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Mucosal Microbiota Associated With Eosinophilic Esophagitis and Eosinophilic Gastritis.
Furuta, Glenn T; Fillon, Sophie A; Williamson, Kayla M; Robertson, Charles E; Stevens, Mark J; Aceves, Seema S; Arva, Nicoleta C; Chehade, Mirna; Collins, Margaret H; Davis, Carla M; Dellon, Evan S; Falk, Gary W; Gonsalves, Nirmala; Gupta, Sandeep K; Hirano, Ikuo; Khoury, Paneez; Leung, John; Martin, Lisa J; Menard-Katcher, Paul; Mukkada, Vincent A; Peterson, Kathryn; Spergel, Jonathan M; Wechsler, Joshua B; Yang, Guang-Yu; Rothenberg, Marc E; Harris, J Kirk.
Afiliação
  • Furuta GT; From the Section of Pediatric Gastroenterology, Hepatology and Nutrition, Digestive Health Institute, Children's Hospital Colorado, Gastrointestinal Eosinophilic Disease Program, Mucosal Inflammation Program, University of Colorado School of Medicine, Aurora, CO.
  • Fillon SA; From the Section of Pediatric Gastroenterology, Hepatology and Nutrition, Digestive Health Institute, Children's Hospital Colorado, Gastrointestinal Eosinophilic Disease Program, Mucosal Inflammation Program, University of Colorado School of Medicine, Aurora, CO.
  • Williamson KM; the Department of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado School of Medicine, Aurora, CO.
  • Robertson CE; the Division of Infectious Disease, University of Colorado School of Medicine, Aurora, CO.
  • Stevens MJ; the Division of Infectious Disease, University of Colorado School of Medicine, Aurora, CO.
  • Aceves SS; the Division of Allergy/Immunology, Department of Pediatrics, University of California, San Diego, Rady Children's Hospital, San Diego, CA.
  • Arva NC; the Department of Pathology, Ann & Robert H Lurie Children's Hospital of Chicago, Chicago, IL.
  • Chehade M; the Departments of Pediatrics and Medicine, Mount Sinai Center for Eosinophilic Disorders, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Collins MH; the Division of Pathology and Laboratory Medicine, Department of Pediatrics, Cincinnati Children's Hospital Medical Center and the University of Cincinnati, Cincinnati, OH.
  • Davis CM; the Division of Immunology, Allergy and Retrovirology, Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston, TX.
  • Dellon ES; the Center for Esophageal Diseases and Swallowing and Center for Gastrointestinal Biology and Disease, Division of Gastroenterology and Hepatology, Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC.
  • Falk GW; the Division of Gastroenterology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Gonsalves N; the Division of Gastroenterology and Hepatology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
  • Gupta SK; the Division of Pediatric Gastroenterology, Hepatology and Nutrition, Riley Hospital for Children/Indiana University School of Medicine, and Community Health Network, Indianapolis, IN.
  • Hirano I; the Division of Gastroenterology and Hepatology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
  • Khoury P; the Division of Allergy, Immunology, and Transplantation, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD.
  • Leung J; the Human Eosinophil Section, NIAID, Bethesda, MD.
  • Martin LJ; the Divisions of Allergy/Immunology and Gastroenterology, Tuft's Medical Center, Boston, MA.
  • Menard-Katcher P; the Department of Pediatrics, Cincinnati Children's Hospital and the University of Cincinnati College of Medicine, Cincinnati, OH.
  • Mukkada VA; the Division of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center and the University of Cincinnati, Cincinnati, OH.
  • Peterson K; the Division of Gastroenterology, University of Colorado, Aurora, CO.
  • Spergel JM; the Division of Gastroenterology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center and the University of Cincinnati, Cincinnati, OH.
  • Wechsler JB; the Division of Gastroenterology, University of Utah, Salt Lake City, UT.
  • Yang GY; the Division of Allergy and Immunology, The Children's Hospital of Philadelphia, Department of Pediatrics, Perelman School of Medicine of University of Pennsylvania, Philadelphia, PA.
  • Rothenberg ME; the Division of Gastroenterology, Hepatology, and Nutrition, Ann & Robert H Lurie Children's Hospital of Chicago, Chicago, IL.
  • Harris JK; the Division of Gastrointestinal Pathology, Department of Pathology, Fineberg School of Medicine, Northwestern University, Chicago, IL.
J Pediatr Gastroenterol Nutr ; 76(3): 347-354, 2023 03 01.
Article em En | MEDLINE | ID: mdl-36525669
ABSTRACT

OBJECTIVE:

The aim of the study was to determine the mucosal microbiota associated with eosinophilic esophagitis (EoE) and eosinophilic gastritis (EoG) in a geographically diverse cohort of patients compared to controls.

METHODS:

We conducted a prospective study of individuals with eosinophilic gastrointestinal disease (EGID) in the Consortium of Eosinophilic Gastrointestinal Disease Researchers, including pediatric and adult tertiary care centers. Eligible individuals had clinical data, mucosal biopsies, and stool collected. Total bacterial load was determined from mucosal biopsy samples by quantitative polymerase chain reaction (PCR). Community composition was determined by small subunit rRNA gene amplicons.

RESULTS:

One hundred thirty-nine mucosal biopsies were evaluated corresponding to 93 EoE, 17 EoG, and 29 control specimens (18 esophageal) from 10 sites across the United States. Dominant community members across disease activity differed significantly. When comparing EoE and EoG with controls, the dominant taxa in individuals with EGIDs was increased ( Streptococcus in esophagus; Prevotella in stomach). Specific taxa were associated with active disease for both EoE ( Streptococcus , Gemella ) and EoG ( Leptotrichia ), although highly individualized communities likely impacted statistical testing. Alpha diversity metrics were similar across groups, but with high variability among individuals. Stool analyses did not correlate with bacterial communities found in mucosal biopsy samples and was similar in patients and controls.

CONCLUSIONS:

Dominant community members ( Streptococcus for EoE, Prevotella for EoG) were different in the mucosal biopsies but not stool of individuals with EGIDs compared to controls; taxa associated with EGIDs were highly variable across individuals. Further study is needed to determine if therapeutic interventions contribute to the observed community differences.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esofagite Eosinofílica / Microbiota Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esofagite Eosinofílica / Microbiota Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article