Abstract

Objective: We aimed to detect C-reactive protein (CRP) in neonatal saliva and evaluate its diagnostic utility.Study Design: Salivary and serum samples (n = 89) were collected from 40 neonates. Salivary CRP levels were determined using an enzyme-linked immunosorbent assay; serum CRP was measured per hospital protocol. Correlation coefficients with 95% confidence intervals and robust linear regression measured association while receiver–operator characteristic curves described the accuracy of salivary CRP in discriminating abnormal serum CRP thresholds of ≥10 and 5 mg/L. Corresponding sensitivities and specificities were calculated for these salivary cutpoints.Results: The area under the curve for salivary CRP in predicting serum CRP levels of ≥10 and 5 mg/L were 0.81 and 0.76, respectively. The corresponding sensitivity and specificity for raw salivary CRP to discriminate a serum CRP of ≥5 mg/L was 0.54 and 0.95, respectively. The corresponding sensitivity and specificity for raw salivary CRP to discriminate a serum CRP of ≥10 mg/L was 0.64 and 0.94, respectively. A statistically significant correlation was observed between serum and salivary CRP (r = 0.62, p < 0.001).Conclusion: C-reactive protein is detectable in neonatal saliva and can predict abnormal serum CRP thresholds. Salivary CRP analysis represents a feasible screening tool for detecting abnormal serum CRP levels.

Highlights

  • C-reactive protein (CRP) is an extensively utilized biomarker for monitoring sepsis, post-surgical complications, and inflammation in the pediatric and neonatal populations [1]

  • C-reactive protein is detectable in neonatal saliva and can predict abnormal serum CRP thresholds

  • Salivary C-reactive protein levels in neonates no exclusion criteria based on gender, genetic disorder, disease was conducted on the dataset by randomly selecting one paired process, or clinical status

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Summary

Introduction

C-reactive protein (CRP) is an extensively utilized biomarker for monitoring sepsis, post-surgical complications, and inflammation in the pediatric and neonatal populations [1]. Produced in the liver in response to IL-6, CRP levels rise rapidly during infection and/or inflammation [1, 2]. A current limitation to the usefulness of serial CRP monitoring in the neonatal population is its reliance on frequent blood draws in a vulnerable population with limited blood volumes. Developing a non-invasive assay for the quantification of CRP in neonates could reduce neonatal side-effects and improve its clinical utility. Saliva is an excellent biofluid to non-invasively monitor the neonate. Filtered from whole blood in the salivary glands, saliva is an important reservoir of systemic proteins and immunoglobulins, electrolytes, nucleic acids, microorganisms, toxins, and drugs

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