Presepsin as a diagnostic biomarker for sepsis across neonates, children, and adults: A meta-analysis

Sepsis remains a leading global health challenge, with delayed recognition and limited diagnostic accuracy of current tools contributing to high morbidity and mortality. Conventional clinical scores (SOFA/qSOFA), standard biomarkers (CRP, PCT), and blood cultures suffer from delayed responsiveness,...

Full description

Saved in:
Bibliographic Details
Main Authors: Kaicheng Peng, Xiangmin Zhang, Qinyuan Li, Zhengxiu Luo
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2025-08-01
Series:Biomolecules & Biomedicine
Subjects:
Online Access:https://www.bjbms.org/ojs/index.php/bjbms/article/view/12909
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849225517049315328
author Kaicheng Peng
Xiangmin Zhang
Qinyuan Li
Zhengxiu Luo
author_facet Kaicheng Peng
Xiangmin Zhang
Qinyuan Li
Zhengxiu Luo
author_sort Kaicheng Peng
collection DOAJ
description Sepsis remains a leading global health challenge, with delayed recognition and limited diagnostic accuracy of current tools contributing to high morbidity and mortality. Conventional clinical scores (SOFA/qSOFA), standard biomarkers (CRP, PCT), and blood cultures suffer from delayed responsiveness, insufficient specificity, or slow turnaround, underscoring the urgent need for more reliable early diagnostic strategies. Presepsin, a soluble CD14 subtype generated during pathogen recognition by innate immune cells, has emerged as a promising biomarker with potential to reflect infection status earlier and more specifically than traditional markers. This systematic review and meta-analysis quantitatively evaluated the diagnostic accuracy of presepsin across diverse populations. PubMed, EMBASE, Web of Science, and Cochrane Library were searched for studies published between 2015 and 2025. Forty-seven studies involving 7,087 participants were included. Pooled sensitivity, specificity, diagnostic odds ratio (DOR), area under the curve (AUC), and likelihood ratios (PLR/NLR) with 95% confidence intervals (CI) were calculated using random-effects models. Heterogeneity was assessed with I² statistics, meta-regression, and subgroup analyses. Study quality was evaluated using QUADAS-2. Presepsin demonstrated excellent overall diagnostic performance: pooled sensitivity 0.84 (95% CI: 0.81–0.88), specificity 0.86 (95% CI: 0.80–0.90), DOR 32.23 (95% CI: 20.11–51.66), and AUC 0.91 (95% CI: 0.88–0.93). Subgroup analyses confirmed robust performance across settings and populations, with particularly high accuracy in neonates (sensitivity 0.90, specificity 0.92, AUC 0.96), followed by children (sensitivity 0.84, specificity 0.81, AUC 0.88, NLR 0.20) and adults (sensitivity 0.81, specificity 0.82, AUC 0.87). Meta-regression identified year of publication, geographic region, specimen type, population, and diagnostic criteria as key contributors to heterogeneity, but sensitivity analyses confirmed result stability. No significant publication bias was observed (p = 0.33). In conclusion, presepsin is a valuable and highly promising biomarker for sepsis diagnosis, showing favorable diagnostic accuracy across populations, with strongest utility in neonates. Its application in pediatric and adult patients warrants further validation through large, prospective, multi-center studies.
format Article
id doaj-art-ee1d8d08dc354d8aa431f7d2b8373d1c
institution Kabale University
issn 2831-0896
2831-090X
language English
publishDate 2025-08-01
publisher Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
record_format Article
series Biomolecules & Biomedicine
spelling doaj-art-ee1d8d08dc354d8aa431f7d2b8373d1c2025-08-24T16:09:03ZengAssociation of Basic Medical Sciences of Federation of Bosnia and HerzegovinaBiomolecules & Biomedicine2831-08962831-090X2025-08-0110.17305/bb.2025.12909Presepsin as a diagnostic biomarker for sepsis across neonates, children, and adults: A meta-analysisKaicheng Peng0https://orcid.org/0000-0002-8094-9720Xiangmin Zhang1Qinyuan Li2Zhengxiu Luo3Department of Respiratory Medicine, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Children’s Vital Organ Development and Disease of Chongqing Health Commission, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Chongqing, ChinaDepartment of Radiology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China; Chongqing Engineering Research Center of Stem Cell Therapy, Chongqing, China.Department