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Published on: January 27, 2019
Prebiotic supplementation of formula in preterm neonates: a systematic review and meta-analysis of randomised
Ravisha Srinivasjois1, Shripada Rao, Sanjay Patole
1Department of Neonatology, King Edward Memorial Hospital for Women, Perth, Western Australia, Australia.
Insights
Prebiotic oligosaccharide supplementation in preterm infant formula increased beneficial gut bacteria like bifidobacteria. This intervention did not negatively impact infant weight gain.
Area of Science:
- Neonatal nutrition
- Microbiome research
- Gastroenterology
Background:
- Preterm neonates are at high risk for necrotizing enterocolitis (NEC) and sepsis.
- Gut microbiome alterations are implicated in NEC pathogenesis.
- Prebiotic supplementation may modulate the gut microbiota and improve outcomes.
Purpose of the Study:
- To evaluate the efficacy and safety of prebiotic oligosaccharide-supplemented formula in preterm infants.
- To assess the impact on NEC and sepsis incidence.
- To examine effects on growth, gut colonization, and stool characteristics.
Main Methods:
- Systematic review of randomized controlled trials.
- Searched multiple databases including Cochrane, MEDLINE, EMBASE, and CINAHL.
- Included trials with prebiotic-supplemented vs. unsupplemented formula in neonates ≤37 weeks gestation, initiated within 28 days of life and lasting ≥2 weeks.
Main Results:
- One study reported no NEC cases in the prebiotic group; others did not report NEC or sepsis data.
- Meta-analysis showed no significant difference in weight gain between groups.
- Prebiotic supplementation significantly increased Bifidobacterial counts in stool (WMD=0.53; 95% CI: 0.33, 0.73) logCFU/g.
Conclusions:
- Prebiotic-supplemented formula enhances stool Bifidobacteria and Lactobacilli counts in preterm neonates.
- This supplementation appears safe regarding weight gain.
- Further research is needed to confirm effects on NEC and sepsis incidence.
Background & Aims:
Review the efficacy and safety of prebiotic oligosaccharide supplementation of formula in reducing the incidence of NEC and sepsis; study its effect on growth, gut colonisation and stool characteristics in preterm neonates < or =37 weeks.
Methods:
The Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE, CINAHL databases and proceedings of relevant conferences were searched. Only randomised control trials using prebiotic supplemented vs unsupplemented formula milk commenced within 28 days of life and continued for > or =2 weeks were included in the review.
Results:
Only one trial reported that NEC did not occur in any of the enrolled neonates. Others did not report on NEC or sepsis. All trials reported anthropometric parameters. Meta-analysis showed no significant effect on weight gain between the two groups. The two trials reporting on stool flora showed a statistically significant increase in bifidobacterial counts in the prebiotic supplemented group (Weighted mean difference (WMD)=0.53; 95% CI: 0.33, 0.73) logCFU/g of stool.
Conclusion:
Prebiotic supplemented formula increased stool colony counts of bifidobacteria and lactobacilli in preterm neonates without adversely affecting weight gain.
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