Relations between feeding intolerance and stress biomarkers in preterm infants
Tiffany A Moore1, Margaret E Wilson, Kendra K Schmid
1College of Nursing, University of Nebraska Medical Center, Omaha, NE 68198-5330, USA.
Insights
Feeding intolerance in preterm infants may be linked to stress. Biomarker differences in cortisol and 8-hydroxydeoxyguanosine (8-OHdG) were observed between infants with and without feeding intolerance.
Area of Science:
- Neonatal physiology
- Stress biomarkers
- Gastrointestinal disorders
Background:
- Feeding intolerance (FI) is a common complication in preterm infants, with unclear etiology.
- This study investigates FI as a stress-related condition involving brain-gut interactions and the allostatic load model.
Purpose of the Study:
- To describe demographic and medical variables and biomarker levels in preterm infants.
- To compare these variables and biomarker levels between infants with and without FI.
- To compare biomarker distributions (interquartile/interpercentile) between infants with and without FI.
Main Methods:
- Recruited preterm infants (<32 weeks' gestation).
- Defined FI as feeding intolerance by day 7.
- Operationalized allostatic load using cortisol and 8-hydroxydeoxyguanosine (8-OHdG) from cord blood, saliva, and urine on days 1, 7, and 14.
Main Results:
- Seven of 31 infants developed FI.
- Infants with FI showed lower median urinary cortisol on day 1 and trended lower in cord blood cortisol.
- Significant differences in biomarker distributions (cortisol, 8-OHdG) were found between groups on days 1 and 14.
Conclusions:
- Findings support the allostatic load model for FI in preterm infants.
- Further research should investigate cellular mechanisms and prenatal factors.
- Larger sample sizes are recommended for future studies.
Objectives:
Feeding intolerance (FI) in preterm infants is common but the etiology remains unclear. This study examined FI as a stress-related disease involving brain-gut interactions and tested the model of allostatic load and complications of prematurity. Specific aims were to describe demographic/medical variables and biomarker levels at each time and over time for the sample; describe/compare variables and biomarker levels at each time for infants with/without FI; and compare biomarker interquartile/interpercentile distributions between infants with/without FI.
Methods:
Preterm infants <32 weeks' gestation were recruited. The primary outcome was FI by day 7 defined as a feeding withheld, discontinued, or decreased because the infant was not tolerating enteral feedings. Allostatic load was operationalized using cortisol and 8-hydroxydeoxyguanosine (8-OHdG) from cord blood and from saliva and urine on days 1, 7, and 14. Descriptive statistics and comparative analyses were performed.
Results:
Seven of 31 infants enrolled met criteria for FI. Infants with FI had lower median urinary cortisol on day 1 (P = 0.007) and trended to have lower cortisol in the cord blood (P = 0.056). Interquartile distributions were significantly different between infants with/without FI for urinary cortisol on day 1 (P = 0.034) and trended for differences in 8-OHdG on day 14 (P = 0.087). Interpercentile distributions were significantly different in salivary cortisol on day 14 (P = 0.034) and trended for differences in 8-OHdG on day 1 (P = 0.079).
Conclusions:
Results support further testing of the model in a larger sample; investigation of the cellular mechanisms associated with the stress and the free radical/antioxidant systems; and inclusion of prenatal factors.
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