Tolerance and Safety of an Anti-Regurgitation Formula Containing Locust Bean Gum, Pre-, and Postbiotics: A Multi-Country Multi-Center Prospective Randomized Controlled Study in Infants with Regurgitation

Author:

Salvatore Silvia1,Klymenko Viktoriia2ORCID,Karpushenko Yuliia2ORCID,Durczak-Hilleman Maria3,Loboda Andrii4ORCID,Petrashenko Viktoriia4,Olechowski Wiesław5,Lista Gianluca6ORCID,Meneghin Fabio6ORCID,Amodio Sonia7ORCID,Bongers Anke7,Ludwig Thomas7,Vandenplas Yvan8ORCID

Affiliation:

1. Pediatric Department, Hospital “F. Del Ponte”, University of Insubria, 21100 Varese, Italy

2. Propaedeutics of Paediatrics No. 2, Communal Nonprofit Enterprise “City Children’s Clinical Hospital # 19” of Kharkiv City Council, 61051 Kharkiv, Ukraine

3. EPOKA Niepubliczny Zaklad Opieki Zdrowotnej Piotr Chodkiewicz Sp. z o.o., 88-400 Znin, Poland

4. Department of Pediatrics, Sumy State University, 40000 Sumy, Ukraine

5. Alergo-Med Specjalistyczna Przychodnia Lekarska Sp. z o.o., 33-100 Tarnow, Poland

6. SC Neonatologia e Terapia Intensiva Neonatale, Ospedale dei Bambini “V. Buzzi”, 20154 Milano, Italy

7. Specialised Nutrition, Danone Nutricia Research, 3584 CT Utrecht, The Netherlands

8. KidZ Health Castle, UZ Brussel, Vrije Universiteit Brussel (VUB), 1090 Brussels, Belgium

Abstract

This multi-center prospective randomized controlled trial was a tolerance and safety study investigating the thickener locust bean gum (LBG) in infants with regurgitation, to support the re-evaluation of the safety of LBG in infant formula. The primary objective was to demonstrate that after an 8-week intervention, stool consistency was not inferior (i.e., was not looser or more watery) in infants fed an anti-regurgitation (AR) formula containing LBG vs. the stool consistency of infants fed with an unthickened control formula. A total of 103 full-term infants with regurgitation were randomized to the test or control formula. The test formula contained LBG (0.4 g/100 mL), short-chain galacto-oligosaccharides, and long-chain fructo-oligosaccharides (scGOS/lcFOS; 9:1; 0.4 g/100 mL) and postbiotics and the control formula contained scGOS/lcFOS (0.8 g/100 mL), the same amount of postbiotics, and did not contain LBG. The average stool consistency score at the 8th intervention week was the primary outcome parameter. Secondary outcome parameters were stool consistency at other timepoints, stool frequency, Infant Gastrointestinal Symptom Questionnaire (IGSQ) score, growth, (serious) adverse events ([S]AEs), regurgitation severity, and infant well-being. Overall, the infants were 36.9 ± 12.9 [mean ± SD] days old, 62.7% girls in the test, and 50.0% girls in the control group. The primary analysis showed that the test group did not have looser or more watery stools than the control group. IGSQ sum scores decreased comparably in both groups. The frequency of regurgitation was significantly lower in the test group compared to the control group (mixed model repeated measurement, p ≤ 0.028) and parent-reported well-being scores were favorable. Adequate growth was observed in both groups. Both products were well-tolerated and safe and the AR formula with LBG was efficacious in reducing regurgitation frequency. This study provides further evidence for the dietary management of regurgitation by LBG-containing formulae in infants who are not exclusively breastfed, and the reassurance it can bring to parents.

Funder

Danone Nutricia Research, Utrecht, The Netherlands

Publisher

MDPI AG

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