Evidence map›Paper›PMID 41964342›Full record

SynthesisMovement disorders : official journal of the Movement Disorder Society2026

Prognosis in Parkinson's Disease: An Individual Patient Data Meta-Analysis of Six European Incidence Cohorts.

Angus D Macleod, David J McLernon, Marta Camacho, Caroline H Williams-Gray, Rachael A Lawson, Alison J Yarnall, David Bäckström, Lars Forsgren, Jodi Maple-Grødem, Guido Alves and 3 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Movement disorders : official journal of the Movement Disorder Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Angus D MacleodInstitute of Applied Health Sciences, University of Aberdeen, Aberdeen, UK.ORCID https://orcid.org/0000-0002-6284-4239
David J McLernonInstitute of Applied Health Sciences, University of Aberdeen, Aberdeen, UK.ORCID https://orcid.org/0000-0001-8905-2429
Marta CamachoJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Caroline H Williams-GrayJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Rachael A LawsonNewcastle NIHR BRC, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Alison J YarnallNewcastle NIHR BRC, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
David BäckströmDepartment of Clinical Science, Neurosciences, Umeå University, Umeå, Sweden.
Lars ForsgrenDepartment of Clinical Science, Neurosciences, Umeå University, Umeå, Sweden.
Jodi Maple-GrødemThe Norwegian Center for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.
Guido AlvesThe Norwegian Center for Movement Disorders, Stavanger University Hospital, Stavanger, Norway.
Ole-Bjørn TysnesDepartment of Clinical Medicine, University of Bergen, Bergen, Norway.
Carl E CounsellInstitute of Applied Health Sciences, University of Aberdeen, Aberdeen, UK.
Parkinson's Incidence Cohorts Collaboration

Funding

Academy of Medical SciencesBritish Medical Association Doris HillierBUPA FoundationChief Scientist Office, Scottish Government Health and Social Care Directorate CAF/12/05Chief Scientist Office, Scottish Government Health and Social Care Directorate PCL/17/10Erling-Persson FoundationHjärnfonden, Umeå UniversityKempe FoundationKing Gustaf V and Queen Victoria Freemason FoundationLockhart Parkinson's Disease Research FundMedical Research Council MR/W029235/1National Institute for Health and Care Research (NIHR) Cambridge Biomedical Research Centre BRC-1215-20014National Institute for Health and Care Research (NIHR) Cambridge Biomedical Research Centre NIHR203312National Institute for Health and Care Research (NIHR) Cambridge Biomedical Research Centre NIHR203312BRC-1215-20014Newcastle University, and the CumbriaNHS Grampian EndowmentsNIHRNorthumberland and Tyne and Wear (CNTW) NHS Foundation TrustNorwegian Association for Public HealthNorwegian Parkinson's Research FoundationParkinson Research FoundationParkinson's UK G-1301Parkinson's UK G-1507Parkinson's UK J-0802Patrick Berthoud TrustReberg's LegacyResearch Council of Norway 177966RS Macdonald TrustSwedish Medical Research CouncilSwedish Parkinson FoundationSwedish PD Associationthe Newcastle upon Tyne Hospitals NHS Foundation TrustVästerbotten County CouncilWellcome TrustWestern Norway Regional Health Authority 911218
6 · The paper itself

Abstract

backgroundAn accurate understanding of prognosis in Parkinson's disease (PD) is important for patient information provision, personalized treatment, and clinical trial design, but most previous research has been biased towards younger, healthier patients.

objectivesTo describe key clinical outcomes longitudinally and identify baseline prognostic factors (predictors) for these outcomes using population-representative PD cohorts.

methodsWe meta-analyzed individual patient data from six incidence cohorts in Western Europe (Norway, Sweden, and UK). Each cohort aimed to recruit and follow up all newly diagnosed cases in defined population/incidence periods (between 2000 and 2011). We described postural instability (Hoehn & Yahr Stage 3), functional dependency (needing help with daily activities), dementia, and death with up to 12 years' follow-up and investigated clinical and genetic predictors using frailty Cox models.

resultsIn 883 population-based incident patients, median age at motor symptom onset was 69.2 years. Median time to postural instability and functional dependency was 7.4 years. Dementia affected 49.6% by 10 years and 54.7% had died by 12 years (median survival 9.4 years). Older age, higher Movement Disorder Society-Unified Parkinson's Disease Rating Scale-Part III (MDS-UPDRS-III) score, and lower Mini-Mental State Examination (MMSE) were significantly associated with all outcomes; cognitive symptoms and GBA polymorphisms with each outcome except mortality; and APOE ε4 with increased mortality and dementia.

conclusionsThis first individual patient data meta-analysis of population-based incidence cohorts provides robust prognostic data, with fewer selection biases than previous PD studies, for informing people with PD about prognosis. In incidence cohorts, overall PD prognosis is worse than previously suggested, with key outcomes often occurring early. Further work should develop validated prognostic models for objective stratification of prognostic risk and for personalized medicine. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Parkinson DiseaseAgedAged, 80 and overCohort StudiesDementiaEuropeFemaleHumansIncidenceMaleMiddle AgedPrognosis

Identifiers

PMID41964342
PMCPMC13387983

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.