Oral Insulin Delay of Stage 3 Type 1 Diabetes Revisited in HLA DR4-DQ8 Participants in the TrialNet Oral Insulin Prevention Trial (TN07)

Author:

Zhao Lue Ping12ORCID,Papadopoulos George K.3ORCID,Skyler Jay S.4ORCID,Parikh Hemang M.5,Kwok William W.6,Bondinas George P.7,Moustakas Antonis K.7,Wang Ruihan8,Pyo Chul-Woo8,Nelson Wyatt C.8,Geraghty Daniel E.8,Lernmark Åke9ORCID

Affiliation:

1. 1Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA

2. 2School of Public Health, University of Washington, Seattle, WA

3. 3Laboratory of Biophysics, Biochemistry, Biomaterials and Bioprocessing, Faculty of Agricultural Technology, Technological Educational Institute of Epirus, Arta, Greece

4. 4Diabetes Research Institute and Division of Endocrinology, Diabetes, and Metabolism, University of Miami Miller School of Medicine, Miami, FL

5. 5Health Informatics Institute, Morsani College of Medicine, University of South Florida, Tampa, FL

6. 6Benaroya Research Institute, Seattle, WA

7. 7Department of Food Science and Technology, Faculty of Environmental Sciences, Ionian University, Argostoli, Cephalonia, Greece

8. 8Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA

9. 9Department of Clinical Sciences, Lund University CRC, Skåne University Hospital, Malmö, Sweden

Abstract

OBJECTIVE To explore if oral insulin could delay onset of stage 3 type 1 diabetes (T1D) among patients with stage 1/2 who carry HLA DR4-DQ8 and/or have elevated levels of IA-2 autoantibodies (IA-2As). RESEARCH AND METHODS Next-generation targeted sequencing technology was used to genotype eight HLA class II genes (DQA1, DQB1, DRB1, DRB3, DRB4, DRB5, DPA1, and DPB1) in 546 participants in the TrialNet oral insulin preventative trial (TN07). Baseline levels of autoantibodies against insulin (IAA), GAD65 (GADA), and IA-2A were determined prior to treatment assignment. Available clinical and demographic covariables from TN07 were used in this post hoc analysis with the Cox regression model to quantify the preventive efficacy of oral insulin. RESULTS Oral insulin reduced the frequency of T1D onset among participants with elevated IA-2A levels (HR 0.62; P = 0.012) but had no preventive effect among those with low IA-2A levels (HR 1.03; P = 0.91). High IA-2A levels were positively associated with the HLA DR4-DQ8 haplotype (OR 1.63; P = 6.37 × 10−6) and negatively associated with the HLA DR7–containing DRB1*07:01-DRB4*01:01-DQA1*02:01-DQB1*02:02 extended haplotype (OR 0.49; P = 0.037). Among DR4-DQ8 carriers, oral insulin delayed the progression toward stage 3 T1D onset (HR 0.59; P = 0.027), especially if participants also had high IA-2A level (HR 0.50; P = 0.028). CONCLUSIONS These results suggest the presence of a T1D endotype characterized by HLA DR4-DQ8 and/or elevated IA-2A levels; for those patients with stage 1/2 disease with such an endotype, oral insulin delays the clinical T1D onset.

Funder

Division of Diabetes, Endocrinology, and Metabolic Diseases

Publisher

American Diabetes Association

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