Srivastava Apurva, Mittal Balraj, Prakash Jai, Srivastava Pranjal, Srivastava Nimisha, Srivastava Neena
a Department of Physiology , King George's Medical University , Chowk, Lucknow, Uttar Pradesh , India .
b Department of Medical Genetics , Sanjay Gandhi Post Graduate Institute of Medical Sciences , Lucknow, Uttar Pradesh , India .
Ann Hum Biol. 2016 Sep;43(5):451-6. doi: 10.3109/03014460.2015.1103902. Epub 2015 Nov 3.
Obesity is an increasingly important health problem worldwide as well as in developing countries like India. Recent genetic studies suggest that obesity associated FTO and IRX3 are functionally linked and many effects due to genetic variants in FTO gene act through IRX3.
To evaluate the association of FTO and IRX3 genetic variants towards obesity risk.
North Indian individuals categorised as non-obese (BMI < 30 kg/m(2)) and obese (BMI ≥ 30 kg/m(2)) were selected. FTO rs8050136, rs1421085, rs9939609, rs17817449 and IRX3 rs3751723 were genotyped by means of validated Taqman® allelic discrimination to evaluate their association with obesity by means of single locus logistic regression by SPSS ver. 19 and multi-locus linkage and haplotype analysis by SNPStats and gene-gene interaction with Generalised Multifactor Dimensionality Reduction (GMDR) ver.6.
In single locus analysis, FTO rs8050136 CA (p = 0.0001; OR (95% CI) = 2.4 (1.7-3.4) and AA (p = 0.0001; OR (95% CI) = 3.1 (1.9-5.2); FTO rs1421085 TA (p = 0.0001; OR (95% CI) = 2.1 (1.4-3.0) and AA (p = 0.0001; OR (95% CI) = 3.0 (1.8-5.0); FTO rs9939609 TC (p = 0.0001; OR (95% CI) = 2.1 (1.5-3.1) and CC (p = 0.0001; OR (95% CI) = 4.2 (2.5-7.3) along with TG (p = 0.001; OR (95% CI) = 2.1 (1.3-3.2) and GG (p = 0.021; OR (95% CI) = 3.8 (1.2-11.8) genotypes of FTO rs17817449 with GT (p = 0.0001; OR (95% CI) = 2.1 (1.5-3.1) and TT (p = 0.012; OR (95% CI) = 3.3 (1.8-3.6) genotypes of IRX3 rs3751723 were significantly associated with obesity. In multi-locus analysis, SNPs of FTO and IRX3 were in strong linkage disequilibrium and in haplotype and GMDR analysis the SNPs were significantly associated with obesity risk (p < 0.05).
This is the first study to reveal that genetic variants of both FTO and IRX3 genes are in high linkage disequilibrium (LD) and are associated with obesity risk in North Indians.
肥胖在全球范围内以及在印度等发展中国家都是一个日益重要的健康问题。最近的基因研究表明,与肥胖相关的FTO和IRX3在功能上存在联系,FTO基因中的许多遗传变异效应是通过IRX3起作用的。
评估FTO和IRX3基因变异与肥胖风险的关联。
选取北印度非肥胖个体(BMI<30kg/m²)和肥胖个体(BMI≥30kg/m²)。通过经过验证的Taqman®等位基因鉴别法对FTO rs8050136、rs1421085、rs9939609、rs17817449以及IRX3 rs3751723进行基因分型,使用SPSS 19版通过单基因座逻辑回归评估它们与肥胖的关联,并通过SNPStats进行多基因座连锁和单倍型分析,以及使用广义多因素降维法(GMDR)6.0版进行基因-基因相互作用分析。
在单基因座分析中,FTO rs8050136的CA基因型(p = 0.0001;OR(95%CI)= 2.4(1.7 - 3.4))和AA基因型(p = 0.0001;OR(95%CI)= 3.1(1.9 - 5.2));FTO rs1421085的TA基因型(p = 0.0001;OR(95%CI)= 2.1(1.4 - 3.0))和AA基因型(p = 0.0001;OR(95%CI)= 3.0(1.8 - 5.0));FTO rs9939609的TC基因型(p = 0.0001;OR(95%CI)= 2.1(1.5 - 3.1))和CC基因型(p = 0.0001;OR(95%CI)= 4.2(2.5 - 7.3)),以及FTO rs17817449的TG基因型(p = 0.001;OR(95%CI)= 2.1(1.3 - 3.2))和GG基因型(p = 0.021;OR(95%CI)= 3.8(1.2 - 11.8)),IRX3 rs3751723的GT基因型(p = 0.0001;OR(95%CI)= 2.1(1.5 - 3.1))和TT基因型(p = 0.012;OR(95%CI)= 3.3(1.8 - 3.6))均与肥胖显著相关。在多基因座分析中,FTO和IRX3的单核苷酸多态性处于强连锁不平衡状态,在单倍型和GMDR分析中,这些单核苷酸多态性与肥胖风险显著相关(p<0.05)。
这是第一项揭示FTO和IRX3基因的遗传变异处于高度连锁不平衡(LD)状态且与北印度人肥胖风险相关的研究。