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Heparin-binding protein as a biomarker of severe sepsis in the pediatric intensive care unit: A multicenter,
Pengcheng Liu1, Dapeng Chen2, Jintu Lou3
1Department of Clinical Laboratory, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai 201102, China.
Insights
Heparin-binding protein (HBP) shows promise as a biomarker for severe sepsis in children. Declining HBP levels at 72 hours predict lower in-hospital mortality in the pediatric intensive care unit (PICU).
Area of Science:
- Pediatric critical care medicine
- Biomarker discovery
- Sepsis diagnostics
Background:
- Severe sepsis is a critical condition in pediatric intensive care units (PICUs).
- Accurate diagnostic and prognostic biomarkers are crucial for timely intervention.
- Heparin-binding protein (HBP) is being investigated for its potential role.
Purpose of the Study:
- To evaluate Heparin-binding protein (HBP) as a diagnostic and prognostic biomarker for severe sepsis in the PICU.
- To compare HBP with established sepsis markers like procalcitonin (PCT) and C-reactive protein (CRP).
Main Methods:
- A prospective, multicenter study involving 355 children with sepsis in nine Chinese PICUs.
- Plasma HBP, PCT, CRP, lactate, and white blood cell (WBC) counts were measured at enrollment and 72 hours.
- Statistical analysis was performed to assess diagnostic and prognostic capabilities.
Main Results:
- Patients with severe sepsis exhibited significantly higher HBP levels than those with non-severe sepsis (170.5 vs. 74.1 ng/mL).
- Incorporating HBP into diagnostic models improved severe sepsis detection.
- Declining HBP levels at 72 hours were strongly associated with reduced in-hospital mortality (aOR 0.242).
- HBP showed positive correlations with PCT, CRP, and WBC count.
Conclusions:
- HBP serves as an independent indicator for diagnosing severe sepsis upon enrollment in the PICU.
- Dynamic changes in HBP levels at 72 hours are a significant predictor of in-hospital mortality.
- HBP offers valuable insights into sepsis severity and patient outcomes.
Objectives:
The aim of this study is to assess Heparin-binding protein (HBP) as a diagnostic and prognostic biomarker of severe sepsis in the pediatric intensive care unit (PICU).
Methods:
A multicenter, prospective study was conducted among children with sepsis in nine PICUs in China from October 2019 to June 2021. Plasma levels of HBP, procalcitonin (PCT), C-reactive protein (CRP), lactate, and white blood cell (WBC) count were determined at enrollment and 72 h after enrollment.
Results:
Of 355 included patients, 132 patients were diagnosed with non-severe sepsis (referred to as sepsis), 223 patients had severe sepsis. Patients with severe sepsis had significantly elevated levels of HBP compared with sepsis (median 170.5 vs. 74.1 ng/mL, P < 0.001). Adding HBP to a diagnostic model with PCT and lactate could significantly improve the diagnostic capability for severe sepsis. The plasma levels of HBP correlated positively with the number of dysfunctional organs. After adjusting for confounding factors, the declined levels of HBP at 72 h had a significant association with decreased in-hospital mortality (adjusted odds ratio (aOR) 0.242, P < 0.001). The levels of HBP showed weak positive correlations with PCT, CRP, WBC, and no correlation to lactate.
Conclusions:
HBP at enrollment can be an independent indicator for severe sepsis and the dynamic changes at 72 h can be a predictor for in-hospital mortality in PICU.
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