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

Kenneth Marek(Institute for Neurodegenerative Disorders), Sohini Chowdhury(Michael J. Fox Foundation), Andrew Siderowf(University of Pennsylvania), Shirley Lasch(Institute for Neurodegenerative Disorders), Christopher S. Coffey(University of Iowa), Chelsea Caspell‐Garcia(University of Iowa), Tanya Simuni(Northwestern University), Danna Jennings(Eli Lilly (United States)), Caroline M. Tanner(University of California, San Francisco), John Q. Trojanowski(University of Pennsylvania), Leslie M. Shaw(University of Pennsylvania), John Seibyl(Institute for Neurodegenerative Disorders), Norbert Schuff(University of California, San Francisco), Andrew Singleton(National Institute on Aging), Karl Kieburtz(University of Rochester), Arthur W. Toga(National Institute on Aging), Brit Mollenhauer(Paracelsus Elena Klinik Kassel), Doug Galasko(University of California San Diego), Lana M. Chahine(University of Pennsylvania), Daniel Weintraub(University of Pennsylvania), Tatiana Foroud(Indiana University Indianapolis), Duygu Tosun(University of California, San Francisco), Kathleen L. Poston(Stanford Medicine), Vanessa Arnedo(Michael J. Fox Foundation), Mark Frasier(Michael J. Fox Foundation), Todd Sherer(Michael J. Fox Foundation), the Parkinson's Progression Markers Initiative
Annals of Clinical and Translational Neurology
October 31, 2018
Cited by 680Open Access
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Abstract

Abstract 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 www.ppmi-info.org . 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) α‐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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