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Clinical value of serum miR‐320‐3p expression in predicting the prognosis of sepsis‐induced acute kidney injury

BACKGROUND: For investigating the expression of miR‐320‐3p in children with sepsis‐induced acute kidney injury (AKI) and its prognostic value. METHODS: A total of 142 patients were grouped into a survival group (n = 95) and death group (n = 47), which was based on their 28‐day survival. Serum degree...

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Detalles Bibliográficos
Autores principales: Ji, Jian, Luo, Hong, Shi, Jufen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102729/
https://www.ncbi.nlm.nih.gov/pubmed/35334494
http://dx.doi.org/10.1002/jcla.24358
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author Ji, Jian
Luo, Hong
Shi, Jufen
author_facet Ji, Jian
Luo, Hong
Shi, Jufen
author_sort Ji, Jian
collection PubMed
description BACKGROUND: For investigating the expression of miR‐320‐3p in children with sepsis‐induced acute kidney injury (AKI) and its prognostic value. METHODS: A total of 142 patients were grouped into a survival group (n = 95) and death group (n = 47), which was based on their 28‐day survival. Serum degrees of miR‐320‐3p, neutrophil gelatinase‐associated lipid carrier protein (NGAL) and kidney injury molecule‐1 (KIM‐1) were detected. The Acute Physiology and Chronic Health scoring system Ⅱ (APACHE Ⅱ) marks were recorded. Target gene forecast and functional enrichment discussion of miR‐320‐3p were performed, and a protein–protein interaction (PPI) network diagram was plotted by applying bioinformatics methods. Multivariate logistic regression, ROC curve and Pearson correlation analysis were applied. RESULTS: The death group showed greatly higher serum levels of miR‐320‐3p, KIM‐1 and APACHE Ⅱ scores than the survival group (p < 0.01). Multivariate logistic regression analysis showed that levels of miR‐320‐3p, NGAL, KIM‐1 and APACHE Ⅱ scores were independent risk elements for death in sepsis children with AKI (p < 0.01). According to ROC curve analysis, the region under the curve (0.963, 95% CI: 0.908–0.996) of miR‐320‐3p, NGAL, KIM‐1 levels and APACHE Ⅱ scores combined to forecast the death of kids suffering from sepsis and AKI were the biggest. According to correlation analysis, the expression degree of serum miR‐320‐3p in the death group was positively correlated with NGAL, KIM‐1 and APACHE Ⅱ scores (all p < 0.01). CONCLUSIONS: The expression level of serum miR‐320‐3p in children with sepsis‐induced AKI was significantly increased, and the combination of NGAL, KIM‐1 and APACHE Ⅱ scores has good value for prognosis prediction in children.
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spelling pubmed-91027292022-05-18 Clinical value of serum miR‐320‐3p expression in predicting the prognosis of sepsis‐induced acute kidney injury Ji, Jian Luo, Hong Shi, Jufen J Clin Lab Anal Research Articles BACKGROUND: For investigating the expression of miR‐320‐3p in children with sepsis‐induced acute kidney injury (AKI) and its prognostic value. METHODS: A total of 142 patients were grouped into a survival group (n = 95) and death group (n = 47), which was based on their 28‐day survival. Serum degrees of miR‐320‐3p, neutrophil gelatinase‐associated lipid carrier protein (NGAL) and kidney injury molecule‐1 (KIM‐1) were detected. The Acute Physiology and Chronic Health scoring system Ⅱ (APACHE Ⅱ) marks were recorded. Target gene forecast and functional enrichment discussion of miR‐320‐3p were performed, and a protein–protein interaction (PPI) network diagram was plotted by applying bioinformatics methods. Multivariate logistic regression, ROC curve and Pearson correlation analysis were applied. RESULTS: The death group showed greatly higher serum levels of miR‐320‐3p, KIM‐1 and APACHE Ⅱ scores than the survival group (p < 0.01). Multivariate logistic regression analysis showed that levels of miR‐320‐3p, NGAL, KIM‐1 and APACHE Ⅱ scores were independent risk elements for death in sepsis children with AKI (p < 0.01). According to ROC curve analysis, the region under the curve (0.963, 95% CI: 0.908–0.996) of miR‐320‐3p, NGAL, KIM‐1 levels and APACHE Ⅱ scores combined to forecast the death of kids suffering from sepsis and AKI were the biggest. According to correlation analysis, the expression degree of serum miR‐320‐3p in the death group was positively correlated with NGAL, KIM‐1 and APACHE Ⅱ scores (all p < 0.01). CONCLUSIONS: The expression level of serum miR‐320‐3p in children with sepsis‐induced AKI was significantly increased, and the combination of NGAL, KIM‐1 and APACHE Ⅱ scores has good value for prognosis prediction in children. John Wiley and Sons Inc. 2022-03-25 /pmc/articles/PMC9102729/ /pubmed/35334494 http://dx.doi.org/10.1002/jcla.24358 Text en © 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Ji, Jian
Luo, Hong
Shi, Jufen
Clinical value of serum miR‐320‐3p expression in predicting the prognosis of sepsis‐induced acute kidney injury
title Clinical value of serum miR‐320‐3p expression in predicting the prognosis of sepsis‐induced acute kidney injury
title_full Clinical value of serum miR‐320‐3p expression in predicting the prognosis of sepsis‐induced acute kidney injury
title_fullStr Clinical value of serum miR‐320‐3p expression in predicting the prognosis of sepsis‐induced acute kidney injury
title_full_unstemmed Clinical value of serum miR‐320‐3p expression in predicting the prognosis of sepsis‐induced acute kidney injury
title_short Clinical value of serum miR‐320‐3p expression in predicting the prognosis of sepsis‐induced acute kidney injury
title_sort clinical value of serum mir‐320‐3p expression in predicting the prognosis of sepsis‐induced acute kidney injury
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102729/
https://www.ncbi.nlm.nih.gov/pubmed/35334494
http://dx.doi.org/10.1002/jcla.24358
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