Lack of association between the interleukin-1 alpha (-889) polymorphism and early-onset Parkinson's disease

被引:17
|
作者
Möller, JC
Depboylu, C
Kölsch, H
Lohmüller, F
Bandmann, O
Gocke, P
Du, YS
Paus, S
Wüllner, U
Gasser, T
Oertel, WH
Klockgether, T
Dodel, RC [1 ]
机构
[1] Univ Bonn, Dept Neurol & Psychiat, D-5300 Bonn, Germany
[2] Univ Marburg, Dept Neurol, Marburg, Germany
[3] Indiana Univ, Sch Med, Dept Neurol, Indianapolis, IN 46204 USA
[4] Univ Tubingen, Hertie Inst Brain Res, Dept Neurodegenerat Dis, Tubingen, Germany
关键词
Parkinson's disease; inflammation; interleukins; genes;
D O I
10.1016/j.neulet.2004.01.058
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
An increasing number of studies have shown that an inflammatory process is part of Parkinson's disease (PD) brain pathology. Interleukin-1 (IL-1) is a multifunctional cytokine and is considered to contribute to several inflammatory diseases. Recently, we detected an associated risk in a subgroup of PD patients with a disease onset <50 years and a C to T transition in the IL-1alpha promoter (-889). One-hundred-seventy-six German PD patients (42.1 +/- 6.4 years; 42.4% male) and 170 unrelated age-matched control individuals (40.4 +/- 8.7 years; 57.6% male) were investigated for the presence of the IL-1alpha (-889C/T) polymorphism. No significant difference in the allelic distribution of the analyzed IL-1alpha polymorphism has been found between PD and controls. We conclude that the C/T polymorphism in the IL-1alpha promoter region at -889 does not increase the risk to develop PD. (C) 2004 Elsevier Ireland ltd. All rights reserved.
引用
收藏
页码:195 / 197
页数:3
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