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Genetic and environmental interactions modify the risk of diabetes-related autoimmunity by 6 years of age: The teddy study

  • Jeffrey P. Krischer(corresponding author)
    ,
  • Kristian F. Lynch
    ,
  • Ake Lernmark
    ,
  • William A. Hagopian
    ,
  • Marian J. Rewers
    ,
  • Jin Xiong She
*Corresponding author for this work
  • University of South Florida
    ,
  • Lund University
    ,
  • Pacific Northwest Diabetes Research Institute
    ,
  • Barbara Davis Center for Childhood Diabetes
    ,
  • ,
  • University of Turku
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

OBJECTIVE We tested the associations between genetic background and selected environmental exposures with respect to islet autoantibodies and type 1 diabetes. RESEARCH DESIGN AND METHODS Infants with HLA-DR high-risk genotypes were prospectively followed for diabetesrelated autoantibodies. Single nucleotide polymorphisms (SNPs) came from the Illumina ImmunoChip and environmental exposure data were by parental report. Children were followed to age 6 years. RESULTS Insulin autoantibodies occurred earlier than GAD antibody (GADA) and then declined, while GADA incidence rose and remained constant (significant in HLA-DR4 but not in the DR3/3 children). The presence of SNPs rs2476601 (PTPN22) and rs2292239 (ERBB3) demonstrated increased risk of both autoantibodies to insulin (IAA) only and GADA only. SNP rs689 (INS) was protective of IAA only, but not of GADA only. The rs3757247 (BACH2) SNP demonstrated increased risk of GADA only. Male sex, father or sibling as the diabetic proband, introduction of probiotics under 28 days of age, and weight at age 12 monthswere associated with IAA only, but only father as the diabetic proband and weight at age 12 months were associated with GADA only. Mother as the diabetic proband was not a significant risk factor. CONCLUSIONS These results show clear differences in the initiation of autoimmunity according to genetic factors and environmental exposures that give rise to IAAorGADA as the first appearing indication of autoimmunity.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1194-1202 (9 pages)

Journal (Volume, Issue Number)

Diabetes Care (Volume 40, Issue 9)

Publication milestones

  • Published - 09/01/2017

Publication status

Published - 09/01/2017

ISSN

0149-5992

Publication IDs

  • Scopus: 85028082327
  • PubMed: 28646072

Publication metrics

Metrics

SciVal
citations
71
Scopus
citations
SciVal
FWCI
6.75
SciVal
Author count
9
SciVal
Paper percentile
98
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.11
Fractional count
8
Fractional count
0.89
Fractional count
1
Fractional count
1

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Captures
134
Citation count
177
Mentions
1

Funding Details

acknowledgment to the TEDDY families for their continued participation in this wonderful study. Duality of Interest. No potential conflicts of interest relevant to this article were reported. Author Contributions. All authors attest to meetingtheInternationalCommitteeofMedical Journal Editors uniform requirements for authorship by making substantial contributions to the conception and design of the manuscript; acquisition, analysis, and interpretation of data; drafting or revising the article for intellectual content; and giving final approval of the published version. J.P.K. designed the study, proposed the analysis, interpreted the findings, and wrote the manuscript. K.F.L. performed the analysis and drafted and revised the manuscript. \u00C5.L., W.A.H., M.J.R., J.-X.S., J.T., A.-G.Z., and B.A. designed the study and reviewed and edited the manuscript. J.P.K. and K.F.L. are the guarantors of this work and, as such, had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Funding. This study was funded by grants U01-DK-63829, U01-DK-63861, U01-DK-63821, U01-DK-63865, U01-DK-63863, U01-DK-63836, U01-DK-63790, UC4-DK-63829, UC4-DK-63861, UC4-DK-63821, UC4-DK-63865, UC4-DK-63863, UC4-DK-63836, and UC4-DK-95300 and contract no. HHSN267200700014C from the National Institute of Diabetes and Digestive and Kidney Diseases,NationalInstituteofAllergyandInfectious Diseases, National Institute of Child Health and Human Development, National Institute of Environmental Health Sciences, JDRF, and Centers for Disease Control and Prevention. This work was also supported in part by National Institutes of Health/National Center for Advancing Translational Sciences Clinical and Translational Science Awards to the University of Florida (UL1 TR000064) and the University of Colorado (UL1 TR001082).
FundersFunding numbers
National Institute for Child Health and Human Development
-
University of Colorado Colorado Springs
-
UC4-DK-63821
-
Centers for Disease Control and Prevention
-
UC4-DK-63861
-
UC4-DK-63865
-
UC4-DK-63836
-
UC4-DK-63829
-
UC4-DK-95300
-
University of Southern Florida
-
Foundation for Neurologic Diseases
-
National Institute of Environmental Health Sciences
-
JDRF
-
UC4-DK-63863
-
NCATS
UL1TR001082, UL1TR001427, UL1TR000064
NIDDK
P30DK048520, UC4DK106955, UC4DK095300, U01DK063829, U01DK063861, U01DK063863, UC4DK063836, U01DK063790, UC4DK112243, UC4DK100238, UC4DK063821, UC4DK063865, UC4DK117483