Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease

被引:156
作者
Ross, Owen A. [1 ]
Wu, Yih-Ru [2 ,3 ]
Lee, Mei-Ching [4 ]
Funayama, Manabu [5 ]
Chen, Meng-Ling [6 ]
Soto, Alexandra I. [1 ]
Mata, Ignacio F. [7 ]
Lee-Chen, Guey-Jen [8 ]
Chen, Chiung Mei [2 ,3 ]
Tang, Michelle [9 ]
Zhao, Yi [9 ]
Hattori, Nobutaka [5 ,10 ]
Farrer, Matthew J. [1 ]
Tan, Eng-King [9 ,11 ]
Wu, Ruey-Meei [6 ]
机构
[1] Mayo Clin, Coll Med, Dept Neurosci, Jacksonville, FL 32224 USA
[2] Chang Gung Mem Hosp, Dept Neurol, Taipei 10591, Taiwan
[3] Chang Gung Univ, Coll Med, Taipei, Taiwan
[4] Cathay Gen Hosp, Dept Neurol, Taipei, Taiwan
[5] Juntendo Univ, Sch Med, Res Inst Dis Old Ages, Bunkyo Ku, Tokyo 113, Japan
[6] Natl Taiwan Univ, Coll Med, Natl Taiwan Univ Hosp, Dept Neurol, Taipei, Taiwan
[7] Univ Washington, Sch Med, Dept Neurol, Seattle, WA USA
[8] Natl Taiwan Normal Univ, Dept Life Sci, Taipei, Taiwan
[9] Singapore Gen Hosp, Dept Neurol, Natl Neurosci Inst Singapore, Singapore, Singapore
[10] Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 113, Japan
[11] Duke NUS Grad Med Sch, Singapore, Singapore
关键词
D O I
10.1002/ana.21405
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Common genetic variants that increase the risk for Parkinson's disease may differentiate patient subgroups and influence future individualized therapeutic strategies. Herein we show evidence for leucine-rich repeat kinase 2 (LRRK2) c.4883G > C (R1628P) as a risk factor in ethnic Chinese populations. A study of 1,986 individuals from 3 independent centers in Taiwan and Singapore demonstrates that Lrrk2 R1628P increases risk for Parkinson's disease (odds ratio, 1.84; 95% confidence interval, 1.20-2.83; P = 0.006). Haplotype analysis suggests an ancestral founder for carriers approximately 2,500 years ago. These findings support the importance of LRRK2 variants in sporadic Parkinson's disease.
引用
收藏
页码:88 / 92
页数:5
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