Recommendations made by the USPSTF are independent of the U.S. government. They should not be construed as an official position of the Agency for Healthcare Research and Quality or the U.S. Department of Health and Human Services.
Importance: The prevalence of type 2 diabetes mellitus is increasing – about 9% of the adult U.S. population currently has this disorder. Diabetes is a leading cause of blindness, renal disease, and amputation and leads to increased mortality, primarily from cardiovascular events.
Detection: The USPSTF found convincing evidence that available screening tests accurately detect type 2 diabetes during an early, asymptomatic phase.
Benefits of Detection and Early Treatment:
- Adults with sustained blood pressure greater than 135/80 mm Hg: The USPSTF found adequate evidence that, in adults who have hypertension and diabetes, lowering blood pressure below conventional target values reduces the incidence of cardiovascular events and cardiovascular mortality.
- Adults with blood pressure 135/80 mm Hg or lower: The USPSTF found convincing evidence that intensive glycemic control in persons with clinically detected (as opposed to screening-detected) diabetes can reduce progression of microvascular disease. However, the benefits of tight glycemic control on microvascular clinical outcomes, such as severe visual impairment or end-stage renal disease, take years to become apparent. There is inadequate evidence that early diabetes control as a result of screening provides an incremental benefit for microvascular clinical outcomes compared with initiating treatment after clinical diagnosis.
There is inadequate evidence that tight glycemic control significantly reduces macrovascular complications, such as myocardial infarction and stroke.
Harms of Detection and Early Treatment: The USPSTF found adequate evidence that the short-term harms of screening for diabetes, such as anxiety, are small. However, the longer-term effects of labeling a large proportion of the adult U.S. population as abnormal are unknown.
USPSTF Assessment: The USPSTF concludes that for adults with sustained blood pressure greater than 135/80 mm Hg, there is moderate certainty that the net benefit of screening for diabetes is substantial.
The USPSTF concludes that for adults with blood pressure of 135/80 mm Hg or less, evidence of the value of screening for diabetes is lacking, and the balance of benefits and harms cannot be determined.
Patient Population Under Consideration: This recommendation concerns adults without symptoms of diabetes or evidence of possible diabetes complications. Symptoms of diabetes include polyuria, polydipsia, and polyphagia. Possible diabetes complications include nonhealing ulcers or infections and established vascular disease (for example, coronary artery disease, stroke, and peripheral artery disease). Persons with these symptoms or conditions should be tested for diabetes.
Suggestions for Practice Regarding the I Statement: In persons with blood pressure of 135/80 mm Hg or lower, screening may be considered on an individual basis if knowledge of diabetes status would help inform decisions about coronary heart disease (CHD) prevention strategies, including assessment of CHD risk and subsequent consideration of lipid-lowering agents or aspirin.
For example, consider a patient for whom lipid-lowering treatment would be recommended if his or her 10-year CHD risk was 20% or greater (found in Risk Assessment section directly below). If the patient's calculated risk was 17% without diabetes and greater than 20% with diabetes, then screening for diabetes would be useful in determining lipid treatment. However, if the calculated risk was 10% without diabetes and 15% with diabetes, then the screening test result would have no effect on the decision whether to use lipid-lowering treatment.
Risk Assessment: Blood pressure is an important predictor of complications of cardiovascular disease (CVD) (including CHD and stroke) in persons with type 2 diabetes mellitus and should be measured as the first step in applying this recommendation. The examination of global CHD and stroke risk allows the clinician to determine how aggressive treatment for CVD risk factors needs to be. In making this assessment, clinicians should use any of several validated CHD risk assessment calculators, such as the calculator based on Framingham Heart Study data (available at http://hp2010.nhlbihin.net/atpiii/calculator.asp).
Screening Tests: Three tests have been used to screen for diabetes: fasting plasma glucose, 2-hour postload plasma glucose, and hemoglobin A1c. Each has advantages and disadvantages. The American Diabetes Association has recommended the fasting plasma glucose test for screening because it is easier and faster to perform, more convenient and acceptable to patients, and less expensive than other screening tests. The fasting plasma glucose test has more reproducible results than does the 2-hour postload plasma glucose test, has less intraindividual variation, and has similar predictive value for development of microvascular complications of diabetes. The American Diabetes Association defines diabetes as a fasting plasma glucose level of 126 mg/dL or greater and recommends confirmation with a repeated screening test on a separate day, especially for people with borderline results.
Treatment of Persons with Sustained Blood Pressure of 135/80 mm Hg or Greater: Blood pressure targets should be lower for persons who have type 2 diabetes mellitus than for those who do not. Lower blood pressure targets for persons with diabetes and high blood pressure reduce CVD events compared with higher targets. Attention to other risk factors for CVD, such as physical inactivity, lipid levels, diet, and obesity, is also important, both to decrease risk for CHD and to improve glucose control.
