This site is intended for healthcare professionals only

DiabetesontheNet Logo
×

Diabetes &
Primary Care

Issue:

Share this article
Share on facebook
Share on twitter
Share on email
Share on print

Screening for type 2 diabetes in primary care: Is it feasible?

There are more than 1.75 million people with type 2 diabetes in the UK, and the number of people diagnosed with type 2 diabetes is set to rise dramatically over the next decade. The UK Prospective Diabetes Study (UKPDS) provided evidence to support early active treatment of type 2 diabetes in order to reduce the risk of future complications (UKPDS Group, 1998). This article assesses the feasibility of screening for type 2 diabetes at the GP practice level.

Standard 2 of the National Service Framework (NSF) for diabetes (Department of Health [DoH], 2001) relates to the development and implementation of strategies to identify people with diabetes. The aim is to ensure that people with diabetes are identified as early as possible. Moreover, the NSF concludes that population-wide screening would not be cost-effective, and instead recommends screening sub-groups with multiple risk factors. Diabetes UK also supports the introduction of a screening programme, recommending systematic and opportunistic screening of people with two or more risk factors every 3 years (Diabetes UK, 2002).

It would seem to be a sensible step forward, then, to actively screen for diabetes, but how practical is this in primary care? The National Screening Committee (http://www.nsc.nhs.uk/ [accessed 23.09.2005]) has been asked to research the feasibility of a screening programme and is due to report later this year.

The scale of the problem in the UK
More than 100 000 people are diagnosed with diabetes every year (which is roughly one person every 5 minutes; Diabetes UK, 2004). Furthermore, rising levels of obesity (Chan et al, 1994), trends towards more sedentary lifestyles and an ageing population are all likely to increase the numbers rapidly. And the much talked about ‘missing million’ is likely to be an underestimate of the number of people who remain undiagnosed.

The National Health Service (NHS) currently spends more than £10million a day on diabetes-related care (Diabetes UK, 2004); put another way, around 5% of total NHS resources are used for the care of people with diabetes.

Prevention is better than cure
Insulin resistance is now widely recognised as the common underlying link between environmental and genetic factors that give rise to type 2 diabetes (Turner and Clapham, 1998). It precedes clinical development of the condition by 10–20 years. During this period, many people will have developed impaired glucose tolerance (IGT), which is a ‘pre-diabetic state’.

Fuller et al (1980) have shown that people with IGT are at an increased risk of developing cardiovascular disease and that IGT is an independent risk factor for coronary heart disease. Subsequently, Lundblad and Eliasson (2003) have also demonstrated that IGT is associated with electrocardiogram findings indicating silent myocardial infarction in women in a middle-aged general population in northern Sweden. The results persisted even after adjusting for known risk factors.

Twenty to fifty per cent of people with IGT go on to develop diabetes over a 10-year period (Alberti, 1998). There is evidence, however, that lifestyle intervention (Tuomilehto et al, 2001; Ryan and the Diabetes Prevention Program Research Group, 2003) and drug treatment with metformin (Knowler et al, 2002; Diabetes Prevention Program Research Group, 2003) can significantly reduce the risk of going on to develop diabetes.

Early detection of diabetes
More than 50% of people with newly diagnosed diabetes will already have evidence of some form of complication (Figure 1). Harris et al (1992) demonstrated that the onset of type 2 diabetes occurs at least 4–7 years before clinical diagnosis. Detecting the condition at an early stage or during the pre-diabetes phase of IGT may reduce the burden of these complications.

Criteria for a screening test
The National Screening Committee has requested further evidence that would support the introduction of a screening programme. Below is a summary of the core criteria by which a potential screening programme could be evaluated. It is by no means an exhaustive list of all the criteria that would be applied.

The condition should be an important health problem
There is little doubt about this point. Nationally collated Quality and Outcomes Framework data (Health and Social Care Information Centre, 2005) indicate a known prevalence of diabetes in England of 3.3%. The prevalence of undiagnosed cases is of a similar order to previously known prevalences (Forrest et al, 1986; Williams et al, 1995). The prevalence of the condition increases with age (Williams 1995) and is higher in certain ethnic groups (Hamman, 1992). The condition itself results in a significant burden of premature morbidity and mortality, with attendant costs to the individual and society as a whole. For example, 21% of people with newly diagnosed diabetes have evidence of retinopathy and 18% have evidence of nephropathy at the time of diagnosis (UK Prospective Diabetes Study Group, 1990; Figure 1). Holmes et al (2003) demonstrated the significant impact in terms of finance and quality of life of diabetes on those with the condition.

