Evidence map›Paper›PMID 33543247›Full record

Observational studyBrain : a journal of neurology2021

Sequence of clinical and neurodegeneration events in Parkinson's disease progression.

Neil P Oxtoby, Louise-Ann Leyland, Leon M Aksman, George E C Thomas, Emma L Bunting, Peter A Wijeratne, Alexandra L Young, Angelika Zarkali, Manuela M X Tan, Fion D Bremner and 5 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Brain : a journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 2 pooled it
7.9field-weighted citation impact, top 2% of its field
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

60 citing papers in PubMed, 2 syntheses or guidelines pooled it, 98 citations in OpenAlex.

  1. Digital Outcomes as Biomarkers of Disease Progression in Early Parkinson's Disease: A Systematic Review.Movement disorders : official journal of the Movement Disorder Society · 2025
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  18. Dynamics of retinal changes in early-stage Parkinson's disease.Acta neuropathologica communications · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 1 country.

Neil P OxtobyCentre for Medical Image Computing, Department of Computer Science and Department of Medical Physics and Biomedical Engineering, UCL, London, UK.
Louise-Ann LeylandDementia Research Centre, UCL Institute of Neurology, UCL, London, UK.
Leon M AksmanCentre for Medical Image Computing, Department of Computer Science and Department of Medical Physics and Biomedical Engineering, UCL, London, UK.
George E C ThomasDementia Research Centre, UCL Institute of Neurology, UCL, London, UK.
Emma L BuntingDementia Research Centre, UCL Institute of Neurology, UCL, London, UK.
Peter A WijeratneCentre for Medical Image Computing, Department of Computer Science and Department of Medical Physics and Biomedical Engineering, UCL, London, UK.
Alexandra L YoungCentre for Medical Image Computing, Department of Computer Science and Department of Medical Physics and Biomedical Engineering, UCL, London, UK.
Angelika ZarkaliDementia Research Centre, UCL Institute of Neurology, UCL, London, UK.
Manuela M X TanDepartment of Clinical and Movement Neuroscience, UCL Queen Square Institute of Neurology, UCL, London, UK.
Fion D BremnerNeuro-ophthalmology, National Hospital for Neurology and Neurosurgery, University College London Hospitals, London, UK.
Pearse A KeaneInstitute of Ophthalmology, UCL, London, UK.
Huw R MorrisDepartment of Clinical and Movement Neuroscience, UCL Queen Square Institute of Neurology, UCL, London, UK.
Anette E SchragDepartment of Clinical and Movement Neuroscience, UCL Queen Square Institute of Neurology, UCL, London, UK.
Daniel C AlexanderCentre for Medical Image Computing, Department of Computer Science and Department of Medical Physics and Biomedical Engineering, UCL, London, UK.
Rimona S WeilDementia Research Centre, UCL Institute of Neurology, UCL, London, UK.
UK Dementia Research Institute · GBUniversity College London · GBNational Hospital for Neurology and Neurosurgery · GBKing's College London · GBMoorfields Eye Hospital · GBRoyal London Hospital · GBWellcome Centre for Human Neuroimaging · GB

Funding

Department of Health CS-2014-14-023Medical Research Council MR/N013867/1Medical Research Council MR/S03546X/1Medical Research Council MR/T019050/1Medical Research Council MR/T027770/1Medical Research Council MR/T027800/1Wellcome Trust 201567/Z/16/ZWellcome Trust 205167/Z/16/Z
6 · The paper itself

Abstract

Dementia is one of the most debilitating aspects of Parkinson's disease. There are no validated biomarkers that can track Parkinson's disease progression, nor accurately identify patients who will develop dementia and when. Understanding the sequence of observable changes in Parkinson's disease in people at elevated risk for developing dementia could provide an integrated biomarker for identifying and managing individuals who will develop Parkinson's dementia. We aimed to estimate the sequence of clinical and neurodegeneration events, and variability in this sequence, using data-driven statistical modelling in two separate Parkinson's cohorts, focusing on patients at elevated risk for dementia due to their age at symptom onset. We updated a novel version of an event-based model that has only recently been extended to cope naturally with clinical data, enabling its application in Parkinson's disease for the first time. The observational cohorts included healthy control subjects and patients with Parkinson's disease, of whom those diagnosed at age 65 or older were classified as having high risk of dementia. The model estimates that Parkinson's progression in patients at elevated risk for dementia starts with classic prodromal features of Parkinson's disease (olfaction, sleep), followed by early deficits in visual cognition and increased brain iron content, followed later by a less certain ordering of neurodegeneration in the substantia nigra and cortex, neuropsychological cognitive deficits, retinal thinning in dopamine layers, and further deficits in visual cognition. Importantly, we also characterize variation in the sequence. We found consistent, cross-validated results within cohorts, and agreement between cohorts on the subset of features available in both cohorts. Our sequencing results add powerful support to the increasing body of evidence suggesting that visual processing specifically is affected early in patients with Parkinson's disease at elevated risk of dementia. This opens a route to earlier and more precise detection, as well as a more detailed understanding of the pathological mechanisms underpinning Parkinson's dementia.

Indexed as

Models, NeurologicalAgedAge of OnsetDementiaDisease ProgressionFemaleHumansMaleMiddle AgedNerve DegenerationParkinson Diseasedementiadisease progressionevent-based modelParkinson’s diseasevision

Identifiers

PMID33543247
PMCPMC8041043
OpenAlexW3128740055

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.