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首页|期刊导航|中华医学杂志(英文版)|Genetic variability in adapter proteins with APPL1/2 is associated with the risk of coronary artery disease in type 2 diabetes mellitus in Chinese Han population

Genetic variability in adapter proteins with APPL1/2 is associated with the risk of coronary artery disease in type 2 diabetes mellitus in Chinese Han population

MA Xiao-wei DING Shan MA Xiao-dan GU Nan GUO Xiao-hui

中华医学杂志(英文版)2011,Vol.124Issue(22):3618-3621,4.
中华医学杂志(英文版)2011,Vol.124Issue(22):3618-3621,4.DOI:10.3760/cma.j.issn.0366-6999.2011.22.004

Genetic variability in adapter proteins with APPL1/2 is associated with the risk of coronary artery disease in type 2 diabetes mellitus in Chinese Han population

Genetic variability in adapter proteins with APPL1/2 is associated with the risk of coronary artery disease in type 2 diabetes mellitus in Chinese Han population

MA Xiao-wei 1DING Shan 1MA Xiao-dan 1GU Nan 1GUO Xiao-hui1

作者信息

  • 1. Department of Endocrinology, Peking University First Hospital,Beijing 100034, China
  • 折叠

摘要

Abstract

Background Adaptor proteins containing PH domain,PTB domain,and leucine zipper motif 1 and 2 (APPL1/2) play a key role in cell proliferation in many tissues.APPL1 or APPL2 as an adaptor for adiponectin receptors mediates the signaling pathway of adiponectin which acts as an anti-atherosclerotic adipokine.This study aimed to investigate whether genetic variations in the APPL 1/2 genes affect the risk of coronary artery disease (CAD) in Chinese patients with type 2 diabetes mellitus (T2DM).Methods Seven haplotype-tagging single nucleotide polymorphisms (tag-SNPs) were selected from CHB HapMap database (Phase Ⅱ) and total 203 CAD-positive cases and 106 CAD-negative controls with T2DM were genotyped for the 7 tag-SNPs by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay.Results The minor allele G of rs4640525 at APPL1 locus was protective from CAD in patients with T2DM,with the carriers of genotype CC at higher risk of CAD compared with non-carriers (OR=2.830,95% CI 1.285-6.230,P=0.010;OR'=4.992,95% CI=1.758-14.173,P'=0.003,after adjustment for the other known CAD risk factors); the homozygotes of AA at rs11112412 in APPL2.gene had higher risk of CAD compared with those of GG (adjusted OR:=5.697,95% CI 1.006-32.257,P'=0.049).Conclusion Genetic variation(s) in APPL1/2 may be associated with CAD risk in T2DM in Chinese population.

关键词

APPL1/APPL2/genes/coronary artery disease/type 2 diabetes mellitus/Chinese

Key words

APPL1/APPL2/genes/coronary artery disease/type 2 diabetes mellitus/Chinese

引用本文复制引用

MA Xiao-wei,DING Shan,MA Xiao-dan,GU Nan,GUO Xiao-hui..Genetic variability in adapter proteins with APPL1/2 is associated with the risk of coronary artery disease in type 2 diabetes mellitus in Chinese Han population[J].中华医学杂志(英文版),2011,124(22):3618-3621,4.

基金项目

This work was supported by grants from the National Basic Research Program of China (973 Program) (No.2006CB503903and 2006CB503908). (973 Program)

中华医学杂志(英文版)

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