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

被引:2
作者
Penes, Ovidiu Nicolae [1 ]
Weber, Bernard [2 ]
Pop, Anca Lucia [3 ]
Bodnarescu-Cobanoglu, Mihaela [4 ]
Varlas, Valentin Nicolae [1 ]
Kucukberksun, Aleksandru Serkan [3 ]
Cretoiu, Dragos [1 ]
Varlas, Roxana Georgiana [1 ]
Zetu, Cornelia [4 ]
机构
[1] Carol Davila Univ Med & Pharm, Fac Med, 37 Dionisie Lupu St, Bucharest 020021, Romania
[2] Univ Hosp, Inst Med Virol, D-60596 Frankfurt, Germany
[3] Carol Davila Univ Med & Pharm, Fac Pharm, 6 Traian Vuia St, Bucharest 020945, Romania
[4] Natl Inst Nutr Diabet & Metab Dis N Paulescu, Bucharest 030167, Romania
关键词
genes; LEP; LEPR; GHRL; 5HTR2A; NPY; FTO; obesity; overweight; biomarkers; genotype; SNP; risk; cardiometabolic; BODY-MASS INDEX; RECEPTOR GENE; ASSOCIATION; CHILDHOOD;
D O I
10.3390/cardiogenetics14020008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:93 / 105
页数:13
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