In recent years there has been an increase in the incidence and prevalence of type 2 diabetes in children, adolescents and young adults.2,3 This early-onset (also called ‘young-onset’) type 2 diabetes is concerning because it results in a longer lifetime exposure to hyperglycaemia and consequent complications. There is also emerging evidence that early-onset type 2 diabetes is a more aggressive disease than later-onset type 2 diabetes and is accompanied by the earlier onset and more rapid progression of macrovascular and microvascular complications.3–6
Table 1. Comparison of type 1 diabetes, type 2 diabetes and monogenic diabetes7–9
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Type 1 diabetes
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Type 2 diabetes
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Monogenic diabetes
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Clinical features
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Usual onset
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Acute
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Insidious
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Variable
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Osmotic symptoms
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Pronounced
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Not evident unless in cases of severe hyperglycaemia
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Variable
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Ketosis
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May be present at diagnosis and risks may be ongoing
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Usually not present but may occur with the use of an SGLT2i
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Common in neonatal forms; rare in others
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Obesity
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Can co-exist as per general population; weight loss is more usual prior to or at diagnosis
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Often obese – up to 85%
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Usually not obese
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Signs of insulin resistance (eg acanthosis nigricans)
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Rare
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Often present
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Rare
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Family history in parents
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2–4%
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80%
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90%
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Diagnostic aid biomarkers
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Antibodies
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IAA, ICA, GAD, IA-2, IA-2β or ZnT8 antibodies present in 85–95% of cases
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Usually not present
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Not present
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C-peptide
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Below normal range (<0.2 nmol/L)9
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Normal or above normal range (>0.2 nmol/L)9
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Normal
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Genetic test
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If family history of diabetes (eg autosomal dominant), see monogenic diabetes for exclusion purposes
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In early onset diabetes (age <30 years) atypical presentations* or autosomal dominant family history of diabetes, consider monogenic diabetes for exclusion purposes or seek specialist endocrinology advice
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Common positive genetic mutations:
HNF4A, HNF1A, GCK
(seek specialist advice)
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*For example, failure to respond to glycaemic management options for type 2 diabetes.
GCK, glucokinase; HNF1A, HNF1 homeobox A; HNF4A, hepatocyte nuclear factor 4 alpha; SGLT2i, sodium–glucose cotransporter 2 inhibitor.
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Definitions and diagnosis
Early-onset type 2 diabetes is usually defined as occurring under the age of 30 years.1 This can be further separated into child and adolescent (<18 years) and young adult (<30 years) onset. However, there is no consistency of definitions across the literature, especially of the upper age limit. Although this handbook refers only to the young adult group, there is clearly a continuum across the age groups.
Unlike older-onset type 2 diabetes, this group can offer a diagnostic challenge for general practitioners to differentiate between type 1 diabetes, latent autoimmune disease of adults, type 2 diabetes and monogenic diabetes (Table 1). Careful diagnostic assessment is required, because this has a major impact on management and outcome.7
For children and adolescents, hyperglycaemia (at levels diagnostic of diabetes) can be a medical emergency, and immediate referral to an emergency department or, if not available, urgent consultation with a specialist is strongly recommended. For more information, refer to The Royal Australian College of General Practitioners’ Emergency management of hyperglycaemia in primary care.
Screening and risk factors
Risk factors for early-onset type 2 diabetes include:1
- a maternal history of type 2 diabetes or gestational diabetes during an individual’s gestation
- a family history of type 2 diabetes in a first-degree relative
- certain ethnicity (Aboriginal and Torres Strait Islander, South Asian, South-East Asian, North African, Latin American, Middle Eastern, Māori or Pacific Islander people [includes individuals of mixed ethnicity])
- clinical evidence of insulin resistance (polycystic ovary syndrome, acanthosis nigricans, dyslipidaemia, hypertension) or existing macrovascular disease, impaired fasting glucose, impaired glucose tolerance or history of gestational diabetes
- the use of antipsychotic medications.
There are no specific tools currently available for the screening or early detection of early-onset type 2 diabetes other than maintaining a high index of suspicion, especially in high-risk groups.
Treatment challenges
Compared with late-onset type 2 diabetes, the early-onset group is more likely to have suboptimal glycaemic management,10 diastolic hypertension, an earlier need to initiate insulin and a greater burden of diabetes-related complications (Box 1), resulting in a reduced quality of life, greater morbidity and premature mortality.
In the cohort of people with early-onset type 2 diabetes, life expectancy is reduced by 14 years for males and 16 years for females compared with those without diabetes.3 An Australian study showed 11% mortality over 20 years in a cohort of young adults diagnosed between the ages of 15 and 30 years.11
Box 1. Complications in early-onset type 2 diabetes compared with older-onset type 2 diabetes3,12
Lifetime risk of complications greater with onset at a younger age
Life expectancy reduced
Non-alcoholic fatty liver disease is twice as common
Earlier onset of microalbuminuria and end-stage renal failure
Earlier onset and greater prevalence of diabetic retinopathy
Earlier onset of neuropathy
Apolipoprotein B concentration is higher despite statin therapy
Risk of myocardial infarction is 14-fold higher compared with same-age counterparts, compared with a two- to fourfold higher risk in older-onset type 2 diabetes
Early onset of diastolic myocardial dysfunction
Reduced fertility and greater pregnancy complications
Risk of premature decline in cognitive function
Higher rate of diabetes-related psychological distress and psychological issues, especially depression
Limited work capacity and consequent socioeconomic impact
Reduced quality of life