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Impact of homogenization of pasteurized human milk on gastric digestion in the preterm infant: A randomized
Samira C de Oliveira1, Amandine Bellanger2, Olivia Ménard1
1STLO, Agrocampus Ouest, INRA, Rennes, France.
Insights
Homogenizing pasteurized human milk (PHM) significantly increased gastric lipolysis and protein digestion in preterm infants. This enhanced digestion may improve fat absorption and infant growth, but further studies on gastrointestinal tolerance are needed.
Area of Science:
- Neonatal nutrition
- Digestive physiology
- Human milk processing
Background:
- Pasteurized human milk (PHM) homogenization may enhance fat absorption and weight gain in preterm infants.
- Previous studies have not investigated the impact of PHM homogenization on digestive kinetics.
Purpose of the Study:
- To determine the effect of PHM homogenization on gastric digestion in preterm infants.
Main Methods:
- A randomized controlled trial involving eight tube-fed preterm infants compared gastric digestion of PHM and homogenized PHM (PHHM).
- Gastric aspirates were collected over six days, analyzing digestion at 35, 60, and 90 minutes post-ingestion.
- A general linear mixed model was used to assess the impact of homogenization on digestive kinetics and disintegration.
Main Results:
- Homogenization increased lipid droplet surface area six-fold and enhanced gastric lipolysis by 22-24% at 35 and 60 minutes.
- Proteolysis of serum albumin was enhanced, while the gastric meal emptying rate was reduced.
- Postprandial gastric pH remained unaffected by homogenization.
Conclusions:
- Homogenization of PHM boosts gastric lipolysis, offering a potential strategy to improve fat absorption and infant development.
- Further investigation into the gastrointestinal tolerance of homogenized PHM in infants is warranted.
Background & Aims:
It has been suggested that homogenization of Holder-pasteurized human milk (PHM) could improve fat absorption and weight gain in preterm infants, but the impact on the PHM digestive kinetics has never been studied. Our objective was to determine the impact of PHM homogenization on gastric digestion in preterm infants.
Methods:
In a randomized controlled trial, eight hospitalized tube-fed preterm infants were their own control to compare the gastric digestion of PHM and of homogenized PHM (PHHM). PHM was obtained from donors and, for half of it, was homogenized by ultrasonication. Over a six-day sequence, gastric aspirates were collected twice a day, before and 35, 60 or 90 min after the start of PHM or PHHM ingestion. The impact of homogenization on PHM digestive kinetics and disintegration was tested using a general linear mixed model. Results were expressed as means ± SD.
Results:
Homogenization leaded to a six-fold increase in the specific surface (P < 0.01) of lipid droplets. The types of aggregates formed during digestion were different between PHM and PHHM, but the lipid fraction kept its initial structure all over the gastric digestion (native globules in PHM vs. blend of droplets in PHHM). Homogenization increased the gastric lipolysis level (P < 0.01), particularly at 35 and 60 min (22 and 24% higher for PHHM, respectively). Homogenization enhanced the proteolysis of serum albumin (P < 0.05) and reduced the meal emptying rate (P < 0.001, half-time estimated at 30 min for PHM and 38 min for PHHM). The postprandial gastric pH was not affected (4.7 ± 0.9 at 90 min).
Conclusions:
Homogenization of PHM increased the gastric lipolysis level. This could be a potential strategy to improve fat absorption, and thus growth and development in infants fed with PHM; however, its gastrointestinal tolerance needs to be investigated further. This trial was registered at clinicaltrials.gov as NCT02112331.
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