Mitochondrial DNA haplogroups J and K are not protective for Parkinson's disease in the Australian community

MtDNA haplogroups J and K have been associated with a decreased risk of developing Parkinson's disease (PD). To confirm this finding, we compared the distribution of mtDNA haplogroups J and K in a large sample of Australian patients with PD (n = 890) to population‐based controls (n = 3,491). We...

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Published inMovement disorders Vol. 24; no. 2; pp. 290 - 292
Main Authors Mehta, Prachi, Mellick, George D., Rowe, Dominic B., Halliday, Glenda M., Jones, Michael M., Manwaring, Neil, Vandebona, Himesha, Silburn, Peter A., Wang, Jie Jin, Mitchell, Paul, Sue, Carolyn M.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 30.01.2009
Wiley
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ISSN0885-3185
1531-8257
1531-8257
DOI10.1002/mds.22389

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Summary:MtDNA haplogroups J and K have been associated with a decreased risk of developing Parkinson's disease (PD). To confirm this finding, we compared the distribution of mtDNA haplogroups J and K in a large sample of Australian patients with PD (n = 890) to population‐based controls (n = 3,491). We assigned subjects to haplogroups J or K using standard PCR/RFLP techniques. Of the 890 subjects with PD, 10.6% were haplogroup J (95% CI 8.6–12.8, n = 94) and 7.1% were haplogroup K (95% CI 5.5–8.9, n = 63). In our controls, 10.2% belonged to haplogroup J (95% CI 9.2–11.2, n = 356), and 7.8% were in haplogroup K (95% CI 6.9–8.7, n = 272). There was no significant difference in the prevalence of mtDNA haplogroup J or K in PD patients compared to population‐based controls. Our findings indicate that mtDNA haplogroups J and K are not associated with a lower risk of PD. © 2008 Movement Disorder Society
Bibliography:NSW Parkinson's Disease Association
Potential conflict of interest: Nothing to report.
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ArticleID:MDS22389
Australian National Health & Medical Research Council, Canberra, Australia - No. 302166
Australian Brain Foundation
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0885-3185
1531-8257
1531-8257
DOI:10.1002/mds.22389