Literature DB >> 9187529

Mortality associated with selegiline in Parkinson's disease. What do the available data mean?

Y Mizuno1, T Kondo.   

Abstract

A recent study by the Parkinson's Disease Research Group of the United Kingdom revealed higher mortality in patients with Parkinson's disease who were treated with selegiline (deprenyl) compared with those who were not. In this article, the methodological limitations of the UK study are discussed. Although several problems exist with this study, the mortality rate was correct, since the data were obtained from a verifiable source. The question then is whether or not the higher mortality rate can be ascribed to selegiline. It is difficult to find answers to this question in the study data, and we will have to wait for the study authors' final report. No other studies have reported higher mortality with selegiline. However, when prescribing selegiline in patients with early-stage Parkinson's disease, it is important to provide them with all the available information so that treatment decisions can be made jointly. Meanwhile, the best indication for selegiline appears to be motor fluctuations in patients with moderately advanced Parkinson's disease.

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Year:  1997        PMID: 9187529     DOI: 10.2165/00002018-199716050-00001

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.228


  43 in total

1.  Effect of adding selegeline to levodopa in early, mild Parkinson's disease. Parkinson's disease is rarely a primary cause of death.

Authors:  M T Silva; P M Watts; P Jenner
Journal:  BMJ       Date:  1996-03-16

2.  Effect of adding selegeline to levodopa in early, mild Parkinson's disease. Other studies have not shown increased mortality.

Authors:  O Mäki-Ikola; O Kilkku; E Heinonen
Journal:  BMJ       Date:  1996-03-16

3.  Metabolism of the neurotoxic tertiary amine, MPTP, by brain monoamine oxidase.

Authors:  K Chiba; A Trevor; N Castagnoli
Journal:  Biochem Biophys Res Commun       Date:  1984-04-30       Impact factor: 3.575

4.  Selegiline as an adjunct to conventional levodopa therapy in Parkinson's disease. Experience with this type B monoamine oxidase inhibitor in 200 patients.

Authors:  T S Elizan; M D Yahr; D A Moros; M R Mendoza; S Pang; C A Bodian
Journal:  Arch Neurol       Date:  1989-12

5.  Multi-center study of Parkinson mortality with early versus later dopa treatment.

Authors:  S G Diamond; C H Markham; M M Hoehn; F H McDowell; M D Muenter
Journal:  Ann Neurol       Date:  1987-07       Impact factor: 10.422

6.  Parkinsonism treated with levodopa: progression and mortality.

Authors:  M M Maier Hoehn
Journal:  J Neural Transm Suppl       Date:  1983

7.  The effect of L-Deprenyl on on-off phenomena in Parkinson's disease.

Authors:  P Brodersen; A Philbert; G Gulliksen; A Stigård
Journal:  Acta Neurol Scand       Date:  1985-06       Impact factor: 3.209

8.  Effect of adding selegeline to levodopa in early, mild Parkinson's disease. Selegeline may be toxic in presence of increased dopamine concentrations.

Authors:  P H Yu; C T Lai; A A Boulton
Journal:  BMJ       Date:  1996-03-16

9.  Deprenyl in the management of response fluctuations in patients with Parkinson's disease on levodopa.

Authors:  M Schachter; C D Marsden; J D Parkes; P Jenner; B Testa
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-11       Impact factor: 10.154

10.  The effect of deprenyl and levodopa on the progression of Parkinson's disease.

Authors:  C W Olanow; R A Hauser; L Gauger; T Malapira; W Koller; J Hubble; K Bushenbark; D Lilienfeld; J Esterlitz
Journal:  Ann Neurol       Date:  1995-11       Impact factor: 10.422

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