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NEUROLOGY 2005;64:87-93
© 2005 American Academy of Neurology

Survival in Parkinson disease

Thirteen-year follow-up of the DATATOP cohort

C. Marras, MD, M. P. McDermott, PhD, P. A. Rochon, MD, MPH, C. M. Tanner, MD, PhD, G. Naglie, MD, A. Rudolph, PhD, A. E. Lang, MD and the Parkinson Study Group*

From the Division of Neurology (Drs. Marras and Lang), Toronto Western Hospital, University Health Network, University of Toronto, Kunin-Lunenfeld Applied Research Unit (Dr. Rochon), Baycrest Centre for Geriatric Care, University of Toronto, Institute for Clinical and Evaluative Sciences (Dr. Rochon), Divisions of Clinical Decision Making and Health Care (Dr. Naglie), Toronto General Research Institute, University Health Network, Division of General Internal Medicine (Dr. Naglie), University Health Network, Geriatrics Program (Dr. Naglie), Toronto Rehabilitation Institute, and Departments of Medicine and Health Policy, Management, and Evaluation (Dr. Naglie), University of Toronto, Ontario, Canada; and Department of Biostatistics and Computational Biology (Dr. McDermott) and Clinical Trials Coordination Center (Dr. Rudolph), University of Rochester Medical Center, NY, and Parkinson’s Institute (Dr. Tanner), Sunnyvale, CA.

Address correspondence and reprint requests to Dr. C. Marras, Movement Disorders Centre, Toronto Western Hospital, 11-MP, 399 Bathurst St., Toronto, Ontario, Canada M5T 2S8; e-mail: connie.marras{at}utoronto.ca

Objective: To investigate predictors of survival in Parkinson disease (PD).

Methods: Vital status was determined in 800 subjects enrolled in a clinical trial of deprenyl (selegiline) and tocopherol 13 years earlier.

Results: Two hundred ninety-six deaths were recorded. There was no difference in the standardized mortality ratios across gender or age group. In univariate analyses, PD-specific variables associated with mortality were increased symmetry of parkinsonism, gait dysfunction as an initial symptom, severity of parkinsonism, and rate of worsening of parkinsonism prior to study enrollment. Cumulative exposure to deprenyl was not associated with mortality. In multivariable analysis, severity of parkinsonism and rate of worsening of parkinsonism remained associated with mortality. A poorer response to levodopa was associated with increased mortality independent of disease severity or dosage of levodopa. Results were unchanged when the analysis was restricted to 747 subjects maintaining a most likely diagnosis of PD throughout 6 years of active follow-up.

Conclusions: Parkinson disease did not affect survival differently across gender or age groups in this selected group of otherwise healthy clinical trial participants. Severity and rate of worsening of parkinsonism and response to levodopa are strongly related to survival.


Received March 16, 2004. Accepted in final form September 15, 2004.

Additional material related to this article can be found on the Neurology Web site. Go to www.neurology.org and scroll down the Table of Contents for the January 11 issue to find the title link for this article.

*See appendix E-1 on the Neurology Web site for a list of Group members.




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