Lactobacillus acidophilus for infant colic and microbiota modulation: a randomized clinical trial

dc.creatorVaz, Sáskia Ribeiro
dc.creatorTofoli, Marise Helena Cardoso
dc.creatorAvelino, Melissa Ameloti Gomes
dc.creatorMota, João Felipe
dc.creatorAraujo Filho, Humberto Bezerra de
dc.creatorCosta, Paulo Sérgio Sucasas da
dc.date.accessioned2026-04-30T13:05:02Z
dc.date.available2026-04-30T13:05:02Z
dc.date.issued2026
dc.description.abstractBackground Infantile colic affects up to 25% of infants during the early weeks of life. Dysbiosis plays a prominent role in its pathogenesis, supporting the potential therapeutic role of probiotics. We aimed to evaluate the efficacy of Lactobacillus acidophilus NCFM versus placebo in infant colic and microbiota modulation. Methods A double-blind, placebo-controlled randomized trial was conducted with 60 infants with colic, randomly assigned to receive five drops of L. acidophilus NCFM (1 × 109 CFU) or placebo for 28 days. Data on responders (subjects with a colicky full-force crying/fussing time reduction of ≥ 50% from baseline), daily fussing and crying time, adverse effects, and maternal and child characteristics were collected. Changes in gut microbiota and fecal calprotectin were also evaluated. The study was registered at ensaiosclinicos.gov.br (RBR-5pp4nks). Results The primary endpoint (proportion of responders at Day 28) was not significantly different between groups (p = 0.240). A higher responder rate was observed in the intervention group at Day 14 in exploratory analyses (p = 0.045); however, this result was attenuated after correction for multiple comparisons. No statistical difference was observed in calprotectin concentration (p = 0.687), infant mood (p = 0.720), fussing and crying time (p = 0.524). A higher diversity was observed in the breastfed and formula-fed groups utilizing probiotics, but not in the formula-fed group receiving placebo. A high relative abundance of Akkermansia was identified in the probiotic group. Ruminococcus was identified in both groups before and after the intervention. Conclusions Intervention did not significantly improve the proportion of responders at Day 28, the primary endpoint. An apparent benefit at Day 14 emerged in secondary. The use of L. acidophilus NCFM was able to improve some aspects of infants’ intestinal microbiota. Also, there was no statistical difference in calprotectin and infant mood. The use of L. acidophilus NCFM was safe for this population.
dc.identifier.citationVAZ, Sáskia Ribeiro et al. Lactobacillus acidophilus for infant colic and microbiota modulation: a randomized clinical trial. BMC Pediatrics, London, 2026. DOI: 10.1186/s12887-026-06883-7. Disponível em: https://link.springer.com/article/10.1186/s12887-026-06883-7. Acesso em: 27 abr. 2026.
dc.identifier.doi10.1186/s12887-026-06883-7
dc.identifier.issn1471-2431
dc.identifier.urihttps://repositorio.bc.ufg.br//handle/ri/30194
dc.language.isoeng
dc.publisher.countryGra-bretanha
dc.publisher.departmentFaculdade de Nutrição - FANUT (RMG)
dc.rightsAcesso Aberto
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectLactobacillus acidophilus
dc.subjectColic
dc.subjectMicrobiota
dc.subjectInfant
dc.subjectProbiotics.
dc.titleLactobacillus acidophilus for infant colic and microbiota modulation: a randomized clinical trial
dc.typeArtigo

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