The efficacy of oral adenosine A(2A) antagonist istradefylline for the treatment of moderate to severe Parkinson's disease

Expert Rev Neurother. 2015;15(12):1383-90. doi: 10.1586/14737175.2015.1113131.

Abstract

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.

Keywords: A2A receptor antagonist; Parkinson’s disease; dyskinesia; istradefylline; levodopa add-on therapy; motor fluctuations; off time; treatment.

MeSH terms

  • Antiparkinson Agents / therapeutic use
  • Catechol O-Methyltransferase Inhibitors / therapeutic use
  • Humans
  • Japan
  • Levodopa / therapeutic use
  • Monoamine Oxidase Inhibitors / therapeutic use
  • Parkinson Disease / drug therapy*
  • Purines / therapeutic use*

Substances

  • Antiparkinson Agents
  • Catechol O-Methyltransferase Inhibitors
  • Monoamine Oxidase Inhibitors
  • Purines
  • istradefylline
  • Levodopa