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Role of citicoline and choline in the treatment of post-stroke depression: an exploratory study

OBJECTIVE: To compare selective serotonin reuptake inhibitors (SSRIs) and nootropic drugs in the reduction of anxiety and depressive symptoms in post-stroke patients. METHODS: This retrospective cohort study included patients diagnosed with post-stroke depression that were treated with either SSRIs...

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Autores principales: Arcadi, Francesca Antonia, Corallo, Francesco, Torrisi, Michele, Scarfì, Chiara, Lo Buono, Viviana, Formica, Caterina, Bramanti, Placido, Marino, Silvia, Bonanno, Lilla, De Cola, Maria Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573512/
https://www.ncbi.nlm.nih.gov/pubmed/34727752
http://dx.doi.org/10.1177/03000605211055036
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author Arcadi, Francesca Antonia
Corallo, Francesco
Torrisi, Michele
Scarfì, Chiara
Lo Buono, Viviana
Formica, Caterina
Bramanti, Placido
Marino, Silvia
Bonanno, Lilla
De Cola, Maria Cristina
author_facet Arcadi, Francesca Antonia
Corallo, Francesco
Torrisi, Michele
Scarfì, Chiara
Lo Buono, Viviana
Formica, Caterina
Bramanti, Placido
Marino, Silvia
Bonanno, Lilla
De Cola, Maria Cristina
author_sort Arcadi, Francesca Antonia
collection PubMed
description OBJECTIVE: To compare selective serotonin reuptake inhibitors (SSRIs) and nootropic drugs in the reduction of anxiety and depressive symptoms in post-stroke patients. METHODS: This retrospective cohort study included patients diagnosed with post-stroke depression that were treated with either SSRIs or nootropic drugs (i.e. citicoline or choline alphoscerate). Depression and anxiety were assessed using the Hamilton Rating Scales. Statistical associations between the use of nootropic drugs and mood disorder improvements were determined by measuring assessment scores at 6-months. RESULTS: A total of 44 post-stroke patients with depression (aged 45–75 years) were enrolled in the study: 20 were treated with SSRIs and 24 received nootropic drugs. From baseline to follow-up, the SSRI group showed a large effect size with regard depression (success rate difference [SRD] 0.57; 95% confidence interval [CI] 0.21, 0.79) and anxiety (SRD 0.49; 95% CI 0.14, 0.74), whereas the nootropic group showed a small effect size for depression (SRD 0.16; 95% CI –0.17, 0.46) and a small effect size for anxiety (SRD 0.36; 95% CI –0.03, 0.62). CONCLUSION: The administration of nootropic drugs could be a valid therapeutic strategy to manage post-stroke patients suffering from mild–moderate anxiety or anxious-depressive syndrome, but this requires further research.
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spelling pubmed-85735122021-11-09 Role of citicoline and choline in the treatment of post-stroke depression: an exploratory study Arcadi, Francesca Antonia Corallo, Francesco Torrisi, Michele Scarfì, Chiara Lo Buono, Viviana Formica, Caterina Bramanti, Placido Marino, Silvia Bonanno, Lilla De Cola, Maria Cristina J Int Med Res Retrospective Clinical Research Report OBJECTIVE: To compare selective serotonin reuptake inhibitors (SSRIs) and nootropic drugs in the reduction of anxiety and depressive symptoms in post-stroke patients. METHODS: This retrospective cohort study included patients diagnosed with post-stroke depression that were treated with either SSRIs or nootropic drugs (i.e. citicoline or choline alphoscerate). Depression and anxiety were assessed using the Hamilton Rating Scales. Statistical associations between the use of nootropic drugs and mood disorder improvements were determined by measuring assessment scores at 6-months. RESULTS: A total of 44 post-stroke patients with depression (aged 45–75 years) were enrolled in the study: 20 were treated with SSRIs and 24 received nootropic drugs. From baseline to follow-up, the SSRI group showed a large effect size with regard depression (success rate difference [SRD] 0.57; 95% confidence interval [CI] 0.21, 0.79) and anxiety (SRD 0.49; 95% CI 0.14, 0.74), whereas the nootropic group showed a small effect size for depression (SRD 0.16; 95% CI –0.17, 0.46) and a small effect size for anxiety (SRD 0.36; 95% CI –0.03, 0.62). CONCLUSION: The administration of nootropic drugs could be a valid therapeutic strategy to manage post-stroke patients suffering from mild–moderate anxiety or anxious-depressive syndrome, but this requires further research. SAGE Publications 2021-11-02 /pmc/articles/PMC8573512/ /pubmed/34727752 http://dx.doi.org/10.1177/03000605211055036 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Retrospective Clinical Research Report
Arcadi, Francesca Antonia
Corallo, Francesco
Torrisi, Michele
Scarfì, Chiara
Lo Buono, Viviana
Formica, Caterina
Bramanti, Placido
Marino, Silvia
Bonanno, Lilla
De Cola, Maria Cristina
Role of citicoline and choline in the treatment of post-stroke depression: an exploratory study
title Role of citicoline and choline in the treatment of post-stroke depression: an exploratory study
title_full Role of citicoline and choline in the treatment of post-stroke depression: an exploratory study
title_fullStr Role of citicoline and choline in the treatment of post-stroke depression: an exploratory study
title_full_unstemmed Role of citicoline and choline in the treatment of post-stroke depression: an exploratory study
title_short Role of citicoline and choline in the treatment of post-stroke depression: an exploratory study
title_sort role of citicoline and choline in the treatment of post-stroke depression: an exploratory study
topic Retrospective Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573512/
https://www.ncbi.nlm.nih.gov/pubmed/34727752
http://dx.doi.org/10.1177/03000605211055036
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