PMID- 17062766 OWN - NLM STAT- MEDLINE DCOM- 20070220 LR - 20221207 IS - 0021-972X (Print) IS - 0021-972X (Linking) VI - 92 IP - 1 DP - 2007 Jan TI - Prevalence of autoantibody-negative diabetes is not rare at all ages and increases with older age and obesity. PG - 88-92 AB - OBJECTIVE: A significant percentage of nonautoimmune forms of diabetes presents among children in all age groups, with a remarkable increase with age. DESIGN: From October 1992 to October 2004, a total of 859 children less than 18 yr of age were newly diagnosed with diabetes at the Barbara Davis Center for Childhood Diabetes and had blood samples obtained within 2 wk of disease onset for analysis of antiislet autoantibodies to glutamic acid decarboxylase-65, insulinoma-associated antigen-2, insulin, and islet cell autoantibodies. The relationship of autoantibody positivity with human leukocyte antigen (HLA) class II, body mass index (BMI), glycosylated hemoglobin, age, and ethnicity was analyzed. RESULTS: Overall 19% (159 of 859) of these children with newly diagnosed diabetes were negative for all autoantibodies, and autoantibody negativity was significantly increased with age (P < 0.01). The Hispanic and Black subjects had significantly increased autoantibody negativity among older children with higher BMI than White subjects. The patients with the highest risk HLA genotype, DR3-DQ2/DR4-DQ8, were significantly less autoantibody negative (P = 0.001), whereas the HLA-protective allele, DQB1*0602, was significantly increased among the autoantibody-negative patients (P < 0.0001). Insulin autoantibodies were dramatically age dependent and were inversely correlated with age in both prevalence (P < 0.0001) and levels (P < 0.0001). Autoantibody positivity was inversely correlated with both BMI and age using multivariate analysis (P < 0.0001 and P = 0.0078, respectively). CONCLUSIONS: A significant percentage of children newly diagnosed with diabetes are negative for all antiislet autoantibodies with a marked increase in obesity-associated autoantibody-negative diabetes after age 10, suggesting diabetes heterogeneity at all ages. FAU - Wang, Jian AU - Wang J AD - Barbara Davis Center for Childhood Diabetes, University of Colorado Health Sciences Center, PO Box 6511, Mail Stop B140, Aurora, Colorado 80045-6511, USA. FAU - Miao, Dongmei AU - Miao D FAU - Babu, Sunanda AU - Babu S FAU - Yu, Jeesuk AU - Yu J FAU - Barker, Jennifer AU - Barker J FAU - Klingensmith, Georgeanna AU - Klingensmith G FAU - Rewers, Marian AU - Rewers M FAU - Eisenbarth, George S AU - Eisenbarth GS FAU - Yu, Liping AU - Yu L LA - eng GR - DK32083/DK/NIDDK NIH HHS/United States GR - N01AI15416/AI/NIAID NIH HHS/United States GR - U19AI050864/AI/NIAID NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20061024 PL - United States TA - J Clin Endocrinol Metab JT - The Journal of clinical endocrinology and metabolism JID - 0375362 RN - 0 (Autoantibodies) RN - 0 (Glycated Hemoglobin A) RN - 0 (HLA-DQ Antigens) RN - 0 (HLA-DQ beta-Chains) RN - 0 (HLA-DQB1 antigen) RN - 0 (HLA-DR Antigens) RN - 0 (islet cell antibody) RN - EC 4.1.1.15 (Glutamate Decarboxylase) SB - IM MH - Adolescent MH - Age Factors MH - Autoantibodies/*blood MH - Body Mass Index MH - Child MH - Child, Preschool MH - Diabetes Mellitus/*immunology MH - Female MH - Glutamate Decarboxylase/immunology MH - Glycated Hemoglobin/analysis MH - HLA-DQ Antigens/genetics MH - HLA-DQ beta-Chains MH - HLA-DR Antigens/genetics MH - Humans MH - Infant MH - Male MH - Obesity/*immunology EDAT- 2006/10/26 09:00 MHDA- 2007/02/21 09:00 CRDT- 2006/10/26 09:00 PHST- 2006/10/26 09:00 [pubmed] PHST- 2007/02/21 09:00 [medline] PHST- 2006/10/26 09:00 [entrez] AID - jc.2006-1494 [pii] AID - 10.1210/jc.2006-1494 [doi] PST - ppublish SO - J Clin Endocrinol Metab. 2007 Jan;92(1):88-92. doi: 10.1210/jc.2006-1494. Epub 2006 Oct 24.