4.7 Article

Motor complications in an incident Parkinson's disease cohort

Journal

EUROPEAN JOURNAL OF NEUROLOGY
Volume 23, Issue 2, Pages 304-312

Publisher

WILEY-BLACKWELL
DOI: 10.1111/ene.12751

Keywords

dyskinesias; levodopa; motor complications; motor fluctuations; Parkinson's disease

Funding

  1. Parkinson's UK
  2. Scottish Chief Scientist Office
  3. BMA Doris Hillier Award
  4. RS Macdonald Trust
  5. BUPA Foundation
  6. NHS Grampian Endowments
  7. SPRING
  8. National Institute of Health Research
  9. Engineering and Physical Sciences Research Council
  10. Chief Scientist Office [CAF/12/05] Funding Source: researchfish
  11. Parkinson's UK [G-0914] Funding Source: researchfish

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Background and purposeLevodopa treatment in Parkinson's disease (PD) causes motor fluctuations and dyskinesias, but few data describe their development or severity in unselected incident cohorts. MethodsDemographic, clinical, treatment, smoking, caffeine and alcohol data from 183 people with PD were gathered from the Parkinsonism Incidence in Northeast Scotland (PINE) study, a community-based, incident cohort. With Kaplan-Meier survival analysis and Cox regression modelling the development, and severity, of dyskinesias and motor fluctuations and which factors independently influenced their onset were assessed. ResultsAfter a mean follow-up of 59months, 39 patients (21.3%) developed motor fluctuations and 52 (28.4%) developed dyskinesias. Kaplan-Meier estimates of the probability of motor fluctuations and dyskinesias after 5years of dopaminergic treatment were 29.2% [95% confidence interval (CI) 21.5%-38.8%] and 37.0% (95% CI 28.5%-47.1%) respectively. 19.8% developed motor fluctuations requiring treatment changes but only 4.0% (95% CI 1.5%-10.4%) developed dyskinesias requiring treatment changes by 5years. Cumulative levodopa dose [hazard ratio (HR) 1.38 (95% CI 1.19-1.60)], female sex [HR 2.41 (1.19-4.89)] and younger age at diagnosis [HR 1.08 (1.04-1.11)] were independently associated with development of motor fluctuations. Cumulative levodopa dose [HR 1.23 (1.08-1.40)] and female sex [HR 2.51 (1.40-4.51)] were independently associated with dyskinesias. In exploratory analyses, moderate caffeine exposure was associated with fewer motor fluctuations, longer symptom duration with more dyskinesias, and tremor at diagnosis with higher rates of both complications. ConclusionsIn this community-based incident PD cohort, severe dyskinesias were rare. Cumulative levodopa dose was the strongest predictor of both dyskinesias and motor fluctuations. Click to view the accompanying paper in this issue.

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