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Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson Disease.

Publication ,  Journal Article
Wang, S; Unnithan, S; Bryant, N; Chang, A; Rosenthal, LS; Pantelyat, A; Dawson, TM; Al-Khalidi, HR; West, AB
Published in: Mov Disord
July 2022

BACKGROUND: Pathogenic leucine-rich repeat kinase 2 LRRK2 mutations may increase LRRK2 kinase activity and Rab substrate phosphorylation. Genetic association studies link variation in LRRK2 to idiopathic Parkinson disease (iPD) risk. OBJECTIVES: Through measurements of the LRRK2 kinase substrate pT73-Rab10 in urinary extracellular vesicles, this study seeks to understand how LRRK2 kinase activity might change with iPD progression. METHODS: Using an immunoblotting approach validated in LRRK2 transgenic mice, the ratio of pT73-Rab10 to total Rab10 protein was measured in extracellular vesicles from a cross-section of G2019S LRRK2 mutation carriers (N = 45 participants) as well as 485 urine samples from a novel longitudinal cohort of iPD and controls (N = 85 participants). Generalized estimating equations were used to conduct analyses with commonly used clinical scales. RESULTS: Although the G2019S LRRK2 mutation did not increase pT73-Rab10 levels, the ratio of pT73-Rab10 to total Rab10 nominally increased over baseline in iPD urine vesicle samples with time, but did not increase in age-matched controls (1.34-fold vs. 1.05-fold, 95% confidence interval [CI], 0.004-0.56; P = 0.046; Welch's t test). Effect estimates adjusting for sex, age, disease duration, diagnosis, and baseline clinical scores identified increasing total Movement Disorder Society-Sponsored Revision of the Unified (MDS-UPDRS) scores (β = 0.77; CI, 0.52-1.01; P = 0.0001) with each fold increase of pT73-Rab10 to total Rab10. Lower Montreal Cognitive Assessment (MoCA) score in iPD is also associated with increased pT73-Rab10. CONCLUSIONS: These results provide initial insights into peripheral LRRK2-dependent Rab phosphorylation, measured in biobanked urine, where higher levels of pT73-Rab10 are associated with worse disease progression. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson Movement Disorder Society.

Duke Scholars

Published In

Mov Disord

DOI

EISSN

1531-8257

Publication Date

July 2022

Volume

37

Issue

7

Start / End Page

1454 / 1464

Location

United States

Related Subject Headings

  • rab GTP-Binding Proteins
  • Phosphorylation
  • Parkinson Disease
  • Neurology & Neurosurgery
  • Mutation
  • Mice, Transgenic
  • Mice
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Humans
  • Animals
 

Citation

APA
Chicago
ICMJE
MLA
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Wang, S., Unnithan, S., Bryant, N., Chang, A., Rosenthal, L. S., Pantelyat, A., … West, A. B. (2022). Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson Disease. Mov Disord, 37(7), 1454–1464. https://doi.org/10.1002/mds.29043
Wang, Shijie, Shakthi Unnithan, Nicole Bryant, Allison Chang, Liana S. Rosenthal, Alexander Pantelyat, Ted M. Dawson, Hussein R. Al-Khalidi, and Andrew B. West. “Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson Disease.Mov Disord 37, no. 7 (July 2022): 1454–64. https://doi.org/10.1002/mds.29043.
Wang S, Unnithan S, Bryant N, Chang A, Rosenthal LS, Pantelyat A, et al. Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson Disease. Mov Disord. 2022 Jul;37(7):1454–64.
Wang, Shijie, et al. “Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson Disease.Mov Disord, vol. 37, no. 7, July 2022, pp. 1454–64. Pubmed, doi:10.1002/mds.29043.
Wang S, Unnithan S, Bryant N, Chang A, Rosenthal LS, Pantelyat A, Dawson TM, Al-Khalidi HR, West AB. Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson Disease. Mov Disord. 2022 Jul;37(7):1454–1464.
Journal cover image

Published In

Mov Disord

DOI

EISSN

1531-8257

Publication Date

July 2022

Volume

37

Issue

7

Start / End Page

1454 / 1464

Location

United States

Related Subject Headings

  • rab GTP-Binding Proteins
  • Phosphorylation
  • Parkinson Disease
  • Neurology & Neurosurgery
  • Mutation
  • Mice, Transgenic
  • Mice
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Humans
  • Animals