Confirmation of the association between LRRK2 R1628P variant and susceptibility to Parkinson's disease in the Thai population

被引:12
作者
Pulkes, Teeratorn [1 ]
Papsing, Chutima [1 ]
Thakkinstian, Ammarin [2 ]
Pongpakdee, Sunsanee [3 ]
Kulkantrakorn, Kongkiat [4 ]
Hanchaiphiboolkul, Suchat [5 ]
Tiamkao, Somsak [6 ]
Boonkongchuen, Pairoj [1 ]
机构
[1] Mahidol Univ, Ramathibodi Hosp, Fac Med, Dept Med,Div Neurol, Bangkok 10400, Thailand
[2] Mahidol Univ, Ramathibodi Hosp, Fac Med, Sect Clin Epidemiol & Biostat, Bangkok 10400, Thailand
[3] Bhumibol Adulyadej Hosp, Dept Med, Div Neurol, Bangkok, Thailand
[4] Thammasat Univ, Fac Med, Dept Med, Div Neurol, Pathum Thani, Thailand
[5] Prasat Neurol Inst, Dept Neurol, Bangkok, Thailand
[6] Khon Kaen Univ, Fac Med, Dept Med, Div Neurol, Khon Kaen, Thailand
关键词
LRRK2; R1628P; Parkinson's disease; Early-onset Parkinson's disease; RISK-FACTOR; EXONIC VARIANTS; TAIWAN;
D O I
10.1016/j.parkreldis.2014.06.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: LRRK2 p.R1628P (c.4883G > C) is associated with Parkinson's disease (PD) in Chinese and Thais. However, some studies in other East Asian ethnic groups did not observe this association. Carriers of p.R1628P are about 3-5% Chinese and Thais. In contrast, Japanese, Koreans and Malays are much less prevalent (0-<1%). The contradictory results may be caused by insufficient sample sizes especially studies in ethnic groups with low prevalence, which, theoretically need a much larger sample size. We conducted a case-control Thai PD study with appropriate size in order to support the role of p.R1628P related to susceptibility to PD. Methods: Estimated total sample size of 958 Thai subjects was needed. 485 PD patients and 480 controls were recruited. The p.R1628P was screened by RFLP and confirmed by direct sequencing. Clinical characteristics were compared between PD patients with and without p.R1628P. Results: 54 PD patients (11%) and 29 control subjects (6%) carried p.R1628P. Multiple logistic regression analysis showed that GC and CC genotypes were significantly higher in PD patients than in controls (OR = 1.81, 95%CI = 1.10-2.97). The PD patients carrying p.R1628P had earlier age at onset (56 +/- 13 vs 60 +/- 12; P = 0.021) and a more rapidly progressive course (P < 0.001) than the patients carrying wild-type nucleotide. Conclusions: We confirm the association between p.R1628P and risk of developing PD in the appropriated sample-sized cohort. Certain LRRK2 variants appear to be generally distributed among East Asians, however, in widely different frequencies. In order to study role of such variants in PD, it should be carefully estimated the appropriate sample size. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1018 / 1021
页数:4
相关论文
共 12 条
  • [1] A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan
    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
    [J]. NEUROGENETICS, 2006, 7 (03) : 133 - 138
  • [2] Leucine-Rich Repeat kinase 2 G238SR variant is a risk factor for Parkinson disease in Asian population
    Funayama, Manabu
    Li, Yuanzhe
    Tomiyama, Hiroyuki
    Yoshino, Hiroyo
    Imamichi, Yoko
    Yamamoto, Mitsutoshi
    Murata, Miho
    Toda, Tatsushi
    Mizuno, Yoshikuni
    Hattori, Nobutaka
    [J]. NEUROREPORT, 2007, 18 (03) : 273 - 275
  • [3] A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan
    Fung, Hon-Chung
    Chen, Chiung-Mei
    Hardy, John
    Singleton, Andrew B.
    Wu, Yih-Ru
    [J]. BMC NEUROLOGY, 2006, 6 (1)
  • [4] ACCURACY OF CLINICAL-DIAGNOSIS OF IDIOPATHIC PARKINSONS-DISEASE - A CLINICOPATHOLOGICAL STUDY OF 100 CASES
    HUGHES, AJ
    DANIEL, SE
    KILFORD, L
    LEES, AJ
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1992, 55 (03) : 181 - 184
  • [5] The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population
    Kim, Jong-Min
    Lee, Jee-Young
    Kim, Hee Jin
    Kim, Ji Seon
    Shin, Eun-Soon
    Cho, Jin-Hwan
    Park, Sung Sup
    Jeon, Beom S.
    [J]. PARKINSONISM & RELATED DISORDERS, 2010, 16 (02) : 85 - 88
  • [6] Frequencies of LRRK2 variants in Thai patients with Parkinson's disease: evidence for an R1628P founder
    Pulkes, Teeratorn
    Papsing, Chutima
    Mahasirimongkol, Surakameth
    Busabaratana, Manisa
    Kulkantrakorn, Kongkiat
    Tiamkao, Somsak
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2011, 82 (10) : 1179 - 1180
  • [7] Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
    Ross, Owen A.
    Wu, Yih-Ru
    Lee, Mei-Ching
    Funayama, Manabu
    Chen, Meng-Ling
    Soto, Alexandra I.
    Mata, Ignacio F.
    Lee-Chen, Guey-Jen
    Chen, Chiung Mei
    Tang, Michelle
    Zhao, Yi
    Hattori, Nobutaka
    Farrer, Matthew J.
    Tan, Eng-King
    Wu, Ruey-Meei
    [J]. ANNALS OF NEUROLOGY, 2008, 64 (01) : 88 - 92
  • [8] Ross OA, 2011, LANCET NEUROL, V10, P898, DOI 10.1016/S1474-4422(11)70175-2
  • [9] Lrrk2 R1628P in Non-Chinese Asian Races
    Tan, Eng-King
    Tang, Michelle
    Tan, Louis C.
    Wu, Yih-Ru
    Wu, Ruey-Meei
    Ross, Owen A.
    Zhao, Yi
    [J]. ANNALS OF NEUROLOGY, 2008, 64 (04) : 472 - 473
  • [10] Quantitative assessment of the effect of LRRK2 exonic variants on the risk of Parkinson's disease: A meta-analysis
    Wu, Xi
    Tang, Ke-Fu
    Li, Yang
    Xiong, Yu-Yu
    Shen, Lu
    Wei, Zhi-Yun
    Zhou, Ke-Jun
    Niu, Jia-Min
    Han, Xia
    Yang, Lun
    Feng, Guo-Yin
    He, Lin
    Qin, Sheng-Ying
    [J]. PARKINSONISM & RELATED DISORDERS, 2012, 18 (06) : 722 - 730