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北印度人群中白细胞介素-1β(-511C/T)和白细胞介素-1受体拮抗剂(86bp重复序列)基因多态性与2型糖尿病的遗传关联。

Genetic association of interleukin-1beta (-511C/T) and interleukin-1 receptor antagonist (86 bp repeat) polymorphisms with Type 2 diabetes mellitus in North Indians.

作者信息

Achyut B R, Srivastava Akanksha, Bhattacharya Sandeep, Mittal Balraj

机构信息

Sanjay Gandhi Postgraduate Institute of Medical Sciences Lucknow-226014, India.

出版信息

Clin Chim Acta. 2007 Feb;377(1-2):163-9. doi: 10.1016/j.cca.2006.09.012. Epub 2006 Oct 27.

Abstract

BACKGROUND

Type 2 diabetes mellitus (T2DM) is associated with a subclinical systemic inflammation and development of complications like nephropathy, retinopathy, neuropathy and hypertension. We studied the genetic association of bi-allelic polymorphism (-511C/T) of interleukin (IL)-1beta and 86 bp variable number tandem repeat (VNTR) polymorphism of natural receptor antagonist (IL-1RN) with T2DM and associated complications in North Indians.

METHODS

We genotyped 200 patients with T2DM and 223 healthy control subjects for IL-1beta (-511C/T) by PCR-RFLP. Genotyping of IL-1RN (VNTR) polymorphism was determined by gel electrophoresis after PCR amplification.

RESULTS

Interleukin-1beta (-511C/T) and IL-1RN (VNTR) polymorphisms were significantly associated with T2DM. IL-1beta -511T, IL-1RN2 and IL-1RN3 alleles were associated with high risk of T2DM whereas; individuals with IL-1beta -511C and IL-1RN1 alleles were at low risk. Haplotype frequency analysis showed that T2 (IL-1beta -511T/IL-1RN2) haplotype was associated with the high risk (p=0.000; OR=2.4, 95% CI 1.68-3.34) and C1 (IL-1beta -511C/IL-1RN*1) haplotype showed low risk (p=0.000; OR=0.38, 95% CI 0.27-0.53). Further, CT, TT genotypes of IL-1beta (-511C/T) and 1/2 genotype of IL-1RN (VNTR) were found to be associated with risk of complications particularly with nephropathy in T2DM.

CONCLUSION

The IL-1beta (-511C/T) and IL-1RN (VNTR) polymorphisms are significantly associated with increased risk of T2DM as well as associated complications in North Indians.

摘要

背景

2型糖尿病(T2DM)与亚临床全身炎症及肾病、视网膜病变、神经病变和高血压等并发症的发生有关。我们研究了白细胞介素(IL)-1β的双等位基因多态性(-511C/T)和天然受体拮抗剂(IL-1RN)的86 bp可变数目串联重复序列(VNTR)多态性与北印度人T2DM及其相关并发症的遗传关联。

方法

我们采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对200例T2DM患者和223例健康对照者的IL-1β(-511C/T)进行基因分型。PCR扩增后通过凝胶电泳确定IL-1RN(VNTR)多态性的基因分型。

结果

白细胞介素-1β(-511C/T)和IL-1RN(VNTR)多态性与T2DM显著相关。IL-1β -511T、IL-1RN2和IL-1RN3等位基因与T2DM高风险相关,而IL-1β -511C和IL-1RN1等位基因个体风险较低。单倍型频率分析显示,T2(IL-1β -511T/IL-1RN2)单倍型与高风险相关(p = 0.000;比值比[OR]=2.4,95%置信区间[CI] 1.68 - 3.34),C1(IL-1β -511C/IL-1RN*1)单倍型显示低风险(p = 0.000;OR = 0.38,95% CI 0.27 - 0.53)。此外,发现IL-1β(-511C/T)的CT、TT基因型和IL-1RN(VNTR)的1/2基因型与并发症风险相关,尤其是T2DM患者的肾病风险。

结论

IL-1β(-511C/T)和IL-1RN(VNTR)多态性与北印度人T2DM风险增加及其相关并发症显著相关。

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