期刊
NEUROSCIENCE LETTERS
卷 489, 期 3, 页码 164-167出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2010.12.008
关键词
Alzheimer's disease; Toll-like receptor 2; Microsatellite polymorphism
资金
- National Natural Science Foundation of China [81000544]
- Qingdao Bureau of Science and Technology [8-2-1-2-nsh, 09-1-1-30-nsh, 10-3-3-4-19-nsh]
- Shandong Provincial Outstanding Medical Academic Professional Program
The amyloid beta protein (A beta) deposits in the brains of patients with Alzheimer's disease (AD) are closely associated with innate immune responses that were assumed to play a pivotal role in the pathogenesis of AD. Toll-like receptor 2 (TLR2) is thought to contribute to A beta clearance. Studies have reported the presence and functional implications of guanine-thymine (GT) repeat microsatellite polymorphisms in intron II of the human TLR2 gene. The present study evaluated the association of the microsatellite polymorphism and sporadic late-onset AD (LOAD) in the Han Chinese population. The numbers of (GT) repeats were counted in 137 AD patients and in 137 non-AD control subjects, using polymerase chain reaction and genescan analysis. The alleles were divided into three subclasses: (GT)16 or less as the S allele, (GT)17 to (GT)22 as the M allele, and (GT)23 or more as the L allele. Patients with AD had more S alleles (P < 0.001; odds ratio (OR) = 2.32; 95% confidence interval (CI) = 1.57-3.42) and fewer L alleles (P = 0.02: OR = 0.66; 95% CI = 0.46-0.93) than did healthy controls. Genotypes SS and SM were more common, whereas ML and SL were less common in patients with AD. In subgroup analyses, the genotypes including S alleles were associated with an increased risk of LOAD (OR = 2.05, 95% CI = 1.26-3.34), and this association was influenced by the presence of APOE epsilon 4 alleles. This study demonstrates an association of microsatellite polymorphisms in intron II of the human TLR2 gene with risk for LOAD in Han Chinese. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据