 1.033-1.149; P = .002), while elevated IL-20RA showed a protective association against HCM (OR = 0.514, 95% CI: 0.302-0.873; P = .014). Mediation analysis indicated that approximately 15.2% of PI's protective effect was mediated through IL-20RA pathways. These findings suggest PI may mitigate HCM risk partially through IL-20RA-mediated mechanisms, highlighting potential therapeutic targets in lipid-inflammatory pathways for HCM intervention. Further research is needed to validate these observational genetic associations.

摘要

这项孟德尔随机化研究调查了磷脂酰肌醇(PI)水平与肥厚型心肌病(HCM)风险之间的因果关系,同时评估了白细胞介素-20受体亚基α(IL-20RA)的潜在中介作用。利用来自芬兰和欧洲人群的全基因组关联研究数据,我们的两样本孟德尔随机化分析显示PI水平与HCM风险之间存在显著的负相关(优势比[OR]=0.686,95%置信区间[CI]:0.512-0.921;P=0.012),且无反向因果关系的证据。分析进一步表明PI与IL-20RA水平之间存在正相关(OR=1.090,95%CI:1.033-1.149;P=0.002),而升高的IL-20RA显示出对HCM的保护作用(OR=0.514,95%CI:0.302-0.873;P=0.014)。中介分析表明,PI的保护作用约15.2%是通过IL-20RA途径介导的。这些发现表明PI可能部分通过IL-20RA介导的机制降低HCM风险,突出了脂质炎症途径中潜在的治疗靶点用于HCM干预。需要进一步的研究来验证这些观察到的基因关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4535/12338210/f2aad9f6a2e7/medi-104-e43432-g001.jpg

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