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Changes in eotaxin-3 and pulmonary and activation-regulated chemokine levels in patients after dupilumab treatment: a systematic review and meta-analysis
INTRODUCTION: Dupilumab is approved for a variety of type 2 inflammatory diseases. Changes in chemokine levels during treatment require further analysis. AIM: We evaluated changes in eotaxin-3 and PARC levels after dupilumab treatment through a meta-analysis, aiming to provide more comprehensive res...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646707/ https://www.ncbi.nlm.nih.gov/pubmed/38028411 http://dx.doi.org/10.5114/ada.2023.132231 |
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author | Wang, Leyi Cheng, Haiyan Zhou, Boyang Li, Linfeng |
author_facet | Wang, Leyi Cheng, Haiyan Zhou, Boyang Li, Linfeng |
author_sort | Wang, Leyi |
collection | PubMed |
description | INTRODUCTION: Dupilumab is approved for a variety of type 2 inflammatory diseases. Changes in chemokine levels during treatment require further analysis. AIM: We evaluated changes in eotaxin-3 and PARC levels after dupilumab treatment through a meta-analysis, aiming to provide more comprehensive results. MATERIAL AND METHODS: Databases were searched to select eligible publications. The study quality was assessed after inclusion. The standardized mean difference (SMD) was used for evaluation. RESULTS: Four studies were included. Eotaxin-3 levels were not seen significantly decreased at weeks 1 and 12, with SMD = –0.39 (95% CI: –1.78, 0.99) and –2.60 (95% CI: –5.77, 0.57), respectively (p > 0.05). Eotaxin-3 levels decreased significantly at weeks 2, 4, 8, 16, 24, 36, and 52, with SMD = –0.94 (95% CI: –1.61, –0.27); –1.17 (95% CI: –1.49, –0.84); –1.20 (95% CI: –1.52, –0.88); –1.31 (95% CI: –1.83, –0.79); –4.57 (95% CI: –6.90, –2.33); –5.28 (95% CI: –5.52, –5.04); and –4.03 (95% CI: –4.22, –3.85) (p < 0.05), respectively. PARC levels decreased significantly at weeks 4, 8, 12, and 16, with SMD = –1.08 (95% CI: –1.59, –0.58); –1.17 (95% CI: –1.68, –0.66); –1.11 (95% CI: –1.61, –0.60); and –1.15 (95% CI: –1.66, –0.64) (p < 0.05), respectively. CONCLUSIONS: Eotaxin-3 and PARC levels can be significantly reduced in patients treated with dupilumab. |
format | Online Article Text |
id | pubmed-10646707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-106467072023-10-01 Changes in eotaxin-3 and pulmonary and activation-regulated chemokine levels in patients after dupilumab treatment: a systematic review and meta-analysis Wang, Leyi Cheng, Haiyan Zhou, Boyang Li, Linfeng Postepy Dermatol Alergol Original Paper INTRODUCTION: Dupilumab is approved for a variety of type 2 inflammatory diseases. Changes in chemokine levels during treatment require further analysis. AIM: We evaluated changes in eotaxin-3 and PARC levels after dupilumab treatment through a meta-analysis, aiming to provide more comprehensive results. MATERIAL AND METHODS: Databases were searched to select eligible publications. The study quality was assessed after inclusion. The standardized mean difference (SMD) was used for evaluation. RESULTS: Four studies were included. Eotaxin-3 levels were not seen significantly decreased at weeks 1 and 12, with SMD = –0.39 (95% CI: –1.78, 0.99) and –2.60 (95% CI: –5.77, 0.57), respectively (p > 0.05). Eotaxin-3 levels decreased significantly at weeks 2, 4, 8, 16, 24, 36, and 52, with SMD = –0.94 (95% CI: –1.61, –0.27); –1.17 (95% CI: –1.49, –0.84); –1.20 (95% CI: –1.52, –0.88); –1.31 (95% CI: –1.83, –0.79); –4.57 (95% CI: –6.90, –2.33); –5.28 (95% CI: –5.52, –5.04); and –4.03 (95% CI: –4.22, –3.85) (p < 0.05), respectively. PARC levels decreased significantly at weeks 4, 8, 12, and 16, with SMD = –1.08 (95% CI: –1.59, –0.58); –1.17 (95% CI: –1.68, –0.66); –1.11 (95% CI: –1.61, –0.60); and –1.15 (95% CI: –1.66, –0.64) (p < 0.05), respectively. CONCLUSIONS: Eotaxin-3 and PARC levels can be significantly reduced in patients treated with dupilumab. Termedia Publishing House 2023-11-09 2023-10 /pmc/articles/PMC10646707/ /pubmed/38028411 http://dx.doi.org/10.5114/ada.2023.132231 Text en Copyright: © 2023 Termedia Sp. z o. o. https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Original Paper Wang, Leyi Cheng, Haiyan Zhou, Boyang Li, Linfeng Changes in eotaxin-3 and pulmonary and activation-regulated chemokine levels in patients after dupilumab treatment: a systematic review and meta-analysis |
title | Changes in eotaxin-3 and pulmonary and activation-regulated chemokine levels in patients after dupilumab treatment: a systematic review and meta-analysis |
title_full | Changes in eotaxin-3 and pulmonary and activation-regulated chemokine levels in patients after dupilumab treatment: a systematic review and meta-analysis |
title_fullStr | Changes in eotaxin-3 and pulmonary and activation-regulated chemokine levels in patients after dupilumab treatment: a systematic review and meta-analysis |
title_full_unstemmed | Changes in eotaxin-3 and pulmonary and activation-regulated chemokine levels in patients after dupilumab treatment: a systematic review and meta-analysis |
title_short | Changes in eotaxin-3 and pulmonary and activation-regulated chemokine levels in patients after dupilumab treatment: a systematic review and meta-analysis |
title_sort | changes in eotaxin-3 and pulmonary and activation-regulated chemokine levels in patients after dupilumab treatment: a systematic review and meta-analysis |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646707/ https://www.ncbi.nlm.nih.gov/pubmed/38028411 http://dx.doi.org/10.5114/ada.2023.132231 |
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