Literature DB >> 31505070

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts.

Hirotaka Iwaki1,2, Cornelis Blauwendraat1, Hampton L Leonard1,2, Jonggeol J Kim1, Ganqiang Liu3,4,5, Jodi Maple-Grødem6,7, Jean-Christophe Corvol8, Lasse Pihlstrøm9, Marlies van Nimwegen10, Samantha J Hutten11, Khanh-Dung H Nguyen12, Jacqueline Rick13, Shirley Eberly14, Faraz Faghri1,15, Peggy Auinger16, Kirsten M Scott17, Ruwani Wijeyekoon17, Vivianna M Van Deerlin18, Dena G Hernandez1, J Raphael Gibbs1, Kumaraswamy Naidu Chitrala19, Aaron G Day-Williams20,21, Alexis Brice22,23,24, Guido Alves6,7,25, Alastair J Noyce26,27, Ole-Bjørn Tysnes28,29, Jonathan R Evans30, David P Breen31,32,33, Karol Estrada12, Claire E Wegel34, Fabrice Danjou22, David K Simon35,36, Ole Andreassen37,38, Bernard Ravina39,40, Mathias Toft9,41, Peter Heutink42,43, Bastiaan R Bloem10, Daniel Weintraub44,45, Roger A Barker46, Caroline H Williams-Gray46, Bart P van de Warrenburg10, Jacobus J Van Hilten47, Clemens R Scherzer4,5, Andrew B Singleton1, Mike A Nalls1,2.   

Abstract

BACKGROUND: Several reports have identified different patterns of Parkinson's disease progression in individuals carrying missense variants in GBA or LRRK2 genes. The overall contribution of genetic factors to the severity and progression of Parkinson's disease, however, has not been well studied.
OBJECTIVES: To test the association between genetic variants and the clinical features of Parkinson's disease on a genomewide scale.
METHODS: We accumulated individual data from 12 longitudinal cohorts in a total of 4093 patients with 22,307 observations for a median of 3.81 years. Genomewide associations were evaluated for 25 cross-sectional and longitudinal phenotypes. Specific variants of interest, including 90 recently identified disease-risk variants, were also investigated post hoc for candidate associations with these phenotypes.
RESULTS: Two variants were genomewide significant. Rs382940(T>A), within the intron of SLC44A1, was associated with reaching Hoehn and Yahr stage 3 or higher faster (hazard ratio 2.04 [1.58-2.62]; P value = 3.46E-8). Rs61863020(G>A), an intergenic variant and expression quantitative trait loci for α-2A adrenergic receptor, was associated with a lower prevalence of insomnia at baseline (odds ratio 0.63 [0.52-0.75]; P value = 4.74E-8). In the targeted analysis, we found 9 associations between known Parkinson's risk variants and more severe motor/cognitive symptoms. Also, we replicated previous reports of GBA coding variants (rs2230288: p.E365K; rs75548401: p.T408M) being associated with greater motor and cognitive decline over time, and an APOE E4 tagging variant (rs429358) being associated with greater cognitive deficits in patients.
CONCLUSIONS: We identified novel genetic factors associated with heterogeneity of Parkinson's disease. The results can be used for validation or hypothesis tests regarding Parkinson's disease.
© 2019 International Parkinson and Movement Disorder Society. © 2019 International Parkinson and Movement Disorder Society.

Entities:  

Keywords:  Apolipoprotein E; GBA; Parkinson's disease; genomewide association study

Mesh:

Substances:

Year:  2019        PMID: 31505070      PMCID: PMC7017876          DOI: 10.1002/mds.27845

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   9.698


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