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Diabetes Care 27:17-20, 2004
© 2004 by the American Diabetes Association, Inc.


Clinical Care/Education/Nutrition
Original Article

Glycemic Control From 1988 to 2000 Among U.S. Adults Diagnosed With Type 2 Diabetes

A preliminary report

Carol E. Koro, PHD1,2, Steven J. Bowlin, DO, PHD1, Nancy Bourgeois, BS1 and Donald O. Fedder, DPH2

1 GlaxoSmithKline, Upper Providence, Pennsylvania
2 University of Maryland, Baltimore, Maryland

Address correspondence and reprint requests to Carol E. Koro, 1250 South Collegeville Rd., UP4305, Collegeville, PA 19426-0989. E-mail: ckoro001{at}umaryland.edu


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
 References
 
OBJECTIVE—To describe the changes in demographics, antidiabetic treatment, and glycemic control among the prevalent U.S. adult diagnosed type 2 diabetes population between the National Health and Nutrition Examination Survey (NHANES) III (1988–1994) and the initial release of NHANES 1999–2000.

RESEARCH DESIGN AND METHODS—The study population was derived from NHANES III (n = 1,215) and NHANES 1999–2000 (n = 372) subjects who reported a diagnosis of type 2 diabetes with available data on diabetes medication and HbA1c. Four therapeutic regimens were defined: diet only, insulin only, oral antidiabetic drugs (OADs) only, or OADs plus insulin. Multiple logistic regression was used to examine changes in antidiabetic regimens and glycemic control rates over time, adjusted for demographic and clinical risk factors. The outcome measure for glycemic control was HbA1c. Glycemic control rates were defined as the proportion of type 2 diabetic patients with HbA1c level <7%.

RESULTS—Dietary treatment in individuals with diabetes decreased as the sole therapy from 27.4 to 20.2% between the surveys. Insulin use also decreased from 24.2 to 16.4%, while those on OADs only increased from 45.4 to 52.5%. Combination of OADs and insulin increased from 3.1 to 11.0%. Glycemic control rates declined from 44.5% in NHANES III (1988–1994) to 35.8% in NHANES 1999–2000.

CONCLUSIONS—Treatment regimens among U.S. adults diagnosed with type 2 diabetes have changed substantially over the past 10 years. However, a decrease in glycemic control rates was also observed during this time period. This trend may contribute to increased rates of macrovascular and microvascular diabetic complications, which may impact health care costs. Our data support the public health message of implementation of early, aggressive management of diabetes.

Abbreviations: OAD, oral antidiabetic drug • NHANES, National Health and Nutrition Examination Survey


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
 References
 
Inadequate glycemic control among individuals with diabetes constitutes a major public health problem in the U.S. Uncontrolled diabetes is associated with premature death and disability as well as decreased quality of life and significantly adds to national medical health care expenditures (1). Recent estimates show that the minimum direct and indirect expenditures attributable to diagnosed diabetes in 2002 were $132 billion (2). Glycemic control remains the major therapeutic objective for prevention of target organ damage and other complications arising from diabetes. Studies have shown that a comprehensive and aggressive management approach is effective in decreasing the rate of progression of microvascular complications (3). Treatment regimens of diet and exercise, insulin, and oral hypoglycemic agents are known to improve glycemia (4,5), and current approaches to disease management that include greater patient self-participation are recommended (6,7).

However, the adequacy of adherence to American Diabetes Association guidelines, as reflected in estimates of glycemic control (8), have not been published recently for the U.S. population. A study of U.S. adults sampled from 1988 to 1994 reported that the glycemic control rate was only 44.6% among patients with diagnosed type 2 diabetes (9). Recently, the initial 1999–2000 National Health and Nutrition Examination Survey (NHANES) data have been released, providing an opportunity for further analysis. This report describes the changes in demographics, general drug treatment, and glycemic control among the prevalent U.S. adult diagnosed type 2 diabetes population between NHANES III (1988–1994) and NHANES 1999–2000.


