Evidence map›Paper›PMID 41388605›Full record

ArticleAnnals of clinical and translational neurology2026

Tracking Motor Progression and Device-Aided Therapy Eligibility in Parkinson's Disease.

David Ledingham, Sahana Sathyanarayana, Charlotte B Stewart, Robyn Iredale, Victoria Foster, Debra Galley, Mark Baker, Nicola Pavese

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

8 authors.

David LedinghamClinical Ageing Research Unit, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.ORCID 0000-0002-6474-2666
Sahana SathyanarayanaClinical Ageing Research Unit, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.
Charlotte B StewartClinical Ageing Research Unit, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.
Robyn IredaleClinical Ageing Research Unit, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.
Victoria FosterClinical Ageing Research Unit, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.
Debra GalleyClinical Ageing Research Unit, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.
Mark BakerNeurosciences, Newcastle Upon Tyne NHS Foundation Trust, Newcastle Upon Tyne, UK.
Nicola PaveseClinical Ageing Research Unit, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo characterise the progression of motor symptoms and identify eligibility for device-aided therapies in Parkinson's disease, using both the 5-2-1 criteria and a refined clinical definition, while examining differences across genetic subgroups.

methodsWe analysed 1205 individuals with sporadic and genetic Parkinson's disease from the Parkinson's Progression Markers Initiative (mean follow-up: 5.6 ± 4.3 years). Kaplan-Meier analysis estimated time to meeting the 5-2-1 criteria (five or more daily levodopa doses, two or more hours of OFF time, or one or more hours of troublesome dyskinesia) and a stricter definition of eligibility for device-aided therapy based on disabling, medication-refractory symptoms and/or tremor. In the sporadic Parkinson's disease subgroup (n = 943), we assessed therapy initiation and clinical suitability, including potential contraindications. Genetic subgroup analyses explored differences in progression, eligibility timing and treatment uptake.

resultsAmong individuals with sporadic Parkinson's disease, 257 (27.3%) met the 5-2-1 criteria, with 25%, 50% and 75% doing so by 5.3, 8.2 and 10.7 years, respectively. A total of 176 (18.6%) met stricter eligibility criteria, with 50% doing so by 12 years. Only 25% of those meeting the 5-2-1 criteria initiated device-aided therapy within 6.8 years. Most had no contraindications. Deep brain stimulation was the most used therapy. GBA and SNCA carriers met criteria earlier. LRRK2 carriers were more likely to initiate therapy, while PRKN carriers were less likely to meet eligibility thresholds.

interpretationEligibility for device-aided therapy is common but underutilised. These findings highlight missed opportunities and support earlier, genotype-informed treatment planning in Parkinson's disease.

Indexed as

Disease ProgressionParkinson DiseaseAgedAntiparkinson AgentsFemaleHumansLevodopaMaleMiddle AgedAntiparkinson AgentsLevodopadevice‐aided therapygenetic subgroupslongitudinal analysismotor complicationsParkinson's disease

Identifiers

PMID41388605
PMCPMC13161881

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.