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1.
Benef Microbes ; 8(5): 717-725, 2017 Oct 13.
Artigo em Inglês | MEDLINE | ID: mdl-28856907

RESUMO

We updated evidence on the effects of the administration of probiotic-supplemented infant formulae (IF) compared with unsupplemented IF. Five databases were searched up to September 2016 for randomised controlled trials. Twenty publications were identified, including five new RCTs. Supplementation of IF with Bifidobacterium lactis Bb12, either alone or with Streptococcus thermophilus, had no effect on growth, respiratory illness, antibiotic use, stool frequency or consistency. However, there was a significant reduction in the number of episodes of gastrointestinal infections (Bb12) and a lower frequency of colic or irritability (when both strains were used). Lactobacillus johnsonii La1 had no effect on growth, gastrointestinal infections, or respiratory illness episodes. There were no effects of supplementation of IF with Bifidobacterium longum BL999, alone or with Lactobacillus rhamnosus LPR. L. rhamnosus GG was associated with better growth; it had no effect on colic/crying, or irritability, and it was associated with greater indexes of loose stools and a higher defecation frequency. Lactobacillus reuteri ATCC 55730 had no effect on growth, colic, crying, irritability, respiratory illness, antibiotic use, stool frequency, or stool consistency; however, it reduced the number of episodes of diarrhoea. L. reuteri DSM 17938 had no effect on growth, night-time sleeping, or flatulence, but it reduced the number of spitting episodes. Lactobacillus salivarius CEC5713 had no effect on growth, colic, crying, or irritability; however, it resulted in a significant reduction in the rate of diarrhoea and the number of episodes of respiratory symptoms. In conclusion, the administration of probiotic-supplemented formulae to healthy infants does not raise safety concerns with regard to growth and adverse effects. Some beneficial clinical effects are possible; however, there is no existing robust evidence to recommend their routine use. The latter conclusion may reflect the small amount of data on a specific probiotic strain(s) and outcomes, rather than a genuine lack of an effect.


Assuntos
Desenvolvimento Infantil , Suplementos Nutricionais , Fórmulas Infantis , Probióticos/administração & dosagem , Bifidobacterium/crescimento & desenvolvimento , Humanos , Lactente , Lactobacillus/crescimento & desenvolvimento , Streptococcus/crescimento & desenvolvimento , Resultado do Tratamento
2.
Aliment Pharmacol Ther ; 41(11): 1038-54, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25819114

RESUMO

BACKGROUND: New evidence emerged on early feeding practices and the risk of coeliac disease. AIM: To systematically update evidence on these practices to find out whether there is a need to revise current recommendations. METHODS: MEDLINE, EMBASE and the Cochrane Library were searched from July 2012 (end of last search) to February 2015 for studies of any design that assessed the effect of gluten consumption and breastfeeding on the development of coeliac disease and/or coeliac disease-related autoimmunity. RESULTS: We identified 21 publications, including two, new, large, randomised controlled trials performed in high-risk infants. Exclusive or any breastfeeding, as well as breastfeeding at the time of gluten introduction, did not reduce the risk of developing coeliac disease during childhood. For infants at high risk of developing coeliac disease, gluten introduction at 4 months of age in very small amounts, or at 6 or 12 months of age, resulted in similar rates of coeliac disease diagnosis in early childhood. Later gluten introduction was associated with later development of coeliac specific autoimmunity and coeliac disease during childhood, but not total risk reduction. Observational studies indicate that consumption of a higher amount of gluten at weaning may increase the risk for coeliac disease development. CONCLUSIONS: Infant feeding practices (breastfeeding, time of gluten introduction) have no effect on the risk of developing coeliac disease during childhood (at least at specific timeframes evaluated in the included studies), necessitating an update of current European recommendations.