    RESEARCH DESIGN AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
 References
 
The study population was derived from both the NHANES III (1988–1994) and the initial release of NHANES 1999–2000 (10). These surveys used a multistage cluster sample design to gather data about the health and nutritional status of the civilian noninstitutionalized population of the U.S. and have been described in detail elsewhere (11). For our analysis, we defined the study sample as the 1,686 subjects in NHANES III (1988–1994) and the 533 subjects in NHANES 1999–2000 aged >=20 years who responded "yes" to the question "Other than during pregnancy, has a doctor ever told you that you had diabetes or sugar diabetes?" and in whom HbA1c had been measured. To limit the analysis to adults with diagnosed type 2 diabetes, we excluded subjects whose age at diagnosis was <30 years and who started insulin therapy within 1 year of diagnosis. We also excluded subjects for whom information on type of diabetes medication, BMI, or duration of diabetes was missing. After applying the exclusions, 1,215 subjects in NHANES III (1988–1994) and 372 subjects in NHANES 1999–2000 remained for analysis. We used the NHANES sampling weights and primary sampling units to estimate the number of individuals with diagnosed diabetes, by various demographic, treatment, and glycemic control groups, in the overall U.S. population.

Four antidiabetic therapeutic regimens were defined for this study: diet, insulin, oral antidiabetic drugs (OADs; monotherapy or in combination), and OADs plus insulin. These were defined according to a "yes" or "no" response to the following questions: "Are you now taking insulin?" and "Are you now taking diabetes pills?" We classified individuals who answered "no" to both of these questions as using diet-only therapy. The number and percent of adults diagnosed with type 2 diabetes on each therapeutic regimen was calculated, as was the estimate of those who achieved glycemic control using a cutpoint HbA1c level <7% (8). Glycemic control rates were calculated as the proportion of type 2 diabetic patients with an HbA1c level <7%. In NHANES III (1988–1994), HbA1c was measured by high-performance liquid chromatography assay, as in the Diabetes Control and Complications Trial (12). The upper limit of normal for HbA1c in the assay system is 6.1%, which is identical to the upper limit of normal recommended by the American Diabetes Association using the same assay system. Glycohemoglobin for NHANES 1999–2000 was measured using a Boronate Affinity High Performance Liquid Chromatography system (Primus, Kansas City, MO) (13), which has been standardized to the reference method used for the Diabetes Control and Complications Trial. Because the HbA1c measurements were standardized to the same reference method, there were no differences in normal range or upper limit for HbA1c in NHANES III (1988–1994) and NHANES 1999–2000.

In addition to univariate analysis, we used multiple logistic regression to examine whether demographics, treatment regimen, and other differences between the survey participants might explain any observed changes in national glycemic control rates between 1988 and 2000. In this logistic model, glycemic control was the dependent variable, the particular NHANES survey was the independent variable, and treatment regimen, age, sex, ethnicity, BMI, and duration of diabetes were potential confounding factors. In similar fashion, logistic models were used to determine whether changes in treatment regimens between the two surveys might be due to demographic and other differences between the surveys’ participants rather than real temporal changes.

SUDAAN software (Research Triangle Institute, Research Triangle Park, NC) was used to account for the nonrandom cluster sample design in calculating variance estimates (14). Standard errors were computed for all prevalence rates via Taylor approximations. Using SAS statistical software (SAS Institute, Cary, NC), logistic regression models were run with sampling weights provided by the NHANES surveys, allowing population-based effect estimates. In the logistic models that included both surveys, it was not possible to calculate CIs for the effect estimates (odds ratios [ORs]), because the sampling methods of the two surveys differ.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
 References
 
Changes in demographic and risk factor information between NHANES III (1988–1994) and NHANES 1999–2000 are described in Table 1. The number of prevalent cases of adults with diagnosed type 2 diabetes increased from 8.1 million in 1988–1994 to 10.3 million in 1999–2000. The proportion of men increased from 45% in NHANES III (1988–1994) to 51% in NHANES 1999–2000; individuals with diabetes in 1999–2000 were slightly younger than those in the earlier survey. The percentage of non-Hispanic whites among patients with diagnosed type 2 diabetes decreased from 74% in NHANES III (1988–1994) to 61% in NHANES 1999–2000. On the other hand, there was a slight increase in the percentage of non-Hispanic blacks and Mexican Americans, and the proportion of ethnic groups other than non-Hispanic whites, non-Hispanic blacks, and Mexican Americans increased from 6 to 17%. Mean BMI increased by 6% from 30.4 to 32.3 kg/m2, the mean duration of diabetes increased by 28% from 9.3 to 11.9 years, and the mean HbA1c increased by 3% from 7.7 to 7.9%.


