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神经降压素U基因的单倍型、基因型和DNA甲基化水平与心脏代谢参数相关:莫利萨尼研究结果

Haplotypes, Genotypes, and DNA Methylation Levels of Neuromedin U Gene Are Associated with Cardio-Metabolic Parameters: Results from the Moli-sani Study.

作者信息

Noro Fabrizia, Marotta Annalisa, Costanzo Simona, Izzi Benedetta, Gialluisi Alessandro, De Curtis Amalia, Pepe Antonietta, Grossi Sarah, Di Castelnuovo Augusto, Cerletti Chiara, Donati Maria Benedetta, de Gaetano Giovanni, Gianfagna Francesco, Iacoviello Licia

机构信息

Research Unit of Epidemiology and Prevention, IRCCS NEUROMED, 86077 Pozzilli, IS, Italy.

EPIMED Research Center, Department of Medicine and Surgery, University of Insubria, 21100 Varese, VA, Italy.

出版信息

Biomedicines. 2025 Aug 5;13(8):1906. doi: 10.3390/biomedicines13081906.

Abstract

Neuromedin U (NMU) is a highly conserved gene encoding a neuropeptide involved in the regulation of feeding behavior and energy homeostasis. We aimed to analyze the association between genetic and epigenetic variations and cardio-metabolic parameters in an Italian population to identify the role of these variants in cardio-metabolic risk. A total of 4028 subjects were randomly selected from the Moli-sani study cohort. haplotypes were estimated using seven SNPs located in the gene body and in the promoter region; DNA methylation levels in the promoter region, previously associated with lipid-related variables in the same population, were also used. : Among the haplotypes inferred, the haplotype carrying the highest number of minor variants (frequency 16.6%), when compared with the most frequent haplotype, was positively associated with insulin levels, HOMA-IR, and diastolic blood pressure, and negatively with HDL-cholesterol. The multivariable analysis that considered methylation levels along with their interactions with SNPs showed that increased methylation levels in two close CpG sites were associated with higher levels of lipid-related variables. : This study supports a role for NMU as a regulator of human metabolism. This finding suggests that NMU could be a potential target for preventive interventions against coronary and cerebrovascular diseases, and that genetic and epigenetic variability may serve as a biomarker for cardio-metabolic risk.

摘要

神经介素U(NMU)是一种高度保守的基因,编码一种参与调节进食行为和能量稳态的神经肽。我们旨在分析意大利人群中基因和表观遗传变异与心血管代谢参数之间的关联,以确定这些变异在心血管代谢风险中的作用。从莫利 - 萨尼研究队列中随机选取了4028名受试者。使用位于基因体和启动子区域的7个单核苷酸多态性(SNP)估计单倍型;还使用了先前在同一人群中与脂质相关变量相关的启动子区域的DNA甲基化水平。在所推断的单倍型中,与最常见单倍型相比,携带次要变异数量最多的单倍型(频率为16.6%)与胰岛素水平、稳态模型评估胰岛素抵抗(HOMA-IR)和舒张压呈正相关,与高密度脂蛋白胆固醇呈负相关。考虑甲基化水平及其与SNP相互作用的多变量分析表明,两个相邻CpG位点甲基化水平的升高与脂质相关变量的较高水平相关。这项研究支持NMU作为人类代谢调节剂的作用。这一发现表明,NMU可能是预防冠状动脉和脑血管疾病干预措施的潜在靶点,并且基因和表观遗传变异可能作为心血管代谢风险的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/140e/12383673/f3b8a347f9e5/biomedicines-13-01906-g001.jpg

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