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. 2010 Jun 11;5(6):e11083.
doi: 10.1371/journal.pone.0011083.

Fecal calprotectin excretion in preterm infants during the neonatal period

Affiliations

Fecal calprotectin excretion in preterm infants during the neonatal period

Carole Rougé et al. PLoS One. .

Abstract

Background: Fecal calprotectin has been proposed as a non-invasive marker of intestinal inflammation in inflammatory bowel disease in adults and children. Fecal calprotectin levels have been reported to be much higher in both healthy full-term and preterm infants than in children and adults.

Objective: To determine the time course of fecal calprotectin (f-calprotectin) excretion in preterm infants from birth until hospital discharge and to identify factors influencing f-calprotectin levels in the first weeks of life, including bacterial establishment in the gut.

Methodology: F-calprotectin was determined using an ELISA assay in 147 samples obtained prospectively from 47 preterm infants (gestational age, and birth-weight interquartiles 27-29 weeks, and 880-1320 g, respectively) at birth, and at 2-week intervals until hospital discharge.

Principal findings: Although median f-calprotectin excretion was 138 microg/g, a wide range of inter- and intra-individual variation in f-calprotectin values (from day 3 to day 78) was observed (86% and 67%, respectively). In multivariate regression analysis, f-calprotectin correlated negatively with ante and per natal antibiotic treatment (p = 0.001), and correlated positively with the volume of enteral feeding (mL/kg/d) (p = 0.009), the need to interrupt enteral feeding (p = 0.001), and prominent gastrointestinal colonization by Clostridium sp (p = 0.019) and Staphylococcus sp (p = 0.047).

Conclusion: During the first weeks of life, the high f-calprotectin values observed in preterm infants could be linked to the gut bacterial establishment.

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Conflict of interest statement

Competing Interests: 1) Carole Rougé was the recipient of a doctoral research fellowship from Nestlé (Vers-chez-les-Blanc, Switzerland), 2) Carole Rougé, Jean-Christophe Rozé, Hugues Piloquet, and Dominique Darmaun have been included along with Nestlé in a patent application for the use of Probiotics in preterm infants, 3) Part of this work was supported by grants from: the Programme Hospitalier de Recherche Clinique (PHRC 2004) from the French Ministry of Health, and the Délégation à la Recherche Clinique (DRC 2004), CHU de Nantes. This does not alter the authors' adherence to all the PLOS ONE policy on sharing data as detailed in the PLOS One guide for authors.

Figures

Figure 1
Figure 1. Fecal calprotectin levels in preterm infants with or without antenatal antibiotherapy.
The boxplot shows the median (central horizontal line) and includes the 25th (lower box border) to 75th percentile (upper box border) of fecal calprotectin (µg/g of feces) in preterm infants with (74 fecal samples) and without (73 fecal samples) antenatal antibiotherapy following the postconceptional age (weeks).
Figure 2
Figure 2. Fecal calprotectin levels in preterm infants without or with poor tolerance to enteral feeding.
Fecal calprotectin in preterm infants without poor tolerance to enteral feeding (i.e. with unplanned enteral feeding interruption, n = 118), and with poor tolerance to enteral feeding (i.e. with unplanned enteral feeding interruption, n = 7). The boxplot shows the median (central horizontal line) and includes the 25th (lower box border) to 75th percentile (upper box border). Dotted line represents cut-off level (205 µg/g of feces) for poor tolerance to enteral feeding (see text for details).
Figure 3
Figure 3. Fecal calprotectin as a function of the tercile of enteral feeding volume and tolerance to enteral feeding.
The median and interquartile range of fecal calprotectin are plotted for each volume of enteral feeding in infants with good (open boxes) or poor (closed boxes) tolerance to feeding. Poor tolerance to feeding was defined as the need for unplanned enteral feeding interruption.

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