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Table 1— Characteristics of the NHANES III (1988–1994) and NHANES 1999–2000 adult individuals with diagnosed type 2 diabetes

 
Changes in therapeutic regimens between NHANES III (1988–1994) and NHANES 1999–2000 are shown in Table 2. The proportion of adults diagnosed with type 2 diabetes treated with insulin only decreased from 24.2% (n = 1,947,176) in NHANES III (1988–1994) to 16.4% (n = 1,679,985) in NHANES 1999–2000. The likelihood of medication use in NHANES 1999–2000 relative to NHANES III, adjusted for potential confounders, is represented by the adjusted ORs in Table 2. The adjusting factors were age, sex, ethnicity, BMI, and duration of diabetes. An adjusted OR of 0.61 for insulin was found, indicating that the odds of being treated with insulin only decreased by 39% among the NHANES 1999–2000 survey participants compared with the NHANES III (1988–1994) participants. The proportion of subjects using only OADs increased over time (from 45.4% [n = 3,655,259] to 52.5% [n = 5,384,943]; OR 1.50). The use of insulin and OADs in combination increased from 3.1% (n = 248,616) to 11.0% (n = 1,128,922) (OR 3.50). Use of diet only decreased from 27.4% (n = 2,207,855) to 20.2% (n = 2,070,771) (OR 0.58).


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Table 2— Treatment of diagnosed adult type 2 diabetes in NHANES III (1988–1994) and NHANES 1999–2000

 
The rate of glycemic control as defined by HbA1c levels <7% was 44.5% for NHANES III (1988–1994) and 35.8% for NHANES 1999–2000. After adjustment for age, ethnicity, sex, BMI, medication use, and duration of diabetes, the odds of glycemic control was 21% lower in NHANES 1999–2000 compared with NHANES III (1988–1994) (OR 0.79; Table 3).


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Table 3— Multiple logistic regression model of glycemic control between adults diagnosed with type 2 diabetes in NHANES 1999–2000 and NHANES III (1988–1994)

 

    CONCLUSIONS
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
 References
 
Our findings show that the proportion of adults in the U.S. with adequately controlled, diagnosed type 2 diabetes decreased between 1988 and 2000. Diabetes is controlled in only 36% of the more recent survey participants, despite recommendations for early diagnosis and aggressive treatment in recent years. We also observed changes in the demographic distribution of the adults with diagnosed type 2 diabetes from NHANES III (1988–1994) to NHANES 1999–2000, such as an increased proportion of men and minority groups other than non-Hispanic blacks and Mexican Americans. In recent years, individuals with diagnosed diabetes tended to be younger, to weigh more, and to have a longer duration of diabetes. However, we found that these demographic differences did not fully explain the lower glycemic control rates seen in recent years. Other reasons might account for the observed declining rates over time, such as changes in patient compliance with treatment programs despite more aggressive management. Another possible explanation for this observation may be surveillance bias due to a preferential increased screening for diabetes in high-risk individuals in the late 1990s compared with the previous decade.

In addition to changes in demographic features among patients over time, we also observed changes in the therapeutic regimen. The proportion of current individuals with diagnosed diabetes following diet-only or insulin-only treatment regimens has decreased since 1988–1994, but the proportion receiving OADs only or OADs in combination with insulin has increased. This change may be due to a larger selection of marketed oral agents. The increase in use of OADs from 1994 to 2000 is likely because only sulfonylureas were available in the earlier time period. By 2000, at least six new products in four new classes of OADs had become available. Another reason for the observed change may be a trend toward more aggressive and earlier treatment with OADs and OAD/insulin combinations.

We have also demonstrated that glycemic control was better in older individuals with diagnosed diabetes, those with higher BMI, and those with a longer duration of diagnosed diabetes (Table 3). Diabetic control was worse in minority ethnic groups and those taking medications (as compared with those on diet only). It is not clear why glycemic control might be better in older individuals, but some studies have suggested that older patients may have better access to medical care, are more motivated to receive care, and are more compliant with medication use (15). This finding is somewhat in contrast to that of the U.K. Prospective Diabetes Study (UKPDS), which suggested that glycemic control rates among individuals with diabetes decrease with disease duration and, thus, with age (16). Also in contrast to the current study, Harris et al. (9) found that obesity was not related to glycemic control. They attributed their results to the cross-sectional design of the survey.

There are several limitations to the current analysis. The sample size from the NHANES 1999–2000 survey is small relative to NHANES III (1988–1994). As the survey continues over the next few years, more subjects will accrue, and the analysis can be repeated. Another limitation is that medication use is self-reported, and this may cause some misclassification in measured treatment regimens. Additionally, because NHANES surveys are cross-sectional in design, some of our findings may be related to survival bias in that individuals with diabetes having the poorest control may have died over time and could not participate in surveys. Also, in 1997, the American Diabetes Association changed the diagnostic criteria for diabetes, which may have influenced prevalence estimates of diagnosed diabetes between the two NHANES surveys (8).