Screening Intervals: The optimal screening interval is not known. The American Diabetes Association, on the basis of expert opinion, recommends a 3-year interval.
Other Approaches to Prevention: There is no evidence of benefit in health outcomes from screening for impaired glucose tolerance (IGT) or impaired fasting glucose (IFG). However, intensive programs of lifestyle modification (diet, exercise, and behavior) do reduce the incidence of diabetes. Regardless of whether the clinician and patient decide to screen for diabetes, people should eat a healthful diet, be active, and maintain a healthy weight-these behaviors have other benefits in addition to preventing or forestalling type 2 diabetes. The USPSTF recommends intensive interventions for obese persons who desire to lose weight. Population-based approaches to increasing physical activity and reducing obesity, as recommended by the Task Force on Community Preventive Services, should be supported.
Useful Resources: Evidence and USPSTF recommendations on blood pressure, diet, physical activity, and obesity are available at https://www.uspreventiveservicestaskforce.org. The reviews and recommendations for the Task Force on Community Preventive Services may be found at https://www.thecommunityguide.org.
Research Needs: The types of studies that would help fill gaps in the evidence include a randomized (or nonrandomized), controlled trial of screening for type 2 diabetes mellitus; extended follow-up of the UKPDS (United Kingdom Prospective Diabetes Study) and other cohort studies; studies of glycemic control, with CHD outcomes, in screening-detected populations; studies of optimal lipid and blood pressure targets for people with screening-detected diabetes; and studies examining the impact of a diagnosis of prediabetes on the effectiveness of lifestyle interventions.
Burden of Disease: Diabetes is a tremendous clinical and public health burden for the U.S. population.1 Data from the NHANES (National Health and Nutrition Examination Survey) indicated that 19.3 million U.S. adults 20 years of age or older (9.3% of the adult population) had diabetes in 2002. Diabetes was undiagnosed in one third of these individuals.2 An additional 26% of the population had IFG. The prevalence of diagnosed diabetes increased from 5.1% from 1988 to 1994 to 6.5% from 1999 to 2002. Prevalence is increasing most rapidly among individuals with a body mass index of 35 kg/m2 or greater.2-3
The prevalence of diabetes (diagnosed and undiagnosed) increases with age, reaching 21.6% for those 65 years of age or older. African Americans, Hispanic or Latino Americans, American Indians, and some Asian Americans and Native Hawaiians or other Pacific Islanders are at particularly high risk for type 2 diabetes mellitus.4 The prevalence of diagnosed diabetes is twice as high in non-Hispanic black and Mexican-American persons as in non-Hispanic white persons.2 Modifiable factors, including reductions in physical activity, dietary changes, and increased frequency of testing, may play a role in the increasing prevalence of diabetes.3
Diabetes was the sixth leading cause of death in 2000.4 Overall, risk for premature death among individuals with diabetes is about twice that for those without. Adults with diabetes have rates of stroke and death from heart disease that are about 2 to 4 times higher than adults without diabetes. Diabetes is the leading cause of new cases of blindness among adults age 20 to 74 years and the leading cause of end-stage renal disease, accounting for 44% of new cases of end-stage renal disease. More than 60% of lower-limb amputations not due to trauma occur among individuals with diabetes.4
Scope of Review: The USPSTF reviewed the evidence on screening for type 2 diabetes mellitus in 2003. For the current recommendation, the USPSTF reviewed the evidence from new trials as well as updates of previously included studies. The current review focused on screening for IGT and IFG in asymptomatic adults and screening for type 2 diabetes mellitus in asymptomatic adults at increased and average risk for diabetes complications. Interventions were reviewed for effects on health outcomes, including cardiovascular morbidity, symptomatic neuropathy, nonhealing ulcers, lower-limb amputation, chronic kidney disease, severe visual impairment, mortality, and quality of life. The USPSTF review focused on the risk for complications from type 2 diabetes mellitus, especially CVD, because the goal of screening—improvement of health and well-being—is contingent on decreasing the complications of type 2 diabetes mellitus and not primarily on decreasing the prevalence of the disease. The risk factors identified as important predictors of cardiovascular complications among persons with type 2 diabetes mellitus included older age, smoking, hypertension, hyperlipidemia, higher glycemic burden, and membership in certain high-risk ethnic groups.
