| Literature DB >> 33302331 |
Amnon A Berger1, Ariel Winnick2,3, Alexandra Welschmeyer4, Alicia Kaneb4, Kevin Berardino4, Elyse M Cornett5, Alan D Kaye5, Omar Viswanath5,6,7,8, Ivan Urits5,9.
Abstract
Parkinson's disease (PD) is a common neurodegenerative disorder that leads to significant morbidity and disability. PD is caused by a loss of dopaminergic, cholinergic, serotonergic, and noradrenergic neurons in the central nervous system (CNS), and peripherally; the syndromic parkinsonism symptoms of movement disorder, gait disorder, rigidity and tremor are mostly driven by the loss of these neurons in the basal ganglia. Unfortunately, a significant proportion of patients taking levodopa, the standard of care treatment for PD, will begin to experience a decrease in effectiveness at varying times. These periods, referred to as "off episodes", are characterized by increased symptoms and have a detrimental effect on quality of life and disability. Istradefylline, a novel adenosine A2A receptor antagonist, is indicated as a treatment addition to levodopa/carbidopa in patients experiencing "off episodes". It promotes dopaminergic activity by antagonizing adenosine in the basal ganglia. This review will discuss istradefylline as a treatment for PD patients with off episodes.Entities:
Keywords: carbidopa; catechol-o-methyl transferase (COMT); levodopa; neurodegenerative; parkinsonism
Year: 2020 PMID: 33302331 PMCID: PMC7768423 DOI: 10.3390/neurolint12030017
Source DB: PubMed Journal: Neurol Int ISSN: 2035-8385