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      Evaluation of the safety, tolerance and efficacy of 1-year consumption of infant formula supplemented with Lactobacillus fermentum CECT5716 Lc40 or Bifidobacterium breve CECT7263: a randomized controlled trial

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          Abstract

          Background

          The microorganism present in breast milk, added to other factors, determine the colonization of infants. The objective of the present study is to evaluate the safety, tolerance and effects of the consumption of a milk formula during the first year of life that is supplemented with L. fermentum CECT5716 or Bifidobacterium breve CECT7263, two strains originally isolated from breast milk.

          Methods

          A randomized, double blind, controlled, parallel group study including healthy, formula-fed infants was conducted. Two hundred and thirty-six 1-month-old infants were selected and randomly divided into three study groups according to a randomization list. Infants in the control group received a standard powdered infant formula until 12 months of age. Infants in the probiotic groups received the same infant formula but supplemented with L. fermentum CECT5716 Lc40 or B. breve CECT7263. Main outcome was weigh-gain of infants as safety marker.

          Results

          One hundred and eighty-nine infants completed the eleven months of intervention (61 in control group, 65 in Lf group and 63 in Bb group). The growth of infants in the three groups was consistent with standards. No significant differences were observed in the main outcome, weight-gain (Control group: 5.77 Kg ± 0.95, Lf group: 5.77 Kg ± 1.31, Bb group: 5.58 Kg ± 1.10; p = 0.527). The three milk formulae were well tolerated, and no adverse effects were related to the consumption of any of the formula. Infants receiving B. breve CECT7263 had a 1.7 times lower risk of crying than the control group (OR = 0.569, CI 95% 0.568–0.571; p = 0.001). On the other hand, the incidence of diarrhoea in infants receiving the formula supplemented with L. fermentum CECT5716 was a 44% lower than in infants receiving the control formula ( p = 0.014). The consumption of this Lactobacillus strain also reduced the duration of diarrhoea by 2.5 days versus control group ( p = 0.044).

          Conclusions

          The addition of L. fermentum CECT5716 Lc40 or B. breve CECT7263, two probiotic strains naturally found in breast milk, to infant formulae is safe and induces beneficial effects on the health of infants.

          Trial registration

          The trial was retrospectively registered in the US Library of Medicine ( www.clinicaltrial.gov) with the number NCT03204630. Registered 11 August 2016.

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          Most cited references31

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          Human milk is a source of lactic acid bacteria for the infant gut.

          To investigate whether human breast milk contains potentially probiotic lactic acid bacteria, and therefore, whether it can be considered a synbiotic food. Study design Lactic acid bacteria were isolated from milk, mammary areola, and breast skin of eight healthy mothers and oral swabs and feces of their respective breast-fed infants. Some isolates (178 from each mother and newborn pair) were randomly selected and submitted to randomly amplified polymorphic DNA (RAPD) polymerase chain reaction analysis, and those that displayed identical RAPD patterns were identified by 16S rDNA sequencing. Within each mother and newborn pair, some rod-shaped lactic acid bacteria isolated from mammary areola, breast milk, and infant oral swabs and feces displayed identical RAPD profiles. All of them, independently from the mother and child pair, were identified as Lactobacillus gasseri. Similarly, among coccoid lactic acid bacteria from these different sources, some shared an identical RAPD pattern and were identified as Enterococcus faecium. In contrast, none of the lactic acid bacteria isolated from breast skin shared RAPD profiles with lactic acid bacteria of the other sources. Breast-feeding can be a significant source of lactic acid bacteria to the infant gut. Lactic acid bacteria present in milk may have an endogenous origin and may not be the result of contamination from the surrounding breast skin.
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            Distinct gut microbiota profiles in patients with primary sclerosing cholangitis and ulcerative colitis

