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IL-33/ST2 immunobiology in coronary artery disease: A systematic review and meta-analysis

The IL-33/ST2 axis is reported to be controversially associated with coronary artery disease (CAD). A systematic review of the association between the IL-33/ST2 axis and CAD revealed that IL-33/ST2 plays a protective role in CAD and serum sST2 and IL-33 levels are increased in patients with cardiova...

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Autores principales: Liu, Renli, Liu, Liping, Wei, Chaojie, Li, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630943/
https://www.ncbi.nlm.nih.gov/pubmed/36337880
http://dx.doi.org/10.3389/fcvm.2022.990007
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author Liu, Renli
Liu, Liping
Wei, Chaojie
Li, Dong
author_facet Liu, Renli
Liu, Liping
Wei, Chaojie
Li, Dong
author_sort Liu, Renli
collection PubMed
description The IL-33/ST2 axis is reported to be controversially associated with coronary artery disease (CAD). A systematic review of the association between the IL-33/ST2 axis and CAD revealed that IL-33/ST2 plays a protective role in CAD and serum sST2 and IL-33 levels are increased in patients with cardiovascular disease. Therefore, the association of IL-33/ST2 single nucleotide polymorphisms (SNPs) with CAD prevalence, prognosis, and risk factors was assessed by performing a meta-analysis. Through a literature search of relevant articles in various databases using the relevant keywords, seven studies were included in the analysis. The meta-analysis showed that the IL-33/ST2 axis was associated with increased CAD risk [pooled odds ratio (OR) = 1.17, 95% confidence interval (CI): 1.13–1.20]. Gene subgroup analysis showed a close association of IL1RL1 (OR = 1.25, 95% CI: 1.20–1.30; I(2) = 85.9%; p = 0.000) and IL1RAcP (OR = 1.42, 95% CI: 1.26–1.60; I(2) = 27.1%; p = 0.203) with increased CAD risk. However, the association for the IL-33 gene was not statistically significant. SNPs rs7044343 (T), rs10435816 (G), rs11792633 (C) in IL-33 gene were associated with a protective effect in CAD. However, rs7025417 (T) in IL-33, rs11685424 (G) in IL1RL1, rs950880 (A) in sST2, and rs4624606 (A) in IL1RAcP were related to increased CAD risk. Overall, polymorphisms in IL-33/ST2 axis components were associated with increased CAD risk. These results may help identify key features of IL-33/ST2 immunobiology in CAD along with potential treatment strategies to lower disease burden.
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spelling pubmed-96309432022-11-04 IL-33/ST2 immunobiology in coronary artery disease: A systematic review and meta-analysis Liu, Renli Liu, Liping Wei, Chaojie Li, Dong Front Cardiovasc Med Cardiovascular Medicine The IL-33/ST2 axis is reported to be controversially associated with coronary artery disease (CAD). A systematic review of the association between the IL-33/ST2 axis and CAD revealed that IL-33/ST2 plays a protective role in CAD and serum sST2 and IL-33 levels are increased in patients with cardiovascular disease. Therefore, the association of IL-33/ST2 single nucleotide polymorphisms (SNPs) with CAD prevalence, prognosis, and risk factors was assessed by performing a meta-analysis. Through a literature search of relevant articles in various databases using the relevant keywords, seven studies were included in the analysis. The meta-analysis showed that the IL-33/ST2 axis was associated with increased CAD risk [pooled odds ratio (OR) = 1.17, 95% confidence interval (CI): 1.13–1.20]. Gene subgroup analysis showed a close association of IL1RL1 (OR = 1.25, 95% CI: 1.20–1.30; I(2) = 85.9%; p = 0.000) and IL1RAcP (OR = 1.42, 95% CI: 1.26–1.60; I(2) = 27.1%; p = 0.203) with increased CAD risk. However, the association for the IL-33 gene was not statistically significant. SNPs rs7044343 (T), rs10435816 (G), rs11792633 (C) in IL-33 gene were associated with a protective effect in CAD. However, rs7025417 (T) in IL-33, rs11685424 (G) in IL1RL1, rs950880 (A) in sST2, and rs4624606 (A) in IL1RAcP were related to increased CAD risk. Overall, polymorphisms in IL-33/ST2 axis components were associated with increased CAD risk. These results may help identify key features of IL-33/ST2 immunobiology in CAD along with potential treatment strategies to lower disease burden. Frontiers Media S.A. 2022-10-20 /pmc/articles/PMC9630943/ /pubmed/36337880 http://dx.doi.org/10.3389/fcvm.2022.990007 Text en Copyright © 2022 Liu, Liu, Wei and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Liu, Renli
Liu, Liping
Wei, Chaojie
Li, Dong
IL-33/ST2 immunobiology in coronary artery disease: A systematic review and meta-analysis
title IL-33/ST2 immunobiology in coronary artery disease: A systematic review and meta-analysis
title_full IL-33/ST2 immunobiology in coronary artery disease: A systematic review and meta-analysis
title_fullStr IL-33/ST2 immunobiology in coronary artery disease: A systematic review and meta-analysis
title_full_unstemmed IL-33/ST2 immunobiology in coronary artery disease: A systematic review and meta-analysis
title_short IL-33/ST2 immunobiology in coronary artery disease: A systematic review and meta-analysis
title_sort il-33/st2 immunobiology in coronary artery disease: a systematic review and meta-analysis
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630943/
https://www.ncbi.nlm.nih.gov/pubmed/36337880
http://dx.doi.org/10.3389/fcvm.2022.990007
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