Evidence map›Paper›PMID 22300470›Full record

ArticleBritish journal of clinical pharmacology2012

Disease progress and response to treatment as predictors of survival, disability, cognitive impairment and depression in Parkinson's disease.

Thuy C Vu, John G Nutt, Nicholas H G Holford

Abstract read
In one paragraph

Article in British journal of clinical pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Development and validation of prognostic survival models in newly diagnosed Parkinson's disease.Movement disorders : official journal of the Movement Disorder Society · 2018
    Article
  13. Article
  14. Dynamics of change in self-reported disability among persons with Parkinson's disease after 2 years of follow-up.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2017
    Article
  15. Article
  16. Article
  17. Article
  18. Clinical pharmacology = disease progression + drug action.British journal of clinical pharmacology · 2015
    Review
  19. Disease progression and neuroscience.Journal of pharmacokinetics and pharmacodynamics · 2013
    Review
  20. A time to event tutorial for pharmacometricians.CPT: pharmacometrics & systems pharmacology · 2013
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Thuy C VuDepartment of Pharmacokinetics and Drug Metabolism, Amgen Inc., Thousand Oaks, CA, USA.
John G Nutt
Nicholas H G Holford

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo describe the time to clinical events (death, disability, cognitive impairment and depression) in Parkinson's disease using the time course of disease status and treatment as explanatory variables.

methodsDisease status based on the Unified Parkinson's Disease Rating Scale (UPDRS) and the time to clinical outcome events were obtained from 800 patients who initially had early Parkinson's disease. Parametric hazard models were used to describe the time to the events of interest.

resultsTime course of disease status (severity) was an important predictor of clinical outcome events. There was an increased hazard ratio for death 1.4 (95% CI 1.31, 149), disability 2.75 (95% CI 2.30, 3.28), cognitive impairment 4.35 (95% CI 1.94, 9.74), and depressive state 1.43 (95% CI 1.26, 1.63) with each 10 unit increase of UPDRS. Age at study entry increased the hazard with hazard ratios of 49.1 (95% CI 8.7, 278) for death, 4.76 (95% CI 1.10, 20.6) for disability and 90.0 (95% CI 63.3-128) for cognitive impairment at age 60 years. Selegiline treatment had independent effects as a predictor of death at 8 year follow-up with a hazard ratio of 2.54 (95% CI 1.51, 4.25) but had beneficial effects on disability with a hazard ratio of 0.363 (95% CI 0.132, 0.533) and depression with a hazard ratio of 0.372 (95% CI 0.12, 0.552).

conclusionsOur findings show that the time course of disease status based on UPDRS is a much better predictor of future clinical events than any baseline disease characteristic. Continued selegiline treatment appears to increase the hazard of death.

Indexed as

Disability EvaluationAdultAgedAnalysis of VarianceAntiparkinson AgentsChi-Square DistributionCognitionCognition DisordersDepressionDisease ProgressionHumansKaplan-Meier EstimateMiddle AgedParkinson DiseasePatient DropoutsPredictive Value of TestsAntiparkinson AgentsSelegilineTocopherols

Identifiers

PMID22300470
PMCPMC3630748

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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.