Accuracy of Screening Tests: The assessment of screening tests for type 2 diabetes mellitus is complicated by uncertainty regarding the most appropriate gold standard for comparison. Definitions of diabetes were originally developed by using results of 2-hour postload plasma glucose testing to identify a population at substantially increased risk for retinopathy. The criterion for an abnormal fasting plasma glucose level was developed on the basis of 2-hour postload plasma glucose testing and revised downward (from 140 mg/dL to 126 mg/dL) to make the sensitivity of fasting plasma glucose testing comparable with that of 2-hour postload plasma glucose testing. However, a study using NHANES III data has demonstrated that, compared with fasting plasma glucose testing, the 2-hour postload plasma glucose screening test leads to diagnosis of diabetes in more individuals.5.
Large population-based studies have examined the test characteristics of 2-hour postload plasma glucose, fasting plasma glucose, and hemoglobin A1c for identifying individuals with retinopathy. Sensitivity and specificity for detecting retinopathy were in the range of 75% to 80% for all 3 tests when using the following thresholds: fasting plasma glucose test, 126 mg/dL or greater; 2-hour postload plasma glucose test, 200 mg/dL or greater; or hemoglobin A1c test, 6.4% or greater.6-8 Other studies have examined whether these tests predict future CVD events.
A meta-regression analysis of 20 observational studies found that the results of both fasting plasma glucose and 2-hour postload plasma glucose tests were statistically significantly associated with future CVD events in a continuously graded fashion, beginning at levels consistent with IGT and IFG and increasing more steeply at the highest glucose levels.9
In the past, the utility of hemoglobin A1c testing was limited in part by relatively poor reproducibility and lack of standardization across laboratories. More recently, widespread adoption of standardized hemoglobin A1c measurements has occurred, and newer techniques for measurement are generally highly reproducible.10 A systematic review in 1996 found that a hemoglobin A1c cutoff value of 6.4% was 66% sensitive and 98% specific and was associated with a positive predictive value of 63% in a population with a diabetes prevalence of 6%.11 Increasing the cutoff value to 7.0% increased the positive predictive value to 90%. Hemoglobin A1c values in the high-normal range (5.6% to 6.0%) seem to predict a higher incidence of future diabetes.12-13
Effectiveness of Early Detection and/or Treatment: No trial has been done to establish whether systematic screening for diabetes and early treatment improves health outcomes compared with clinical diagnosis. The ADDITION (Anglo-Danish-Dutch Study of Intensive Treatment in People with Screen Detected Diabetes in Primary Care), currently in progress, may shed light on differences in baseline characteristics and long-term health outcomes between persons with screening-detected type 2 diabetes mellitus and those who present with symptoms.14 The USPSTF attempted to compare the expected health outcomes from a strategy of systematic screening with those from usual care. In the absence of direct evidence from a trial of screening, the USPSTF examined indirect evidence to estimate whether screening, early diagnosis, and treatment of screening-detected or early type 2 diabetes mellitus were associated with improved health outcomes.
The USPSTF reviewed the evidence on early treatment of type 2 diabetes mellitus in preventing long-term adverse outcomes, including cardiovascular events, visual impairment, renal failure, and amputations. Four treatments to reduce the incidence of CVD events among persons with diabetes have been studied in high-quality, randomized, controlled trials: tight glycemic control, tight blood pressure control, treatment of dyslipidemia, and aspirin therapy. No randomized, controlled trial has demonstrated a statistically significant reduction in total CVD events from tight glycemic control. The UKPDS (after 10 years of follow-up) showed a trend toward reduced CVD events in participants randomly assigned to tight glycemic control.15 These participants had lower rates of myocardial infarction (14.7 vs. 17.4 events per 1000 patient-years) and sudden death (0.9 vs. 1.6 events per 1000 patient-years) than those receiving conventional management. There were no reductions in stroke (relative risk (RR), 1.11), heart failure (RR, 0.91), angina (RR, 1.02), or all-cause mortality (RR, 0.94) associated with tighter glycemic control.
A number of recent randomized, controlled trials have examined various aspects of treatment for hypertension among persons with type 2 diabetes. Principal findings indicate that an aggressive approach to blood pressure control among persons with type 2 diabetes mellitus reduces CVD events by 50%; 16-17 treatment of isolated systolic hypertension among persons older than 60 years of age with type 2 diabetes mellitus reduces CVD events by 34% to 69%;18-19 treatment of persons with type 2 diabetes mellitus and at least 1 other CVD risk factor with ramipril (regardless of whether they have hypertension) reduces CVD events by 22% and all-cause mortality by 16%;20 and angiotensin-converting enzyme inhibitors and angiotensin-receptor blockers are useful antihypertensive agents for type 2 diabetes mellitus.16,21 Although there is evidence that lowering blood pressure in individuals with diabetes improves outcomes, no clear evidence has shown that persons with type 2 diabetes detected by screening would respond differently to specific antihypertensive regimens than would those without diabetes.