            AIM To characterize the gut bacterial microbiota of patients with primary sclerosing cholangitis (PSC) and ulcerative colitis (UC). METHODS Stool samples were collected and relevant clinical data obtained from 106 study participants, 43 PSC patients with (n = 32) or without (n = 11) concomitant inflammatory bowel disease, 32 UC patients, and 31 healthy controls. The V3 and V4 regions of the 16S ribosomal RNA gene were sequenced on Illumina MiSeq platform to cover low taxonomic levels. Data were further processed in QIIME employing MaAsLin and LEfSe tools for analysis of the output data. RESULTS Microbial profiles in both PSC and UC were characterized by low bacterial diversity and significant change in global microbial composition. Rothia, Enterococcus, Streptococcus, Veillonella, and three other genera were markedly overrepresented in PSC regardless of concomitant inflammatory bowel disease (IBD). Rothia, Veillonella and Streptococcus were tracked to the species level to identify Rothia mucilaginosa, Streptococcus infantus, S. alactolyticus, and S. equi along with Veillonella parvula and V. dispar. PSC was further characterized by decreased abundance of Adlercreutzia equolifaciens and Prevotella copri. Decrease in genus Phascolarctobacterium was linked to presence of colonic inflammation regardless of IBD phenotype. Akkermansia muciniphila, Butyricicoccus pullicaecorum and Clostridium colinum were decreased in UC along with genus Roseburia. Low levels of serum albumin were significantly correlated with enrichment of order Actinomycetales. CONCLUSION PSC is associated with specific gut microbes independently of concomitant IBD and several bacterial taxa clearly distinguish IBD phenotypes (PSC-IBD and UC).
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              Paroxysmal fussing in infancy, sometimes called colic.

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                Author and article information

                Contributors
                jmaldon@ugr.es
                mercedes_gil_campos@yahoo.es
                joseantonio.maldonadolobon@biosearchlife.com
                rosibenavidesr@yahoo.es
                katherine1.flores@gmail.com
                reyes.jaldo@gmail.com
                inmaculadajbj@hotmail.com
                vbolivarg@gmail.com
                advalero@biosearchlife.com
                pradosguerrero@hotmail.com
                fonchopenalver@yahoo.es
                molivares@biosearchlife.com
                Journal
                BMC Pediatr
                BMC Pediatr
                BMC Pediatrics
                BioMed Central (London )
                1471-2431
                21 October 2019
                21 October 2019
                2019
                : 19
                : 361
                Affiliations
                [1 ]ISNI 0000 0000 8771 3783, GRID grid.411380.f, Pediatric Unit, , University Hospital Virgen de las Nieves, ; Granada, Spain
                [2 ]ISNI 0000000121678994, GRID grid.4489.1, Pediatric Department, , University of Granada, ; Granada, Spain
                [3 ]Biosanitary Research Institute (IBS), Granada, Spain
                [4 ]ISNI 0000 0000 9314 1427, GRID grid.413448.e, Maternal and Child Health and Development Network (SAMID), , Health Institute Carlos III, ; Madrid, Spain
                [5 ]Unit of Metabolism and Pediatric Research (IMIBIC), Reina Sofia University Hospital, University of Córdoba, Cordoba, Spain
                [6 ]ISNI 0000 0004 5930 4615, GRID grid.484042.e, CIBEROBN, ; Cordoba, Spain
                [7 ]GRID grid.490622.b, Biosearch Life, Research Department, ; Granada, Spain
                [8 ]Pediatric Clinic Roquetas, Roquetas de Mar, Almería, Spain
                [9 ]GRID grid.418355.e, Andalusian Health Service, ; Andalusia, Spain
                [10 ]Clinic “Cristo de la Salud” Albolote, Granada, Spain
                Author information
                http://orcid.org/0000-0002-8596-9923
                Article
                1753
                10.1186/s12887-019-1753-7
                6802336
                e17f4e7e-0e04-4be9-ac2a-4d4c52cfe4bc
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 28 August 2018
                : 27 September 2019
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Pediatrics
                infant formula,probiotics,safety,diarrhoea,colic
                Pediatrics
                infant formula, probiotics, safety, diarrhoea, colic

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