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rs17817449变异体增加巴西队列中严重肥胖风险:一项病例对照研究

rs17817449 Variant Increases the Risk of Severe Obesity in a Brazilian Cohort: A Case-Control Study.

作者信息

Salum Kaio Cezar Rodrigues, Assis Izadora Sthephanie da Silva, Kopke Úrsula de Almeida, Palhinha Lohanna, Abreu Gabriella de Medeiros, Gouvêa Laura Wendling, Teixeira Myrela Ribeiro, Mattos Fernanda Cristina C, Nogueira Neto José Firmino, Felício Rafaela de Freitas Martins, Rosado Eliane Lopes, Zembrzuski Verônica Marques, Campos Junior Mario, Maya-Monteiro Clarissa Menezes, Cabello Pedro Hernán, Carneiro João Regis Ivar, Bozza Patrícia Torres, Kohlrausch Fabiana Barzotto, da Fonseca Ana Carolina Proença

机构信息

Medical Clinic Department, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.

Human Genetics Laboratory, Oswaldo Cruz Institute, Rio de Janeiro, Brazil.

出版信息

Diabetes Metab Syndr Obes. 2025 Jan 31;18:283-303. doi: 10.2147/DMSO.S451401. eCollection 2025.

Abstract

PURPOSE

Obesity is a complex disease caused by a combination of genetic, environmental, and epigenetic factors, and is associated with an increased risk of chronic diseases. The leptin-melanocortin pathway integrates peripheral signals about the body's energy stores with a central neuronal circuit in the hypothalamus. This pathway has been extensively studied over the years, as genetic variations in genes related to it may play a crucial role in determining an individual's susceptibility to obesity. Therefore, we analyzed the association between obesity and specific polymorphisms in leptin-melanocortin-related genes such as rs1137101, rs1042571, rs7799039, rs6265, rs17817449, rs121909065, and rs16147/rs5574.

PATIENTS AND METHODS

The study enrolled 501 participants from Rio de Janeiro, Brazil, with obesity class II or greater (BMI ≥ 35 kg/m2) and normal weight controls (18.5≤ BMI ≤24.9 kg/m2). We collected demographic, body composition, biochemical, and genotyping data by real-time PCR, and performed logistic and linear regression analyses to investigate the association of polymorphisms with severe obesity status and obesity-related quantitative parameters.

RESULTS

Individuals with severe obesity had significantly higher anthropometric measures, blood pressure, and biochemical levels. The rs17817449 TT genotype was associated with a significantly higher risk of developing severe obesity, and distinct cytokine expression was observed across the rs17817449 genotypes. The rs6265 dominant-model and rs16147 CC genotypes were associated with triglyceride levels and childhood obesity, respectively. Finally, individuals with obesity were more likely to carry a greater number of risk alleles than those without obesity.

CONCLUSION

Our study observed an important association between rs17817449 polymorphism with obesity and obesity-related traits. Additionally, rs6265 dominant-model was associated with triglyceride serum levels, and rs16147 may have a role in obesity onset.

摘要

目的

肥胖是一种由遗传、环境和表观遗传因素共同导致的复杂疾病,与慢性疾病风险增加相关。瘦素-黑皮质素通路将有关身体能量储备的外周信号与下丘脑的中枢神经回路整合在一起。多年来,该通路已得到广泛研究,因为与其相关基因的遗传变异可能在决定个体对肥胖的易感性方面发挥关键作用。因此,我们分析了肥胖与瘦素-黑皮质素相关基因(如rs1137101、rs1042571、rs7799039、rs6265、rs17817449、rs121909065以及rs16147/rs5574)中特定多态性之间的关联。

患者与方法

该研究招募了来自巴西里约热内卢的501名参与者,包括II级或更严重肥胖者(BMI≥35kg/m²)以及正常体重对照者(18.5≤BMI≤24.9kg/m²)。我们通过实时聚合酶链反应收集了人口统计学、身体成分、生化和基因分型数据,并进行了逻辑回归和线性回归分析,以研究多态性与严重肥胖状态及肥胖相关定量参数之间的关联。

结果

严重肥胖个体的人体测量指标、血压和生化水平显著更高。rs17817449 TT基因型与发生严重肥胖的风险显著更高相关,并且在rs17817449各基因型中观察到不同的细胞因子表达。rs6265显性模型和rs16147 CC基因型分别与甘油三酯水平和儿童肥胖相关。最后,肥胖个体比非肥胖个体更有可能携带更多的风险等位基因。

结论

我们的研究观察到rs17817449多态性与肥胖及肥胖相关特征之间存在重要关联。此外,rs6265显性模型与血清甘油三酯水平相关,并且rs16147可能在肥胖发病中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9298/11792641/5e394a7d384e/DMSO-18-283-g0001.jpg

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