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Published on: July 28, 2022
Decreased Acetic Acid in the Stool of Preterm Infants Is Associated with an Increased Risk of Bronchopulmonary
Lauren C Frazer1, William Yakah2, Camilia R Martin3
1Department of Pediatrics, Division of Neonatal-Perinatal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Insights
Low levels of acetic acid in preterm infants' stool are linked to a higher risk of bronchopulmonary disease (BPD). This suggests a connection between gut health and lung development in premature babies.
Area of Science:
- Neonatal pathophysiology
- Microbiome research
- Gastroenterology and Pulmonology
Background:
- Short-chain fatty acids (SCFAs), microbial metabolites, are understudied in neonatal diseases but linked to adult outcomes.
- Investigating SCFA levels in maternal breastmilk and preterm infant stool is crucial for understanding neonatal morbidities.
- Preterm infants (< 28 weeks gestation) are a vulnerable population requiring focused research on factors influencing their health.
Purpose of the Study:
- To determine if SCFA levels in maternal breastmilk (BM) and preterm infant stool correlate with neonatal morbidities.
- To assess the impact of specific SCFAs, particularly acetic acid, on the risk of bronchopulmonary disease (BPD) and retinopathy of prematurity (ROP).
- To explore the relationship between gut microbiome metabolites and the development of common neonatal complications.
Main Methods:
- Quantification of SCFA levels using liquid chromatography with tandem mass spectrometry.
- Analysis of maternal BM and preterm infant stool samples (N=72) at postnatal days 14 and 28.
- Comparison of SCFA levels in infants with and without BPD and ROP, employing logistic regression for association analysis.
Main Results:
- SCFA levels, including acetic, propionic, and others, showed an increase in BM and infant stool from day 14 to 28.
- A significant inverse relationship was found between fecal acetic acid levels and the odds of developing BPD.
- Each quartile increase in fecal acetic acid was associated with reduced odds of BPD (OR 0.41 on day 14, 0.28 on day 28), but not ROP.
Conclusions:
- Lower levels of acetic acid in preterm infant stool are associated with increased odds of bronchopulmonary disease.
- These findings highlight a potential link between intestinal health, indicated by SCFA profiles, and pulmonary outcomes in preterm neonates.
- The study supports the hypothesis that gut microbiome-derived metabolites play a role in neonatal health and disease development.
Abstract:
Background: Short-chain fatty acids (SCFAs), microbial metabolites, have been minimally studied in neonatal pathophysiology but have been associated with disease outcomes in adults. The objective of this manuscript was to determine if SCFA levels in maternal breastmilk (BM) and stool from preterm neonates impacted the risk of neonatal morbidities. Methods: SCFA levels were quantified by liquid chromatography with tandem mass spectrometry on maternal BM and neonatal stool for preterm infants < 28 weeks’ gestation (N = 72) on postnatal days 14 and 28. SCFA levels in BM and stool of infants with and without bronchopulmonary disease (BPD) and retinopathy of prematurity (ROP) were compared. Logistic regression was applied to determine the association between stool acetic acid levels and disease. Results: Acetic, propionic, isobutyric, 2-methylbutyric, and isovaleric acid levels increased in BM and neonatal stool between days 14 and 28. Logistic regression demonstrated an inverse relationship between the quartile of fecal acetic acid level and the odds of BPD but not ROP on days 14 and 28. For each quartile increase in fecal acetic acid, the odds ratio (95% CI) of BPD was 0.41 (0.18, 0.83) for day 14 and 0.28 (0.09, 0.64) for day 28. Conclusions: Low acetic acid levels in the stool of preterm infants are associated with increased odds of BPD. These findings support a relationship between intestinal and pulmonary health in preterm infants.
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