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Licensed Unlicensed Requires Authentication Published by De Gruyter March 30, 2018

Utility of serum resistin in the diagnosis of neonatal sepsis and prediction of disease severity in term and late preterm infants

  • Ahmed Anwar Khattab , Muhammad Said El-Mekkawy ORCID logo EMAIL logo , Mohamed Ahmed Helwa and Ehab Seif Omar

Abstract

Introduction

Resistin is a proinflammatory hormone recently proposed as a sepsis biomarker. Our aim was to evaluate the diagnostic and prognostic values of this marker in neonatal sepsis.

Methods

This is a prospective observational study that includes 60 term and late preterm neonates with proven and possible sepsis besides 30 healthy controls. Resistin and other biomarkers, like C-reactive protein (CRP), were measured within 2 h of neonatal intensive care unit (NICU) admission. Infants were monitored and the primary outcome was 30-day mortality.

Results

Resistin was higher among septic neonates compared with controls (P<0.001). Resistin had an area under the receiver operating characteristic (ROC) curve of 0.994 for differentiating septic infants from controls. The area under the curve (AUC) for differentiating infants with culture-proven sepsis from controls was 0.999 compared with an AUC of 1 for CRP. The other markers, like platelet count, were inferior to resistin and CRP. Resistin was positively correlated with CRP [Spearman’s correlation coefficient (rs)=0.55, P<0.001]. No significant differences in resistin levels were noted between survivors and non-survivors but resistin was higher among infants with severe sepsis (P=0.015) and among those who needed mechanical ventilation (P<0.001).

Conclusion

Resistin is useful for the diagnosis of neonatal sepsis. Resistin failed to predict mortality but was associated with indicators of disease severity.


Corresponding author: Muhammad Said El-Mekkawy, MD, Department of Pediatrics, Faculty of Medicine, Menoufia University, Menoufia 32511, Egypt, Mobile: +00201015359228

  1. Author’s statement

  2. Conflict of interest: Authors state no conflict of interest.

  3. Material and methods: Informed consent: Informed consent has been obtained from all individuals included in this study.

  4. Ethical approval: The research related to human subject use has complied with all the relevant national regulations, and institutional policies, and is in accordance with the tenets of the Helsinki Declaration, and has been approved by the authors’ institutional review board or equivalent committee.

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Received: 2018-01-11
Accepted: 2018-02-27
Published Online: 2018-03-30
Published in Print: 2018-10-25

©2018 Walter de Gruyter GmbH, Berlin/Boston

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