Poul Henning Jensen

Phosphorylated α-synuclein in Parkinson's disease: correlation depends on disease severity

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  • Tessandra Stewart
  • ,
  • Vesna Sossi
  • ,
  • Jan O Aasly
  • ,
  • Zbigniew K Wszolek
  • ,
  • Ryan J Uitti
  • ,
  • Kazuko Hasegawa
  • ,
  • Teruo Yokoyama
  • ,
  • Cyrus P Zabetian
  • ,
  • James B Leverenz
  • ,
  • Alexander Jon Stoessl
  • ,
  • Yu Wang
  • ,
  • Carmen Ginghina
  • ,
  • Changqin Liu
  • ,
  • Kevin C Cain
  • ,
  • Peggy Auinger
  • ,
  • Un Jung Kang
  • ,
  • Poul Henning Jensen
  • Min Shi
  • ,
  • Jing Zhang

INTRODUCTION: α-Synuclein (α-syn) is a key protein in Parkinson's disease (PD), and one of its phosphorylated forms, pS129, is higher in PD patients than healthy controls. However, few studies have examined its levels in longitudinally collected cerebrospinal fluid (CSF) or in preclinical cases. In this study, CSF and clinical data were contributed by >300 subjects from three cohorts (the longitudinal DATATOP cohort, a large cross-sectional cohort, and a cohort of LRRK2 mutation carriers).

RESULTS: Consistent with our previous observation that CSF pS129 positively correlated with Unified Parkinson's Disease Rating Scale (UPDRS) scores, CSF pS129 in the DATATOP cohort increased over approximately two years of disease progression (mean change 5.60 pg/ml, p = 0.050). Intriguingly, in the DATATOP cohort, pS129 negatively correlated with UPDRS scores at the baseline (R = -0.244, p = 0.017), but not final point, suggesting that this association may depend on disease stage. Reanalysis of our previous cohort with stratification by PD stage, and addition of a cohort of LRRK2 mutation carriers with very early/preclinical PD, supported the idea that the relationship between CSF pS129 and disease severity over a wider range of PD stages might be represented with a U-shaped curve, in which lower pS129 levels correlated with worse clinical condition at early stages, but better condition at later stages.

CONCLUSION: The observation of a negative-to-positive transition of correlation of pS129 to disease severity as PD progresses could have profound impact on how pS129 is used as a biomarker clinically as well as in modeling PD experimentally.

Original languageEnglish
JournalActa Neuropathologica Communications
Volume3
Issue7
Number of pages11
ISSN2051-5960
DOIs
Publication statusPublished - 2015

    Research areas

  • Aged, Biomarkers, Cohort Studies, Cross-Sectional Studies, Disease Progression, Female, Humans, Male, Middle Aged, Mutation, Parkinson Disease, Phosphorylation, Positron-Emission Tomography, Protein-Serine-Threonine Kinases, ROC Curve, Severity of Illness Index, Statistics as Topic, Time Factors, alpha-Synuclein

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