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CMAJ
CMAJ - June 1, 1999JAMC - le 1 juin 1999

Controversy
The folly of population screening for type 2 diabetes

Kenneth G. Marshall, MD

CMAJ 1999;160:1592-3


See also:
Articles under the Controversy flag appear in the form of a debate. An invited response to Dr. Marshall's article, by Drs. Hertzel C. Gerstein and Sara Meltzer, begins on  page 1593. Dr. Marshall's rebuttal follows on page 1595. Drs. Gerstein and Meltzer's rebuttal follows on page 1596.

In 1994 the Canadian Task Force on the Periodic Health Examination concluded that there was fair evidence not to screen the general adult population for diabetes mellitus (grade D recommendation).1 In 1996 the US Preventive Health Services found insufficient evidence to make a recommendation for or against such screening (grade C recommendation).2 In 1997 the American Diabetes Association3 and in 1998 the Canadian Diabetes Association4 recommended that the entire adult population over the age of 45 be screened for diabetes. The Canadian Diabetes Association specified that this recommendation was based on opinion, not evidence.4

In the absence of evidence, why make such a recommendation? The argument for doing so is the estimate that 30% to 50% of cases of type 2 diabetes are undiagnosed,4 and that detecting these cases might help to prevent illness and death. But such an undertaking is acceptable only if there is reasonable evidence that a significant number of people will benefit5 and if the potential benefits clearly outweigh the harms.6,7 Screening the entire adult population over the age of 45 for diabetes does not meet these criteria.

The therapeutic interventions of choice for most patients with type 2 diabetes are diet and exercise, with the aim of decreasing body weight and insulin resistance. Since it is well documented that very few people are able to achieve and maintain weight loss,8,9 it is wishful thinking to suppose that screening for diabetes will make people change their lifestyles.

If screening does not lead to weight loss, could it lead to earlier intervention with intensive pharmacological therapy to decrease the risk of macrovascular and microvascular disease? Although no published studies have dealt specifically with this issue, the results of the United Kingdom Prospective Diabetes Study (UKPDS)10­12 suggest that earlier pharmacological interventions are unlikely to diminish the risk of clinically significant diabetic complications.

The UKPDS documented that intensive treatment of type 2 diabetes with insulin or sulfonylureas over a 10-year period did not decrease illness or deaths from macrovascular causes — a rather discouraging result, in view of the fact that 60% of people with diabetes die as a result of macrovascular complications.10 A ray of hope comes from another UKPDS report, which showed that intensive metformin therapy for obese people with type 2 diabetes decreased the risk of macrovascular disease. Unfortunately, such patients treated with a combination of metformin and sulfonylureas had higher rates of death compared to controls who received conventional therapy.11 Although tight glucose control using insulin or sulfonylureas therapy does not by itself decrease the risk of macrovascular disease, aggressive treatment of other risk factors such as hypertension13 or dyslipidemia14 in type 2 diabetes does. However, because the assessment of blood sugar should be an integral part of the work-up of patients with hypertension or dyslipidemia, it seems unlikely that screening the general population for diabetes would be of additional value.

Microvascular complications develop far less frequently in people with type 2 diabetes than do macrovascular complications.15 The UKPDS reported a 25% reduction of microvascular disease with intensive treatment; this was measured primarily by a surrogate outcome, namely, a decrease in the progression of retinopathy as determined by ophthalmologic examination. No difference was seen in the more important clinical outcome of vision loss between patients treated intensively and those who received conventional treatment. One small benefit of intensive treatment was that, on an annual basis, 1 in 323 patients were able to avoid retinal photocoagulation. Intensive treatment did not prevent the development of impotence.10

It seems unlikely that population screening for diabetes would decrease the incidence of blindness. In the UKPDS, retinopathy at the time of clinical diagnosis was mild in over 92% of cases among men and in 95% of cases among women, and in the remaining cases it was moderate. No cases of advanced retinopathy (preproliferative or proliferative) requiring photocoagulation were detected. Many people who had moderate retinopathy also had hypertension,12 but if testing for diabetes is indeed included as an integral part of the work-up for hypertension, the retinopathy should have been detected at that time.