The epidemiology and natural history of the condition should be understood
Population studies have identified the incidence of the condition and risk factors for progression to diabetes (e.g. Hamman, 1992). Köbberling and Tillil (1982) calculated that the lifetime risk of diabetes for someone with a parental history of diabetes was as high as 40%. Morris et al (1989) showed that this is affected by other factors, including a sedentary lifestyle and obesity. The natural history of the condition is now well understood, with several established risk factors such as a history of IGT and obesity. Up to 5% of people with IGT will progress to diabetes every year. Diabetes is also strongly associated with metabolic disturbances such as insulin resistance (which is seen in 92% of people with type 2 diabetes) and dyslipidaemia, as shown by Haffner et al (1990).

There should be an identifiable latent period or early symptomatic stage
As is already known from Harris et al (1992), many people with diabetes remain asymptomatic and undiagnosed for a number of years. At diagnosis, around 50% will have some evidence of a complication. Eriksson and Lindgarde (1991) showed that in at-risk groups such as those with IGT – which, as mentioned earlier, can be considered a pre-diabetic state – lifestyle interventions (including diet modification and exercise) reduced the incidence of progression to type 2 diabetes by over 50%.

There should be an acceptable safe and reliable screening test available
Several tests could be employed, including random and fasting plasma glucose levels, HbA1c levels, dipstick urinalysis and the glucose tolerance test (GTT). Andersson et al (1993) showed that urinalysis for glycosuria has a high specificity (proportion of true negatives; 96–100%) but a low sensitivity (proportion of true positives; 16–43%). Random blood glucose testing was also shown to be specific but non-sensitive.

McCance et al (1994) compared fasting glucose, HbA1c and the 2-hour post-challenge GTT and found that they all predicted the future risk of microvascular complications and potentially have a role in both screening and diagnosis. The tests appear to be acceptable to the patients using them, as reflected in the high uptake of testing in some of the screening studies undertaken. Diagnostic criteria have been quite clearly set out by Alberti and Zimmet (1998) in the World Health Organization consultation document on the definition, diagnosis and classification of diabetes mellitus and its complications.

Several trials have looked at the utility in screening of HbA1c specifically. Rohlfing et al (2000) found a cut-off HbA1c of 6.1% to be highly specific (97.4%) but the sensitivity was noted to be only 63.2%. Kilpatrick et al (1998) questioned the use of HbA1c as a screening test because of inter- and intra-individual assay variability. At present, the sensitivity and specificity of HbA1c alone offers no advantage over other methods for screening for type 2 diabetes.

There should be clear evidence-based guidance for directing the treatment of people found to have the condition through a screening programme
There is an accumulating evidence base for the various interventions that can be applied, including reduction of macrovascular and microvascular complications by achieving control of hyperglycaemia as well hypertension and hyperlipidaemia. Although it remains a challenge to improve care for people who already have diabetes, careful consideration should be made of resource expansion of services as an ever-increasing number of people are diagnosed with the condition. Disease management targets within the Quality and Outcomes Framework of the new General Medical Services (DoH, 2004) contract have given the impetus, as well as the resources, to provide organised evidence-based care for patients on practice diabetes registers.

There should be evidence from high-quality randomised controlled trials that the screening programme is effective in reducing morbidity and mortality
At present, there is no evidence from trials that a screening programme would be effective.

The cost of case finding by screening and subsequent treatment is acceptable and economically balanced in relation to health expenditure as a whole
There is no evidence from any trials on screening programmes, although some evidence from observational studies has been used to model cost-effectiveness. As these are based on certain assumptions and reach differing conclusions it is difficult to base the case for a screening programme on this evidence (Hoerger et al, 2004).

Targeted screening
Currently, there appears to be good evidence to support early case finding and treatment but there is no evidence to support a population-based screening programme. Various studies have looked at developing risk scores (e.g. Griffin et al, 2000) or questionnaires (e.g. Ruige et al, 1997) to identify patients for further screening. These have been found to be relatively specific (55–72%) and sensitive (59–77%), depending on the system used in study populations.

There is some evidence to support targeted screening aimed at people with multiple risk factors. Lawrence et al (2001), for instance, looked at a general practice population who were over 45 years old and not known to have diabetes. They found that prevalence of diabetes in patients with age as a sole risk factor was 0.2%, while prevalence of diabetes in patients with age and one or more other risk factors (hypertension, obesity or a family history of diabetes) was 2.8%.