Results from studies of intensive lipid-lowering treatment in persons with and without type 2 diabetes mellitus are mixed about whether those with type 2 diabetes mellitus benefit more than those without. Several secondary prevention trials of treatments for people with lipid abnormalities reported that lipid treatment reduced the incidence of CHD events by about the same relative percentage among those with type 2 diabetes mellitus and those without (RR reduction, 19% to 42%).22-24 The HPS (Heart Protection Study) found that including simvastatin in the treatment regimen of persons with diabetes reduces major vascular events (myocardial infarction, stroke, and revascularization) from 25% to 20%; that is, using simvastatin prevents 1 major vascular event in 20 persons over a 5-year period.25 This benefit was seen regardless of initial low-density lipoprotein cholesterol level.26
Aspirin reduces CHD in persons with and without diabetes, with a similar RR reduction (about 30%) in both groups.27-29 Aspirin lowers the risk for ischemic stroke in women, but the benefits do not seem to be greater in women with diabetes than in those without.30
Although there is evidence that retinal photocoagulation is effective in reducing the incidence of visual impairment among people with diabetes who have severe retinopathy or macular edema, most people with type 2 diabetes mellitus detected by routine screening will not require this intervention. Furthermore, although tight glycemic control reduces the development and progression of retinopathy, its effects on serious visual impairment are less clear and probably occur 10 years or more after the diagnosis of diabetes. There is less certainty about the degree to which tight glycemic control during the preclinical period (between screening and clinical detection), when glucose levels are lower than at later stages of the disease, reduces retinopathy and later visual impairment.31
In reviewing the evidence on screening and its possible impact on chronic renal failure, the USPSTF concluded that, although tight glycemic and blood pressure control and use of angiotensin-converting enzyme inhibitors and angiotensin-receptor blockers reduce development and progression of albuminuria, it could not determine whether initiating these treatments earlier as a result of screening would have an important impact on chronic renal failure.31 Lower-limb amputation in persons with diabetes occurs primarily as late complications related to development of distal sensory neuropathy and peripheral vascular disease, both of which take years to develop. Although foot care programs, and perhaps tight glycemic and blood pressure control, may reduce lower-limb amputation over the long term, the USPSTF found no evidence that early implementation of these interventions during the time between screening and clinical detection would affect this outcome.31
Modeling diabetes interventions is a relatively young field; models vary in their perspectives, methods, and results. Some models suggest that aggressive blood pressure, lipid level, and glycemic control in persons with diabetes may be effective and relatively cost-effective, and that older persons benefit more than younger persons. However, the assumptions in the models are based on data from trials that included both clinically and screening-detected persons with diabetes; therefore, the models do not directly address the question of screening or whether persons with type 2 diabetes mellitus should be treated differently from those without.1
A number of studies suggest that intensive lifestyle and various pharmacotherapeutic interventions in persons with IGT or IFG decrease the incidence of type 2 diabetes mellitus over follow-up periods of up to 7 years.1,32 However, there are few data on prevention or delay of cardiovascular and other long-term health outcomes, including CVD events or death. There are also few data on treatments for cardiovascular risk factors among persons with IGT or IFG compared with normoglycemic populations.
Potential Harms of Screening and Treatment: Observational studies report no serious long-term adverse psychological effects from receiving a new diagnosis of type 2 diabetes mellitus from screening. Data are limited, however, and studies vary in outcome measures, characteristics of the screened and comparison populations, and methodological quality. One cohort study compared persons with type 2 diabetes mellitus diagnosed in a general practitioner's office (most of whom had diabetes-related symptoms) with those diagnosed via screening. The researchers found that the former group had worse psychological measures, although the negative effects diminished over time. No studies reported adverse effects of receiving a diagnosis of IFG or IGT, and no studies examined the psychological effects of the actual screening test or of labeling a large proportion of the population with IFG or IGT.
Treatments for diabetes are relatively safe. However, tight glycemic control at a time when glucose levels are relatively low (that is, the time between screening and clinical diagnosis) can induce hypoglycemia. In the UKPDS, 2.3% of people receiving insulin had a major hypoglycemic episode each year, as did 0.4% to 0.6% of those receiving oral hypoglycemic agents.15 Angiotensin-converting enzyme inhibitors and statins have reasonably low levels of serious adverse effects.33 New information has recently been published linking rosiglitazone use to increased risk for myocardial infarction.36
Estimate of Magnitude of Net Benefit: When there is no direct evidence on the effectiveness of screening, the USPSTF looks to indirect evidence of benefit. The USPSTF found that available screening tests accurately identify asymptomatic diabetes and that in adults with hypertension and diabetes, more intensive blood pressure treatment leads to a substantial reduction—approximately 50%—in CVD events over 5 years. The USPSTF did not find evidence in other populations that screening and treatment of early diabetes or screening for IGT or IFG would lead to improved health outcomes compared with waiting to treat diabetes once it becomes symptomatic. Therefore, the USPSTF concluded that there was moderate certainty that screening for diabetes in adults with hypertension would lead to substantial benefit but that there is insufficient evidence to determine the benefit of screening in other populations.
