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

作者：Ma Xiao wei^*; Ding Shan; Ma Xiao dan; Gu Nan; Guo Xiao hui

来源：Chinese Medical Journal, 2011, 124(22): 3618-3621.

DOI：10.3760/cma.j.issn.0366-6999.2011.22.004

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

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 APPL1/2 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. Chin Med J 2011;124(22):3618-3621

• 出版日期2011-11-20
• 单位北京大学