It is not known to what extent characteristics of individuals modify C-peptide changes prior to T1D diagnosis. Thus, we assessed whether 4 characteristics [age, BMIZ, autoantibodies (abs), and HLA genotype] modified changes in 2-hr OGTT indices [AUC C-peptide and 30-0 minutes (early) C-peptide in ng/ml] during the progression to T1D. We studied 519 progressors to T1D (mean±SD age at first OGTT: 14.2±11.0 yo; BMIZ: 0.8±1.2; 50.0% male). Slopes were derived for changes in C-peptide indices from 36 to 6 months before diagnosis using mixed effects regression models. Slopes differed significantly by DR3/DR4 both (more inverse) vs. not both (30-0 minutes: p=0.005; AUC: p=0.034) and by ≥12.0 (more inverse) vs. <12.0 yo (30-0 minutes: p=0.002; AUC: p=0.001) with narrowed differences in C-peptide at 6 months. In contrast, the slopes were similar in 1 vs. ≥2 abs and BMIZ ≤1.0 vs. >1.0 comparisons. The Figures show curves for the changes in the C-peptide indices according to age and BMIZ categories from 36 to 6 months (* indicates significant differences at the 36 and 6 months time points). These novel findings indicate that slopes of C-peptide change vary according to DR3/DR4 and age during the progression to T1D, resulting in smaller differences at 6 months. BMIZ and ab slopes have little variation. Attributes of individuals should be considered when studying β-cell function decline during the progression to T1D.
Disclosure

H.M. Ismail: None. M.A. Cleves: None. S.E. Gitelman: Advisory Panel; Self; Avortes, Intermountain Therapeutics, Lilly Diabetes, Tolerion, Inc. Research Support; Self; Caladrius Biosciences, Inc., Janssen Research & Development. Other Relationship; Self; Novo Nordisk Inc. J.S. Skyler: Advisory Panel; Self; ADOCIA, Applied Therapeutics, Dance Biopharm Holdings Inc., Orgenesis Ltd., Tolerion, Inc., Viacyte, Inc. Board Member; Self; Dexcom, Inc., Intarcia Therapeutics, Inc., Moerae Matrix, Inc. Consultant; Self; AstraZeneca, Boehringer Ingelheim Pharmaceuticals, Inc., Dalcor, Dialogics, Elcelyx Therapeutics, Inc., Esperion, GeNeuro Innovation, Ideal Life, Immunomolecular Therapeutics, Intrexon, Kamada, Nestlé, Sanofi, Valeritas, Inc., Zafgen, Inc. Stock/Shareholder; Self; Dexcom, Inc., Ideal Life, Intarcia Therapeutics, Inc., Intrexon, Moerae Matrix, Inc. A. Steck: None. H. Rodriguez: Research Support; Self; Boehringer Ingelheim Pharmaceuticals, Inc., Bristol-Myers Squibb Company, Daiichi Pharm Corp, MannKind Corporation, Medtronic MiniMed, Inc. Research Support; Spouse/Partner; Medtronic MiniMed, Inc. Research Support; Self; Takeda Pharmaceutical Company Limited. Other Relationship; Self; Merck & Co., Inc., Novartis Pharmaceuticals Corporation, Novo Nordisk Inc. M.A. Atkinson: None. B.M. Nathan: None. M.J. Redondo: None. K.C. Herold: Consultant; Self; Provention Bio, Roche Pharma. J.P. Palmer: None. C. Evans-Molina: None. L. DiMeglio: Research Support; Self; Amgen Inc., Caladrius Biosciences, Inc., Janssen Research & Development, Medtronic, Sanofi. Other Relationship; Self; Dexcom, Inc. J.M. Sosenko: None.

Funding

National Institutes of Health

Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at http://www.diabetesjournals.org/content/license.