Rainero I, Bo M, Ferrero M, Valfrè W, Vaula G, Pinessi L
Neurology III-Headache Center, Department of Neuroscience, University of Turin, Via Cherasco, 15-10126 Torino, Italy.
Neurobiol Aging. 2004 Nov-Dec;25(10):1293-8. doi: 10.1016/j.neurobiolaging.2004.02.011.
Inflammatory processes are involved in the pathogenesis of Alzheimer's disease (AD). Several studies have addressed the effects of interleukin-1 (IL-1) genes polymorphisms on the risk of developing AD. The results are not in full agreement on whether these polymorphisms are associated with the disease. To clarify this issue, we performed a meta-analysis of all the association studies between IL-1 genes and AD. Due to the relatively small number of published articles, the meta-analysis was restricted to the association of the IL-1alpha -889 C/T gene polymorphism and AD. Under a random effects model, the risk for the disease was significantly higher in subjects with the T/T genotype in comparison with both C/T (OR: 1.51; 95% C.I.: 1.15-1.99) and C/C (OR: 1.49; 95% C.I.: 1.09-2.03) subjects. There was modest heterogeneity for these effect estimates. Analysis of subgroups showed a significant association in patients with early-onset AD but not in late-onset AD. Our data support a significant but modest association between the T/T genotype of the IL-1alpha gene and AD.
炎症过程参与了阿尔茨海默病(AD)的发病机制。多项研究探讨了白细胞介素-1(IL-1)基因多态性对患AD风险的影响。关于这些多态性是否与该疾病相关,研究结果并未完全一致。为阐明这一问题,我们对所有关于IL-1基因与AD的关联研究进行了荟萃分析。由于已发表文章数量相对较少,荟萃分析仅限于IL-1α -889 C/T基因多态性与AD的关联。在随机效应模型下,与C/T(比值比:1.51;95%置信区间:1.15 - 1.99)和C/C(比值比:1.49;95%置信区间:1.09 - 2.03)受试者相比,T/T基因型受试者患该疾病的风险显著更高。这些效应估计值存在适度的异质性。亚组分析显示,早发型AD患者存在显著关联,而晚发型AD患者则不然。我们的数据支持IL-1α基因的T/T基因型与AD之间存在显著但适度的关联。