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. 2017 Dec:45:39-43.
doi: 10.1016/j.parkreldis.2017.09.021. Epub 2017 Sep 29.

Genetic risk factors in Finnish patients with Parkinson's disease

Susanna Ylönen  1 , Ari Siitonen  1 , Michael A Nalls  2 , Pauli Ylikotila  3 , Jaana Autere  4 , Johanna Eerola-Rautio  5 , Raphael Gibbs  2 , Mikko Hiltunen  6 , Pentti J Tienari  5 , Hilkka Soininen  6 , Andrew B Singleton  2 , Kari Majamaa  7
Affiliations

Genetic risk factors in Finnish patients with Parkinson's disease

Susanna Ylönen et al. Parkinsonism Relat Disord. 2017 Dec.

Abstract

Introduction: Variation contributing to the risk of Parkinson's disease (PD) has been identified in several genes and at several loci including GBA, SMPD1, LRRK2, POLG1, CHCHD10 and MAPT, but the frequencies of risk variants seem to vary according to ethnic background. Our aim was to analyze how variation in these genes contributes to PD in the Finnish population.

Methods: The subjects consisted of 527 Finnish patients with early-onset PD, 325 patients with late-onset PD and 403 population controls. We screened for known genetic risk variants in GBA, SMPD1, LRRK2, POLG1, CHCHD10 and MAPT. In addition, DNA from 225 patients with early-onset Parkinson's disease was subjected to whole exome sequencing (WES).

Results: We detected a significant difference in the length variation of the CAG repeat in POLG1 between patients with early-onset PD compared to controls. The p.N370S and p.L444P variants in GBA contributed to a relative risk of 3.8 in early-onset PD and 2.5 in late-onset PD. WES revealed five variants in LRRK2 and SMPD1 that were found in the patients but not in the Finnish ExAC sequences. These are possible risk variants that require further confirmation. The p.G2019S variant in LRRK2, common in North African Arabs and Ashkenazi Jews, was not detected in any of the 849 PD patients.

Conclusions: The POLG1 CAG repeat length variation and the GBA p.L444P variant are associated with PD in the Finnish population.

Keywords: Gene; Mitochondrial; Molecular epidemiology; Mutation; Neurodegenerative diseases.

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Conflict of interest statement

Conflicts of interest

None.

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