Please use this identifier to cite or link to this item: https://doi.org/10.1001/archneur.62.3.460
Title: Effect of MDR1 haplotype on risk of Parkinson disease
Authors: Tan, E.-K.
Chan, D.K.-Y.
Ng, P.-W.
Woo, J.
Teo, Y.Y.
Tang, K.
Wong, L.-P.
Chong, S.S. 
Tan, C.
Shen, H.
Zhao, Y.
Lee, C.G.L. 
Issue Date: Mar-2005
Citation: Tan, E.-K., Chan, D.K.-Y., Ng, P.-W., Woo, J., Teo, Y.Y., Tang, K., Wong, L.-P., Chong, S.S., Tan, C., Shen, H., Zhao, Y., Lee, C.G.L. (2005-03). Effect of MDR1 haplotype on risk of Parkinson disease. Archives of Neurology 62 (3) : 460-464. ScholarBank@NUS Repository. https://doi.org/10.1001/archneur.62.3.460
Abstract: Background: MDR1, a multidrug transporter, encodes a P-glycoprotein that regulates the bioavailability of xenobiotics and is highly expressed at the blood-brain-barrier. Two single nucleotide polymorphisms (SNPs) (e21/ 2677[G/T/A] and e26/3435[C/T]) in the MDR1 gene can lead to differences in MDR1 expression and function. Specific MDR1 alleles of the 2 SNPs are positively selected among ethnic Chinese but not in the white population. Objective: To determine whether specific haplotypes formed by SNPs e21/2677 and e26/3435 may protect against Parkinson disease (PD) among ethnic Chinese in Hong Kong. Design: Case-control study. Setting: Tertiary referral centers in Hong Kong. Subjects: One hundred eighty-five patients with PD and 206 control subjects. Interventions: The two SNPs were amplified in a single multiplex polymerase chain reaction. Five other SNPs that span 100 kilobases of the gene were also analyzed. Main Outcome Measures: Haplotypes frequencies, degree of haplotype association with the disease status, and estimated odds ratio for each haplotype with associated 95% confidence intervals. Results: In addition to 2677 G→T/A (exon 21) and 3435 C→T (exon 26), the other SNPs that were analyzed were -41 A→G (intron-1), -145 C→G (exon 1), -129 T→C (exon 1), 1236 T→C (exon 12), and 4036 A→G (exon 28). Haplotypes containing SNPs e21/2677 and e26/ 3435 were found to be significantly associated with risk of PD. In particular, the 2677T-3435T haplotype was strongly associated with a reduced risk of PD (P<.001; χ 2 = 14.521; odds ratio, 0.33; 95% confidence interval, 0.19-0.59). Conclusions: An MDR1 haplotype containing SNPs e21/ 2677T and e26/3435T protects against PD in ethnic Chinese, compatible with the observation of a recent positive selection of the T alleles of these 2 SNPs in this ethnic population.
Source Title: Archives of Neurology
URI: http://scholarbank.nus.edu.sg/handle/10635/107792
ISSN: 00039942
DOI: 10.1001/archneur.62.3.460
Appears in Collections:Staff Publications
Elements

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
archneur.62.3.460.pdf77.12 kBAdobe PDF

OPEN

PublishedView/Download

SCOPUSTM   
Citations

64
checked on Aug 11, 2022

WEB OF SCIENCETM
Citations

56
checked on Sep 27, 2021

Page view(s)

371
checked on Aug 4, 2022

Download(s)

1
checked on Aug 4, 2022

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.