DOI: 10.31832/smj.1925439 ISSN: 2146-409X

Short-Term Effects of Bedtime Levodopa Regimens on Subjective Sleep Quality in Parkinson's Disease: A Randomized Crossover Study

Hilal İlbars, Ömer Akbudak, Aysu Akbaş Korucu, Osman Korucu, Emine Emektar
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Objective: To compare the short-term effects of levodopa-benserazide prolonged-release and levodopa-carbidopa-entacapone on subjective sleep quality in patients with idiopathic Parkinson's disease and nocturnal hypokinesia.Methods: In this prospective, randomized, open-label, two-period crossover study conducted in a tertiary hospital movement disorders unit, thirty patients with idiopathic Parkinson's disease, daily levodopa dose ≥1000 mg, and nocturnal hypokinesia received levodopa-carbidopa-entacapone (100/25/200 mg) and levodopa-benserazide prolonged-release (125 mg) on two consecutive nights in randomized order, about one hour before bedtime. Subjective sleep quality was assessed with the Pittsburgh Sleep Quality Index (PSQI) at baseline and by structured telephone interview the following mornings. Scores were compared across assessments and sequences using the Friedman test, with Wilcoxon signed-rank tests and Bonferroni correction for pairwise comparisons.Results: Median PSQI scores decreased from eight at baseline to six after the first treatment night and 6.5 after the second treatment night. No statistically significant difference was observed across the three assessment periods in the overall cohort (p=0.157). A significant overall difference across assessments was observed only in the levodopa-benserazide prolonged-release-first sequence (p=0.001); however, none of the pairwise comparisons remained statistically significant after Bonferroni correction (p<0.016).Conclusions: In this study, PSQI scores decreased following short-term bedtime dopaminergic therapy in patients with Parkinson's disease. Although the reduction was more pronounced when levodopa-benserazide prolonged-release was administered first, the difference did not reach statistical significance. This finding may have been influenced by the imbalance in concomitant long-acting dopaminergic medication use between treatment sequences and the relatively small sample size.

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