Metabolomic Profile in Breastfed Late Preterm Infants

Sponsor
Ospedale Buon Consiglio Fatebenefratelli (Other)
Overall Status
Recruiting
CT.gov ID
NCT06052592
Collaborator
University of Salerno (Other)
54
2
20
27
1.3

Study Details

Study Description

Brief Summary

Exclusive breast milk is recommended from birth to 6 months of life to promote the development of a balanced intestinal microbiota. Human milk provides several bioactive components, from natural probiotics such as Bifidobacterium spp. and Lactobacillus spp., to their metabolites which colonize the intestine of the newborn. However, if breast milk is not available or insufficient, it is used formula milk as a substitute. Infant formula can be supplemented with postbiotics to promote maturation of immune, metabolic and microbial components, similar to breast milk. Postbiotics are preparations composed of both microbial constituents and their metabolites, produced during fermentation.

Condition or Disease Intervention/Treatment Phase
  • Other: Milk

Detailed Description

A balanced nutrition starting from early childhood significantly influences growth and psychomotor development. Exclusive breast milk is the recommended nutritional choice from birth to 6 months of life, as it guarantees everything necessary for growth, maturation, protection from infections, promoting the development of a balanced intestinal microbiota. Several prenatal and perinatal factors including the type of delivery, the use of antibiotics, diet and other environmental factors, can influence the microbial colonization of the newborn. Thus, it is generally accepted that the gut microbiota of the healthy, full-term, vaginally born, breastfed infant is the gold standard for a favorable microbial composition in the early years of life. Human milk provides several bioactive components, from natural probiotics such as Bifidobacterium spp. and Lactobacillus spp., to their metabolites ("natural postbiotics"), which colonize the intestine of the newborn. These metabolites regulate the development of the immune system and attenuate the inflammatory processes. However, if breast milk is not available or insufficient to meet the nutritional needs of the infant, formula milk is proposed and used as a substitute. Given the benefits, it is essential that infant formula is as close to human milk as possible, providing bioactive substances that target gut and immune system health. Current research focuses on optimizing artificial formulas, with the aim of resembling human milk in composition and functionality, with some on the market already including probiotics, prebiotics, synbiotics and postbiotics. However, it still remains to be clarified which is the best formulation and the exact consequences on the immune, metabolic and microbial system of the newborn. In particular, postbiotics are preparations composed of both microbial constituents and their metabolites, produced during fermentation. It has already been highlighted in the literature that the enrichment of formula milk with post-biotics would seem to offer advantages for feeding term infants. Furthermore, it promotes an immune, metabolic and microbial component maturation, similarly to human milk, thus making postbiotic supplements very promising and interesting in the nutrition of newborns and infants.

Study Design

Study Type:
Observational
Anticipated Enrollment :
54 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Metabolomic Profile in Breastfed Late Preterm Infants Versus Standard Formula Milk or Postbiotic-supplemented Formula Milk
Actual Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
Nov 1, 2023
Anticipated Study Completion Date :
Nov 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Group A

Newborns fed with formula milk supplemented with 20 mg/day of fermented FOS from Lactobacillus paracasei strain CNCM I-5220 and Vitamin D (0.5 ml of SMART D3 MATRIX)

Other: Milk
Newborns will be fed with breast milk, formula milk or postbiotic formula milk

Group B

Newborns fed with formula milk

Other: Milk
Newborns will be fed with breast milk, formula milk or postbiotic formula milk

Group C

Newborns fed with exclusive breast milk

Other: Milk
Newborns will be fed with breast milk, formula milk or postbiotic formula milk

Outcome Measures

Primary Outcome Measures

  1. Evaluation of metabolomic profile by liquid chromatography mass spectrometry in breastfed late preterm infants [5 days after delivery]

    To detect the differences in the metabolome of the newborns

  2. Evaluation of metabolomic profile by liquid chromatography mass spectrometry in breastfed late preterm infants [1 month after delivery]

    To detect the differences in the metabolome of the newborns

  3. Evaluation of metabolomic profile by liquid chromatography mass spectrometry in breastfed late preterm infants [3 months after delivery]

    To detect the differences in the metabolome of the newborns

Eligibility Criteria

Criteria

Ages Eligible for Study:
34 Weeks to 37 Weeks
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Weight appropriate to gestational age (percentiles >10th and <90th)

  • Written informed consent

Exclusion Criteria:
  • Cardiological diseases

  • Liver disease

  • Gastrointestinal diseases with malabsorption

  • Endocrinological diseases

  • Perinatal infections

  • Metabolic and genetic diseases

  • Born to mothers with endocrinological and metabolic diseases

  • Withdrawal of informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Pharmacy, University of Salerno Salerno Naples Italy 84084
2 Department of Woman and Child, Buon Consiglio Fatebenefratelli Hospital Napoli Italy 80123

Sponsors and Collaborators

  • Ospedale Buon Consiglio Fatebenefratelli
  • University of Salerno

Investigators

  • Principal Investigator: Giuseppe De Bernardo, MD, Ospedale Buon Consiglio Fatebenefratelli

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Giuseppe De Bernardo, Head of Department of Woman and Child, Ospedale Buon Consiglio Fatebenefratelli
ClinicalTrials.gov Identifier:
NCT06052592
Other Study ID Numbers:
  • 1680
First Posted:
Sep 25, 2023
Last Update Posted:
Sep 25, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Giuseppe De Bernardo, Head of Department of Woman and Child, Ospedale Buon Consiglio Fatebenefratelli

Study Results

No Results Posted as of Sep 25, 2023