Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson’s disease

Authors: Ross, Jay P.; Dupré, Nicolas; Dauvilliers, Yves; Strong, Stephanie; Ambalavanan, Amirthagowri; Spiegelman, Dan; Dionne-Laporte, Alexandre; Pourcher, EmmanuelleLanglois, MélanieBoivin, Michel; Leblond, Claire S.; Dion, Patrick A.; Rouleau, Guy A.; Gan-Or, Ziv
Abstract: DNAJC13 mutations have been suggested to cause Parkinson's disease (PD), yet subsequent studies reported conflicting results on this association. In the present study, we sequenced the coding region of DNAJC13 in a French-Canadian/French cohort of 528 PD patients and 692 controls. A total of 62 (11.7%) carriers of rare DNAJC13 variants were identified among the PD patients compared with 82 (11.8%) among controls (p = 1.0). Two variants that were previously suggested to be associated with PD, p.R1516H and p.L2170W, were identified with similar directions of association as previously reported. The p.R1516H was found in 2 (0.4%) patients versus 6 (0.9%, nonsignificant) controls and the p.L2170W variant was found in 9 (1.7%) patients and 5 (0.7%, nonsignificant) controls. Meta-analysis with previous reports resulted in odds ratios of 0.32 (95% confidence interval = 0.15–0.68, p = 0.0037) and 2.68 (95% confidence interval = 1.32–5.42, p = 0.007), respectively. Our results provide some support for the possibility that specific DNAJC13 variants may play a minor role in PD susceptibility, although studies in additional populations are necessary.
Document Type: Article de recherche
Issue Date: 3 May 2016
Open Access Date: 3 May 2017
Document version: AM
Permalink: http://hdl.handle.net/20.500.11794/13593
This document was published in: Neurobiology of Aging, Vol. 45, 212.e13–212.e17 (2016)
https://doi.org/10.1016/j.neurobiolaging.2016.04.023
Elsevier
Alternative version: 10.1016/j.neurobiolaging.2016.04.023
27236598
Collection:Articles publiés dans des revues avec comité de lecture

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