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

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Authors: Mirjam I Sauter, Josefin Emelie Kaufmann, Lukas Boos, Annaelle V. Zietz, Simon Trüssel, Andreas Rüdiger Luft, Alexandros A. Polymeris, Valerian L. Altersberger, Karin Wiesner, Martina Wiegert, Jeremia P. O. Held, Yannik Rottenberger
+44 more Anne Schwarz, Friedrich Medlin, Ettore A. Accolla, Sandrine Foucras, Georg Kägi, Gian Marco De Marchis, Svetlana Politz, Matthias Greulich, Alexander Andrea Tarnutzer, Rolf Sturzenegger, Katan Mira, Marcel Arnold, Krassen Nedeltchev, Janine Schär, Katrien Van Den Keybus, Pierre-André Rapin, Alexander Salerno, David Julian Seiffge, Elias Auer, Julian Lippert, Leo Hermann Bonati, Corina Schuster‐Amft, Szabina Gäumann, Joëlle Nsimire Chabwine, Andrea Monika Humm, Jens Carsten Möller, Raoul Schweinfurther, Bartosz Bujan, Piotr Jedrysiak, Peter Stephan Sándor, Roman Rudolf Gonzenbach, Veit Mylius, Dietmar Lutz, Carmen Lienert, Nils Peters, Patrik Michel, René M. Müri, Sabine Schädelin, Lars G. Hemkens, Gary A. Ford, Philippe A. Lyrer, Henrik Gensicke, Christopher Traenka, Stefan T. Engelter
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References: 39

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).

Fields of Study & Subjects

Stroke Rehabilitation and Recovery Treatment of Major Depression Transcranial Magnetic Stimulation Studies

Publication details

Journal / source
European Stroke Journal
Volume
11
Issue
2
Publication date
1 January 2026
Language
EN