These two scenarios outline the clinical implications and management of early-onset type 2 diabetes, as well as the challenges inherent in correctly diagnosing younger adults who present with symptoms of diabetes.
Resources
At a glance factsheet: Early-onset and youth-onset type 2 diabetes. Diabetes & Primary Care 23: 69–70. Click here to access
How to correctly diagnose and classify diabetes. Diabetes & Primary Care 24: 107–10. Click here to access
Early-onset type 2 diabetes: Clinical implications, diagnosis and management. Journal of Diabetes Nursing 26: JDN267. Click here to access
References
Al-Saeed AH, Constantino MI, Molyneaux L et al (2016) An inverse relationship between age of type 2 diabetes onset and complication risk and mortality: the impact of youth-onset type 2 diabetes. Diabetes Care 39: 823–9
Buzzetti R, Tuomi T, Mauricio D et al (2020) Management of latent autoimmune diabetes in adults: a consensus statement from an international expert panel. Diabetes 69: 2037–47
Copeland KC, Zeitler P, Geffner M et al; TODAY Study Group (2011) Characteristics of adolescents and youth with recent-onset type 2 diabetes: The TODAY cohort at baseline. J Clin Endocrinol Metab 96: 159–67
Duggan SN, Conlon KC (2017) Pancreatogenic type 3c diabetes: Underestimated, underappreciated and poorly managed. Practical Gastroenterology 41: 14–23
ElSayed NA, Aleppo G, Aroda VR et al; American Diabetes Association (2023) 2. Classification and diagnosis of diabetes: Standards of Care in Diabetes – 2023. Diabetes Care 46(Suppl 1): S19–40
Lascar N, Brown J, Pattison H et al (2018) Type 2 diabetes in adolescents and young adults. Lancet Diabetes Endocrinol 6: 69–80
Misra S, Holman N, Barron E et al (2023) Characteristics and care of young people with type 2 diabetes included in the national diabetes audit datasets for England. Diabet Med 40: e14940
Morris D (2022a) The evolving role of SGLT2 inhibitors. Journal of Diabetes Nursing 26: JDN243
Morris D (2022b) Early-onset type 2 diabetes: Clinical implications, diagnosis and management. Journal of Diabetes Nursing 26: JDN267
Naik RG, Palmer JP (2003) Latent autoimmune diabetes in adults (LADA). Rev Endocr Metab Disord 4: 233–41
NICE (2022) Type 2 diabetes in adults: management [NG28]. Available at: https://www.nice.org.uk/guidance/ng28
NICE (2023a) Obesity: identification, assessment and management [CG189]. Available at: https://www.nice.org.uk/guidance/cg189
NICE (2023b) Diabetes (type 1 and type 2) in children and young people: diagnosis and management [NG18]. Available at: https://www.nice.org.uk/guidance/ng18
Thanabalasingham G, Owen KR (2011) Diagnosis and management of maturity onset diabetes of the young (MODY). BMJ 343: d6044
University of Exeter (2022) Diabetes Genes: What is maturity-onset diabetes of the young? Available at: http://www.diabetesgenes.org/what-is-mody/
Wilmot E, Idris I (2014) Early onset type 2 diabetes: Risk factors, clinical impact and management. Ther Adv Chronic Dis 5: 234–44
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Question 1 of 20
1. Question
Section 1 – Naseem
Naseem is a 37-year-old man of Asian ethnic origin who has made an appointment with the Nurse Practitioner. He reports increased frequency of micturition over a period of weeks, but when asked denies dysuria, abdominal pain, haematuria or fever.
A urine dipstick is performed and this shows an absent reaction for the presence of white cells, nitrite, blood or protein but does reveal glucose +++.
What further immediate test could you perform to help with a diagnosis?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 2 of 20
2. Question
Section 2
A fingerprick blood glucose reading would be useful in establishing the presence of hyperglycaemia and clarifying the likely diagnosis of diabetes.
Naseem’s capillary blood glucose reading is 15.6 mmol/L.
What further symptoms might you ask Naseem about to support the diagnosis of diabetes?
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Question 3 of 20
3. Question
Section 3
Ask about other osmotic symptoms: thirst and weight loss. Has Naseem been feeling unduly tired and has there been any evidence of recurrent or persistent infection – most notably genital thrush or skin eruptions such as boils?
Naseem reports feeling thirsty and tired and thinks he may have lost weight. He has not suffered from any unusual infections recently.