A recent observational study was undertaken by Greaves et al (2004) across 16 GP practices in Devon and Somerset to investigate the feasibility and performance of a practical method for identifying patients with type 2 diabetes and impaired fasting glycaemia (IFG). The practices were asked to sample 100 patients, 25 from each of four groups with different entry criteria relating to body mass index (BMI) and age (BMI ≥33kg/m2 and age >70 years; BMI ≥31kg/m2 and age >65 years; BMI ≥29kg/m2 and age >60 years; BMI ≥27kg/m2 and age >50 years). Selection of patients within the practices was done randomly. Those with previously diagnosed diabetes were excluded, and only Caucasians were screened, which left 1287 patients across the 16 practices. Fasting plasma glucose was measured in the local NHS laboratory and repeated if abnormal to determine the prevalence of new cases of diabetes or IFG in each group.

The response rate from the 1287 patients was 60% and the prevalence of new cases of type 2 diabetes was 4.7% (95% confidence interval [CI], 2.8–7.7%), 5.7% (95% CI, 4.0–8.2%), 3.8% (95% CI, 2.4–6.0%) and 2.6% (95% CI, 1.4–4.7%), in the groups ranging from highest BMI and age cut-offs to lowest cut-offs. An additional 5.2–8.4% had IFG. The number needed to test to find one new diagnosis of diabetes or IFG in any of the four patient groups was low (7–13 people).

These screening strategies discovered significant numbers of people with previously undiagnosed type 2 diabetes: undiagnosed rates were about 2.0% of the level of diagnosed rates.

This example demonstrates that targeted screening can be relatively simple and effective. Practices could choose what criteria they might wish to adopt based on perceived workload and on the resources available. Lower age and BMI criteria could be employed to identify people earlier, so that lifestyle changes may be more effective, especially in those with IFG.

In the author’s practice
In 2004, it was decided in the author’s practice to actively find cases of type 2 diabetes (Table 1). From the patient list of 12400 individuals, a search was carried out for adults aged 35–75 years with a BMI above 28kg/m2 recorded in the last 12 months. Patients with diabetes (n=332) and IGT or IFG (n=47) were excluded; 384 patients were identified. It was felt that this was too large a group of patients to screen for diabetes at one time.

From this group a search was conducted for patients with concurrent hypertension or hypercholesterolaemia and identified 82 individuals. (It was noted that 122 patients did not have a blood pressure measurement recorded in the last 5 years and 197 did not have a cholesterol measurement recorded). Of the 82 people identified for screening, 25 were excluded from screening for clinical reasons (terminal illness or clinical inappropriateness, as determined by the patients’ GPs).

Fifty-seven patients were invited for screening and 47 patients (82% uptake) went on to have a laboratory fasting blood glucose test, of which 17 were abnormal (two patients did not respond to the invitation for screening and eight declined). Of the 17 patients with abnormal results, 13 had repeat fasting blood glucose tests because of a raised fasting blood glucose level over 7.1mmol/l. Glucose tolerance tests were arranged for four people with a fasting blood glucose level of above 6.1mmol/l but below 7.1mmol/l; these were people who might have had IGT but for whom diabetes could not be excluded. Three patients had two fasting blood glucose tests and a GTT because of repeat borderline fasting test results.

Seven patients (15% of those screened) were found to have type 2 diabetes; this is equivalent to 2.1% of our existing diabetes register. A further six (13% of those screened) were found to have IGT.

This simple approach enabled the practice to handle the screening procedure without an unmanageable increase in workload. The entire process took 3 months to complete. It was not taken into account that those patients without recorded hypertension or hypercholesterolaemia may have had either of these conditions if measurements had been taken. The number of people in the target group would also rise with 100% recording of BMI. This amply illustrates the point that a high-quality targeted screening programme relies upon high-quality data recording.

The aim is to repeat the process in stages to screen all adult patients over 35 years old with a BMI greater than 28kg/m2. A protocol for managing people with IGT is also being developed.

Conclusion
An explosion in the number of people with type 2 diabetes is beginning to be seen as the population ages and more sedentary lifestyles with richer diets are adopted. There are many people with the condition who remain undiagnosed. There exists a dual challenge of improving the care of those who have already been diagnosed with type 2 diabetes as well as detecting those who have not been diagnosed at a stage where early intervention may prevent future complications. The health economy will need to evaluate the clinical effectiveness and cost-effectiveness of screening for diabetes before further guidance is published.

