Types 1 & 2
- Type 1 - absolute insulin deficiency due to autoimmune pancreatic destruction, typically diagnosed at a young age and requires insulin therapy
- Type 2 - insulin resistance and relative deficiency, with both genetic and environmental components that often coalesces with metabolic syndrome
Type 3, 4 and others
- Type 3 diabetes
- 3a - Monogenetic defects of β-cell function or insulin action e.g. MODY, neonatal diabetes
- 3b - Disease of the exocrine pancreas
- As part of other inherited disease states e.g. cystic fibrosis, haemochromatosis
- Following trauma, pancreatitis, infection, malignancy
- Post-pancreatectomy
- 3c - Endocrinopathies
- Cushing's disease
- Acromegaly
- Phaeochromocytoma
- Glucagonoma
- 3d - Drug-induced diabetes
- Thiazide diuretics
- Glucocorticoids
- β-blockers
- Post-organ transplant
- Type 4 - Gestational diabetes i.e. glucose intolerance during pregnancy
- Late-onset autoimmune diabetes in adults (LADA)