Genetic Predisposition to Parkinson’s Disease: CYP2D6 and HFE in the Faroe Islands
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2008/03/01
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Details
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Personal Author:Brosen K ; Grandjean P ; Halling J ; Petersen MS ; Weihe P ; Brosen K ; Grandjean P ; Halling J ; Petersen MS ; Weihe P
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Description:OBJECTIVE: To investigate whether the genetic variants of CYP2D6 and HFE are more frequent in Parkinson's disease (PD) patients compared with controls in a population where the prevalence of these variants and PD are increased. METHODS: Blood samples were collected from 79 PD patients and 154 controls in the Faroe Islands. Genotyping for the 'CYP2D6*3, *4, *6 and *9' alleles and for the C282Y and H63D mutations were performed by real-time polymerase chain reaction before Taqman assessment. RESULTS: The frequency of CYP2D6 poor metabolizers among the patients was not higher compared with the frequency found in the control group (chi2 test, P=0.86). The odds ratio was 0.92 (95% confidence interval: 0.44-1.90). Neither was a difference in HFE genotype or allele frequencies found between the patients and the controls, and the C282Y and H63D mutation carrier frequencies did not reveal any difference (chi2 test, P=0.50 and 0.60, respectively). CONCLUSION: This study does not support an association between PD and mutations of the CYP2D6 and HFE genes, although a weak association cannot be excluded. The high frequency of PD in the Faroes is most likely the result of interactions between multiple genetic and environmental factors, still to be identified. [Description provided by NIOSH]
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ISSN:1744-6872
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Pages in Document:209-212
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Volume:18
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Issue:3
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NIOSHTIC Number:nn:20056306
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Citation:Pharmacogenet Genomics 2008 Mar; 18(3):209-212
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Contact Point Address:Jo'nrit Halling, MSc, Clinical Pharmacology, Faculty of Health Sciences, Institute of Public Health, University of Southern Denmark, Winslowparken 19, DK-5000 Odense C, Denmark
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Email:jhalling@health.sdu.dk
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Federal Fiscal Year:2008
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Performing Organization:Harvard School of Public Health
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Peer Reviewed:True
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Start Date:20050701
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Source Full Name:Pharmacogenetics and Genomics
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End Date:20280630
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Main Document Checksum:urn:sha-512:225b018e77bd600b1c8999606201a6ecb7a6723e1dab986520ca0839055b655b83d492895f34efb7821860c25d38bb14e9db3e9f1ab5b844b504adcea9ea5069
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