What is the most important type of diabetes to exclude here?
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Question 4 of 20
4. Question
Section 4
You should consider types of diabetes other than type 2 diabetes, especially in a younger person, and most importantly the possibility of type 1 diabetes.
What test would you perform to exclude an acute presentation of type 1 diabetes?
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Question 5 of 20
5. Question
Section 5
You need to check for diabetic ketoacidosis (DKA) by testing for ketones. Blood ketones are a more accurate and contemporaneous measure of ketosis than urinary ketones, so only resort to the latter if blood ketone measurement is not available. Table 1 helps you to interpret ketone levels and direct management (Morris, 2022a).
Table 1. Blood and urine ketone test results and interpretation.
Blood ketone concentration
Urine ketones dipstick
Interpretation
<0.6 mmol/L
Negative
Normal range
0.6–1.5 mmol/L
Trace or +
Potential problem; keep monitoring; seek medical advice if unwell
1.5–3.0 mmol/L
++
High risk of diabetic ketoacidosis; seek medical advice urgently
>3.0 mmol/L
+++/++++
Likely diabetic ketoacidosis; immediate medical review needed
Naseem’s blood ketone level is 0.2 mmol/L, ruling out DKA and making type 1 diabetes unlikely.
So what is the most likely form of diabetes that Naseem has? What further information should you seek that would support this diagnosis?
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Question 6 of 20
6. Question
Section 6
Type 2 diabetes seems the most likely diagnosis, and Naseem’s ethnicity would be a clear risk factor for this condition. You should check Naseem’s BMI and ask about family history of type 2 diabetes.
Naseem’s BMI is 28.6 kg/m2 which, given his ethnicity, would place him in a similar overweight category as an obese Caucasian with a BMI of 30 kg/m2 or more (NICE, 2023a).
Both Naseem’s father and mother have been diagnosed with type 2 diabetes, at around the ages of 50 and 60 years, respectively.
What would you consider to be “early-onset” type 2 diabetes?
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Question 7 of 20
7. Question
Section 7
Early-onset type 2 diabetes is generally accepted as being that which occurs below the age of 40 years (Misra et al, 2023), with a further division often made between children/adolescents (<18 years) and younger adults (18 years or more). Whilst these are somewhat arbitrary cut-offs, there is no doubt that the population distribution of type 2 diabetes has shifted to include those of a younger age.
Early-onset type 2 diabetes is a rapidly developing problem. Why do you think this is the case?
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Question 8 of 20
8. Question
Section 8
The principal driver of the increased incidence of early-onset type 2 diabetes is the epidemic of overweight and obesity.
Can you make a list of the risk factors for early-onset type 2 diabetes?
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Question 9 of 20
9. Question
Section 9
Box 1 lists the key risk factors for developing early-onset type 2 diabetes, which are very similar to those for type 2 diabetes in older adults. Most prominently, they include obesity (in around 90% of cases), family history (again, in nearly 90% of cases, reflecting both genetic predisposition and similar living environment) and ethnicity (Copeland et al, 2011; Wilmot and Idris, 2014).
Box 1. Risk factors for development of early-onset type 2 diabetes (Morris, 2022b). - Obesity
- Physical inactivity
- Strong family history of type 2 diabetes
- Black, Asian and Hispanic ethnicity
- Female sex
- Socioeconomic deprivation
- Personal or maternal history of gestational diabetes
- Polycystic ovarian syndrome
In the absence of ketosis, what clinical features might make you suspect underlying type 1 diabetes?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 10 of 20
10. Question
Section 10
Rapid progress of osmotic symptoms (thirst, polyuria, weight loss) typically feature in type 1 diabetes. A family history of type 1 diabetes and a personal or family history of other autoimmune conditions (e.g. thyroid disease) increase the likelihood of type 1 diabetes.
If you do clinically suspect type 1 diabetes, how would you manage this situation?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 11 of 20
11. Question
Section 11
As previously indicated, the presence of significant ketosis requires immediate hospital admission. In the absence of ketosis then urgent referral to the specialist diabetes team is indicated for further investigations and consideration of insulin initiation.
In the case of children and young people with new-onset diabetes, it is safer to assume type 1 diabetes (even if there are good reasons to suspect type 2 diabetes) until proven otherwise, and to arrange same-day assessment with the paediatric diabetes team. Insulin can be commenced whilst the outcomes of further investigations are awaited, after which the condition can be safely re-assessed (NICE, 2023b).
