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The efficacy of oral adenosine A2A antagonist istradefylline for the treatment of moderate to severe Parkinson's disease

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EXPERT REVIEW OF NEUROTHERAPEUTICS
卷 15, 期 12, 页码 1383-1390

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TAYLOR & FRANCIS LTD
DOI: 10.1586/14737175.2015.1113131

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A(2A) receptor antagonist; dyskinesia; istradefylline; levodopa add-on therapy; motor fluctuations; off time; Parkinson's disease; treatment

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The moderate and severe stages of Parkinson's disease (PD) are marked by motor and non-motor complications that still remain difficult to control with the currently available therapy. Adenosine A(2A) receptor antagonists target non-dopaminergic systems, and have emerged as promising add-on therapy in the management of PD, a little more than a decade ago. While the development of this new drug class was slower than initially expected, istradefylline was recently registered in Japan, because it provides reduction of the off-time, when given in association with levodopa. Effects on some non-motor features have also been suggested, and preliminary studies further suggest a potential neuroprotective effect. Associations of A(2A) receptor antagonists with dopaminergic agents, as well as enzyme blockers like catechol-O-methyltransferase (COMT) and monoamine oxidase-B (MAO-B) inhibitors, should provide even greater benefit in advanced PD patients, and, thus, a more individualized treatment approach would be at hand.

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