PMID- 17032199 OWN - NLM STAT- MEDLINE DCOM- 20061219 LR - 20220419 IS - 0002-9270 (Print) IS - 0002-9270 (Linking) VI - 101 IP - 10 DP - 2006 Oct TI - Rotavirus infection frequency and risk of celiac disease autoimmunity in early childhood: a longitudinal study. PG - 2333-40 AB - OBJECTIVE: Few studies have assessed the role of specific gastrointestinal infections in celiac disease. We investigated whether increased frequency of rotavirus infection, a common cause of gastrointestinal infection and inflammation, predicts increased risk of celiac disease autoimmunity. METHODS: A cohort of 1,931 children from the Denver metropolitan area who carried celiac disease human leukocyte antigen (HLA) risk alleles were followed from infancy for development of celiac disease autoimmunity, defined as positivity at two or more subsequent clinic visits for tissue transglutaminase (tTG) autoantibodies measured using a radioimmunoassay with human recombinant tTG. Blood samples were obtained at ages 9, 15, and 24 months, and annually thereafter. Rotavirus antibodies were assayed using an indirect enzyme immunoassay in serial serum samples from each case and two matched controls. Frequency of infections were estimated by the number of increases (> 2 assay coefficient of variation) in rotavirus antibody between clinic visits. RESULTS: Fifty-four cases developed celiac disease autoimmunity at a median age of 4.4 yr. Thirty-six had an intestinal biopsy, of which 27 (75%) were positive for celiac disease. Frequent rotavirus infections predicted a higher risk of celiac disease autoimmunity (compared with zero infections, rate ratio 1.94, 95% confidence interval [CI] 0.39-9.56, for one infection and rate ratio 3.76, 95% CI 0.76-18.7, for > or = 2 infections, rate ratio for trend per increase in number of infections = 1.94, 95% CI 1.04-3.61, p = 0.037). The result was similar after adjustment for gender, ethnic group, maternal education, breast-feeding, day-care attendance, number of siblings, season of birth, and number of HLA DR3-DQ2 haplotypes. CONCLUSIONS: This prospective study provides the first indication that a high frequency of rotavirus infections may increase the risk of celiac disease autoimmunity in childhood in genetically predisposed individuals. FAU - Stene, Lars C AU - Stene LC AD - Barbara Davis Center for Childhood Diabetes, University of Colorado School of Medicine, Aurora, Colorado 80045-6511, USA. FAU - Honeyman, Margo C AU - Honeyman MC FAU - Hoffenberg, Edward J AU - Hoffenberg EJ FAU - Haas, Joel E AU - Haas JE FAU - Sokol, Ronald J AU - Sokol RJ FAU - Emery, Lisa AU - Emery L FAU - Taki, Iman AU - Taki I FAU - Norris, Jill M AU - Norris JM FAU - Erlich, Henry A AU - Erlich HA FAU - Eisenbarth, George S AU - Eisenbarth GS FAU - Rewers, Marian AU - Rewers M LA - eng GR - AI 50864/AI/NIAID NIH HHS/United States GR - DK 32083/DK/NIDDK NIH HHS/United States GR - DK 32493/DK/NIDDK NIH HHS/United States GR - DK 50979/DK/NIDDK NIH HHS/United States GR - M01 RR00069/RR/NCRR NIH HHS/United States GR - P30 DK 57516/DK/NIDDK NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PL - United States TA - Am J Gastroenterol JT - The American journal of gastroenterology JID - 0421030 RN - 0 (Antibodies, Viral) RN - 0 (Autoantibodies) RN - 0 (HLA Antigens) RN - EC 2.3.2.13 (Transglutaminases) SB - IM CIN - Am J Gastroenterol. 2007 Aug;102(8):1831. PMID: 17686081 MH - Antibodies, Viral/*blood MH - Autoantibodies/blood MH - Autoimmunity/*physiology MH - Case-Control Studies MH - Celiac Disease/*blood/*etiology/pathology MH - Child MH - Child, Preschool MH - Female MH - HLA Antigens/genetics MH - Humans MH - Infant MH - Longitudinal Studies MH - Male MH - Rotavirus/*immunology MH - Rotavirus Infections/blood/complications/*epidemiology MH - Transglutaminases/immunology EDAT- 2006/10/13 09:00 MHDA- 2006/12/21 09:00 CRDT- 2006/10/13 09:00 PHST- 2006/10/13 09:00 [pubmed] PHST- 2006/12/21 09:00 [medline] PHST- 2006/10/13 09:00 [entrez] AID - AJG741 [pii] AID - 10.1111/j.1572-0241.2006.00741.x [doi] PST - ppublish SO - Am J Gastroenterol. 2006 Oct;101(10):2333-40. doi: 10.1111/j.1572-0241.2006.00741.x.