Assuntos
Aleitamento Materno , Doença Celíaca/epidemiologia , Comportamento Alimentar/fisiologia , Doença Celíaca/etiologia , Glutens/administração & dosagem , Glutens/efeitos adversos , Humanos , Lactente , Fatores de Tempo , Desmame
3.
Aliment Pharmacol Ther ; 37(3): 289-303, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23190209

RESUMO

BACKGROUND: In 2008, the European Society for Paediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) and the European Society of Paediatric Infectious Disease (ESPID) developed evidence-based guidelines for the management of acute gastroenteritis (AGE) in children in Europe. AIM: To summarise data published subsequently to the ESPGHAN/ESPID guidelines. METHODS: MEDLINE and The Cochrane Library were searched in August 2012 for randomised controlled trials (RCTs) or their meta-analyses published after 2008. RESULTS: Efforts to improve the taste and/or efficacy of oral rehydration solution (ORS) continue, and some interventions are promising. While standard (over 24 h) nasogastric rehydration is still being used, new evidence confirms that rapid (over 4 h) rehydration is also effective. For intravenous rehydration, new evidence is available regarding rapid or ultrarapid and large-volume vs. standard-volume rehydration; as the new evidence is not consistent, until more data are available, the administration of 20 mL/kg seems appropriate. Convincing evidence has accumulated showing that ondansetron reduces the risk for vomiting; however, a clearance on safety in children is needed. New evidence has reconfirmed that in Europe, where zinc deficiency is rare, there is no benefit from the use of zinc. New data, although mainly from outside of Europe, have reconfirmed that either smectite or racecadotril is an effective adjunctive therapy to oral rehydration. There is a clear effect of using certain probiotics, such as Lactobacillus GG or S. boulardii. CONCLUSIONS: The update of current ESPGHAN/ESPID recommendations is warranted.


Assuntos
Antieméticos/uso terapêutico , Desidratação/tratamento farmacológico , Diarreia/tratamento farmacológico , Hidratação/métodos , Gastroenterite/tratamento farmacológico , Vômito/tratamento farmacológico , Pré-Escolar , Desidratação/etiologia , Diarreia/etiologia , Relação Dose-Resposta a Droga , Gastroenterite/complicações , Humanos , Lactente , Metanálise como Assunto , Probióticos/uso terapêutico , Ensaios Clínicos Controlados Aleatórios como Assunto , Soluções para Reidratação/administração & dosagem , Vômito/etiologia , Zinco/administração & dosagem
4.
Aliment Pharmacol Ther ; 36(7): 607-18, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22905651

RESUMO

BACKGROUND: PREVENTCD, Prevent Coeliac Disease, is an international project investigating the hypothesis of possible induction of tolerance to gluten in genetically predisposed children through introducing small quantities of gluten during the period of breastfeeding. AIM: To summarise current knowledge on the possible relationship between early feeding practices and the risk of coeliac disease (CD). METHODS: The Cochrane Library, MEDLINE, and EMBASE databases were searched in May 2011, and the search was updated in January 2012, and again in July 2012. RESULTS: Breastfeeding (BF) and CD: some studies show a protective effect of BF, while others show no effect. No studies have shown a long-term preventive effect. BF at the time of gluten introduction and CD: Results from a meta-analysis of five observational case-control studies suggest that BF at gluten introduction is associated with a lower risk of CD compared with formula feeding. It is unclear whether BF provides a permanent protection or only delays the onset of CD. Timing of gluten introduction: The data suggest that both early (≤4 months) and late (≥7 months) introduction of gluten may increase the risk of CD. Amount of gluten at weaning (and later) and CD: One incident case-referent study documented that the introduction of gluten in large amounts compared with small or medium amounts increased the risk of CD. CONCLUSIONS: In the absence of clear evidence, in order to decrease the risk of later coeliac disease, it is reasonable to avoid both early (<4 months) and late (≥7 months) introduction of gluten, and to introduce gluten while the infant is still being breastfed. Future studies may clarify the remaining uncertainties.


Assuntos
Aleitamento Materno/métodos , Doença Celíaca/prevenção & controle , Estudos de Casos e Controles , Doença Celíaca/etiologia , Doença Celíaca/fisiopatologia , Predisposição Genética para Doença , Glutens/administração & dosagem , Glutens/efeitos adversos , Humanos , Lactente , Fatores de Risco , Fatores de Tempo , Desmame
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