4.8 Article

Metagenomics of the faecal virome indicate a cumulative effect of enterovirus and gluten amount on the risk of coeliac disease autoimmunity in genetically at risk children: the TEDDY study

期刊

GUT
卷 69, 期 8, 页码 1416-1422

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/gutjnl-2019-319809

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资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institute of 2 Allergy and Infectious Diseases (NIAID), Eunice Kennedy Shriver National Institute of Child Health 3 and Human Development (NICHD) [U01 DK63829, U01 6 DK63861, U01 DK63821, U01 42 DK63865, U01 DK63863, U01 DK63836, 7 U01 DK63790, UC4 DK63829, UC4 DK63861, UC4 43 DK63821, UC4 8 DK63865, UC4 DK63863, UC4 DK63836, UC4 DK95300, UC4 DK100238, 44 UC4 DK106955, UC4 DK112243, UC4 DK117483, HHSN267200700014C]
  2. National Institute of Environmental Health Sciences (NIEHS), 4 Centers for Disease Control and Prevention (CDC)
  3. JDRF
  4. 5 NIH/NCATS Clinical and Translational Science Awards to the University of Florida [UL1 6 TR000064]
  5. University of Colorado
  6. [UL1 TR001082]

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Objective Higher gluten intake, frequent gastrointestinal infections and adenovirus, enterovirus, rotavirus and reovirus have been proposed as environmental triggers for coeliac disease. However, it is not known whether an interaction exists between the ingested gluten amount and viral exposures in the development of coeliac disease. This study investigated whether distinct viral exposures alone or together with gluten increase the risk of coeliac disease autoimmunity (CDA) in genetically predisposed children. Design The Environmental Determinants of Diabetes in the Young study prospectively followed children carrying the HLA risk haplotypes DQ2 and/or DQ8 and constructed a nested case-control design. From this design, 83 CDA case-control pairs were identified. Median age of CDA was 31 months. Stool samples collected monthly up to the age of 2 years were analysed for virome composition by Illumina next-generation sequencing followed by comprehensive computational virus profiling. Results The cumulative number of stool enteroviral exposures between 1 and 2 years of age was associated with an increased risk for CDA. In addition, there was a significant interaction between cumulative stool enteroviral exposures and gluten consumption. The risk conferred by stool enteroviruses was increased in cases reporting higher gluten intake. Conclusions Frequent exposure to enterovirus between 1 and 2 years of age was associated with increased risk of CDA. The increased risk conferred by the interaction between enteroviruses and higher gluten intake indicate a cumulative effect of these factors in the development of CDA.

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