Please use this identifier to cite or link to this item: https://doi.org/10.1001/archneur.62.3.460
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dc.titleEffect of MDR1 haplotype on risk of Parkinson disease
dc.contributor.authorTan, E.-K.
dc.contributor.authorChan, D.K.-Y.
dc.contributor.authorNg, P.-W.
dc.contributor.authorWoo, J.
dc.contributor.authorTeo, Y.Y.
dc.contributor.authorTang, K.
dc.contributor.authorWong, L.-P.
dc.contributor.authorChong, S.S.
dc.contributor.authorTan, C.
dc.contributor.authorShen, H.
dc.contributor.authorZhao, Y.
dc.contributor.authorLee, C.G.L.
dc.date.accessioned2014-11-10T09:52:33Z
dc.date.available2014-11-10T09:52:33Z
dc.date.issued2005-03
dc.identifier.citationTan, 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
dc.identifier.issn00039942
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/107792
dc.description.abstractBackground: 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1001/archneur.62.3.460
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOCHEMISTRY
dc.contributor.departmentPAEDIATRICS
dc.description.doi10.1001/archneur.62.3.460
dc.description.sourcetitleArchives of Neurology
dc.description.volume62
dc.description.issue3
dc.description.page460-464
dc.description.codenARNEA
dc.identifier.isiut000227446000017
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