Your browser doesn't support javascript.
loading
Compromised gut microbiota networks in children with anti-islet cell autoimmunity.
Endesfelder, David; zu Castell, Wolfgang; Ardissone, Alexandria; Davis-Richardson, Austin G; Achenbach, Peter; Hagen, Michael; Pflueger, Maren; Gano, Kelsey A; Fagen, Jennie R; Drew, Jennifer C; Brown, Christopher T; Kolaczkowski, Bryan; Atkinson, Mark; Schatz, Desmond; Bonifacio, Ezio; Triplett, Eric W; Ziegler, Anette-G.
Affiliation
  • Endesfelder D; Scientific Computing Research Unit, Helmholtz Zentrum München, GermanyInstitute of Diabetes Research, Helmholtz Zentrum München, and Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München, Germany.
  • zu Castell W; Scientific Computing Research Unit, Helmholtz Zentrum München, Germany.
  • Ardissone A; Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL.
  • Davis-Richardson AG; Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL.
  • Achenbach P; Institute of Diabetes Research, Helmholtz Zentrum München, and Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München, Germany.
  • Hagen M; Scientific Computing Research Unit, Helmholtz Zentrum München, Germany.
  • Pflueger M; Institute of Diabetes Research, Helmholtz Zentrum München, and Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München, Germany.
  • Gano KA; Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL.
  • Fagen JR; Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL.
  • Drew JC; Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL.
  • Brown CT; Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL.
  • Kolaczkowski B; Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL.
  • Atkinson M; Department of Pediatrics, University of Florida, Gainesville, FL.
  • Schatz D; Department of Pediatrics, University of Florida, Gainesville, FL.
  • Bonifacio E; Center for Regenerative Therapies, Dresden, and Paul Langerhans Institute Dresden, Technische Universität Dresden, GermanyInstitute for Diabetes and Obesity, Helmholtz Zentrum München, Germany.
  • Triplett EW; Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL.
  • Ziegler AG; Institute of Diabetes Research, Helmholtz Zentrum München, and Forschergruppe Diabetes, Klinikum rechts der Isar, Technische Universität München, Germany anette-g.ziegler@helmholtz-muenchen.de.
Diabetes ; 63(6): 2006-14, 2014 Jun.
Article in En | MEDLINE | ID: mdl-24608442
ABSTRACT
The gut microbiome is suggested to play a role in the pathogenesis of autoimmune disorders such as type 1 diabetes. Evidence of anti-islet cell autoimmunity in type 1 diabetes appears in the first years of life; however, little is known regarding the establishment of the gut microbiome in early infancy. Here, we sought to determine whether differences were present in early composition of the gut microbiome in children in whom anti-islet cell autoimmunity developed. We investigated the microbiome of 298 stool samples prospectively taken up to age 3 years from 22 case children in whom anti-islet cell autoantibodies developed, and 22 matched control children who remained islet cell autoantibody-negative in follow-up. The microbiome changed markedly during the first year of life, and was further affected by breast-feeding, food introduction, and birth delivery mode. No differences between anti-islet cell autoantibody-positive and -negative children were found in bacterial diversity, microbial composition, or single-genus abundances. However, substantial alterations in microbial interaction networks were observed at age 0.5 and 2 years in the children in whom anti-islet cell autoantibodies developed. The findings underscore a role of the microbiome in the pathogenesis of anti-islet cell autoimmunity and type 1 diabetes.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Islets of Langerhans / Gastrointestinal Tract / Diabetes Mellitus, Type 1 / Feces / Microbiota / Milk, Human Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Infant / Male Language: En Journal: Diabetes Year: 2014 Document type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Islets of Langerhans / Gastrointestinal Tract / Diabetes Mellitus, Type 1 / Feces / Microbiota / Milk, Human Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans / Infant / Male Language: En Journal: Diabetes Year: 2014 Document type: Article Affiliation country: Germany