PNPLA3 rs738409 polymorphism and kidney dysfunction: an association beyond nonalcoholic fatty liver disease?

Alessandro Mantovani, Giovanni Targher
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引用次数: 0

Abstract

This commentary is primarily devoted to a recent observational study by Mantovani and colleagues (Aliment Pharmacol Ther. 2023; 57: 1093-102) examining the adverse effect of the patatin-like phospholipase domain-containing protein-3 (PNPLA3 ) rs738409 G allele on the kidney function in a cohort of 1,144 middle-aged Italian individuals with metabolic dysfunction. In this study, the authors found that the PNPLA3 rs738409 G allele was significantly associated with lower levels of estimated glomerular filtrate rate (eGFR), even after adjusting for not only common anthropometric and cardiometabolic risk factors but also ethnicity, serum liver enzymes, use of drugs against dyslipidemia and chronic kidney disease polygenic risk score. Additionally, in a subgroup of 144 patients followed for a median of 17 months, the authors also found that the PNPLA3 rs738409 G allele was independently associated with a faster eGFR decline. Commenting on the cohort study by Mantovani et al ., we also summarized the rapidly expanding evidence linking the PNPLA3 rs738409 variant with the risk of kidney disease. Furthermore, we discussed the potential research implications of these findings.
PNPLA3 rs738409多态性与肾功能障碍:非酒精性脂肪肝以外的关联?
这篇评论主要是针对Mantovani及其同事最近的一项观察性研究(alment Pharmacol Ther. 2023;[57](93-102)研究了1144名意大利中年代谢功能障碍患者中patatin样磷脂酶结构域蛋白-3 (PNPLA3) rs738409g等位基因对肾功能的不良影响。在这项研究中,作者发现PNPLA3 rs738409 G等位基因与较低水平的估计肾小球滤过率(eGFR)显著相关,即使在调整了常见的人体测量学和心脏代谢危险因素,以及种族、血清肝酶、使用抗血脂异常药物和慢性肾脏疾病多基因风险评分后也是如此。此外,在144名患者中位随访17个月的亚组中,作者还发现PNPLA3 rs738409g等位基因与eGFR的快速下降独立相关。在评论Mantovani等人的队列研究时,我们也总结了将PNPLA3 rs738409变异与肾脏疾病风险联系起来的迅速扩大的证据。此外,我们还讨论了这些发现的潜在研究意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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