Outcomes in Long‐Term Follow‐Up of Sporadic Parkinson's Disease in the Parkinson's Progression Markers Initiative

The Parkinson's Progression Markers Initiative (PPMI) has addressed a key gap in the availability of long-term longitudinal data in sporadic Parkinson's disease (sPD) with extensive biological characterization. With biological characterization in the neuronal synuclein disease (NSD) framework, longitudinal outcomes are observed in cohorts defined by biological characteristics rather than based on conventional clinical diagnostic criteria. We recently reported our observations on 5 years of follow up in this cohort, and here, we provide our earliest findings on a comprehensive long-term description of disease progression in 344 sPD participants followed for up to 11 years. Although data collection is ongoing, these early findings highlight the heterogeneity in the early PD population as defined by clinical diagnostic criteria and affirm the importance of shifting to biologically and functionally based criteria in clinical research studies. ANN NEUROL 2026.

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Publication Details

Journal
Annals of Neurology
Published
2026-05-18
DOI
https://doi.org/10.1002/ana.78248
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
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article

Outcomes in Long‐Term Follow‐Up of Sporadic Parkinson's Disease in the Parkinson's Progression Markers Initiative

Annals of Neurology
Parkinson's Disease Mechanisms and Treatments
article

Outcomes in Long‐Term Follow‐Up of Sporadic Parkinson's Disease in the Parkinson's Progression Markers Initiative

article en

Abstract

The Parkinson's Progression Markers Initiative (PPMI) has addressed a key gap in the availability of long-term longitudinal data in sporadic Parkinson's disease (sPD) with extensive biological characterization. With biological characterization in the neuronal synuclein disease (NSD) framework, longitudinal outcomes are observed in cohorts defined by biological characteristics rather than based on conventional clinical diagnostic criteria. We recently reported our observations on 5 years of follow up in this cohort, and here, we provide our earliest findings on a comprehensive long-term description of disease progression in 344 sPD participants followed for up to 11 years. Although data collection is ongoing, these early findings highlight the heterogeneity in the early PD population as defined by clinical diagnostic criteria and affirm the importance of shifting to biologically and functionally based criteria in clinical research studies. ANN NEUROL 2026.

Annals of Neurology
Northwestern University (US), University of Iowa (US), University of Salerno (IT), University of Pittsburgh (US), University of California, San Francisco (US), Michael J. Fox Foundation (US), University of California San Diego (US), Institute for Neurodegenerative Disorders (US), University of Rochester (US), University of Pennsylvania (US), Stanford University (US)
Openalex Percentile: Top 5%
Parkinson's Disease Mechanisms and Treatments
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