Normal Growth of Healthy Infants Born from HIV+ Mothers Fed a Reduced Protein Infant Formula Containing the Prebiotics Galacto-Oligosaccharides and Fructo-Oligosaccharides: A Randomized Controlled Trial

Author:

Da Costa Ribeiro Júnior Hugo1,Ribeiro Tereza Cristina Medrado2,De Mattos Angela Peixoto1,Pontes Mariana2,Sarni Roseli Oselka Saccardo3,Cruz Maria Letícia Santos4,Nogueira-De-Almeida Carlos Alberto5,Mussi-Pinhata Marisa M.6,De Carvalho Norton Rocksane7,Steenhout Philippe8

Affiliation:

1. Pediatrics, Federal University of Bahia School of Medicine, Salvador de Bahia, Brazil.

2. Fima Lifshitz Research Center, University Hospital Complex at Federal University of Bahia, Salvador de Bahia, Brazil.

3. Faculdade de Medicina do ABC, Santo André, de São Paulo, Brazil.

4. Infectious Diseases Department, Hospital Federal dos Servidores do Estado, Rio de Janeiro, Brazil.

5. Nutrology Department, University of Ribeirão Preto, Ribeirão Preto, Brazil.

6. Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto de São Paulo, Brazil.

7. Pediatrics, Federal University of Minas Gerais School of Medicine, Belo Horizontede Minas Gerais, Brazil.

8. Nestlé Clinical Development Unit, Vevey, Switzerland.

Abstract

Objective The aim of the current study was to evaluate the safety of a new reduced protein (2.1 g/100 kcal) infant formula containing 4 g/L of 90% galacto-oligosaccharides (GOS) and 10% fructo-oligosaccharides (FOS). Methods Healthy term infants from Brazil were enrolled. Those born to human immunodeficiency virus (HIV)-positive mothers were randomized to a test ( n = 65) or control ( n = 63) formula group. Infants born to HIV-negative mothers were either exclusively breast-fed ( n = 79) or received a mixed diet (breast milk and test formula, n = 65). Between 2 weeks and 4 months of age, infants were exclusively fed according to their assigned group. Anthropometric measurements were taken at baseline, 1, 2, 3, 4, 6, 8, 10, and 12 months. Digestive tolerance was evaluated during the first 4 months. The primary outcome was mean daily weight gain between 2 weeks and 4 months in the test formula and breast-fed groups. Results Data from all infants ( N = 272) were used in the intention-to-treat (ITT) analysis and data from 230 infants were used in the per-protocol (PP) analysis. The difference in mean daily weight gain between 2 weeks and 4 months in the test formula and breast-fed groups was 1.257 g/day (onesided 95% confidence interval [CI]: -0.705 to inf, P < 0.001) in the PP analysis, showing that the lower bound of the 95% CI was above the -3.0 g/day non-inferiority margin. Results were similar in the ITT analysis. Symptoms of digestive tolerance and frequency of adverse events were similar in the two groups. Conclusions The formula containing 2.1 g/100 kcal protein and GOS and FOS was safe and tolerated well.

Publisher

SAGE Publications

Subject

Media Technology

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