NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

C reactive protein and procalcitonin: reference intervals for preterm and term newborns during the early neonatal period.

Author(s): Chiesa C, Natale F, Pascone R, Osborn JF, Pacifico L, Bonci E, De Curtis M

Publication: Clin Chim Acta, 2011, Vol. 412, Page 1053-9

PubMed ID: 21338596 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of maternal and neonatal characteristics on the expression of C reactive protein (CRP) and procalcitonin (PCT) in serum.

Conclusion of Paper

CRP increased significantly with gestational age in weeks, and with increasing birth weight, but was uninfluenced by gender. CRP levels peaked in term neonates when infants were 56-70 h old, however, CRP levels peaked in preterm neonates when infants were 27-36 h old. CRP levels significantly increased with duration of active labor, use of prenatal steroids, intrapartum antimicrobial prophylaxis, and duration of ruptured membranes, and vaginal delivery compared to cesarean section. PCT was negatively influenced by gestational age in weeks, and increasing birth weight, but was unaffected by gender. PCT levels peaked in term neonates when infants were 24 h old and in preterm neonates when infants were 21-22 h old. None of the other antenatal and perinatal variables analyzed significantly affected PCT levels.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of length of gestation, newborn age, birth weight, gender, and other maternal and neonatal characteristics on the expression of CRP and PCT in serum which was frozen at -80 degrees C until analysis.

    Summary of Findings:

    CRP increased significantly with gestational age in weeks (p<0.01), and with increasing birth weight (p<0.01), but was unaffected by gender. CRP levels peaked in term neonates when infants were 56-70 h old, but in preterm neonates, CRP peaked when infants were 27-36 h old. The authors report average levels of CRP in preterm infants increased again between 100 and 120 h neonatal age, but there were a limited number of observations at these ages. Other prenatal and antenatal variables significantly increased CRP levels including duration of active labor, use of prenatal steroids, intrapartum antimicrobial prophylaxis, and duration of ruptured membranes. In addition, vaginal delivery significantly increased CRP concentrations compared to cesarean section (p<0.05), especially when the cesarean section was elective (p<0.01). PCT was negatively influenced by gestational age in weeks (p<0.0001), and increasing birth weight (p<0.05), but was unaffected by gender. PCT levels peaked in term neonates when infants were 24 h old, but PCT levels peaked in preterm neonates when infants were 21-22 h old. None of the other antenatal and perinatal variables analyzed significantly affected PCT levels.

    Biospecimens
    Preservative Types
    • Frozen
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Protein Clinical chemistry/auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Preaquisition Patient gender Female
    Male
    Preaquisition Patient age 0-120 h
    Maternal age at delivery (unspecified range)
    Preaquisition Diagnosis/ patient condition Preterm birth (30-36 weeks)
    Term birth (37-39 weeks)
    Vaginal birth
    Elective cesarean section
    Emergency cesarean section
    Maternal complications during pregnancy
    No maternal complications during pregnancy
    Birth weight (unspecified range)
    Intrapartum antimicrobial prophylaxis
    No antimicrobial prophylaxis
    Intrapartum fetal distress
    No fetal distress
    Duration of active labor (unspecified range)
    Length of time of ruptured membranes (unspecified range)
    Preaquisition Other drugs Maternal use of antenatal steroids
    No use of antenatal steroids

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