Publication Date:
2018
abstract:
Levodopa-induced dyskinesia is a common complication in Parkinson disease. Pathogenic mechanisms include phasic stimulation of dopamine receptors, nonphysiological levodopa-to-dopamine conversion in serotonergic neurons, hyperactivity of corticostriatal glutamatergic transmission, and overstimulation of nicotinic acetylcholine receptors on dopamine-releasing axons. Delay in initiating levodopa is no longer recommended, as dyskinesia development is a function of disease duration rather than cumulative levodopa exposure. We review current and in-development treatments for peak-dose dyskinesia but suggest that improvements in levodopa delivery alone may reduce its future prevalence. Ann Neurol 2018;84:797–811.
Iris type:
14.a.1 Articolo su rivista
Keywords:
Animals; Antiparkinson Agents; Dose-Response Relationship, Drug; Drug Administration Schedule; Humans; Levodopa; Parkinson Disease; Dyskinesia, Drug-Induced
List of contributors:
Espay, A. J.; Morgante, F.; Merola, A.; Fasano, A.; Marsili, L.; Fox, S. H.; Bezard, E.; Picconi, B.; Calabresi, P.; Lang, A. E.
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