The α1-antichymotrypsin A-allele in German Parkinson disease patients

被引:11
作者
Grasbon-Frodl, EM
Egensperger, R
Kösel, S
Krüger, R
Riess, O
Mehraein, P
Graeber, MB
机构
[1] Max Planck Inst Neurobiol, Dept Neuromorphol, Mol Neuropathol Lab, D-85152 Martinsried, Germany
[2] Hannover Med Sch, Inst Neuropathol, Hannover, Germany
[3] Ruhr Univ Bochum, Dept Human Mol Genet, D-4630 Bochum, Germany
[4] Max Planck Inst Neurobiol, Dept Neuromorphol, Mol Neuropathol Lab, Martinsried, Germany
关键词
Alzheimer disease; apolipoprotein E; genetics; neurodegeneration; susceptibility allele;
D O I
10.1007/s007020050193
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
An increased frequency of the A-allele of the alpha(1)-antichymotrypsin (ACT) gene has been recently described in Japanese patients suffering from Parkinson disease (PD). In the present study, we have analyzed 62 German PD patients with regard to their ACT and APOE genotypes and compared them to 53 controls without clinical or pathological evidence of neurodegenerative disease. The A-allele frequency was 47% in PD patients compared to 54% in control cases excluding ACT as a major susceptibility factor for PD in the Caucasian population. Yet, ACT-A allele frequencies were significantly different (p < 0.001) between Japanese and German controls. Therefore, although our data do not suggest that the alpha(1)-ACT polymorphism is a significant risk factor for the development of PD, a consideration of differences in genetic background seems warranted when evaluating susceptibility factors for neurodegenerative disease.
引用
收藏
页码:729 / 736
页数:8
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