How Does Evidence Fit with Biological Understanding? Type 2 diabetes mellitus may remain undiagnosed for several years because hyperglycemia develops gradually and may not cause symptoms.3,37 However, at some unknown level of hyperglycemia, risk for macrovascular complications increases in persons with undiagnosed diabetes. The prevalence of advanced microvascular complications, such as proliferative retinopathy, is low at clinical diagnosis, and duration of diabetes and degree of hyperglycemia are associated with increasing risk for these complications over time.38-41 The epidemiology of macrovascular complications differs from that of microvascular complications: Cardiovascular morbidity and mortality are substantially elevated well before diagnosis of diabetes and are also elevated in persons with IFG or IGT.9,42-49
Update of Previous USPSTF Recommendation: This recommendation updates the one released in 2003. The major change in the current recommendation is that routine screening for type 2 diabetes mellitus in adults with hyperlipidemia is no longer part of the grade B recommendation. As discussed in the Clinical Considerations section, clinicians should perform an assessment of global CVD risk, including the risk in those with hyperlipidemia, and if the patient's risk is near a threshold for treatment with lipid-lowering medications, they should screen for diabetes to adequately assess the patient's CVD risk.
The American Academy of Family Physicians recommends screening for type 2 diabetes in adults with hypertension and hyperlipidemia; it found insufficient evidence to recommend for or against screening adults who are at low risk for coronary vascular disease.50 The American College of Obstetricians and Gynecologists recommends fasting glucose testing for women beginning at age 45 years, with an interval of 3 years. The Canadian Task Force on Preventive Health Care found fair evidence to recommend screening adults with hypertension and hyperlipidemia for type 2 diabetes mellitus to prevent cardiovascular events and death (a grade B recommendation).51 On the basis of expert opinion, the American Diabetes Association recommends consideration of screening to detect prediabetes (IFG or IGT) or diabetes in persons 45 years of age and older, particularly in those with a body mass index of 25 kg/m2 or greater. Such testing should also be considered in people who are younger than 45 years of age and overweight if they have another risk factor for diabetes, including inactivity, family history of type 2 diabetes mellitus, membership in a high-risk ethnic group, gestational diabetes, hypertension, dyslipidemia, IGT or IFG, or a history of vascular disease.52
Corresponding Author: Ned Calonge, MD, MPH, Chair, U.S. Preventive Services Task Force, c/o Program Director, USPSTF, Agency for Healthcare Research and Quality, 540 Gaither Road, Rockville, MD 20850, e-mail: firstname.lastname@example.org.
Members of the U.S. Preventive Services Task Force*: Ned Calonge, MD, MPH, Chair (Colorado Department of Public Health and Environment, Denver, CO); Diana B. Petitti, MD, MPH, Vice-Chair (Keck School of Medicine, University of Southern California, Sierra Madre, CA); Thomas G. DeWitt, MD (Children's Hospital Medical Center, Cincinnati, OH); Allen J. Dietrich, MD (Dartmouth Medical School, Hanover, NH); Leon Gordis, MD, MPH, DrPH (Johns Hopkins Bloomberg School of Public Health, Baltimore, MD); Kimberly D. Gregory, MD, MPH (Cedars-Sinai Medical Center, Los Angeles, CA); Russell Harris, MD, MPH (University of North Carolina School of Medicine, Chapel Hill, NC); George Isham, MD, MS, (HealthPartners, Minneapolis, MN); Rosanne Leipzig, MD, PhD (Mount Sinai School of Medicine, New York, NY); Michael L. LeFevre, MD, MSPH (University of Missouri School of Medicine, Columbia, MO); Carol Loveland-Cherry, PhD, RN (University of Michigan School of Nursing, Ann Arbor, MI); Lucy N. Marion, PhD, RN (Medical College of Georgia, Augusta, GA); Virginia A. Moyer, MD, MPH (University of Texas Health Science Center, Houston, TX); Judith K. Ockene, PhD (University of Massachusetts Medical School, Worcester, MA); George F. Sawaya, MD (University of California, San Francisco, CA); and Barbara P. Yawn, MD, MSPH, MSc (Olmsted Medical Center, Rochester, MN).
*Members of the Task Force at the time this recommendation was finalized. For a list of current Task Force members, go to https://www.uspreventiveservicestaskforce.org/Page/Name/our-members.
Disclaimer: Recommendations made by the USPSTF are independent of the U.S. Government. They should not be construed as an official position of the Agency for Healthcare Research and Quality or the U.S. Department of Health and Human Services.