Primary care can adopt pragmatic approaches to screening based on existing resources and perceived workload. Targeted screening appears to be practical and has the support of Diabetes UK.

Alberti KG (1998) Impaired glucose tolerance: what are the clinical implications? Diabetes Research and Clinical Practice40(Suppl): S3–8
Alberti KG, Zimmet PZ (1998) Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabetic Medicine 15(7): 539–53
Andersson DK, Lundblad E, Svardsudd K (1993) A model for early diagnosis of type 2 diabetes mellitus in primary health care. Diabetic Medicine 10(2): 167–73
Chan JM, Rimm EB, Colditz GA, Stampfer MJ, Willett WC (1994) Obesity, fat distribution, and weight gain as risk factors for clinical diabetes in men. Diabetes Care 17(9): 961–9
Department of Health (DoH; 2001) National Service Framework for Diabetes: Standards. DoH, London. Available at http://www.dh.gov.uk/assetRoot/04/05/89/38/04058938.pdf (accessed 23.09.2005)
DoH (2004) General Medical Services contract. DoH, London. Available at http://www.dh.gov.uk/PolicyAndGuidance/OrganisationPolicy/PrimaryCare/PrimaryCareContracting/PrimaryCareContractingArticle/fs/en?CONTENT_ID=4079003&chk=5nnqaMDate (accessed 23.09.2005)
Diabetes Prevention Program Research Group (2003) Effects of withdrawal from metformin on the development of diabetes in the diabetes prevention program. Diabetes Care 26(4): 977–80 
Diabetes UK (2002) Position Statement: Early identification of people with Type 2 diabetes. Diabetes UK, London. Available at www.diabetes.org.uk/infocentre/state/downloads/earlyid.doc (accessed 23.09.2005)
Diabetes UK (2004) Diabetes in the UK. Diabetes UK, London. Available at http://www.diabetes.org.uk/infocentre/reports/in_the_uk_2004.doc (accessed 23.09.2005)
Eriksson KF, Lindgarde F (1991) Prevention of type 2 (non-insulin-dependent) diabetes mellitus by diet and physical exercise. The 6-year Malmo feasibility study. Diabetologia 34(12): 891–8
Forrest RD, Jackson CA, Yudkin JS (1986) Glucose intolerance and hypertension in north London: the Islington Diabetes Survey. Diabetic Medicine 3(4): 338–42
Fuller JH, Shipley MJ, Rose G, Jarrett RJ, Keen H (1980) Coronary-heart-disease risk and impaired glucose tolerance: The Whitehall study. Lancet 1(8183): 1373–6
Greaves CJ, Stead JW, Hattersley AT, Ewings P, Brown P, Evans PH (2004) A simple pragmatic system for detecting new cases of type 2 diabetes and impaired fasting glycaemia in primary care. Family Practice 21(1): 57–62
Griffin SJ, Little PS, Hales CN, Kinmonth AL, Wareham NJ (2000) Diabetes risk score: towards earlier detection of type 2 diabetes in general practice. Diabetes/Metabolism Research and Reviews 16(3): 164–71
Haffner SM, Stern MP, Hazuda HP, Mitchell BD, Patterson JK (1990) Cardiovascular risk factors in confirmed prediabetic individuals. Does the clock for coronary heart disease start ticking before the onset of clinical diabetes? Journal of the American Medical Association 263(21): 2893–8
Hamman RF (1992) Genetic and environmental determinants of non-insulin-dependent diabetes mellitus.Diabetes/Metabolism Reviews 8(4): 287–99
Harris MI, Klein R, Welborn TA, Knuiman MW (1992) Onset of NIDDM occurs at least 4-7 yr before clinical diagnosis.Diabetes Care 15(7): 815–9
Health and Social Care Information Centre (2005) Quality and Outcomes Framework, 2004/05. HSCIC, London. Available at http://www.ic.nhs.uk/services/qof/data (accessed 23.09.05)
Hoerger TJ, Harris R, Hicks KA, Donahue K, Sorensen S, Engelgau M (2004) Screening for type 2 diabetes mellitus: a cost-effectiveness analysis. Annals of Internal Medicine 140(9): 689–99 
Holmes J, Gear E, Bottomley J, Gillam S, Murphy M, Williams R (2003) Do people with type 2 diabetes and their carers lose income? (T2ARDIS-4) Health Policy 64(3): 291–6
Hypertension in Diabetes Study (1993) Prevalence of hypertension in newly presenting type 2 diabetic patients and the association with risk factors for cardiovascular and diabetic complications. Journal of Hypertension 11(3): 309–17
Kilpatrick ES, Maylor PW, Keevil BG (1998) Biological variation of glycated hemoglobin. Implications for diabetes screening and monitoring. Diabetes Care 21(2): 261–4
