PPMI
Parkinson's Progression Markers Initiative (now Parkinson's Precision Medicine Initiative)
Longitudinal multi-site observational study of early untreated Parkinson's disease, prodromal and genetic at-risk people and healthy controls, with DaTscan SPECT, MRI including DTI, biofluids, genetics and clinical assessments shared through LONI.
Overview
PPMI is an observational natural history study that follows people with Parkinson's disease, people at risk of it and healthy volunteers over many years to find markers of onset and progression for use in therapeutic trials. The Michael J. Fox Foundation launched it in 2010 together with academic and industry partners, and it has since been renamed the Parkinson's Precision Medicine Initiative. Clinical, imaging, biofluid, genetic and sensor data are released to approved researchers as they are collected, through the LONI Image and Data Archive.
Composition
The first phase enrolled 423 people with recently diagnosed, untreated Parkinson's disease, 196 healthy controls and 64 people whose clinical signs suggested Parkinson's but whose dopamine transporter scan was normal (SWEDD), at 24 sites in the US, Europe and Australia. About two thirds of each group were men, and mean age was around 61. The study has since added people with Parkinson's carrying LRRK2, GBA or SNCA variants (294 in the initial genetic phase), a prodromal cohort with risk features such as REM sleep behaviour disorder or reduced smell, and a further 600 untreated sporadic cases. The study design page plans about 5,500 clinical participants at around 50 sites. The counts in this entry cover the first phase only.
Acquisition
All participants had a brain MRI at baseline. Ten sites with a 3 T Siemens Trio followed a standardized protocol with a 3D MPRAGE and a cardiac-gated DTI sequence, repeated at follow-up for roughly half of the cohort; resting-state fMRI is flagged in the MRI metadata. Dopaminergic imaging used [123I]ioflupane SPECT (DaTscan), or [18F]AV-133 PET for VMAT-2 at the Australian site. Parkinson's participants were rescanned at 12, 24 and 48 months, healthy controls only at baseline.
Annotations
There are no voxel-level labels. The imaging core provides visual reads of each dopaminergic scan and striatal specific binding ratios for left and right caudate and putamen. Diagnoses, MDS-UPDRS and other clinical scores, biomarker results and genetic status are linked by participant number.
Known limitations
- The database is updated continuously without version control, so analyses must record the download date.
- Protocols, eligibility criteria and visit schedules changed between study phases.
- Only part of the cohort has the standardized MRI protocol; other sites acquired MRI to exclude non-Parkinson pathology.
- More than 90% of first-phase participants were white.
Cohort
Aggregate numbers from the sources below. Bars are relative to the 683 subjects.
Sex
- Male 443 65%
- Female 240 35%
Condition
subjects, values can overlap
- Parkinson's disease 423 62%
- Healthy control 196 29%
Country
subjects
- United States 553 81%
- Australia 6 <1%
License and access
Our reading of the license, not legal advice. Before you use the data, read the original license and confirm that your use is allowed. We take no responsibility for how you use a dataset. Full disclaimer
A research proposal is reviewed and approved
PPMI Data Use Agreement
Access for scientific investigation, teaching or planning clinical research after an online application reviewed by the PPMI Data and Publications Committee. No disclosure beyond the approved use, a review of every manuscript before submission, a required data acknowledgement, and no IP claims on the data or on inventions arising from it. Model training is allowed, but not on third-party AI services that retain inputs.
What you can do
- Not stated
- Not stated
- Conditional
- Yes
- Conditional
What you can share
- No
- Conditional
- Conditional
What you must do
- Yes
- Share alike No
- Yes
- Conditional
- Yes
- Release code No
- Conditional
- Delete after use No
Limits
- Yes
- No
Citation
State "Data used in the preparation of this article was obtained on [YYYY-MM-DD] from the Parkinson's Progression Markers Initiative (PPMI) database (www.ppmi-info.org/access-data-specimens/download-data), RRID:SCR_006431" and the funding statement from the PPMI Publication Policy. Cohort reference: Marek K, et al. The Parkinson Progression Marker Initiative (PPMI). Progress in Neurobiology 95(4):629-635 (2011). doi:10.1016/j.pneurobio.2011.09.005
All numbers
Every number on this page, as stored in stats.csv, with its source.
| Measure | Breakdown | Value | Source |
|---|---|---|---|
| Subjects | total initial phase only: sum of the three disjoint enrollment cohorts (423 PD + 196 healthy controls + 64 SWEDD, scans without evidence of dopaminergic deficit), enrolled from June 2010 over about 32 months; later expansion cohorts are not counted | 683 | marek2018 Table 1 |
| Subjects | condition=parkinsons untreated, within 2 years of diagnosis, with a dopaminergic deficit on DAT SPECT or VMAT-2 PET | 423 | marek2018 Table 1 |
| Subjects | condition=healthy | 196 | marek2018 Table 1 |
| Subjects | sex=male sum of 277 PD + 126 healthy controls + 40 SWEDD | 443 | marek2018 Table 1 |
| Subjects | sex=female sum of 146 PD + 70 healthy controls + 24 SWEDD | 240 | marek2018 Table 1 |
| Subjects | condition=parkinsons;sex=male | 277 | marek2018 Table 1 |
| Subjects | condition=parkinsons;sex=female | 146 | marek2018 Table 1 |
| Subjects | condition=healthy;sex=male | 126 | marek2018 Table 1 |
| Subjects | condition=healthy;sex=female | 70 | marek2018 Table 1 |
| Subjects | country=US enrolled at 18 US sites; a further 124 were enrolled at 5 European sites whose countries the paper does not list | 553 | marek2018 Results |
| Subjects | country=AU enrolled at 1 Australian site | 6 | marek2018 Results |
| Mean age | condition=parkinsons | 61.7 | marek2018 Table 1 |
| Minimum age | condition=parkinsons | 33 | marek2018 Table 1 |
| Maximum age | condition=parkinsons | 85 | marek2018 Table 1 |
| Mean age | condition=healthy | 60.8 | marek2018 Table 1 |
| Minimum age | condition=healthy | 31 | marek2018 Table 1 |
| Maximum age | condition=healthy | 84 | marek2018 Table 1 |
| Minimum age | total lowest of the three cohort minimums (PD 33; healthy controls 31; SWEDD 38) | 31 | marek2018 Table 1 |
| Maximum age | total highest of the three cohort maximums (PD 85; healthy controls 84; SWEDD 79) | 85 | marek2018 Table 1 |
Sources
The keys used in the table above.
- marek2011 Marek K et al. 2011, The Parkinson Progression Marker Initiative (PPMI), Progress in Neurobiology paper
- marek2018 Marek K et al. 2018, The Parkinson's progression markers initiative (PPMI) - establishing a PD biomarker cohort, Annals of Clinical and Translational Neurology paper
- ppmi-study-design PPMI website, Study Design website
- ppmi-study-cohorts PPMI website, Study Cohorts website
- ppmi-data-user-guide PPMI Data User Guide, updated 6 August 2026 website