Requests for linking or to incorporate content in electronic resources should be sent via the USPSTF contact form.
Source: U.S. Preventive Services Task Force. Screening for Type 2 Diabetes Mellitus in Adults: U.S. Preventive Services Task Force Recommendation Statement. Originally in Ann Intern Med 2008;148:846-854.
- Norris SL, Kansagara D, Bougatsos C, Fu R. Screening adults for type 2 diabetes: a review of the evidence for the U.S. Preventive Services Task Force. Ann Intern Med. 2008;148:855-68.
- Cowie CC, Rust KF, Byrd-Holt DD, Eberhardt MS, Flegal KM, Engelgau MM, et al. Prevalence of diabetes and impaired fasting glucose in adults in the U.S. population: National Health and Nutrition Examination Survey 1999-2002. Diabetes Care. 2006;29:1263-8. [PMID: 16732006]
- Gregg EW, Cadwell BL, Cheng YJ, Cowie CC, Williams DE, Geiss L, et al. Trends in the prevalence and ratio of diagnosed to undiagnosed diabetes according to obesity levels in the U.S. Diabetes Care. 2004;27:2806-12. [PMID: 15562189]
- Centers for Disease Control and Prevention. National Diabetes Fact Sheet: General Information and National Estimates on Diabetes in the United States, 2005. Atlanta: U.S. Department of Health and Human Services, Centers for Disease Control and Prevention, 2005. Accessed at www.cdc.gov/diabetes/pubs/pdf/ndfs_2005.pdf on 21 April 2008.
- Harris MI, Flegal KM, Cowie CC, Eberhardt MS, Goldstein DE, Little RR, et al. Prevalence of diabetes, impaired fasting glucose, and impaired glucose tolerance in U.S. adults. The Third National Health and Nutrition Examination Survey, 1988-1994. Diabetes Care. 1998;21:518-24. [PMID: 9571335]
- Engelgau MM, Thompson TJ, Herman WH, Boyle JP, Aubert RE, Kenny SJ, et al. Comparison of fasting and 2-hour glucose and HbA1c levels for diagnosing diabetes. Diagnostic criteria and performance revisited. Diabetes Care. 1997;20:785-91. [PMID: 9135943]
- Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care. 1997;20:1183-97. [PMID: 9203460]
- McCance DR, Hanson RL, Charles MA, Jacobsson LT, Pettitt DJ, Bennett PH, et al. Comparison of tests for glycated haemoglobin and fasting and two hour plasma glucose concentrations as diagnostic methods for diabetes. BMJ. 1994;308:1323-8. [PMID: 8019217]
- Coutinho M, Gerstein HC, Wang Y, Yusuf S. The relationship between glucose and incident cardiovascular events. A metaregression analysis of published data from 20 studies of 95,783 individuals followed for 12.4 years. Diabetes Care. 1999;22:233-40. [PMID: 10333939]
- Little RR, Rohlfing CL, Wiedmeyer HM, Myers GL, Sacks DB, Goldstein DE. NGSP Steering Committee. The national glycohemoglobin standardization program: a five-year progress report. Clin Chem. 2001;47:1985-92. [PMID: 11673367]
- Peters AL, Davidson MB, Schriger DL, Hasselblad V. A clinical approach for the diagnosis of diabetes mellitus: an analysis using glycosylated hemoglobin levels. Meta-analysis Research Group on the Diagnosis of Diabetes Using Glycated Hemoglobin Levels. JAMA. 1996;276:1246-52. [PMID: 8849753]
- Edelman D, Olsen MK, Dudley TK, Harris AC, Oddone EZ. Utility of hemoglobin A1c in predicting diabetes risk. J Gen Intern Med. 2004;19:1175-80. [PMID: 15610327]
- Norberg M, Eriksson JW, Lindahl B, Andersson C, Rolandsson O, Stenlund H, et al. A combination of HbA1c, fasting glucose and BMI is effective in screening for individuals at risk of future type 2 diabetes: OGTT is not needed. J Intern Med. 2006;260:263-71. [PMID: 16918824]
- Lauritzen T, Griffin S, Borch-Johnsen K, Wareham NJ, Wolffenbuttel BH, Rutten G. Anglo-Danish-Dutch Study of Intensive Treatment in People with Screen Detected Diabetes in Primary Care. The ADDITION study: proposed trial of the cost-effectiveness of an intensive multifactorial intervention on morbidity and mortality among people with type 2 diabetes detected by screening. Int J Obes Relat Metab Disord. 2000;24 Suppl 3:S6-11. [PMID: 11063279]
- 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. [PMID: 9742976]
