Nutrients· 2026Q1
Efficacy of a Limosilactobacillus reuteri DSM 17938 and BG-R46™ Formulation in Predominantly Breastfed Infants with Infant Distress Syndrome: A Randomized Double-Blind Placebo-Controlled Trial
- 0citations
- Q1SCImago
- 2026year
Short summary
A combination of Limosilactobacillus reuteri DSM 17938 and BG-R46™ reduced infant distress time by 43% within 7 days in a trial of 48 infants, compared to a 13% reduction with placebo.
AI-generated from the title and abstract; the full text is not read.
Key points
- A probiotic blend of L. reuteri DSM 17938 and BG-R46™ reduced infant distress time by 43% at Day 7 and 62% at Day 21.
- The placebo group showed only a 13% reduction at Day 7 and 26% at Day 21.
- The study included 48 predominantly breastfed infants diagnosed with infant distress syndrome (colic).
- The probiotic formulation was well-tolerated and showed no safety concerns.
AI-generated from the title and abstract; the full text is not read.
Abstract
Background: Infant distress syndrome, previously termed Infantile colic, is a common disorder of gut–brain interaction characterized by excessive crying and impaired behavioral regulation. Although Limosilactobacillus reuteri DSM 17938 has shown efficacy in predominantly breastfed infants, treatment responses remain variable, highlighting the need to investigate alternative probiotic formulations. BG-R46™, a strain derived from DSM 17938, exhibits distinct properties in preclinical models, providing a rationale for evaluating the combined formulation. This study investigated the efficacy and tolerability of DSM 17938 plus BG-R46™ compared with placebo in infants with infantile colic. Methods: In this randomized, double-blind, placebo-controlled trial, 50 infants were randomized to receive either the probiotic formulation or placebo for 21 days. Forty-eight infants (24 per group) were included in the intention-to-treat and per-protocol analyses. The primary endpoint was the change from baseline to Day 7 in total infant distress time, defined as the sum of awake fussing, crying, and inconsolable crying recorded using the Baby’s Day Diary®. Secondary outcomes included crying time, infant behavioral regulation (sleep duration, awake and content behavior, awake fussing, and inconsolable crying), maternal emotional well-being assessed using the Edinburgh Postnatal Depression Scale (EPDS), and safety. Results: Baseline infant distress time was comparable between groups. At Day 7, infant distress time decreased by 43% in the probiotic group versus 13% in the placebo group (−236.0 ± 111.5 vs. −66.7 ± 100.1 min/day; p < 0.001). At Day 21, reductions reached 62% and 26%, respectively. The probiotic formulation was well tolerated throughout the study. Conclusions: Supplementation with L. reuteri DSM 17938 plus L. reuteri BG-R46™ significantly reduced infant distress compared with placebo.
The authors' abstract, as published at the source. Nutrients, 2026 · DOI ↗
Continue with a free account
Ask the paper: 3 free questions a day about this paper; save it, get its citation, new summaries every day for your field. Takeaways are Premium.
Continue free on the webSign in with Google or Apple; no card needed. You come back to this paper.
On your phone:
Field: Pharmacy
PharmacyHealth Professions