Lack of Association between the LRRK2 A419V Variant and Asian Parkinson's Disease

被引:0
作者
Gopalai, Aroma Agape [1 ]
Lim, Shen Yang [2 ]
Aziz, Zariah Abdul
Lim, Soo Kun [2 ]
Tan, Li Ping [2 ]
Chong, Yip Boon [2 ]
Tan, Chong Tin [2 ]
Puvanarajah, Santhi [3 ]
Viswanathan, Shanti [3 ]
Kuppusamy, Rishikesan [2 ]
Tan, Ai Huey [2 ]
Lim, Thien Thien [4 ]
Eow, Gaik Bee [4 ]
Norlinah, Mohamed Ibrahim [5 ]
Li, Hui Hua [6 ,7 ]
Zhao, Yi [6 ,7 ]
Ahmad-Annuar, Azlina [1 ]
机构
[1] Univ Malaya, Fac Med, Dept Biomed Sci, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Fac Med, Dept Med, Kuala Lumpur 50603, Malaysia
[3] Hosp Kuala Lumpur, Dept Neurol, Kuala Lumpur, Malaysia
[4] Hosp Pulau Pinang, Dept Neurol, George Town, Malaysia
[5] Univ Kebangsaan Malaysia, Dept Med, Bangi 43600, Malaysia
[6] Singapore Gen Hosp, Natl Neurosci Inst, Dept Neurol, Singapore, Singapore
[7] Singapore Gen Hosp, Natl Neurosci Inst, Dept Clin Res, Singapore, Singapore
关键词
Asian; A419V; Genetics; LRRK2; Parkinson's disease; RISK-FACTOR; GLY2385ARG; CHINESE; G2019S; SUSCEPTIBILITY;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The G2385R and R1628P LRRK2 gene variants have been associated with an increased risk of Parkinson's disease (PD) in the Asian population. Recently, a new LRRK2 gene variant, A419V, was reported to be a third risk variant for PD in Asian patients. Our objective was to investigate this finding in our cohort of Asian subjects. Materials and Methods: Eight hundred and twenty-eight subjects (404 PD patients, and 424 age and gender-matched control subjects without neurological disorders) were recruited. Genotyping was done by Taqman (R) allelic discrimination assay on an Applied Biosystems 7500 Fast Real-Time PCR machine. Results: The heterozygous A419V genotype was found in only 1 patient with PD, compared to 3 in the control group (0.4% vs 1.3%), giving an odds ratio of 0.35 (95% confidence interval (CI), 0.01 to 3.79; P = 0.624). Conclusion: A419V is not an important LRRK2 risk variant in our Asian cohort of patients with PD. Our data are further supported by a literature review which showed that 4 out of 6 published studies reported a negative association of this variant in PD.
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页码:237 / 240
页数:4
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