性别特异性DNA甲基化与循环尿酸水平和bcg诱导的尿酸变化相关。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Zhaoli Liu, Tania O Crișan, Cancan Qi, Manoj Kumar Gupta, Xuan Liu, Simone J C F M Moorlag, Valerie A C M Koeken, Xun Jiang, Mohamad Ballan, L Charlotte J de Bree, Vera P Mourits, Xu Gao, Andrea Baccarelli, Joel Schwartz, Frank Pessler, Carlos A Guzmán, Yang Li, Mihai G Netea, Leo A B Joosten, Cheng-Jian Xu
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引用次数: 0

摘要

背景:尿酸浓度和生理调节尿酸体内平衡表现出明显的性别差异。DNA甲基化已被证明可以解释血清尿酸盐差异的很大一部分,介导尿酸盐浓度的遗传效应,并与心脏代谢性状共同调节。然而,尿酸盐浓度是否以性别依赖的方式与DNA甲基化相关尚不清楚。此外,值得研究的是,接种疫苗等扰动后的尿酸变化是否以性别特异性的方式与DNA甲基化有关。方法:我们研究了荷兰325名健康个体的DNA甲基化和血清尿酸浓度之间的关系。在卡介苗接种前后测量尿酸浓度和DNA甲基化,作为与痛风发作增加相关的扰动。关联分析包括联合分析、相互作用分析和性别分层分析。结果:215个CpG位点与男性血清尿酸相关,而5个CpG位点与女性血清尿酸相关,表明性别特异性关联。卡介苗接种后循环尿酸浓度显著增加,基线DNA甲基化与接种前后尿酸浓度差异以性别特异性方式相关。在男性中,与尿酸盐浓度相关的CpG位点在神经保护通路中富集,而在女性中,与尿酸盐变化相关的CpG位点与脂质和葡萄糖代谢有关。结论:我们的研究增强了对表观遗传因素如何以性别特异性方式调节血清尿酸水平的理解。这些见解突出了医学中个性化和针对性别的方法的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex-specific DNA methylation associations with circulating urate levels and BCG-induced urate changes.

Background: Urate concentration and the physiological regulation of urate homeostasis exhibit clear sex differences. DNA methylation has been shown to explain a substantial proportion of serum urate variance, mediate the genetic effect on urate concentration, and co-regulate with cardiometabolic traits. However, whether urate concentration is associated with DNA methylation in a sex-dependent manner is unknown. Additionally, it is worth investigating if urate changes after perturbations, such as vaccination, are associated with DNA methylation in a sex-specific manner.

Methods: We investigated the association between DNA methylation and serum urate concentrations in a Dutch cohort of 325 healthy individuals. Urate concentration and DNA methylation were measured before and after Bacillus Calmette-Guérin (BCG) vaccination, used as a perturbation associated with increased gout flares. The association analysis included united, interaction, and sex-stratified analysis.

Results: 215 CpG sites are associated with serum urate in males, while 5 CpG sites are associated with serum urate in females, indicating sex-specific associations. Circulating urate concentrations significantly increase after BCG vaccination, and baseline DNA methylation is associated with differences in urate concentration before and after vaccination in a sex-specific manner. The CpG sites associated with urate concentration in males are enriched in neuro-protection pathways, whereas in females, the urate change-associated CpG sites are related to lipid and glucose metabolism.

Conclusions: Our study enhances the understanding of how epigenetic factors contribute to regulating serum urate levels in a sex-specific manner. These insights highlight the importance of personalized and sex-specific approaches in medicine.

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