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Thymosin alpha1 use in adult COVID-19 patients: A systematic review and meta-analysis on clinical outcomes

OBJECTIVE: Thymosin alpha1 (Ta1) is widely used to treat patients with coronavirus disease 2019 (COVID-19), however, its effect remains unclear. This systematic review and meta-analysis aimed to evaluate the effect of Ta1 as a COVID-19 therapy. METHODS: PubMed, EMBASE, the Cochrane library, Web of S...

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Detalles Bibliográficos
Autores principales: Shang, Weifeng, Zhang, Bo, Ren, Yali, Wang, Weina, Zhou, Dengfeng, Li, Yuanyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9754924/
https://www.ncbi.nlm.nih.gov/pubmed/36527881
http://dx.doi.org/10.1016/j.intimp.2022.109584
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author Shang, Weifeng
Zhang, Bo
Ren, Yali
Wang, Weina
Zhou, Dengfeng
Li, Yuanyuan
author_facet Shang, Weifeng
Zhang, Bo
Ren, Yali
Wang, Weina
Zhou, Dengfeng
Li, Yuanyuan
author_sort Shang, Weifeng
collection PubMed
description OBJECTIVE: Thymosin alpha1 (Ta1) is widely used to treat patients with coronavirus disease 2019 (COVID-19), however, its effect remains unclear. This systematic review and meta-analysis aimed to evaluate the effect of Ta1 as a COVID-19 therapy. METHODS: PubMed, EMBASE, the Cochrane library, Web of Science, and the reference lists of relevant articles were searched to identify eligible studies. Assessment of heterogeneity was done using the I-squared (I(2)) test and random/fixed effect analysis was done to determine the risk ratio (RR). We polled the data related to mortality mainly by using Review Manager 5.4. Predefined subgroup analyses and sensitivity analyses were also performed. RESULTS: A total of 9 studies were included, on a total of 5352 (Ta1 = 1152, control = 4200) patient outcomes. Meta-analysis results indicated that Ta1 therapy had no statistically significant effect on mortality [RR 1.03 (0.60, 1.75), p = 0.92, I(2) = 90 %]. Subgroup analyses demonstrated that the beneficial effect in mortality was associated with mean age>60 years in the Tα1 group [RR 0.68 (0.58, 0.78), p < 0.0000.1, I(2) = 0 %], the proportion of female ≤ 40 % in the Tα1 group [RR 0.67 (0.58, 0.77), p < 0.0000.1, I(2) = 0 %], and severe/critical COVID-19 patients [RR 0.66 (0.57, 0.76), p < 0.0000.1, I(2) = 0 %]. Sensitivity analysis further demonstrated the results to be robust. CONCLUSIONS: The results of this meta-analysis do not support the use of Ta1 in hospitalized adult COVID-19 patients.
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spelling pubmed-97549242022-12-16 Thymosin alpha1 use in adult COVID-19 patients: A systematic review and meta-analysis on clinical outcomes Shang, Weifeng Zhang, Bo Ren, Yali Wang, Weina Zhou, Dengfeng Li, Yuanyuan Int Immunopharmacol Article OBJECTIVE: Thymosin alpha1 (Ta1) is widely used to treat patients with coronavirus disease 2019 (COVID-19), however, its effect remains unclear. This systematic review and meta-analysis aimed to evaluate the effect of Ta1 as a COVID-19 therapy. METHODS: PubMed, EMBASE, the Cochrane library, Web of Science, and the reference lists of relevant articles were searched to identify eligible studies. Assessment of heterogeneity was done using the I-squared (I(2)) test and random/fixed effect analysis was done to determine the risk ratio (RR). We polled the data related to mortality mainly by using Review Manager 5.4. Predefined subgroup analyses and sensitivity analyses were also performed. RESULTS: A total of 9 studies were included, on a total of 5352 (Ta1 = 1152, control = 4200) patient outcomes. Meta-analysis results indicated that Ta1 therapy had no statistically significant effect on mortality [RR 1.03 (0.60, 1.75), p = 0.92, I(2) = 90 %]. Subgroup analyses demonstrated that the beneficial effect in mortality was associated with mean age>60 years in the Tα1 group [RR 0.68 (0.58, 0.78), p < 0.0000.1, I(2) = 0 %], the proportion of female ≤ 40 % in the Tα1 group [RR 0.67 (0.58, 0.77), p < 0.0000.1, I(2) = 0 %], and severe/critical COVID-19 patients [RR 0.66 (0.57, 0.76), p < 0.0000.1, I(2) = 0 %]. Sensitivity analysis further demonstrated the results to be robust. CONCLUSIONS: The results of this meta-analysis do not support the use of Ta1 in hospitalized adult COVID-19 patients. Elsevier B.V. 2023-01 2022-12-13 /pmc/articles/PMC9754924/ /pubmed/36527881 http://dx.doi.org/10.1016/j.intimp.2022.109584 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Shang, Weifeng
Zhang, Bo
Ren, Yali
Wang, Weina
Zhou, Dengfeng
Li, Yuanyuan
Thymosin alpha1 use in adult COVID-19 patients: A systematic review and meta-analysis on clinical outcomes
title Thymosin alpha1 use in adult COVID-19 patients: A systematic review and meta-analysis on clinical outcomes
title_full Thymosin alpha1 use in adult COVID-19 patients: A systematic review and meta-analysis on clinical outcomes
title_fullStr Thymosin alpha1 use in adult COVID-19 patients: A systematic review and meta-analysis on clinical outcomes
title_full_unstemmed Thymosin alpha1 use in adult COVID-19 patients: A systematic review and meta-analysis on clinical outcomes
title_short Thymosin alpha1 use in adult COVID-19 patients: A systematic review and meta-analysis on clinical outcomes
title_sort thymosin alpha1 use in adult covid-19 patients: a systematic review and meta-analysis on clinical outcomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9754924/
https://www.ncbi.nlm.nih.gov/pubmed/36527881
http://dx.doi.org/10.1016/j.intimp.2022.109584
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