Systematic review of prognostic models in Parkinson’s disease

Predicting outcomes for people with Parkinson's (PwP) can enable better information provision, personalised treatments, and enhanced trial design. It is unclear what prognostic models are optimal for use. We systematically reviewed previously published prognostic models for PwP, assessed quality, and made recommendations. We searched MEDLINE and EMBASE for studies developing/validating models predicting clinical outcomes in PwP. We assessed risk of bias and applicability using the PROBAST tool. We screened 1024 references and identified 25 studies (41 prognostic models). The most common outcomes were falls (11 studies), dementia (7) and motor complications (4). Most models made short-term predictions (60% ≤2 years). All studies had concerns about bias, e.g., inadequate population details (n = 16), suboptimal methods for missing data (n = 21), and no external validation (n = 22). 13 models had sufficient information to be used in practice. Further development and validation of prognostic models is needed which follows existing guidelines to reduce risk of bias.

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Publication Details

Journal
npj Parkinson s Disease
Published
2025-08-29
DOI
https://doi.org/10.1038/s41531-025-01112-x
Citations
2
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
2.78
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article

Systematic review of prognostic models in Parkinson’s disease

Angus D. Macleod, David J. McLernon, Y Li, Carl Counsell et al.
2 citations
npj Parkinson s Disease
Parkinson's Disease Mechanisms and Treatments
2.78
article

Systematic review of prognostic models in Parkinson’s disease

Angus D. Macleod, David J. McLernon, Y Li, Carl Counsell, Millie McDonald-Webb
article en
2 citations

Abstract

Predicting outcomes for people with Parkinson's (PwP) can enable better information provision, personalised treatments, and enhanced trial design. It is unclear what prognostic models are optimal for use. We systematically reviewed previously published prognostic models for PwP, assessed quality, and made recommendations. We searched MEDLINE and EMBASE for studies developing/validating models predicting clinical outcomes in PwP. We assessed risk of bias and applicability using the PROBAST tool. We screened 1024 references and identified 25 studies (41 prognostic models). The most common outcomes were falls (11 studies), dementia (7) and motor complications (4). Most models made short-term predictions (60% ≤2 years). All studies had concerns about bias, e.g., inadequate population details (n = 16), suboptimal methods for missing data (n = 21), and no external validation (n = 22). 13 models had sufficient information to be used in practice. Further development and validation of prognostic models is needed which follows existing guidelines to reduce risk of bias.

npj Parkinson s DiseaseVol. 11(1)
University of Aberdeen (GB)
Openalex Percentile: Top 9%
Parkinson's Disease Mechanisms and Treatments
2.78
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