4.6 Article

The Parkinson's progression markers initiative (PPMI) - establishing a PD biomarker cohort

Journal

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY
Volume 5, Issue 12, Pages 1460-1477

Publisher

WILEY
DOI: 10.1002/acn3.644

Keywords

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Funding

  1. Michael J. Fox Foundation for Parkinson's Research (MJFF)
  2. MJFF
  3. Abbvie
  4. Allergan
  5. Avid Radiopharmaceuticals
  6. Biogen
  7. BioLegend
  8. Bristol-Myers Squibb Eli Lilly Co.
  9. F. Hoffman-La Roche, Ltd.
  10. GE Healthcare
  11. Genentech
  12. GlaxoSmithKline
  13. Lundbeck
  14. Merck
  15. MesoScale
  16. Piramal
  17. Pfizer
  18. Sanofi Genzyme
  19. Servier
  20. Takeda
  21. Teva
  22. UCB

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Objective The Parkinson's Progression Markers Initiative (PPMI) is an observational, international study designed to establish biomarker-defined cohorts and identify clinical, imaging, genetic, and biospecimen Parkinson's disease (PD) progression markers to accelerate disease-modifying therapeutic trials. Methods A total of 423 untreated PD, 196 Healthy Control (HC) and 64 SWEDD (scans without evidence of dopaminergic deficit) subjects were enrolled at 24 sites. To enroll PD subjects as early as possible following diagnosis, subjects were eligible with only asymmetric bradykinesia or tremor plus a dopamine transporter (DAT) binding deficit on SPECT imaging. Acquisition of data was standardized as detailed at . Results Approximately 9% of enrolled subjects had a single PD sign at baseline. DAT imaging excluded 16% of potential PD subjects with SWEDD. The total MDS-UPDRS for PD was 32.4 compared to 4.6 for HC and 28.2 for SWEDD. On average, PD subjects demonstrated 45% and 68% reduction in mean striatal and contralateral putamen Specific Binding Ratios (SBR), respectively. Cerebrospinal fluid (CSF) was acquired from >97% of all subjects. CSF (PD/HC/SWEDD pg/mL) alpha-synuclein (1845/2204/2141) was reduced in PD vs HC or SWEDD (P < 0.03). Similarly, t-tau (45/53) and p-tau (16/18) were reduced in PD versus HC (P < 0.01), Interpretation PPMI has detailed the biomarker signature for an early PD cohort defined by clinical features and imaging biomarkers. This strategy provides the framework to establish biomarker cohorts and to define longitudinal progression biomarkers to support future PD treatment trials.

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