Apart from type 1 diabetes, what other types of diabetes could you consider in a younger adult you think has type 2 diabetes?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 12 of 20
12. Question
Section 12
Possibilities include:
- Latent autoimmune disease in adults (LADA, or slowly evolving immune-mediated diabetes).
- Maturity-onset diabetes of the young (MODY).
- Pancreatogenic (type 3c) diabetes.
Can you think of any clinical features that might suggest these alternative diagnoses?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 13 of 20
13. Question
Section 13
LADA, like type 1 diabetes, is an autoimmune condition in which antibodies are directed against pancreatic beta-cells, so review personal and family history of autoimmune disease. However, in contrast to type 1 diabetes, the progression to insulin dependence in LADA can take several years and, initially at least, the condition can be managed with oral glucose-lowering agents; thus, LADA is often initially mislabelled as type 2 diabetes (Naik and Palmer, 2003; Buzzetti et al, 2020).
A strong family history of diabetes across multiple generations is to be expected with MODY, as the inheritance pattern is autosomal dominant (i.e. there is a 50% chance of passing on the condition to the next generation; Thanabalasingham and Owen, 2011). If MODY is initially diagnosed as type 2 diabetes then response to metformin is usually poor, whilst there can be marked sensitivity to sulfonylurea therapy. Referral for genetic testing allows a definitive diagnosis of MODY (University of Exeter, 2022).
A further possibility is pancreatogenic diabetes. A past history of pancreatitis (responsible for 75% of cases) may be suggestive of this diagnosis, although if this is the pathology then diabetes usually occurs over the age of 40 years. You could seek a history of upper abdominal pain and establish alcohol consumption.
Pancreatogenic diabetes can, however, occur at a younger age with genetic conditions such as cystic fibrosis. Look out for gastrointestinal symptoms such as upper abdominal pain, steatorrhoea and weight loss, which could indicate malabsorption secondary to pancreatic enzyme insufficiency, which usually precedes the onset of diabetes (Duggan and Conlon, 2017; ElSayed et al, 2023).
Characteristics of these different types of diabetes are summarised in Table 2 (Morris, 2022b).
Referral to secondary care is indicated to establish these diagnoses.
Table 2. Features of early-onset diabetes diagnoses.
Clinical feature
Early onset type 2 diabetes
Type 1 diabetes
MODY
LADA
Pancreatogenic
diabetes
Age of onset
>10 years; increasing incidence with age
Any age from early childhood; commonly young children and adolescents
Commonly 10–30 years
Usually >30 years
Chronic pancreatitis: usually >40 years;
Cystic fibrosis: usually before 30 years
Family history
Type 2 diabetes in family very common
Can be type 1 diabetes or other autoimmune disease in family but often absent
Very strong: autosomal dominant inheritance
May be history of autoimmune disease in family
Relevant only in inherited cases
Ethnicity
Increased risk in Black African, African–Caribbean, South Asian, American Hispanic
All ethnicities affected, more common in Caucasians
All ethnicities affected, more common in Caucasians
All ethnicities affected
All ethnicities affected
Obesity
Very common
Uncommon (but increasing)
Uncommon (but increasing)
Uncommon (but increasing)
Uncommon (but increasing)
Gender
Female > Male
Female = Male
Female = Male
Female = Male
Gender independent
Presentation with DKA
Uncommon
Common
Rarely
May occur several years after diagnosis
Rarely
Islet cell autoantibodies
Uncommon
Common
Uncommon
Common
Uncommon
C-peptide (insulin) levels
Normal
Low
Normal
Lower than type 2 diabetes, greater than type 1 diabetes
Low
DKA=diabetic ketoacidosis; LADA=latent autoimmune disease in adults; MODY=maturity-onset diabetes of the young.
It looks like Naseem has type 2 diabetes. How would you confirm this diagnosis?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 14 of 20
14. Question
Section 14
We need just one HbA1c reading of 48 mmol/mol or more to confirm the diagnosis of diabetes because Naseem is symptomatic.
Naseem is given dietary advice and asked to monitor fingerprick blood glucose readings. A baseline set of blood tests are arranged.
Naseem’s HbA1c comes back at 73 mmol/mol, confirming the diagnosis of diabetes. Urea and electrolytes, eGFR, liver function tests, thyroid function tests and full blood counts are all within the normal range; however, there is an adverse lipid profile. Fingerprick glucose readings have been in the range of 10–18 mmol/L.
