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K121Q ENPP1基因多态性在糖尿病及其并发症中的作用。

The role of K121Q ENPP1 polymorphism in diabetes mellitus and its complications.

作者信息

Leitão C B, Nabinger G B, Krahe A L, Bolson P B, Gerchman F, Friedman R, Gross J L, Canani L H

机构信息

Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brasil.

出版信息

Braz J Med Biol Res. 2008 Mar;41(3):229-34. doi: 10.1590/s0100-879x2006005000202. Epub 2007 Dec 20.

Abstract

The aim of the present study was to analyze the frequency of K121Q polymorphism in the ENPP1 gene of Brazilian subjects according to ethnic origin and to determine its possible association with diabetes mellitus (DM) and/or diabetic complications. A cross-sectional study was conducted on 1027 type 2 DM patients and 240 anonymous blood donors (BD). Ethnicity was classified based on self-report of European and African descent. The Q allele frequency was increased in African descendant type 2 DM patients (KK = 25.9%, KQ = 48.2%, and QQ = 25.9%) and BD (KK = 22.0%, KQ = 53.8%, and QQ = 24.2%) compared to European descendant type 2 DM patients (KK = 62.7%, KQ = 33.3%, and QQ = 4.1%) and BD (KK = 61.0%, KQ = 35.6%, and QQ = 3.4%). However, there was no difference in genotype distribution or Q allele frequency between diabetic and non-diabetic subjects (European descendants: DM = 0.21 vs BD = 0.21, P = 0.966, and African descendants: DM = 0.50 vs BD = 0.51, P = 0.899). In addition, there were no differences in clinical, laboratory or insulin resistance indices among the three genotypes. The prevalence of DM complications was also similar. In conclusion, K121Q polymorphism is more common among Afro-Brazilian descendants regardless of glycemic status or insulin sensitivity indices. Likewise, insulin sensitivity and DM chronic complications appear not to be related to the polymorphism in this sample.

摘要

本研究的目的是根据种族起源分析巴西受试者ENPP1基因中K121Q多态性的频率,并确定其与糖尿病(DM)和/或糖尿病并发症的可能关联。对1027例2型糖尿病患者和240名匿名献血者(BD)进行了横断面研究。种族根据欧洲和非洲血统的自我报告进行分类。与欧洲血统的2型糖尿病患者(KK = 62.7%,KQ = 33.3%,QQ = 4.1%)和BD(KK = 61.0%,KQ = 35.6%,QQ = 3.4%)相比,非洲血统的2型糖尿病患者(KK = 25.9%,KQ = 48.2%,QQ = 25.9%)和BD(KK = 22.0%,KQ = 53.8%,QQ = 24.2%)的Q等位基因频率增加。然而,糖尿病患者和非糖尿病患者之间的基因型分布或Q等位基因频率没有差异(欧洲血统:糖尿病患者= 0.21,BD = 0.21,P = 0.966;非洲血统:糖尿病患者= 0.50,BD = 0.51,P = 0.899)。此外,三种基因型在临床、实验室或胰岛素抵抗指标方面没有差异。糖尿病并发症的患病率也相似。总之,无论血糖状态或胰岛素敏感性指标如何,K121Q多态性在非裔巴西后裔中更为常见。同样,胰岛素敏感性和糖尿病慢性并发症似乎与该样本中的多态性无关。

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