LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson's disease compared to late-onset patients

被引:9
作者
Chan, Daniel Kam Yin [1 ,2 ]
Ng, Ping Wing [3 ]
Mok, Vincent [4 ]
Yeung, Jonas [5 ]
Fang, Zhi Ming [6 ]
Clarke, Raymond [6 ]
Leung, Edward [3 ]
Wong, Lawrence [4 ]
机构
[1] Bankstown Lidcombe Hosp, Dept Aged Care & Rehabil, Bankstown, NSW 2200, Australia
[2] Univ New S Wales, Fac Med, Kensington, NSW 2033, Australia
[3] United Christian Hosp, Dept Med & Geriatr, Hong Kong, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Div Neurol, Hong Kong, Hong Kong, Peoples R China
[5] AHML Nethersole Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
[6] St George Hosp, Canc Care Ctr, Kogarah, NSW, Australia
关键词
early-onset Parkinson's disease; LRRK2 Gly2385Arg mutation; Chinese;
D O I
10.1007/s00702-008-0065-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The frequency of LRRK2 Gly2385Arg mutation in Hong Kong Chinese with early-onset (age <= 45 years) Parkinson's disease was identified and compared with late-onset patients (age > 50 years) and controls. The mutation prevalence were 8.8, 8.3, and 0% for early-onset, late-onset, and controls, respectively. The mean age of onset among LRRK2 G2385R carriers was 42.7 years old for early-onset compared to 74.3 for late-onset patients. LRRK2 G2385R mutation appears to be as prevalent among early-onset as late-onset patients.
引用
收藏
页码:1275 / 1277
页数:3
相关论文
共 13 条
[1]   Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease [J].
Berg, D ;
Schweitzer, KJ ;
Leitner, P ;
Zimprich, A ;
Lichtner, P ;
Belcredi, P ;
Brüssel, T ;
Schulte, C ;
Maass, S ;
Nägele, T ;
Wszolek, ZK ;
Gasser, T .
BRAIN, 2005, 128 :3000-3011
[2]  
Cao L., 2007, MOVEMENT DISORD, V22, P2439
[3]   Comparison of environmental and genetic factors for Parkinson's disease between Chinese and Caucasians [J].
Chan, DKY ;
Cordato, D ;
Bui, T ;
Mellick, G ;
Woo, J .
NEUROEPIDEMIOLOGY, 2004, 23 (1-2) :13-22
[4]  
CHAN DKY, 2008, J NEURAL TRANSM
[5]   A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan [J].
Di Fonzo, Alessio ;
Wu-Chou, Yah-Huei ;
Lu, Chin-Song ;
van Doeselaar, Marina ;
Simons, Erik J. ;
Rohe, Christan F. ;
Chang, Hsiu-Chen ;
Chen, Rou-Shayn ;
Weng, Yi-Hsin ;
Vanacore, Nicola ;
Breedveld, Guido J. ;
Oostra, Ben A. ;
Bonifati, Vincenzo .
NEUROGENETICS, 2006, 7 (03) :133-138
[6]   Leucine-Rich Repeat kinase 2 G238SR variant is a risk factor for Parkinson disease in Asian population [J].
Funayama, Manabu ;
Li, Yuanzhe ;
Tomiyama, Hiroyuki ;
Yoshino, Hiroyo ;
Imamichi, Yoko ;
Yamamoto, Mitsutoshi ;
Murata, Miho ;
Toda, Tatsushi ;
Mizuno, Yoshikuni ;
Hattori, Nobutaka .
NEUROREPORT, 2007, 18 (03) :273-275
[7]   A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan [J].
Fung, Hon-Chung ;
Chen, Chiung-Mei ;
Hardy, John ;
Singleton, Andrew B. ;
Wu, Yih-Ru .
BMC NEUROLOGY, 2006, 6 (1)
[8]   Common LRRK2 mutation in idiopathic Parkinson's disease [J].
Gilks, WP ;
Abou-Sleiman, PM ;
Gandhi, S ;
Jain, S ;
Singleton, A ;
Lees, AJ ;
Shaw, K ;
Bhatia, KP ;
Bonifati, V ;
Quinn, NP ;
Lynch, J ;
Healy, DG ;
Holton, JL ;
Revesz, T ;
Wood, NW .
LANCET, 2005, 365 (9457) :415-416
[9]   The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease [J].
Lu, CS ;
Simons, EJ ;
Wu-Chòu, YH ;
Di Fonzo, A ;
Chang, HC ;
Chen, RS ;
Weng, YH ;
Rohé, CF ;
Breedveld, GJ ;
Hattori, N ;
Gasser, T ;
Oostra, BA ;
Bonifati, V .
PARKINSONISM & RELATED DISORDERS, 2005, 11 (08) :521-522
[10]   Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease [J].
Paisán-Ruíz, C ;
Jain, S ;
Evans, EW ;
Gilks, WP ;
Simón, J ;
van der Brug, M ;
de Munain, AL ;
Aparicio, S ;
Gil, AM ;
Khan, N ;
Johnson, J ;
Martinez, JR ;
Nicholl, D ;
Carrera, IM ;
Pena, AS ;
de Silva, R ;
Lees, A ;
Martí-Massó, JF ;
Pérez-Tur, J ;
Wood, NW ;
Singleton, AB .
NEURON, 2004, 44 (04) :595-600