首页> 外文期刊>International Journal of Experimental Diabetes Research: Experimental Diabesity Research >Association of HLA-B Gene Polymorphisms with Type 2 Diabetes in Pashtun Ethnic Population of Khyber Pakhtunkhwa, Pakistan
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Association of HLA-B Gene Polymorphisms with Type 2 Diabetes in Pashtun Ethnic Population of Khyber Pakhtunkhwa, Pakistan

机译:HLA-B基因多态性与2型糖尿病在巴基斯坦,巴基斯坦,巴基斯坦

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Human leukocyte antigen (HLA) system is the most polymorphic and gene dense region of human DNA that has shown many disease associations. It has been further divided into HLA classes I, II, and III. Polymorphism in HLA class II genes has been reported to play an important role in the pathogenesis of type 1 diabetes (T1D). It also showed association with T2D in different ethnic populations. However, a little is known about the relationship of HLA class I gene polymorphism and T2D. This study has evaluated the association of HLA-B (class I gene) variants with T2D in Pashtun ethnic population of Khyber Pakhtunkhwa. In the first phase of the study, whole exome sequencing (WES) of 2 pooled DNA samples was carried out, and DNA pools used were constructed from 100 diabetic cases and 100 control subjects. WES results identified a total of SNPs in HLA-B gene. In the next phase, first 5 out of reported SNPs were genotyped using MassARRAY? system in order to validate WES results and to confirm association of selected SNPs with T2D. Minor allele frequencies (MAFs) and selected SNPs×T2D association were determined using chi-square test and logistic regression analysis. The frequency of minor C allele was significantly higher in the T2D group as compared to control group (45.0% vs. 13.0%) ( ) for rs2308655 in HLA-B gene. No significant difference in MAF distribution between cases and controls was observed for rs1051488, rs1131500, rs1050341, and rs1131285 ( ). Binary logistic regression analyses showed significant results for SNP rs2308655 ( , , and ), while no considerable association was observed for the other 4 SNPs. However, when adjusted for these variants, the association of rs2308655 further strengthened significantly ( , , and ), except for rs1131500, which has no additive effect. In conclusion, the finding of this study suggests rs2308655 variant in HLA-B gene as risk variant for T2D susceptibility in Pashtun population.
机译:人白细胞抗原(HLA)系统是人DNA最多态性和基因浓密区域,其具有许多疾病关联。它进一步分为HLA课程I,II和III。据报道,HLA II类基因中的多态性在1型糖尿病(T1D)的发病机制中发挥着重要作用。它还显示出与不同种族种群的T2D相关联。然而,关于HLA I类基因多态性和T2D的关系,稍微熟知。该研究评估了HLA-B(I类基因)变体与T2D在帕什屯族族群Khyber Pakhtunkhwa的族族的关联。在研究的第一阶段,进行了2个合并的DNA样品的全外壳测序(WES),使用的DNA池由100例糖尿病病例和100种对策进行。 WES结果鉴定了HLA-B基因中的SNP。在下阶段,先报告的SNP中的前5个使用MassArray进行基因分型?系统为了验证WES结果并确认所选SNP与T2D的关联。使用Chi-Square测试和Logistic回归分析确定了次要等位基因频率(MAF)和所选SNPS×T2D关联。与HLA-B基因的RS2308655的对照组(45.0%Vs.13.0%)()相比,T2D组的次要C等位基因的频率显着高。对于RS1051488,RS1131500,RS1050341和RS1131285(),观察到病例和控制之间的MAF分布没有显着差异。二进制逻辑回归分析对SNP RS2308655(和)显示出显着的结果,而另外4个SNP没有观察到相当大的关联。然而,在调整这些变体时,除了RS1131500之外,RS2308655的关联进一步强化了(和),除了RS1131500,没有添加效果。总之,本研究的发现表明HLA-B基因的RS2308655变体作为Pashtun人口T2D易感性的风险变量。

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