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Islet Autoimmunity and HLA Markers of Presymptomatic and Clinical Type 1 Diabetes : Joint Analyses of Prospective Cohort Studies in Finland, Germany, Sweden, and the U.S

Anand, Vibha (author)
IBM Thomas J. Watson Research Center
Li, Ying (author)
IBM Thomas J. Watson Research Center
Liu, Bin (author)
IBM Thomas J. Watson Research Center
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Ghalwash, Mohamed (author)
IBM Thomas J. Watson Research Center,Ain Shams University
Koski, Eileen (author)
IBM Thomas J. Watson Research Center
Ng, Kenney (author)
IBM Thomas J. Watson Research Center
Dunne, Jessica L (author)
Juvenile Diabetes Research Foundation
Jönsson, Josefine (author)
Lund University,Lunds universitet,Diabetes - epigenetik,Forskargrupper vid Lunds universitet,Diabetes - Epigenetics,Lund University Research Groups,Skåne University Hospital
Winkler, Christiane (author)
Technical University of Munich,Helmholtz Zentrum München
Knip, Mikael (author)
Tampere University Hospital,University of Helsinki,Folkhälsan Research Center,Helsinki University Central Hospital
Toppari, Jorma (author)
Turku University Hospital,University of Turku
Ilonen, Jorma (author)
Turku University Hospital,University of Turku
Killian, Michael B (author)
Pacific Northwest Research Institute
Frohnert, Brigitte I (author)
University of Colorado
Lundgren, Markus (author)
Helmholtz Zentrum München
Ziegler, Anette-Gabriele (author)
Helmholtz Zentrum München,Technical University of Munich
Hagopian, William (author)
Pacific Northwest Research Institute
Veijola, Riitta (author)
University of Oulu,Oulu University Hospital
Rewers, Marian (author)
University of Colorado
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IBM Thomas J Watson Research Center Ain Shams University (creator_code:org_t)
 
2021-06-23
2021
English 8 s.
In: Diabetes Care. - : American Diabetes Association. - 1935-5548 .- 0149-5992. ; 44, s. 2269-2276
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • OBJECTIVE: To combine prospective cohort studies, by including HLA harmonization, and estimate risk of islet autoimmunity and progression to clinical diabetes.RESEARCH DESIGN AND METHODS: For prospective cohorts in Finland, Germany, Sweden, and the U.S., 24,662 children at increased genetic risk for development of islet autoantibodies and type 1 diabetes have been followed. Following harmonization, the outcomes were analyzed in 16,709 infants-toddlers enrolled by age 2.5 years.RESULTS: In the infant-toddler cohort, 1,413 (8.5%) developed at least one autoantibody confirmed at two or more consecutive visits (seroconversion), 865 (5%) developed multiple autoantibodies, and 655 (4%) progressed to diabetes. The 15-year cumulative incidence of diabetes varied in children with one, two, or three autoantibodies at seroconversion: 45% (95% CI 40-52), 85% (78-90), and 92% (85-97), respectively. Among those with a single autoantibody, status 2 years after seroconversion predicted diabetes risk: 12% (10-25) if reverting to autoantibody negative, 30% (20-40) if retaining a single autoantibody, and 82% (80-95) if developing multiple autoantibodies. HLA-DR-DQ affected the risk of confirmed seroconversion and progression to diabetes in children with stable single-autoantibody status. Their 15-year diabetes incidence for higher- versus lower-risk genotypes was 40% (28-50) vs. 12% (5-38). The rate of progression to diabetes was inversely related to age at development of multiple autoantibodies, ranging from 20% per year to 6% per year in children developing multipositivity in ≤2 years or >7.4 years, respectively.CONCLUSIONS: The number of islet autoantibodies at seroconversion reliably predicts 15-year type 1 diabetes risk. In children retaining a single autoantibody, HLA-DR-DQ genotypes can further refine risk of progression.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

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