Chandak Giriraj R, Ward Kirsten J, Yajnik Chittaranjan S, Pandit Anand N, Bavdekar Ashish, Joglekar Charu V, Fall Caroline H D, Mohankrishna P, Wilkin Terence J, Metcalf Bradley S, Weedon Michael N, Frayling Timothy M, Hattersley Andrew T
Genome Research Group, Centre for Cellular and Molecular Biology, Hyderabad, India.
BMC Med Genet. 2006 Oct 10;7:76. doi: 10.1186/1471-2350-7-76.
The APOA5 gene variants, -1131T>C and S19W, are associated with altered triglyceride concentrations in studies of subjects of Caucasian and East Asian descent. There are few studies of these variants in South Asians. We investigated whether the two APOA5 variants also show similar association with various lipid parameters in Indian population as in the UK white subjects.
We genotyped 557 Indian adults from Pune, India, and 237 UK white adults for -1131T>C and S19W variants in the APOA5 gene, compared their allelic and genotype frequency and determined their association with fasting serum triglycerides, total cholesterol, HDL and LDL cholesterol levels using univariate general linear analysis. APOC3 SstI polymorphism was also analyzed in 175 Pune Indian subjects for analysis of linkage disequilibrium with the APOA5 variants.
The APOA5 -1131C allele was more prevalent in Indians from Pune (Pune Indians) compared to UK white subjects (allele frequency 20% vs. 4%, p = 0.00001), whereas the 19W allele was less prevalent (3% vs. 6% p = 0.0015). Patterns of linkage disequilibrium between the two variants were similar between the two populations and confirmed that they occur on two different haplotypes. In Pune Indians, the presence of -1131C allele and the 19W allele was associated with a 19% and 15% increase respectively in triglyceride concentrations although only -1131C was significant (p = 0.0003). This effect size was similar to that seen in the UK white subjects. Analysis of the APOC3 SstI polymorphism in 175 Pune Indian subjects showed that this variant is not in appreciable linkage disequilibrium with the APOA5 -1131T>C variant (r2 = 0.07).
This is the first study to look at the role of APOA5 in Asian Indian subjects that reside in India. The -1131C allele is more prevalent and the 19W allele is less prevalent in Pune Indians compared to UK Caucasians. We confirm that the APOA5 variants are associated with triglyceride levels independent of ethnicity and that this association is similar in magnitude in Asian Indians and Caucasians. The -1131C allele is present in 36% of the Pune Indian population making it a powerful marker for looking at the role of elevated triglycerides in important conditions such as pancreatitis, diabetes and coronary heart disease.
在对白种人和东亚裔受试者的研究中,载脂蛋白A5(APOA5)基因变异体-1131T>C和S19W与甘油三酯浓度改变有关。针对南亚人的此类变异体研究较少。我们调查了这两种APOA5变异体在印度人群中是否也如在英国白人受试者中一样,与各种脂质参数存在相似的关联。
我们对来自印度浦那的557名印度成年人以及237名英国白人成年人的APOA5基因-1131T>C和S19W变异体进行基因分型,比较它们的等位基因和基因型频率,并使用单变量一般线性分析确定它们与空腹血清甘油三酯、总胆固醇、高密度脂蛋白和低密度脂蛋白胆固醇水平的关联。还对175名浦那印度受试者的载脂蛋白C3(APOC3)SstI多态性进行了分析,以研究其与APOA5变异体的连锁不平衡情况。
与英国白人受试者相比,APOA5 -1131C等位基因在来自浦那的印度人(浦那印度人)中更为普遍(等位基因频率分别为20%和4%,p = 0.00001),而19W等位基因则不太普遍(3%对6%,p = 0.0015)。两种变异体之间的连锁不平衡模式在两个人群中相似,并证实它们位于两种不同的单倍型上。在浦那印度人中,-1131C等位基因和19W等位基因的存在分别与甘油三酯浓度升高19%和15%相关,尽管只有-1131C具有统计学意义(p = 0.0003)。这种效应大小与在英国白人受试者中观察到的相似。对175名浦那印度受试者的APOC3 SstI多态性分析表明,该变异体与APOA5 -1131T>C变异体不存在明显的连锁不平衡(r2 = 0.07)。
这是第一项研究APOA5在居住在印度的亚洲印度人受试者中的作用的研究。与英国白种人相比,-1131C等位基因在浦那印度人中更为普遍,而19W等位基因则不太普遍。我们证实,APOA5变异体与甘油三酯水平相关,且不受种族影响,这种关联在亚洲印度人和白种人中的程度相似。-1131C等位基因存在于36%的浦那印度人群中,使其成为研究甘油三酯升高在胰腺炎、糖尿病和冠心病等重要疾病中作用的有力标志物。