The complications of established diabetes are extremely serious. Primary prevention of type 2 diabetes and its main complications is the ideal therapeutic intervention — plenty of exercise and a sensible diet — but one doesn't have to be screened for diabetes to be aware of this. Obviously, patients with other conditions such as hypertension or known hyperlipidemia that put them at risk for cardiovascular disease should be assessed for diabetes and vigorously treated for all detected risk factors.

There is no evidence that screening the entire adult population over the age of 45 for diabetes will decrease morbidity or mortality. What is certain is that screening will do a great deal of harm. Not only will thousands of Canadians who thought they were well find out they are sick, but our society as a whole will be subjected to yet another voice fostering our burgeoning and anxiety-provoking obsession with health.6,16-23

Competing interests: None declared.

Comments Send a letter to the editor
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Dr. Marshall is with the Department of Family Medicine at the University of Western Ontario.

Correspondence to: Dr. Kenneth G. Marshall, 452 William St., Stratford ON N5A 4Y7


References
  1. Canadian Task Force on the Periodic Health Examination. The Canadian guide to clinical preventive health care. Ottawa: Health Canada; 1994. p. 602-9.
  2. US Preventive Services Task Force. Guide to clinical preventive services, 2nd ed. Baltimore: Williams and Wilkins; 1996. p. 193-208.
  3. American Diabetes Association. Standards of medical care for patients with diabetes mellitus. Diabetes Care 1997;20(Suppl 1):1S-70S.
  4. Meltzer S, Leiter L, Daneman D, Gerstein HC, Lau D, Ludwig S, et al. 1998 clinical practice guidelines for the management of diabetes in Canada. CMAJ 1998;159(8 Suppl): 1S-29S.
  5. Cochrane AL, Holland WW. Validation of screening procedures. Br Med Bull 1971;27:3-8.
  6. Marshall KG. Prevention. How much harm? How much benefit? 3. Physical, psychological and social harm. CMAJ 1996;155(2):169-76.
  7. Marshall KG. Prevention. How much harm? How much benefit? 4. The ethics of informed consent for preventive screening programs. CMAJ 1996;155(4):377-83.
  8. Wing R, Venditti E, Jakicic J, Polly BA, Lang W. Lifestyle intervention in overweight individuals with a family history of diabetes. Diabetes Care 1998;21:350-60.
  9. Foreyt J, Goodrick K. The ultimate triumph of obesity [editorial]. Lancet 1995;346:134-5.
  10. UK Prospective Diabetes Study (UKPDS) Group. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet 1998;352:837-53.
  11. UK Prospective Diabetes Study (UKPDS) Group. Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34). Lancet 1998;352:854-65.
  12. United Kingdom Prospective Diabetes Study 30. Diabetic retinopathy at diagnosis of non-insulin-dependent diabetes mellitus and associated risk factors. Arch Ophthalmol 1998;116:297-303.
  13. UK Prospective Diabetes Study Group. Tight blood pressure control and risk of macrovascular and microvascular complications in type 2 diabetes: UKPDS 38. BMJ 1998;317:703-13.
  14. Pyorala K, Pedersen TR, Kjekshus J, Faegeman O, Olsson AG, Thorgeirsson G, for the Scandinavian Simvastatin Survival Study (45) Group. Cholesterol lowering with simvastatin improves prognosis of diabetic patients with coronary heart disease. Diabetes Care 1997;20:614-20.
  15. Goyder E, Irwig L. Screening for diabetes: What are we really doing? BMJ 1998;317:1644-6.
  16. Meador CK. The last well person. N Engl J Med 1994;330:440-1.
  17. Barsky AJ. The paradox of health. N Engl J Med 1988;318:414-8.
  18. Thomas L. Notes of a biology-watcher. The health-care system. N Engl J Med 1975;293:1245-6.
  19. Annas GJ. Reframing the debate on health care reform by replacing our metaphors. N Engl J Med 1995;332:744-7.
  20. Fitzgerald FT. The tyranny of health. N Engl J Med 1994;331:196-8.
  21. Scrabanek P. The death of humane medicine and the rise of coercive healthism. Bury Saint Edmunds (UK): Crowley Esmonde; 1994.
  22. Herman J. The ethics of prevention: old twists and new. Br J Gen Pract 1996;46:547-9.
  23. Førde OH. Is imposing risk awareness cultural imperialsim? Soc Sci Med 1998;47:1155-9.

© 1999 Canadian Medical Association