A Randomized Double Blind Controlled Safety Trial Evaluating D-Lactic Acid Production in Healthy Infants Fed a -containing Formula

Background D-Lactic acidosis in infants fed lactic acid bacteria-containing products is a concern. Methods The primary objective of this non-inferiority trial was to compare urinary D-lactic acid concentrations during the first 28 days of life in infants fed formula containing Lactobacillus reuteri...

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Main Authors: Konstantinos Papagaroufalis, Aikaterini Fotiou, Delphine Egli, Liên-Anh Tran, Philippe Steenhout
Format: Article
Language:English
Published: SAGE Publishing 2014-01-01
Series:Nutrition and Metabolic Insights
Online Access:https://doi.org/10.4137/NMI.S14113
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spelling doaj-63faa746e4534baba099978d9a71fba02020-11-25T01:25:46ZengSAGE PublishingNutrition and Metabolic Insights1178-63882014-01-01710.4137/NMI.S14113A Randomized Double Blind Controlled Safety Trial Evaluating D-Lactic Acid Production in Healthy Infants Fed a -containing FormulaKonstantinos Papagaroufalis0Aikaterini Fotiou1Delphine Egli2Liên-Anh Tran3Philippe Steenhout4Maternity Helena Venizelou, Athens, Greece.Maternity Helena Venizelou, Athens, Greece.Nestec Ltd, Vevey, Switzerland.Nestec Ltd, Vevey, Switzerland.Nestec Ltd, Vevey, Switzerland.Background D-Lactic acidosis in infants fed lactic acid bacteria-containing products is a concern. Methods The primary objective of this non-inferiority trial was to compare urinary D-lactic acid concentrations during the first 28 days of life in infants fed formula containing Lactobacillus reuteri (1.2 x 10 6 colony forming units (CFU)/ml) with those fed a control formula. The non-inferiority margin was set at a two-fold increase in D-lactic acid (0.7 mmol/mol creatinine, log-transformed). Healthy term infants in Greece were enrolled between birth and 72 hours of age, and block randomized to a probiotic ( N = 44) or control ( N = 44) group. They were exclusively fed their formulae until 28 days of age and followed up at 7, 14, 28, 112, and 168 ± 3 days. Anthropometric measurements were taken at each visit and tolerance recorded until 112 days. Urine was collected before study formula intake and at all visits up to 112 days and blood at 14 days. Results D-Lactic acid concentration in the probiotic group was below the non-inferiority margin at 28 days: treatment effect -0.03 (95% confidence interval [CI]: [-0.48 to 0.41]) mmol/mol creatinine but was above the non-inferiority margin at 7 and 14 days–-treatment effect 0.50 (95% CI: [0.05-0.96]) mmol/mol creatinine and 0.45 (95% CI: [0.00-0.90]) mmol/mol creatinine, respectively. Blood acid excess and pH, anthropometry, tolerance, and adverse events (AEs) were not significantly different between groups. Conclusion Intake of L. reuteri -containing formula was safe and did not cause an increase in D-lactic acid beyond two weeks. Trial Registration ClinicalTrials.gov NCT01119170.https://doi.org/10.4137/NMI.S14113
collection DOAJ
language English
format Article
sources DOAJ
author Konstantinos Papagaroufalis
Aikaterini Fotiou
Delphine Egli
Liên-Anh Tran
Philippe Steenhout
spellingShingle Konstantinos Papagaroufalis
Aikaterini Fotiou
Delphine Egli
Liên-Anh Tran
Philippe Steenhout
A Randomized Double Blind Controlled Safety Trial Evaluating D-Lactic Acid Production in Healthy Infants Fed a -containing Formula
Nutrition and Metabolic Insights
author_facet Konstantinos Papagaroufalis
Aikaterini Fotiou
Delphine Egli
Liên-Anh Tran
Philippe Steenhout
author_sort Konstantinos Papagaroufalis
title A Randomized Double Blind Controlled Safety Trial Evaluating D-Lactic Acid Production in Healthy Infants Fed a -containing Formula
title_short A Randomized Double Blind Controlled Safety Trial Evaluating D-Lactic Acid Production in Healthy Infants Fed a -containing Formula
title_full A Randomized Double Blind Controlled Safety Trial Evaluating D-Lactic Acid Production in Healthy Infants Fed a -containing Formula
title_fullStr A Randomized Double Blind Controlled Safety Trial Evaluating D-Lactic Acid Production in Healthy Infants Fed a -containing Formula
title_full_unstemmed A Randomized Double Blind Controlled Safety Trial Evaluating D-Lactic Acid Production in Healthy Infants Fed a -containing Formula
title_sort randomized double blind controlled safety trial evaluating d-lactic acid production in healthy infants fed a -containing formula
publisher SAGE Publishing
series Nutrition and Metabolic Insights
issn 1178-6388
publishDate 2014-01-01
description Background D-Lactic acidosis in infants fed lactic acid bacteria-containing products is a concern. Methods The primary objective of this non-inferiority trial was to compare urinary D-lactic acid concentrations during the first 28 days of life in infants fed formula containing Lactobacillus reuteri (1.2 x 10 6 colony forming units (CFU)/ml) with those fed a control formula. The non-inferiority margin was set at a two-fold increase in D-lactic acid (0.7 mmol/mol creatinine, log-transformed). Healthy term infants in Greece were enrolled between birth and 72 hours of age, and block randomized to a probiotic ( N = 44) or control ( N = 44) group. They were exclusively fed their formulae until 28 days of age and followed up at 7, 14, 28, 112, and 168 ± 3 days. Anthropometric measurements were taken at each visit and tolerance recorded until 112 days. Urine was collected before study formula intake and at all visits up to 112 days and blood at 14 days. Results D-Lactic acid concentration in the probiotic group was below the non-inferiority margin at 28 days: treatment effect -0.03 (95% confidence interval [CI]: [-0.48 to 0.41]) mmol/mol creatinine but was above the non-inferiority margin at 7 and 14 days–-treatment effect 0.50 (95% CI: [0.05-0.96]) mmol/mol creatinine and 0.45 (95% CI: [0.00-0.90]) mmol/mol creatinine, respectively. Blood acid excess and pH, anthropometry, tolerance, and adverse events (AEs) were not significantly different between groups. Conclusion Intake of L. reuteri -containing formula was safe and did not cause an increase in D-lactic acid beyond two weeks. Trial Registration ClinicalTrials.gov NCT01119170.
url https://doi.org/10.4137/NMI.S14113
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