☰ Table of contents
Types 1 and 2 diabetes are multifactorial, and there are currently no indications for genetic testing.
Approximately 2% of people with diabetes have maturity onset diabetes of the young (MODY), which is caused by a dominantly inherited variant in one of several known genes. It is important to identify these patients and family members, as there are implications for clinical management, including choice of treatment, prognosis and reproduction.1
What do I need to know?
MODY typically presents in the second to fourth decade of life, and does not fit the clinical picture of either types 1 or 2 diabetes. Presentation is often subacute or incidental. Many cases are misdiagnosed as types 1 or 2 diabetes.2,3
MODY is the only type of diabetes caused by a single gene mutation. Mutations in 13 genes are known to cause MODY. The most prevalent mutations are in the HNF1A, GCK and HNF4A genes. GCK-MODY constitutes 10–60% of all MODY cases.2
Testing for MODY should be considered in individuals with early onset diabetes with atypical features (ie not clearly type 1 or type 2):1
- atypical type 1 diabetes
- no history of diabetic ketoacidosis
- prandial plasma C-peptide >200 pmol/L and >5 years post-diagnosis of type 1 diabetes
- atypical type 2 diabetes
- <35 years of age
- absence of features of insulin resistance
- no obesity
- no dyslipidaemia
- no hypertension
- no polycystic ovary syndrome
- strong family history of diabetes.
If MODY is suspected, assess risk using the calculator available.
When should I refer?
Individuals with suspected MODY should be referred to an endocrinologist for assessment and consideration of genetic testing.
Resource for general practitioners
McElduff A. Non-type 1, non-type 2 diabetes: What’s in a name?
Resource for patients
Centre for Genetics Education, Fact sheet 48: Diabetes types 1 and 2 and inherited predisposition