King’s Fund Policy Institute (1996) Counting the cost: the real impact of non-insulin-dependent diabetes. British Diabetic Association, London
Knowler WC, Barrett-Connor E, Fowler SE, Hamman RF, Lachin JM, Walker EA et al (2002) Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. New England Journal of Medicine 346(6): 393–403
Köbberling J, Tillil H (1982) Empirical risk figures for first-degree relatives of non-insulin dependent diabetes. In: J Köbberling, RB Tattersall, eds. The genetics of diabetes mellitus. Academic Press, London, 201–9
Lawrence JM, Bennett P, Young A, Robinson AM (2001) Screening for diabetes in general practice: cross sectional population study. British Medical Journal 323(7312): 548–51
Lundblad D, Eliasson M (2003) Silent myocardial infarction in women with impaired glucose tolerance: The Northern Sweden MONICA study. Cardiovascular Diabetology 2:  9–15
McCance DR, Hanson RL, Charles MA, Jacobsson LT, Pettitt DJ, Bennett PH, Knowler WC (1994) Comparison of tests for glycated haemoglobin and fasting and two hour plasma glucose concentrations as diagnostic methods for diabetes. British Medical Journal 308(6940): 1323–8
Morris RD, Rimm DL, Hartz AJ, Kalkhoff RK, Rimm AA (1989) Obesity and heredity in the etiology of non-insulin-dependent diabetes mellitus in 32,622 adult white women. American Journal of Epidemiology 130(1): 112–21
Rohlfing CL, Little RR, Wiedmeyer HM, England JD, Madsen R, Harris MI et al (2000) Use of GHb (HbA1c) in screening for undiagnosed diabetes in the U.S. population. Diabetes Care 23(2): 187–91
Ruige JB, de Neeling JN, Kostense PJ, Bouter LM, Heine RJ (1997) Performance of an NIDDM screening questionnaire based on symptoms and risk factors. Diabetes Care 20(4): 491–6
Ryan DH; Diabetes Prevention Program Research Group (2003) Diet and exercise in the prevention of diabetes.International Journal of Clinical Practice. Supplement (134): 28–35
Tuomilehto J, Lindstrom J, Eriksson JG, Valle TT, Hamalainen H, Ilanne-Parikka P, et al (2001) Prevention of type 2 diabetes mellitus by changes in lifestyle among subjects with impaired glucose tolerance. Finnish Diabetes Prevention Study. New England Journal of Medicine 344(18): 1343–50
Turner NC, Clapham JC (1998) Insulin resistance, impaired glucose tolerance and non-insulin-dependent diabetes, pathologic mechanisms and treatment: current status and therapeutic possibilities. Progress in Drug Research 51: 33–94
UK Prospective Diabetes Study (UKPDS) Group (1990) UK Prospective Diabetes Study 6. Complications in newly diagnosed type 2 diabetic patients and their association with different clinical and biochemical risk factors. Diabetes Research 13(1): 1–11
UKPDS Group (1998) Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34). Lancet 352(9131): 854–65 
Williams DR, Wareham NJ, Brown DC, Byrne CD, Clark PM, Cox BD et al (1995) Undiagnosed glucose intolerance in the community: the Isle of Ely Diabetes Project. Diabetic Medicine 12(1): 30–5
Wingard DL, Barrett-Connor EL, Scheidt-Nave C, McPhillips JB (1993) Prevalence of cardiovascular and renal complications in older adults with normal or impaired glucose tolerance or NIDDM. A population-based study. Diabetes Care 16(7):1022–5

Share this article
Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on whatsapp
Related content
For the latest news and articles

Sign up to all DiabetesontheNet journals

© Copyright Omniamed Communications. All Rights Reserved​
108 Cannon Street, London, EC4N 6EU. Registered in the United Kingdom​
Omniamed logo white
DiabetesontheNet Logo
For the latest news and articles

Sign up to all DiabetesontheNet journals

 

By clicking ‘Subscribe’, you are agreeing that DiabetesontheNet.com are able to email you periodic newsletters. You may unsubscribe from these at any time. Your info is safe with us and we will never sell or trade your details. For information please review our Privacy Policy.

DiabetesontheNet Logo

This website is for UK healthcare professionals only. To continue, please confirm that you are a UK healthcare professional below.