4.3 Article

Islet autoantibodies can discriminate maturity-onset diabetes of the young (MODY) from Type 1 diabetes

期刊

DIABETIC MEDICINE
卷 28, 期 9, 页码 1028-1033

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1464-5491.2011.03287.x

关键词

autoantibodies; GAD antibodies; GAD65; IA-2 antibodies; maturity-onset diabetes of the young

资金

  1. European Community [HEALTH-F2-2008-223211]
  2. Health Innovation Challenge Fund
  3. Wellcome Trust [091985/HICF 1009-041]
  4. Department of Health [091985/HICF 1009-041]
  5. NIHR Peninsula Clinical Research Facility, University of Exeter
  6. NIHR
  7. National Institute for Health Research [PDA/02/06/098] Funding Source: researchfish
  8. National Institutes of Health Research (NIHR) [PDA/02/06/098] Funding Source: National Institutes of Health Research (NIHR)

向作者/读者索取更多资源

Aim Maturity-onset diabetes of the young is amonogenic form of familial, young-onset diabetes. It is rare (similar to 1% diabetes) and may be misdiagnosed as Type 1 diabetes and inappropriately treated with insulin. Type 1 diabetes is characterized by the presence of islet autoantibodies, including glutamate decarboxylase (GAD) and islet antigen-2 (IA-2) antibodies. The prevalence of islet autoantibodies is unknown inmaturity-onset diabetes of the young and may have the potential to differentiate this form of diabetes from Type 1 diabetes. The aim of this study was to determine the prevalence of GAD and IA-2 antibodies in patients with maturity-onset diabetes of the young and Type 1 diabetes. Methods We measured plasma GAD and IA-2 antibodies in 508 patients with the most common forms of maturity-onset diabetes of the young (GCK: n = 227; HNF1A: n = 229; HNF4A: n = 52) and 98 patients with newly diagnosed Type 1 diabetes (diagnosed < 6 months). Autoantibodies were considered positive if >= 99th centile of 500 adult control subjects. Results GAD and/or IA-2 antibodies were present in 80/98 (82%) patients with Type 1 diabetes and 5/508 (< 1%) patients with maturity-onset diabetes of the young. In the cohort with Type 1 diabetes, both GAD and IA-2 antibodies were detected in 37.8% of patients, GAD only in 24.5% and IA-2 only in 19.4%. All five patients with maturity-onset diabetes of the young with detectable antibodies had GAD antibodies and none had detectable IA-2 antibodies. Conclusion The prevalence of GAD and IA-2 antibodies in maturity-onset diabetes of the young is the same as in control subjects (< 1%). The finding of islet autoantibodies, especially IA-2 antibodies, makes the diagnosis of maturity-onset diabetes of the young very unlikely and genetic testing should only be performed if other clinical characteristics strongly suggest this form of diabetes rather than Type 1 diabetes. This supports routine islet autoantibody testing before proceeding to more expensive molecular genetic testing.

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