| Literature DB >> 30357892 |
Alberto J Espay1, Francesca Morgante2, Aristide Merola1, Alfonso Fasano3,4, Luca Marsili1, Susan H Fox3,4, Erwan Bezard5,6, Barbara Picconi7, Paolo Calabresi8, Anthony E Lang3,4.
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.Entities:
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Year: 2018 PMID: 30357892 DOI: 10.1002/ana.25364
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422