Austin Health

Title
Effect of intravenous alteplase on post-stroke depression in the WAKE UP trial.
Publication Date
2021-06
Author(s)
Königsberg, Alina
Sehner, Susanne
Arlt, Sönke
Cheng, Bastian
Simonsen, Claus Z
Boutitie, Florent
Serena, Joaquin
Thijs, Vincent
Ebinger, Martin
Endres, Matthias
Fiebach, Jochen B
Lemmens, Robin
Muir, Keith W
Nighoghossian, Norbert
Pedraza, Salvador
Gerloff, Christian
Thomalla, Götz
Subject
DWI
MRI
WAKE-UP
Type of document
Journal Article
OrcId
0000-0003-2591-1807
0000-0003-0594-4409
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DOI
10.1111/ene.14797
Abstract
To study the effect of intravenous alteplase on development of post-stroke depression (PSD) in acute stroke patients, and to identify predictors of PSD. This post-hoc analysis included patients with unknown onset stroke randomized to treatment with alteplase or placebo in the WAKE-UP trial (ClinicalTrials.gov number, NCT01525290), in whom a composite endpoint of PSD was defined as a Beck Depression Inventory BDI ≥10, medication with an antidepressant, or depression recorded as an adverse event. We used multiple logistic regression to identify predictors of PSD at 90 days. Structural equation modelling was applied to assess the indirect effect of thrombolysis on PSD mediated by the modified Rankin Scale (mRS). Information on the composite endpoint was available for 438 of 503 randomized patients. PSD was present in 96 of 224 (42.9%) patients in the alteplase group and 115 of 214 (53.7%) in the placebo group (OR 0.63; 95% CI 0.43-0.94; p=0.022; adjusted for age and National Institutes of Health Stroke Scale [NIHSS] at baseline). Prognostic factors associated with PSD included baseline medication with antidepressants, higher lesion volume, history of depression and assignment to placebo. While 65% of the effect of thrombolysis on PSD was caused directly, while 35% where mediated by an improvement of the mRS. Treatment with alteplase in patients with acute stroke resulted in lower rates of depression at 90 days, which was only partially explained by reduced functional disability. Predictors of PSD including history and clinical characteristics may help in identifying patients at risk PSD.
Link
Citation
European Journal of Neurology 2021; 28(6): 2017-2025
Jornal Title
European Journal of Neurology

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