The impact of levodopa on post-stroke depression: the ESTREL-depression-study.

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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Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2026-02-09
DOI
https://doi.org/10.48620/94751
Primary Topic
Stroke Rehabilitation and Recovery
Type
article
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article

The impact of levodopa on post-stroke depression: the ESTREL-depression-study.

Raoul Schweinfurther, Peter S. Sándor, Zorica Suica, Elias Auer et al.
Open Access CRIS of the University of Bern
Stroke Rehabilitation and Recovery
article

The impact of levodopa on post-stroke depression: the ESTREL-depression-study.

Raoul Schweinfurther, Peter S. Sándor, Zorica Suica, Elias Auer, Ettore Accolla, Andreas R. Luft, Annaelle V. Zietz, Piotr Jedrysiak, S. Schädelin, Josefin E. Kaufmann, Andrea M. Humm, Joëlle Nsimire Chabwine, Carmen Lienert, Friedrich Medlin, Yannik Rottenberger, Jeremia P. O. Held, Dietmar Lutz, Lars G Hemkens, Mira Katan, Simon Trüssel, Lukas Boos, René M Müri, Svetlana Politz, Janine Schär, Karin Wiesner, Mirjam I Sauter, Szabina Gäumann, Patrik Michel, Anne Schwarz, Gary A Ford, Alexander A Tarnutzer, Gian Marco De Marchis, Julian Lippert, Philippe A Lyrer, Marcel Arnold, Bartosz Bujan, Nils Peters, Krassen Nedeltchev, David Julian Seiffge, Matthias Greulich, J Carsten Möller, Sandrine Foucras, Alexander Salerno, Georg Kägi, Roman Gonzenbach, Valerian L Altersberger, Leo H Bonati, Stefan T Engelter, Katrien Van Den Keybus Deglon, Rolf Sturzenegger, Martina Wiegert, Alexandros Polymeris, Henrik Gensicke, Pierre-André Rapin
article en

Abstract

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).

Open Access CRIS of the University of Bern
National Center for Geriatrics and Gerontology (JP)
Good health and well-being
Openalex Percentile: Top 51%
Stroke Rehabilitation and Recovery
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