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Clin Chem Lab Med ; 62(8): 1643-1648, 2024 Jul 26.
Article in English | MEDLINE | ID: mdl-38353160

ABSTRACT

OBJECTIVES: Early sepsis detection and diagnosis still constitutes an open issue since the accuracy of standard-of care parameters is biased by a series of perinatal factors including hypoxia. Therefore, we aimed at investigating the effect of fetal chronic hypoxia insult on urine levels of a promising new marker of sepsis, namely presepsin (P-SEP). METHODS: We conducted a prospective case-control study in 22 cases of early-intrauterine growth restriction (E-IUGR) compared with 22 small-for-gestational-age (SGA) newborns and 66 healthy controls. P-SEP urine samples were collected over the first 72 h from birth. Blood culture and C-reactive protein (CRP) blood levels were measured in E-IUGR and SGA infants. Perinatal standard monitoring parameters and main outcomes were also recorded. RESULTS: No significant urinary P-SEP differences (p>0.05, for all) were observed among studied groups. Moreover, no significant correlations (p>0.05, for both) between urinary P-SEP and blood CRP levels in both E-IUGR and SGA groups (R=0.08; R=0.07, respectively) were observed. CONCLUSIONS: The present results showing the lack of influence of fetal chronic hypoxia on urinary P-SEP levels offer additional data to hypothesize the possible use of urinary P-SEP measurement in neonates in daily clinical practice. Further multicenter prospective data are needed, including infants with early-onset sepsis.


Subject(s)
Lipopolysaccharide Receptors , Peptide Fragments , Humans , Infant, Newborn , Female , Case-Control Studies , Prospective Studies , Peptide Fragments/urine , Peptide Fragments/blood , Male , Pregnancy , Fetal Hypoxia/urine , Fetal Hypoxia/diagnosis , Fetal Hypoxia/blood , C-Reactive Protein/analysis , Biomarkers/urine , Biomarkers/blood , Infant, Small for Gestational Age , Fetal Growth Retardation/urine , Fetal Growth Retardation/diagnosis , Fetal Growth Retardation/blood , Sepsis/urine , Sepsis/diagnosis , Sepsis/blood
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