- Hansson L, Zanchetti A, Carruthers SG, Dahlöf B, Elmfeldt D, Julius S, et al. Effects of intensive blood-pressure lowering and low-dose aspirin in patients with hypertension: principal results of the Hypertension Optimal Treatment (HOT) randomised trial. HOT Study Group. Lancet. 1998;351:1755-62. [PMID: 9635947]
- 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. [PMID: 9732337]
- Curb JD, Pressel SL, Cutler JA, Savage PJ, Applegate WB, Black H, et al. Effect of diuretic-based antihypertensive treatment on cardiovascular disease risk in older diabetic patients with isolated systolic hypertension. Systolic Hypertension in the Elderly Program Cooperative Research Group. JAMA. 1996;276: 1886-92. [PMID: 8968014]
- Tuomilehto J, Rastenyte D, Birkenhäger WH, Thijs L, Antikainen R, Bulpitt CJ, et al. Effects of calcium-channel blockade in older patients with diabetes and systolic hypertension. Systolic Hypertension in Europe Trial Investigators. N Engl J Med. 1999;340:677-84. [PMID: 10053176]
- Yusuf S, Sleight P, Pogue J, Bosch J, Davies R, Dagenais G. Effects of an angiotensin-converting-enzyme inhibitor, ramipril, on cardiovascular events in high-risk patients. The Heart Outcomes Prevention Evaluation Study Investigators. N Engl J Med. 2000;342:145-53. [PMID: 10639539]
- Tatti P, Pahor M, Byington RP, Di Mauro P, Guarisco R, Strollo G, et al. Outcome results of the Fosinopril Versus Amlodipine Cardiovascular Events Randomized Trial (FACET) in patients with hypertension and NIDDM. Diabetes Care. 1998;21:597-603. [PMID: 9571349]
- Haffner SM, Alexander CM, Cook TJ, Boccuzzi SJ, Musliner TA, Pedersen TR, et al. Reduced coronary events in simvastatin-treated patients with coronary heart disease and diabetes or impaired fasting glucose levels: subgroup analyses in the Scandinavian Simvastatin Survival Study. Arch Intern Med. 1999;159:2661-7. [PMID: 10597756]
- Rubins HB, Robins SJ, Collins D, Fye CL, Anderson JW, Elam MB, et al. Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high-density lipoprotein cholesterol. Veterans Affairs High-Density Lipoprotein Cholesterol Intervention Trial Study Group. N Engl J Med. 1999; 341:410-8. [PMID: 10438259]
- The Long-Term Intervention with Pravastatin in Ischaemic Disease (LIPID) Study Group. Prevention of cardiovascular events and death with pravastatin in patients with coronary heart disease and a broad range of initial cholesterol levels. N Engl J Med. 1998;339:1349-57. [PMID: 9841303]
- Heart Protection Study Collaborative Group. MRC/BHF Heart Protection Study of cholesterol lowering with simvastatin in 20,536 high-risk individuals: a randomised placebo-controlled trial. Lancet. 2002;360:7-22. [PMID: 12114036]
- Heart Protection Study Collaborative Group. MRC/BHF Heart Protection Study of cholesterol-lowering with simvastatin in 5963 people with diabetes: a randomised placebo-controlled trial. Lancet. 2003;361:2005-16. [PMID: 12814710]
- American Diabetes Association. Aspirin therapy in diabetes. Diabetes Care. 2000;23 Suppl 1:S61-2. [PMID: 12017681]
- Colwell JA. Aspirin therapy in diabetes. Diabetes Care. 1997;20:1767-71. [PMID: 9353620]
- Hayden M, Pignone M, Phillips C, Mulrow C. Aspirin for the primary prevention of cardiovascular events: a summary of the evidence for the U.S. Preventive Services Task Force. Ann Intern Med. 2002;136:161-72. [PMID: 11790072]
- Ridker PM, Cook NR, Lee IM, Gordon D, Gaziano JM, Manson JE, et al. A randomized trial of low-dose aspirin in the primary prevention of cardiovascular disease in women. N Engl J Med. 2005;352:1293-304. [PMID: 15753114]
- U.S. Preventive Services Task Force. Screening for type 2 diabetes mellitus in adults: recommendations and rationale. Ann Intern Med. 2003;138:212-4. [PMID: 12558361]
- Harris R, Donahue K, Rathore SS, Frame P, Woolf SH, Lohr KN. Screening adults for type 2 diabetes: a review of the evidence for the U.S. Preventive Services Task Force. Ann Intern Med. 2003;138:215-29. [PMID: 12558362]
- Bradford RH, Shear CL, Chremos AN, Dujovne CA, Franklin FA, Grillo RB, et al. Expanded Clinical Evaluation of Lovastatin (EXCEL) study results: two-year efficacy and safety follow-up. Am J Cardiol. 1994;74:667-73. [PMID: 7942524]
