拉丁美洲混合人群中FTO和IRX3基因与肥胖及相关代谢疾病的相互作用分析:体重超标的可能风险增加

Pub Date : 2022-06-14 eCollection Date: 2022-04-01 DOI:10.25100/cm.v53i2.4874
María Stephany Ruiz-Díaz, Diana Mena-Yi, Doris Gómez-Camargo, Gustavo Mora-García
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引用次数: 0

摘要

背景:脂肪质量与肥胖相关基因(FTO)一直是与常见肥胖相关的基因之一。FTO的单核苷酸多态性(snp)与IRX3基因有关。目的:本研究旨在验证以下假设:1)FTO和IRX3中常见的snp与肥胖及相关疾病相关;Ii)两个基因之间存在显著的连锁不平衡。方法:在哥伦比亚加勒比海海岸进行横断面研究。测量了人体测量和生化变量,并诊断了肥胖和代谢紊乱。4个snp基因分型:3个位于FTO位点(rs17817449, rs8050136, rs9939609), 1个位于IRX3位点(rs3751723)。估计了这些snp之间的LD。采用逻辑回归模型估计相关性。结果:共纳入受试者792例。FTO和IRX3不在LD中(D′≤0.03;R2≤0.03)。TT基因型(rs9939609)与腰围相关(p= 0.04;adj-p= 0.01), IRX3 SNP与体重超标(BWE)有关(OR= 1.06, adj-p= 0.03)。1个FTO-IRX3单倍型与BWE (G-A-A-T, rs17817449-rs8050136-rs9939609-rs3751723)相关;OR= 0.67, p= 0.04)。对三杂交群体进行混合调整后,这些关系仍具有统计学意义(p= 0.03)。结论:拉丁美洲成年人中,FTO与腰围有关,IRX3与BWE有关。在对性别、年龄和遗传血统进行调整后,这种关系仍然具有统计学意义。尽管这些基因不在LD中,但涉及FTO-IRX3的单倍型的发现表明基因-基因相互作用与BWE风险增加有关。
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Interaction analysis of FTO and IRX3 genes with obesity and related metabolic disorders in an admixed Latin American population: a possible risk increases of body weight excess.

Background: Fat Mass and Obesity-related (FTO) has been one of the genes consistently related to common obesity. Single nucleotide polymorphisms (SNPs) in FTO have been linked with the IRX3 gene.

Aim: This study was designed by testing the hypothesis that: i) common SNPs in FTO and IRX3 are associated with obesity and related disorders; ii) there is significant linkage disequilibrium between both genes.

Methods: A cross-sectional study was carried out on the Colombian Caribbean Coast. Anthropometric and biochemical variables were measured, and obesity and metabolic disorders were diagnosed. Four SNPs were genotyped: 3 at FTO locus (rs17817449, rs8050136, rs9939609) and one at IRX3 locus (rs3751723). LD between these SNPs was estimated. A logistic regression model was applied to estimate associations.

Results: A total of 792 subjects were included. FTO and IRX3 were not in LD (D'≤ 0.03; R2≤ 0.03). TT genotype (rs9939609) was found to be associated with waist circumference (p= 0.04; adj-p= 0.01), and IRX3 SNP with Body Weight Excess (BWE) (OR= 1.06, adj-p= 0.03). One FTO-IRX3 haplotype was associated with BWE (G-A-A-T, rs17817449-rs8050136-rs9939609-rs3751723; OR= 0.67, p= 0.04). The statistical significance of these relations continued after admixture adjustment for a three-hybrid population (p= 0.03).

Conclusions: FTO was related to waist circumference, and IRX3 was associated with BWE in Latin American adults. This relation remained statistically significant after an adjustment for sex, age, and genetic ancestry was performed. Despite that these genes were not in LD, findings of a haplotype involving FTO-IRX3 suggest a gene-gene interaction associated with an increased risk of BWE.

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