of Respiratory Medicine, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Children’s Vital Organ Development and Disease of Chongqing Health Commission, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Chongqing, ChinaDepartment of Respiratory Medicine, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Children’s Vital Organ Development and Disease of Chongqing Health Commission, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Chongqing, China Sepsis remains a leading global health challenge, with delayed recognition and limited diagnostic accuracy of current tools contributing to high morbidity and mortality. Conventional clinical scores (SOFA/qSOFA), standard biomarkers (CRP, PCT), and blood cultures suffer from delayed responsiveness, insufficient specificity, or slow turnaround, underscoring the urgent need for more reliable early diagnostic strategies. Presepsin, a soluble CD14 subtype generated during pathogen recognition by innate immune cells, has emerged as a promising biomarker with potential to reflect infection status earlier and more specifically than traditional markers. This systematic review and meta-analysis quantitatively evaluated the diagnostic accuracy of presepsin across diverse populations. PubMed, EMBASE, Web of Science, and Cochrane Library were searched for studies published between 2015 and 2025. Forty-seven studies involving 7,087 participants were included. Pooled sensitivity, specificity, diagnostic odds ratio (DOR), area under the curve (AUC), and likelihood ratios (PLR/NLR) with 95% confidence intervals (CI) were calculated using random-effects models. Heterogeneity was assessed with I² statistics, meta-regression, and subgroup analyses. Study quality was evaluated using QUADAS-2. Presepsin demonstrated excellent overall diagnostic performance: pooled sensitivity 0.84 (95% CI: 0.81–0.88), specificity 0.86 (95% CI: 0.80–0.90), DOR 32.23 (95% CI: 20.11–51.66), and AUC 0.91 (95% CI: 0.88–0.93). Subgroup analyses confirmed robust performance across settings and populations, with particularly high accuracy in neonates (sensitivity 0.90, specificity 0.92, AUC 0.96), followed by children (sensitivity 0.84, specificity 0.81, AUC 0.88, NLR 0.20) and adults (sensitivity 0.81, specificity 0.82, AUC 0.87). Meta-regression identified year of publication, geographic region, specimen type, population, and diagnostic criteria as key contributors to heterogeneity, but sensitivity analyses confirmed result stability. No significant publication bias was observed (p = 0.33). In conclusion, presepsin is a valuable and highly promising biomarker for sepsis diagnosis, showing favorable diagnostic accuracy across populations, with strongest utility in neonates. Its application in pediatric and adult patients warrants further validation through large, prospective, multi-center studies. https://www.bjbms.org/ojs/index.php/bjbms/article/view/12909Biomarkerspresepsinsepsismeta-analysisdiagnosis
spellingShingle Kaicheng Peng
Xiangmin Zhang
Qinyuan Li
Zhengxiu Luo
Presepsin as a diagnostic biomarker for sepsis across neonates, children, and adults: A meta-analysis
Biomolecules & Biomedicine
Biomarkers
presepsin
sepsis
meta-analysis
diagnosis
title Presepsin as a diagnostic biomarker for sepsis across neonates, children, and adults: A meta-analysis
title_full Presepsin as a diagnostic biomarker for sepsis across neonates, children, and adults: A meta-analysis
title_fullStr Presepsin as a diagnostic biomarker for sepsis across neonates, children, and adults: A meta-analysis
title_full_unstemmed Presepsin as a diagnostic biomarker for sepsis across neonates, children, and adults: A meta-analysis
title_short Presepsin as a diagnostic biomarker for sepsis across neonates, children, and adults: A meta-analysis
title_sort presepsin as a diagnostic biomarker for sepsis across neonates children and adults a meta analysis
topic Biomarkers
presepsin
sepsis
meta-analysis
diagnosis
url https://www.bjbms.org/ojs/index.php/bjbms/article/view/12909
work_keys_str_mv AT kaichengpeng presepsinasadiagnosticbiomarkerforsepsisacrossneonateschildrenandadultsametaanalysis
AT xiangminzhang presepsinasadiagnosticbiomarkerforsepsisacrossneonateschildrenandadultsametaanalysis
AT qinyuanli presepsinasadiagnosticbiomarkerforsepsisacrossneonateschildrenandadultsametaanalysis
AT zhengxiuluo presepsinasadiagnosticbiomarkerforsepsisacrossneonateschildrenandadultsametaanalysis