- Israili ZH, Hall WD. Cough and angioneurotic edema associated with angiotensin-converting enzyme inhibitor therapy. A review of the literature and pathophysiology. Ann Intern Med. 1992;117:234-42. [PMID: 1616218]
- Pierce LR, Wysowski DK, Gross TP. Myopathy and rhabdomyolysis associated with lovastatin-gemfibrozil combination therapy. JAMA. 1990;264:71-5. [PMID: 2355431]
- Nissen SE, Wolski K. Effect of rosiglitazone on the risk of myocardial infarction and death from cardiovascular causes. N Engl J Med. 2007;356:2457-71. [PMID: 17517853]
- Harris MI, Klein R, Welborn TA, Knuiman MW. Onset of NIDDM occurs at least 4-7 yr before clinical diagnosis. Diabetes Care. 1992;15:815-9. [PMID: 1516497]
- Henricsson M, Tyrberg M, Heijl A, Janzon L. Incidence of blindness and visual impairment in diabetic patients participating in an ophthalmological control and screening programme. Acta Ophthalmol Scand. 1996;74:533-8. [PMID: 9017036]
- Klein R, Klein BE, Moss SE, Davis MD, DeMets DL. Glycosylated hemoglobin predicts the incidence and progression of diabetic retinopathy. JAMA. 1988;260:2864-71. [PMID: 3184351]
- Stratton IM, Kohner EM, Aldington SJ, Turner RC, Holman RR, Manley SE, et al. UKPDS 50: risk factors for incidence and progression of retinopathy in Type II diabetes over 6 years from diagnosis. Diabetologia. 2001;44:156-63. [PMID: 11270671]
- Liverpool Diabetic Eye Study. Incidence of sight-threatening retinopathy in patients with type 2 diabetes in the Liverpool Diabetic Eye Study: a cohort study. Lancet. 2003;361:195-200. [PMID: 12547541]
- Davis TM, Stratton IM, Fox CJ, Holman RR, Turner RC. U.K. Prospective Diabetes Study 22. Effect of age at diagnosis on diabetic tissue damage during the first 6 years of NIDDM. Diabetes Care. 1997;20:1435-41. [PMID: 9283793]
- Chowdhury TA, Lasker SS. Complications and cardiovascular risk factors in South Asians and Europeans with early-onset type 2 diabetes. QJM. 2002;95: 241-6. [PMID: 11937651]
- Haffner SM, Stern MP, Hazuda HP, Mitchell BD, Patterson JK. Cardiovascular risk factors in confirmed prediabetic individuals. Does the clock for coronary heart disease start ticking before the onset of clinical diabetes? JAMA. 1990;263:2893-8. [PMID: 2338751]
- Hu FB, Stampfer MJ, Haffner SM, Solomon CG, Willett WC, Manson JE. Elevated risk of cardiovascular disease prior to clinical diagnosis of type 2 diabetes. Diabetes Care. 2002;25:1129-34. [PMID: 12087009]
- Khaw KT, Wareham N, Luben R, Bingham S, Oakes S, Welch A, et al. Glycated haemoglobin, diabetes, and mortality in men in Norfolk cohort of european prospective investigation of cancer and nutrition (EPIC-Norfolk). BMJ. 2001;322:15-8. [PMID: 11141143]
- McPhillips JB, Barrett-Connor E, Wingard DL. Cardiovascular disease risk factors prior to the diagnosis of impaired glucose tolerance and non-insulindependent diabetes mellitus in a community of older adults. Am J Epidemiol. 1990;131:443-53. [PMID: 2301354]
- Meigs JB, Nathan DM, Wilson PW, Cupples LA, Singer DE. Metabolic risk factors worsen continuously across the spectrum of nondiabetic glucose tolerance. The Framingham Offspring Study. Ann Intern Med. 1998;128:524-33. [PMID: 9518396]
- Pan WH, Cedres LB, Liu K, Dyer A, Schoenberger JA, Shekelle RB, et al. Relationship of clinical diabetes and asymptomatic hyperglycemia to risk of coronary heart disease mortality in men and women. Am J Epidemiol. 1986;123: 504-16. [PMID: 3946397]
- American Academy of Family Physicians. AAFP Policy Action: Summary of Recommendations for Clinical Preventive Services. Revision 6.3. March 2007. Leawood, KS: American Academy of Family Physicians; 2007.
- Feig DS, Palda VA, Lipscombe L. Canadian Task Force on Preventive Health Care. Screening for type 2 diabetes mellitus to prevent vascular complications: updated recommendations from the Canadian Task Force on Preventive Health Care. CMAJ. 2005;172:177-80. [PMID: 15655234]
- American Diabetes Association. Standards of medical care in diabetes. Diabetes Care. 2007;30 Suppl 1:S4-41. [PMID: 17192377]