基因多态性 LEP、LEPR、5HT2A、GHRL、NPY 和 FTO--代谢风险评估中的肥胖生物标志物:罗马尼亚超重和肥胖人群的回顾性试点研究

IF 0.5 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiogenetics Pub Date : 2024-05-20 DOI:10.3390/cardiogenetics14020008
O. Peneş, Bernard Weber, A. Pop, M. Bodnarescu-Cobanoglu, V. Varlas, Aleksandru Serkan Kucukberksun, D. Crețoiu, Roxana Georgiana Varlas, Cornelia Zetu
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引用次数: 0

摘要

全基因组关联研究(GWAS)成功揭示了肥胖症的众多易感基因位点。PREDATORR研究(2014年)显示,在罗马尼亚,20-79岁的成年人中有346%超重,31.4%肥胖,具有高心脏代谢并发症风险,这一数字使罗马尼亚近67%的人口处于异常体重组。我们的研究旨在调查与肥胖相关的代谢性疾病的遗传基础现状,并应用于一组试点患者,专门研究已知多态性及其单倍型对六个食物摄入调节基因的影响、这六个基因是瘦素(LEP)、瘦素受体(LEP-R)、5-羟色胺受体(5HTR2A)、胃泌素(GHRL)、神经肽 Y(NPY)和脂肪量与肥胖相关蛋白(FTO):LEP A-2548G、LEPR A-223G、5HTR2A G-1439A、GHRL G-72T、NPY T-29063C、FTO A-T 和体重指数(BMI)。研究发现,LEP-2548 rs7799039 基因的 AG 基因型与肥胖风险之间存在明显联系,尤其是 40-49 岁的男性,肥胖的可能性增加了约 7 倍。5HTR2A rs6311 AA 基因型与较高的体重指数有关,但无统计学意义。FTO rs9939609 基因的 AA 基因型是肥胖风险的重要预测因子。除这些重要发现外,LEPR、5HTR2A、GHRL 和 NPY 基因均未发现实质性关联。单倍型关联分析表明,GRGMLA(rs7799039、rs1137101、rs6311、rs696217、rs16139、rs9939609序列)单倍型对肥胖易感性有提示性作用。连锁不平衡(LD)分析表明,LEP与LEPR基因(p = 0.04)、LEP与GHRL基因(p = 0.0047)以及GHRL与FTO基因(p = 0.03)之间存在统计学意义上的显著关联。据我们所知,我们的研究是为数不多的针对罗马尼亚人群的研究之一,旨在成为进一步研究有针对性的干预策略以降低心脏代谢风险的起点。
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Gene Polymorphisms LEP, LEPR, 5HT2A, GHRL, NPY, and FTO-Obesity Biomarkers in Metabolic Risk Assessment: A Retrospective Pilot Study in Overweight and Obese Population in Romania
Genome-wide association studies (GWAS) have successfully revealed numerous susceptibility loci for obesity. The PREDATORR study (2014) shows that in Romania, 346% of adults aged 20–79 y/o are overweight, and 31.4% are obese with a high risk of cardiometabolic complications, a number that puts almost 67% of Romania’s population in the abnormal weight group. Our study aims to investigate the current status of the genetic foundation in metabolic disease associated with obesity, applied to a pilot group of patients specifically examining the impact of known polymorphisms and their haplotype of six food intake-regulating genes, namely leptin (LEP), leptin receptor (LEP-R), serotonin receptor (5HTR2A), ghrelin (GHRL), neuropeptide Y (NPY), and fat-mass and obesity-associated protein (FTO) with the following polymorphisms: LEP A-2548G, LEPR A-223G, 5HTR2A G-1439A, GHRL G-72T, NPY T-29063C, FTO A-T, and body mass index (BMI). A notable link between the LEP-2548 rs7799039 gene’s AG genotype and the risk of obesity was observed, particularly pronounced in males aged 40–49, with an approximately seven-fold increased likelihood of obesity. The 5HTR2A rs6311 AA genotype was associated with a higher BMI, which was not statistically significant. The FTO rs9939609 gene’s AA genotype emerged as a significant predictor of obesity risk. Besides these significant findings, no substantial associations were observed with the LEPR, 5HTR2A, GHRL, and NPY genes. Haplotype association analysis showed a suggestive indication of GRGMLA (rs7799039, rs1137101, rs6311, rs696217, rs16139, rs9939609 sequence) haplotype with a susceptibility effect towards obesity predisposition. Linkage disequilibrium (LD) analysis showed statistically significant associations between LEP and LEPR gene (p = 0.04), LEP and GHRL gene (p = 0.0047), and GHRL and FTO gene (p = 0.03). Our study, to the best of our knowledge, is one of the very few on the Romanian population, and aims to be a starting point for further research on the targeted interventional strategies to reduce cardiometabolic risks.
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来源期刊
Cardiogenetics
Cardiogenetics CARDIAC & CARDIOVASCULAR SYSTEMS-
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