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1.
Front Immunol ; 11: 1421, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32754153

RESUMO

Background: Infants with ileostomies often suffer from sodium depletion, ultimately leading to a failure to thrive. Moreover, early-infantile microbial dysbiosis may potentially aggravate weight faltering. Given that sodium supplementation has been used to restore weight gain and feeding practices largely determine infantile microbiota, the current study investigated the effect of sodium chloride (NaCl) on weight gain and intestinal microbiome in infants with jejuno- and ileostomies. Methods: A prospective cohort study including 24 neonates with enterostomies compared 19 subjects receiving oral NaCl (5.85%) to five subjects without supplementation with respect to postoperative changes in thrive and the intestinal microbiome. Results: Infants receiving NaCl after enterostomy-surgery showed vastly improved weight gain and an increased abundance of Lactobacillus in fecal samples, as compared to subjects without oral supplement who displayed decreasing percentiles for weight and did not reveal a higher abundance of probiotic strains within the ostomy effluent. Contrarily, Klebsiella was equally enriched in supplemented infants, reflecting a higher susceptibility for infections in preterm neonates. Discussion: Our findings support oral NaCl supplementation as a mainstay of postoperative treatment in infants with small bowel ostomies who are predisposed to suffer from a sodium depletion-associated failure to thrive. Not only does NaCl promote weight gain by increasing glucose resorption, but it also appears to induce microbial restoration by enhancing the abundance of health-promoting probiotic bacteria. This finding has an even greater significance when facing an elevated Klebsiella/Bifidobacteria (K/B) ratio, believed to represent an early-life microbial biomarker for development of allergic disease.


Assuntos
Suplementos Nutricionais , Microbioma Gastrointestinal , Ileostomia/efeitos adversos , Cloreto de Sódio/administração & dosagem , Aumento de Peso/efeitos dos fármacos , Estudos de Coortes , Insuficiência de Crescimento/etiologia , Feminino , Humanos , Recém-Nascido , Masculino , Estudos Prospectivos
2.
Cell Host Microbe ; 26(2): 252-264.e10, 2019 08 14.
Artigo em Inglês | MEDLINE | ID: mdl-31399369

RESUMO

Obesity and type 2 diabetes (T2D) are metabolic disorders that are linked to microbiome alterations. However, their co-occurrence poses challenges in disentangling microbial features unique to each condition. We analyzed gut microbiomes of lean non-diabetic (n = 633), obese non-diabetic (n = 494), and obese individuals with T2D (n = 153) from German population and metabolic disease cohorts. Microbial taxonomic and functional profiles were analyzed along with medical histories, serum metabolomics, biometrics, and dietary data. Obesity was associated with alterations in microbiome composition, individual taxa, and functions with notable changes in Akkermansia, Faecalibacterium, Oscillibacter, and Alistipes, as well as in serum metabolites that correlated with gut microbial patterns. However, microbiome associations were modest for T2D, with nominal increases in Escherichia/Shigella. Medications, including antihypertensives and antidiabetics, along with dietary supplements including iron, were significantly associated with microbiome variation. These results differentiate microbial components of these interrelated metabolic diseases and identify dietary and medication exposures to consider in future studies.


Assuntos
Diabetes Mellitus Tipo 2/complicações , Microbioma Gastrointestinal/fisiologia , Obesidade/complicações , Obesidade/microbiologia , Animais , Bactérias/classificação , Bactérias/genética , Bactérias/isolamento & purificação , Biodiversidade , Dieta , Suplementos Nutricionais , Fezes/microbiologia , Feminino , Alemanha , Humanos , Ferro/metabolismo , Magnésio/metabolismo , Masculino , Doenças Metabólicas/complicações , Metagenômica , Camundongos , Camundongos Endogâmicos C57BL , Análise Multivariada , Avaliação Nutricional , Soro/metabolismo
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