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Chemerin levels in chronic kidney disease: A systematic review and meta-analysis

INTRODUCTION: Chemerin as an inflammatory biomarker has gained attention in its biomarker capability. Several studies measured its levels in chronic kidney disease (CKD), as one of the common non-communicable causes of mortality and morbidity. Hence, this systematic review and meta-analysis aimed to...

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Autores principales: Behnoush, Amir Hossein, Shobeiri, Parnian, Bahiraie, Pegah, Amirkhani, Nikan, Khalaji, Amirmohammad, Peiman, Soheil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9907439/
https://www.ncbi.nlm.nih.gov/pubmed/36761204
http://dx.doi.org/10.3389/fendo.2023.1120774
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author Behnoush, Amir Hossein
Shobeiri, Parnian
Bahiraie, Pegah
Amirkhani, Nikan
Khalaji, Amirmohammad
Peiman, Soheil
author_facet Behnoush, Amir Hossein
Shobeiri, Parnian
Bahiraie, Pegah
Amirkhani, Nikan
Khalaji, Amirmohammad
Peiman, Soheil
author_sort Behnoush, Amir Hossein
collection PubMed
description INTRODUCTION: Chemerin as an inflammatory biomarker has gained attention in its biomarker capability. Several studies measured its levels in chronic kidney disease (CKD), as one of the common non-communicable causes of mortality and morbidity. Hence, this systematic review and meta-analysis aimed to investigate this association. METHODS: PubMed, Scopus, Embase, and the Web of Science databases were systematically searched for studies investigating chemerin levels in any CKD stage (including end-stage renal disease patients undergoing hemodialysis (HD)) and comparing it with healthy controls. Random effect meta-analysis was performed to calculate the standardized mean difference (SMD) and 95% confidence interval (CI). RESULTS: A total of eight studies were included, comprised of 875 individuals, with a mean age of 56.92 ± 11.78 years. All studies had high quality based on the New Castle-Ottawa Scale (NOS). Meta-analysis revealed significantly higher levels of chemerin in CKD patients compared to healthy controls (SMD 2.15, 95% CI 0.83-3.48, p-value<0.01). Additionally, HD patients had statistically higher levels of chemerin than controls (SMD 2.10, 95% CI 0.58-3.62, p-value=0.01). In meta-regression, publication year accounted for 23.50% and 24.17% of heterogeneity for these analyses, respectively. CONCLUSION: Chemerin can be potentially used as a biomarker in CKD patients, which can suggest the inflammatory pathways for the disease. Further research is warranted for the assessment of its clinical applications and enlightening its role in the pathophysiology of CKD.
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spelling pubmed-99074392023-02-08 Chemerin levels in chronic kidney disease: A systematic review and meta-analysis Behnoush, Amir Hossein Shobeiri, Parnian Bahiraie, Pegah Amirkhani, Nikan Khalaji, Amirmohammad Peiman, Soheil Front Endocrinol (Lausanne) Endocrinology INTRODUCTION: Chemerin as an inflammatory biomarker has gained attention in its biomarker capability. Several studies measured its levels in chronic kidney disease (CKD), as one of the common non-communicable causes of mortality and morbidity. Hence, this systematic review and meta-analysis aimed to investigate this association. METHODS: PubMed, Scopus, Embase, and the Web of Science databases were systematically searched for studies investigating chemerin levels in any CKD stage (including end-stage renal disease patients undergoing hemodialysis (HD)) and comparing it with healthy controls. Random effect meta-analysis was performed to calculate the standardized mean difference (SMD) and 95% confidence interval (CI). RESULTS: A total of eight studies were included, comprised of 875 individuals, with a mean age of 56.92 ± 11.78 years. All studies had high quality based on the New Castle-Ottawa Scale (NOS). Meta-analysis revealed significantly higher levels of chemerin in CKD patients compared to healthy controls (SMD 2.15, 95% CI 0.83-3.48, p-value<0.01). Additionally, HD patients had statistically higher levels of chemerin than controls (SMD 2.10, 95% CI 0.58-3.62, p-value=0.01). In meta-regression, publication year accounted for 23.50% and 24.17% of heterogeneity for these analyses, respectively. CONCLUSION: Chemerin can be potentially used as a biomarker in CKD patients, which can suggest the inflammatory pathways for the disease. Further research is warranted for the assessment of its clinical applications and enlightening its role in the pathophysiology of CKD. Frontiers Media S.A. 2023-01-25 /pmc/articles/PMC9907439/ /pubmed/36761204 http://dx.doi.org/10.3389/fendo.2023.1120774 Text en Copyright © 2023 Behnoush, Shobeiri, Bahiraie, Amirkhani, Khalaji and Peiman 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 Endocrinology
Behnoush, Amir Hossein
Shobeiri, Parnian
Bahiraie, Pegah
Amirkhani, Nikan
Khalaji, Amirmohammad
Peiman, Soheil
Chemerin levels in chronic kidney disease: A systematic review and meta-analysis
title Chemerin levels in chronic kidney disease: A systematic review and meta-analysis
title_full Chemerin levels in chronic kidney disease: A systematic review and meta-analysis
title_fullStr Chemerin levels in chronic kidney disease: A systematic review and meta-analysis
title_full_unstemmed Chemerin levels in chronic kidney disease: A systematic review and meta-analysis
title_short Chemerin levels in chronic kidney disease: A systematic review and meta-analysis
title_sort chemerin levels in chronic kidney disease: a systematic review and meta-analysis
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9907439/
https://www.ncbi.nlm.nih.gov/pubmed/36761204
http://dx.doi.org/10.3389/fendo.2023.1120774
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