Development of dyskinesias in a 5-year trial and ropinirole and L-dopa

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

DOI

  • Olivier Rascol, INSERM
  • ,
  • David J. Brooks
  • Amos D. Korczyn, Tel Aviv University Medical School
  • ,
  • Peter P. De Deyn, Dept. of Biology, Universiteit Antwerpen
  • ,
  • C. E. Clarke
  • ,
  • Anthony E. Lang, University of Toronto
  • ,
  • Mona Abdalla, London School of Hygiene and Tropical Medicine
  • ,
  • J. Harmant
  • ,
  • J. Jacquy
  • ,
  • D. King
  • ,
  • W. Martin
  • ,
  • A. Destee
  • ,
  • F. Durif
  • ,
  • J. Aharon-Peretz
  • ,
  • A. Reches
  • ,
  • B. Bergamasco
  • ,
  • F. Bracco
  • ,
  • L. Frattolla
  • ,
  • P. Nordera
  • ,
  • G. Pezzoli
  • ,
  • G. Scarlato
  • ,
  • F. Stocchi
  • ,
  • A. Hovestadt
  • ,
  • R. Abbott
  • ,
  • M. Bakheit
  • ,
  • G. Boddie
  • ,
  • David J. Brooks
  • C. E. Clarke
  • ,
  • R. Corston
  • ,
  • C. Hawkes
  • ,
  • C. Kennard
  • ,
  • L. Loizou
  • ,
  • L. McLellan
  • ,
  • D. Park
  • H. Sagar
  • ,
  • E. Spokes
  • ,
  • C. Ward
  • ,
  • S. V. Wroe

A 5-year trial of ropinirole and levodopa in early Parkinson's disease showed that ropinirole is associated with reduced incidence of dyskinesias. This post hoc analysis investigated whether the dyskinesia-sparing benefit of ropinirole is lost when levodopa is added to the regimen and evaluated other risk factors for developing dyskinesias. Patients receiving levodopa had a significantly higher risk of dyskinesias than those taking ropinirole monotherapy (hazard ratio [HR], 6.67; 95% confidence interval [CI], 3.23-14.29; P < 0.001). When patients randomized to ropinirole were treated with supplementary levodopa, the development of dyskinesias was not significantly different from that in those receiving levodopa from the start (HR, 0.80; 95% CI, 0.48-1.33; P = 0.39). However, the onset of dyskinesias was delayed by around 3 years compared with levodopa monotherapy. Adjusted analyses taking into account baseline and on-treatment factors that influenced use of supplementary levodopa or the development of dyskinesias produced similar results. In conclusion, the risk of developing dyskinesias during maintained initial ropinirole monotherapy is very low. Only once levodopa is added does the risk substantially change. Early use of ropinirole postpones the onset of dyskinesias, but these benefits decline when levodopa therapy is started, with no evidence of a s bsequent rapid "catch-up" or a persisting preventive effect.

Original languageEnglish
JournalMovement Disorders
Volume21
Issue11
Pages (from-to)1844-1850
Number of pages7
ISSN0885-3185
DOIs
Publication statusPublished - 1 Nov 2006

    Research areas

  • Dyskinesia, Levodopa, Parkinson's disease, Ropinirole

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