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1.
J Pediatr Gastroenterol Nutr ; 78(3): 699-703, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38504410

ABSTRACT

The objective of the present study is to assess the rates of acquired tolerance to cow's milk (CM) after 36 months in subjects who consumed amino acid-based formula with synbiotics (AAF-S) or amino acid-based formula without synbiotics (AAF) during a 1-year intervention period in early life as part of the PRESTO study (Netherlands Trial Register number NTR3725). Differences in CM tolerance development between groups were analysed using a logistic regression model. Results show that the proportion of subjects (mean [±SD] age, 3.8 ± 0.27 years) who developed CM tolerance after 36 months was similar in the group receiving AAF-S (47/60 [78%]) and in the group receiving AAF (49/66 [74%]) (p = 0.253), that is, figures comparable to natural outgrowth of CM allergy. Our data suggest that the consumption of AAF and absence of exposure to CM peptides do not slow down CM tolerance acquisition.


Subject(s)
Milk Hypersensitivity , Synbiotics , Child , Female , Animals , Cattle , Humans , Infant , Child, Preschool , Milk , Follow-Up Studies , Amino Acids , Infant Formula , Milk Hypersensitivity/prevention & control , Allergens
2.
J Allergy Clin Immunol ; 149(2): 650-658.e5, 2022 02.
Article in English | MEDLINE | ID: mdl-34224785

ABSTRACT

BACKGROUND: Tolerance development is an important clinical outcome for infants with cow's milk allergy. OBJECTIVE: This multicenter, prospective, randomized, double-blind, controlled clinical study (NTR3725) evaluated tolerance development to cow's milk (CM) and safety of an amino acid-based formula (AAF) including synbiotics (AAF-S) comprising prebiotic oligosaccharides (oligofructose, inulin) and probiotic Bifidobacterium breve M-16V in infants with confirmed IgE-mediated CM allergy. METHODS: Subjects aged ≤13 months with IgE-mediated CM allergy were randomized to receive AAF-S (n = 80) or AAF (n = 89) for 12 months. Stratification was based on CM skin prick test wheal size and study site. After 12 and 24 months, CM tolerance was evaluated by double-blind, placebo-controlled food challenge. A logistic regression model used the all-subjects randomized data set. RESULTS: At baseline, mean ± SD age was 9.36 ± 2.53 months. At 12 and 24 months, respectively, 49% and 62% of subjects were CM tolerant (AAF-S 45% and 64%; AAF 52% and 59%), and not differ significantly between groups. During the 12-month intervention, the number of subjects reporting at least 1 adverse event did not significantly differ between groups; however, fewer subjects required hospitalization due to serious adverse events categorized as infections in the AAF-S versus AAF group (9% vs 20%; P = .036). CONCLUSIONS: After 12 and 24 months, CM tolerance was not different between groups and was in line with natural outgrowth. Results suggest that during the intervention, fewer subjects receiving AAF-S required hospitalization due to infections.


Subject(s)
Amino Acids/administration & dosage , Immune Tolerance , Infant Formula , Milk Hypersensitivity/immunology , Double-Blind Method , Female , Humans , Infant , Infant Formula/adverse effects , Infant, Newborn , Male , Prospective Studies , Synbiotics/administration & dosage
3.
Nutrients ; 11(1)2019 01 17.
Article in English | MEDLINE | ID: mdl-30658383

ABSTRACT

We read with interest the recently published narrative review of seven growth studies in healthy infants fed extensively hydrolyzed protein-based formulas (eHF) and amino acid-based formulas (AAF) [...].


Subject(s)
Infant Formula , Milk Hypersensitivity , Amino Acids , Humans , Infant , Infant, Newborn , Nutrients , Protein Hydrolysates
4.
Pediatr Allergy Immunol ; 26(4): 316-22, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25845680

ABSTRACT

BACKGROUND: Children with cow's milk allergy (CMA) are at risk for inadequate nutritional intake and growth. Dietary management of CMA, therefore, requires diets that are not only hypoallergenic but also support adequate growth in this population. This study assessed growth of CMA infants when using a new amino acid-based formula (AAF) with prebiotics and probiotics (synbiotics) and evaluated its safety in the intended population. METHODS: In a prospective, randomized, double-blind controlled study, full-term infants with diagnosed CMA received either an AAF (control; n = 56) or AAF with synbiotics (oligofructose, long-chain inulin, acidic oligosaccharides, Bifidobacterium breve M-16V) (test; n = 54) for 16 wk. Primary outcome was growth, measured as weight, length and head circumference. Secondary outcomes included allergic symptoms and stool characteristics. RESULTS: Average age (±SD) of infants at inclusion was 4.5 ± 2.4 months. Both formulas equally supported growth according to WHO 2006 growth charts and resulted in similar increases of weight, length and head circumference. At week 16, differences (90% CI) in Z-scores (test-control) were as follows: weight 0.147 (-0.10; 0.39, p = 0.32), length -0.299 (-0.69; 0.09, p = 0.21) and head circumference 0.152 (-0.15; 0.45, p = 0.40). Weight-for-age and length-for-age Z-scores were not significantly different between the test and control groups. Both formulas were well tolerated and reduced allergic symptoms; the number of adverse events was not different between the groups. CONCLUSIONS: This is the first study that shows that an AAF with a specific synbiotic blend, suitable for CMA infants, supports normal growth and growth similar to the AAF without synbiotics. This clinical trial is registered as NCT00664768.


Subject(s)
Child Development , Infant Formula/administration & dosage , Infant Nutrition Disorders/prevention & control , Milk Hypersensitivity/immunology , Synbiotics/administration & dosage , Amino Acids/administration & dosage , Double-Blind Method , Female , Humans , Infant , Infant Formula/statistics & numerical data , Infant, Newborn , Male , Prospective Studies , Synbiotics/statistics & numerical data
5.
Pediatr Res ; 75(2): 343-51, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24216543

ABSTRACT

BACKGROUND: To evaluate the effects of an amino acid-based formula (AAF) with synbiotics on growth and tolerance in healthy infants. The hypoallergenicity of this AAF with synbiotics was evaluated in subjects with cow's milk allergy (CMA). METHODS: Study 1: 115 full-term, healthy infants randomly received an AAF with synbiotics or a commercially available AAF for 16 wk. Subjects' weight, length, and head circumference were primary outcome measures. Stool characteristics and gastrointestinal (GI) symptoms were secondary outcome measures. Clinical examinations, dietary intake, clinical laboratory results, and adverse events were recorded. Study 2: hypoallergenicity of the AAF with synbiotics was evaluated in 30 infants and children with immunoglobulin E (IgE)-mediated CMA using a double-blind, placebo-controlled food challenge, and a 7-d feeding period. RESULTS: Study 1: comparable results in growth parameters and tolerance were observed for both groups. Minimal differences were observed in stool characteristics and GI symptoms throughout the study. Study 2: all 30 subjects with IgE-mediated CMA completed the study with no allergic reactions detected to challenges. CONCLUSION: These studies demonstrate that an AAF with synbiotics is safe and well tolerated and promotes normal growth when fed to healthy full-term infants as the sole source of nutrition and is hypoallergenic in subjects with CMA.


Subject(s)
Amino Acids/chemistry , Infant Formula/chemistry , Milk Hypersensitivity/immunology , Synbiotics , Allergens , Animals , Bifidobacterium/metabolism , Cattle , Double-Blind Method , Female , Humans , Immune Tolerance , Immunoglobulin E/chemistry , Infant , Infant Formula/administration & dosage , Male , Oligosaccharides/chemistry , Probiotics/chemistry
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