Levodopa‐induced dyskinesias in Parkinson's disease: clinical and pharmacological classification

MR Luquin, O Scipioni, J Vaamonde… - … : official journal of the …, 1992 - Wiley Online Library
MR Luquin, O Scipioni, J Vaamonde, O Gershanik, JA Obeso
Movement disorders: official journal of the Movement Disorder Society, 1992Wiley Online Library
Levodopa‐induced dyskinesias (LID) in Parkinson's disease (PD) may be classified into
three main categories:“On” dyskinesias, diphasic dyskinesias (DD), and “off” periods. The
study of 168 parkinsonian patients showed that about half (n= 84) showed one pattern of LID
only. A combination of two was present in 68, and 16 had the three presentation patterns. A
fairly good correlation between type of dyskinesia and presentation pattern was established.
Chorea, myoclonus, and dystonic movements occurred during the “on” period. Dystonic …
Abstract
Levodopa‐induced dyskinesias (LID) in Parkinson's disease (PD) may be classified into three main categories: “On” dyskinesias, diphasic dyskinesias (DD), and “off” periods. The study of 168 parkinsonian patients showed that about half (n = 84) showed one pattern of LID only. A combination of two was present in 68, and 16 had the three presentation patterns. A fairly good correlation between type of dyskinesia and presentation pattern was established. Chorea, myoclonus, and dystonic movements occurred during the “on” period. Dystonic postures, particularly affecting the feet, were mainly present in the “off” period, but a few patients had a diphasic presentation. Repetitive stereotyped movements of the lower limbs always corresponded to DD. Acute pharmacological tests using dopamine agonists 9subcutaneous apomorphine 3–8 mg; intravenous lisuride 0. (1–0. 15 mg) and dopamine antagonists (intravenous sulpiride 200–400 mg and intravenous chlorpromazine 25 mg) were performed in 40 patients. Dopamine agonists enhanced “on” dyskinesias and markedly reduced or abolished “off” period dystonia and DD. Dopamine antagonists reduced all types of LID but usually aggravated parkinsonism. These clinical and pharmacological results indicate that LID in PD are a heterogeneous phenomenon difficult to explain on the basis of a single pathophysiological mechanism.
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