Optimization of oral entacapone administration in patients undergoing levodopa–carbidopa intestinal gel treatment

Levodopa–carbidopa intestinal gel (LCIG) treatment markedly reduces motor fluctuations in patients with Parkinson's disease; however, some patients undergoing LCIG treatment may demonstrate clinical deterioration in the afternoon. Entacapone, a catechol-O-methyltransferase inhibitor, may be a p...

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Veröffentlicht in:Journal of the neurological sciences 2024-02, Vol.457, p.122901-122901, Article 122901
Hauptverfasser: Miyaue, Noriyuki, Ito, Yuko, Yamanishi, Yuki, Tada, Satoshi, Ando, Rina, Yabe, Hayato, Nagai, Masahiro
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Sprache:eng
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Zusammenfassung:Levodopa–carbidopa intestinal gel (LCIG) treatment markedly reduces motor fluctuations in patients with Parkinson's disease; however, some patients undergoing LCIG treatment may demonstrate clinical deterioration in the afternoon. Entacapone, a catechol-O-methyltransferase inhibitor, may be a promising adjunctive option for LCIG-treated patients; however, the optimal timing of oral entacapone administration to ameliorate clinical symptoms in the afternoon remains unexplored. This study aimed to investigate the optimal timing of oral entacapone administration in patients with Parkinson's disease undergoing LCIG treatment. Pharmacokinetic analysis and symptom assessment were performed on three days: a day without entacapone administration, day with oral entacapone administration at 13:00, and day with oral entacapone administration at 15:00. Eight LCIG-treated patients were enrolled, of whom seven completed this study. The relative plasma concentrations of levodopa with entacapone administration at 13:00 were gradually increased, especially at 18:00 and were significantly higher than those without entacapone administration (127.10 ± 25.06% vs. 97.51 ± 22.20%). The relative plasma concentrations of 3-O-methyldopa were gradually increased without entacapone administration, whereas those with entacapone administration at 13:00 were lower than those without entacapone administration, especially at 17:00 (97.47 ± 3.70% vs. 110.71 ± 9.84%). Administering oral entacapone at 15:00 increased and decreased the relative plasma concentrations of levodopa and 3-O-methyldopa, respectively, but without significant difference. The “Off” time was shorter with entacapone administration at 13:00 (0.43 ± 0.79 h) and at 15:00 (0.57 ± 0.79 h) than that without entacapone administration (1.14 ± 1.46 h). The concomitant use of oral entacapone in the early afternoon may be effective in improving afternoon symptoms in patients undergoing LCIG treatment. •Motor fluctuations in afternoon are observed in some LCIG-treated patients with PD.•We explored the optimal timing of oral entacapone administration in the afternoon.•Dosing at 13:00 significantly increased levodopa levels and decreased 3-OMD levels.•Dosing at 15:00 tended to increase levodopa levels and decrease 3-OMD levels.•Early-afternoon entacapone administration may be effective in improving symptoms.
ISSN:0022-510X
1878-5883
DOI:10.1016/j.jns.2024.122901