Interleukin-1A polymorphism is not associated with late onset Alzheimer's disease

被引:26
作者
Fidani, L
Goulas, A
Mirtsou, V
Petersen, RC
Tangalos, E
Crook, R
Hardy, J
机构
[1] Aristole Univ, Sch Med, Dept Pharmacol, Thessaloniki 54006, Greece
[2] Mayo Clin, Dept Neurol, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Neurosci, Jacksonville, FL 32224 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; interleukin-1A; polymorphism; genetics;
D O I
10.1016/S0304-3940(02)00114-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Over the past few years, association studies have proposed a number of potential genetic risk factors for Alzheimer's disease (AD). With the exception of the epsilon4 allele of the apolipoprotein E gene, whose association with the late onset type of AD (LOAD) has been confirmed, the relative significance of most of these associations is still in question. A polymorphism in the interleukin-1A gene (IL-1A2) has been suggested as a risk factor for the early onset as well as for LOAD. In this study, the distribution of IL-1A alleles was examined in a cohort of predominantly LOAD patients and in control individuals. No significant difference was detected in genotype or allele frequencies (odds ratios of 0.929 and 0.743, respectively; P > 0.5). We conclude that IL-1A genotype is not a major risk factor for LOAD. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:81 / 83
页数:3
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