Key result
Levodopa during rehabilitation fails to reduce post-stroke depression at 3 months compared to placebo.
Why the study?
Post-stroke depression frequently occurs and impairs rehabilitation, and low dopamine levels are linked to it, but whether levodopa treatment during in-hospital rehabilitation impacts post-stroke depression was unknown.
Does levodopa/carbidopa reduce the occurrence of post-stroke depression in patients with acute ischemic or hemorrhagic stroke?
Does levodopa/carbidopa reduce the occurrence of post-stroke depression in patients with acute ischemic or hemorrhagic stroke?
Levodopa/carbidopa treatment during in-hospital rehabilitation does not reduce the occurrence of post-stroke depression at 3 months compared to placebo.
Does not support levodopa for post-stroke depression prevention; confirms null effect in acute rehabilitation.
Introduction Post-stroke depression (PSD) frequently occurs after acute stroke and negatively affects rehabilitation. Dopamine has beneficial effects on motivation and emotional stability. In stroke patients, low dopamine levels are linked to PSD. This study investigated whether levodopa treatment during in-hospital rehabilitation impacts PSD compared to placebo. Patients and methods ESTREL-Depression was a pre-planned analysis of the multicenter, randomized, double-blind, placebo-controlled ESTREL trial. Participants with an acute ischemic or hemorrhagic stroke were randomly assigned to receive either levodopa/carbidopa (100/25 mg) or placebo three times daily for 39 days. All ESTREL participants with (1) information about the presence or absence of depression at three months and (2) who took at least 80% of the study medication were eligible for the study. Participants with a history of depression were excluded. For the primary outcome, the presence of PSD was defined as having a T-score of ≥55 in the Patient-Reported Outcomes Measurement Information System short-form depression-4a 3 months after randomization. Binary logistic regression was performed to assess the effect of levodopa on PSD. Results The study included 407 ESTREL participants (median age 72, 60% male), 209 receiving levodopa, and 198 receiving placebo. At 3 months, the frequency and odds of PSD did not differ between the levodopa group (26%) and the placebo group (28%) (OR = 0.93, 95% CI, 0.60–1.43). Conclusion In the ESTREL-Depression study, treatment with levodopa had no impact on the occurrence of PSD. Clinical Trial Registration ClinicalTrials.gov: NCT03735901 (https://clinicaltrials.gov/study/NCT03735901).
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Sauter et al. (2026) studied this question. Levodopa treatment during rehabilitation did not reduce post-stroke depression at 3 months (26% vs 28%; OR 0.93, 95% CI 0.60–1.43) compared to placebo.
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