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L.Fermentum CECT5716 and B.Breve CECT7263 on premature infants morbidities: a randomized clinical trial

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dc.contributor.author Hurtado-Suazo, José-Antonio
dc.contributor.author Alonso-Ojembarrena, Almudena
dc.contributor.author Sánchez-Tamayo, Tomas
dc.contributor.author Martín-Álvarez, Estefanía
dc.contributor.author Sáez, María-Eugenia
dc.contributor.author Martínez-Pardo, Luz
dc.contributor.author Diez-Delgado-Rubio, Javier
dc.contributor.author Granero-Asencio, Mercedes
dc.contributor.author Serrano-López, Laura
dc.contributor.author Maldonado-Lobon, José-Antonio
dc.contributor.author Mora-Navarro, David
dc.contributor.author De-Benito-Guerra, María-Teresa
dc.contributor.author Torres-Begara, Eva
dc.contributor.author Ruiz-Moreno, Juan-Antonio
dc.contributor.author Macias-Díaz, Carmen
dc.contributor.author Lloreda-García, José-María
dc.contributor.author Peña-Caballero, Manuela
dc.contributor.author Olivares, Mónica
dc.contributor.author Blanco-Rojo, Ruth
dc.date.accessioned 2026-03-06T14:11:50Z
dc.date.available 2026-03-06T14:11:50Z
dc.date.issued 2025-11-27
dc.identifier.citation Hurtado Suazo JA, Alonso Ojembarrena A, Sánchez Tamayo T, Martín Alvarez E, Saez ME, Martínez Pardo L, et al. L.Fermentum CECT5716 and B.Breve CECT7263 on premature infants morbidities: a randomized clinical trial. Pediatr Res. 27 de noviembre de 2025. doi:10.1038/s41390-025-04633-6
dc.identifier.issn 0031-3998
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/24713
dc.description.abstract BACKGROUND: This study examined the effects of two doses of probiotics isolated from human milk on the incidences of necrotizing enterocolitis (NEC) and mortality in preterm infants. METHODS: This multicenter, randomized, double-blind study involved 583 very low birth weight preterm neonates (?32 6/7 weeks, <1500 g) who started enteral nutrition within 72 h of birth (>5 ml/kg/day) and received either a high-dose (HD, 1 × 10(9) CFU/day per strain) or a low-dose (LD, 1 × 10(6) CFU/day per strain) of Limosilactobacillus fermentum CECT5716 (LC40) and Bifidobacterium breve CECT7263 (BfM26) until 36 6/7 weeks postmenstrual age or discharge. RESULTS: The probiotic combination was well tolerated with no adverse effects. The NEC (2.5% vs. 1.3%; p = 0.156) and mortality (3.9% vs. 3.6%; p = 0.685) rates were not significantly different between the groups (HD vs. LD). These rates were lower than those reported in a co-temporal cohort in the region (SEN1500 cohort). CONCLUSION: No significant differences were found between the HD and the LD of the LC40 and BfM26 combination in the incidence of NEC and all-cause mortality. The incidence rates of death and NEC were lower in this study than in the SEN1500 cohort, suggesting that the low dose may suffice for preterm infants. This study supports the safety and tolerability of these probiotics in preterm infants. IMPACT: The study responds to scientific societies' request for more clinical trials to strengthen the currently low level of evidence on probiotics' safety and benefits for preterm infants. The study presents evidence supporting the safety and the effect of two different doses of a combination of two human milk-derived probiotic strains in preterm infants. The study indicates that a low dose of probiotics may be sufficient to achieve beneficial effects in preterm infants. These findings will inform future research on optimizing probiotic dosing in this population.
dc.language.iso eng
dc.publisher SPRINGERNATURE
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.title L.Fermentum CECT5716 and B.Breve CECT7263 on premature infants morbidities: a randomized clinical trial
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 41310220
dc.relation.publisherversion https://www.nature.com/articles/s41390-025-04633-6
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1038/s41390-025-04633-6
dc.journal.title Pediatric Research
dc.identifier.essn 1530-0447


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