How would you initially manage Naseem’s hyperglycaemia?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 15 of 20
15. Question
Section 15
In line with NICE (2022) NG28 guidance, start metformin at low dose with plans for gradual dose uptitration.
It would also be reasonable to offer low-dose gliclazide (say, 40 mg twice daily) to achieve immediate lowering of blood glucose and provide relief of osmotic symptoms of diabetes. Once glucose control has been established and stabilised with metformin, consideration could be given to withdrawing the gliclazide and, if necessary, adding in a more suitable agent for hyperglycaemia, such as an SGLT2 inhibitor, which will facilitate weight loss and carry a lower risk of hypoglycaemia.
Naseem is commenced on low doses of metformin and gliclazide and given advice on avoiding simple sugars in his diet and restricting starchy carbohydrate intake. He is referred to be seen in the practice diabetes clinic the following week.
What needs to be covered in Naseem’s first diabetes clinic appointment?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 16 of 20
16. Question
Section 16
Firstly, reinforce the importance of lifestyle issues – diet, exercise and weight loss – and offer Naseem referral to a diabetes educational programme (NICE, 2022).
You should also give due consideration to Naseem’s cardiovascular risk factors, controlling his blood pressure to 140/90 mmHg and introducing a statin if indicated by QRISK assessment.
Naseem needs to be enrolled for retinopathy and podiatry screening, and a urine sample should be sent for albuminuria screening.
How aggressive a condition do you think early-onset type 2 diabetes is in comparison to type 2 diabetes developing at a later age?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 17 of 20
17. Question
Section 17
Early-onset type 2 diabetes is regarded as a more aggressive disease than later-onset type 2 diabetes. This is in part due to longer exposure to hyperglycaemia; however, the early-onset form is also thought to be a more rapidly progressive condition in itself. People with early-onset type 2 diabetes are vulnerable to microvascular and macrovascular complications at an earlier age (Al-Saeed et al, 2016; Lascar et al, 2018).
For these reasons, and also if there is any doubt over the correct diagnosis of type 2 diabetes, you should have a low threshold for referring those with early-onset type 2 diabetes to specialist care.
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Question 18 of 20
18. Question
Section 18 – Tamsin
Tamsin is a 29-year-old lady of Caucasian ethnicity without significant past medical history. She sees her GP with thirst, weight loss and recurrent genital thrush and is found to have a raised fingerprick glucose level of 12.7 mmol/L but no indication of ketosis.
Tamsin has a BMI of 25.7 kg/m2. She is physically active, has no history of autoimmune disease, has not been diagnosed with polycystic ovarian syndrome and has never been pregnant. There is no history of pancreatitis, recurrent abdominal pain, loose offensive stools or excessive alcohol consumption. Tamsin’s father receives treatment for type 2 diabetes and her deceased paternal grandmother also suffered from diabetes, although Tamsin is uncertain of the details. She has no siblings.
Blood tests are performed and an HbA1c comes back at 67 mmol/mol.
What are you thinking diagnostically for Tamsin?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 19 of 20
19. Question
Section 19
This may represent early-onset type 2 diabetes, considering Tamsin’s family history, but she is only marginally overweight, not from an ethnic group at high risk of type 2 diabetes and is unusually young to develop type 2 diabetes. You should, therefore, consider other possible types of diabetes that could affect someone of this age.
The absence of ketosis argues against type 1 diabetes, and there are no pointers towards pancreatogenic diabetes. The family history could suggest MODY (three generations affected and always the possibility that her father may have been mislabelled as having type 2 diabetes). LADA is certainly a possibility.
How would you manage Tamsin’s situation?
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This response will be awarded full points automatically, but it can be reviewed and adjusted after submission.
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Question 20 of 20
20. Question
Section 20
It would be wise to refer Tamsin to the specialist diabetes team to clarify this diagnosis. Pancreatic autoantibodies and C-peptide levels would be helpful in these circumstances.
In the meantime, it is reasonable to start treatment for type 2 diabetes, as discussed in Sections 15 and 16. There is always the possibility of decompensation to DKA if the underlying diagnosis is type 1 diabetes or LADA, so Tamsin should be warned of danger symptoms suggesting DKA and asked to monitor her fingerprick glucose readings regularly for any sudden rise. Should these occur, she should seek immediate medical review and be tested for ketones.