We conclude that the proportion of adults in the U.S. with diagnosed type 2 diabetes that is controlled is inadequate and less favorable than in previous years. The cardiovascular and other consequences of inadequate glycemic control warrant serious consideration by treating physicians and others who care for individuals with diabetes. These data lend support to public health initiatives advocating early and aggressive management of diabetes.


    Footnotes
 
A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

Received for publication June 17, 2003. Accepted for publication September 16, 2003.


    References
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
 References
 

  1. Gilmer TP, O’Conner PJ, Manning WG, Rush WA: The cost to health plans of poor glycemic control. Diabetes Care 20: 1847–1853, 1997[Abstract]
  2. Hogan P, Dall T, Nikolov P, American Diabetes Association: Economic costs of diabetes in the U.S. in 2002. Diabetes Care 26: 917–932, 2003[Abstract/Free Full Text]
  3. 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 352: 837–853, 1998[Medline]
  4. Holman RR, Turner RC: Optimising blood glucose control in type 2 diabetes: an approach based on fasting blood glucose measurements. Diabet Med 5: 582–588, 1988[Medline]
  5. Johnson JL, Wolf SL, Kabadi UM: Efficacy of insulin and sulfonylurea combination therapy in type 2 diabetes: a meta-analysis of the randomized placebo-controlled trials. Arch Intern Med 156: 259–264, 1996[Abstract]
  6. Nicolucci A, Cavaliere D, Scorpiglione N, Carinci F, Capani F, Tognoni G, Benedetti MM: A comprehensive assessment of the avoidability of long-term complications of diabetes: a case-control study. Diabetes Care 19: 927–933, 1996[Abstract]
  7. American Diabetes Association: Standards of medical care for patients with diabetes mellitus. Diabetes Care 23 (Suppl. 1): S32–S42, 2000
  8. American Diabetes Association: Standards of medical care for patients with diabetes mellitus (Position Statement). Diabetes Care 21 (Suppl. 1): S23–S31, 1998
  9. Harris MI, Eastman RC, Cowie CC, Flegal KM, Eberhardt MS: Racial and ethnic differences in glycemic control of adults with type 2 diabetes. Diabetes Care 22: 403–408, 1999[Abstract]
  10. Centers for Disease Control and Prevention: NHANES 1999–2000 public data release file documentation [article online], 2000. Available from http://www.cdc.gov/nchs/about/major/nhanes/currentnhanes.htm. Accessed 7 August 2003
  11. Centers for Disease Control and Prevention, National Center for Health Statistics: Vital and Health Statistics, Plan and Operation of the Third National Health and Nutrition and Examination Survey, 1988–1994. Rockville, MD, U.S. Department of Health and Human Services, Public Health Service, 1994, p. 4–485 (DHHS publ. no. PHS 94–1308, series 1, no. 32)
  12. Diabetes Control and Complications Trial Research Group: The effect of intensive treatment of diabetes on the development and progression of long term complications in insulin-dependent diabetes mellitus. N Engl J Med 329: 977–986, 1993[Abstract/Free Full Text]
  13. Primus Corporation: Glycated Hemoglobin and Plasma Protein Analyzer Operator’s Manual for the Diabetes Care Test Package of the CLC330 and CLC385. Kansas City, MO, Primus Corporation, 1999
  14. Shah BV, Barnwell BG, Bieler GS: SUDAAN User’s Manual, Release 6.40. Research Triangle Park, NC, Research Triangle Institute, 1995
  15. El-Kibbi IM, Cook CB, Ziemer DC, Miller CD, Gallina DL, Philips LS: Association of younger age with poor glycemic control and obesity in urban African Americans with type 2 diabetes. Arch Intern Med 163: 69–75, 2003[Abstract/Free Full Text]
  16. Turner RC, Cull CA, Frighi V, Holman RR, for the U.K. Prospective Diabetes Study (UKPDS) Group: Glycemic control with diet, sulfonylurea, metformin, or insulin in patients with type 2 diabetes mellitus: progressive requirement for multiple therapies (UKPDS 49). JAMA 281: 2005–2012, 1999[Abstract/Free Full Text]

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J Am Board Fam MedHome page
D. Hinnen, L. L. Nielsen, A. Waninger, and P. Kushner
Incretin Mimetics and DPP-IV Inhibitors: New Paradigms for the Treatment of Type 2 Diabetes
J Am Board Fam Med, November 1, 2006; 19(6): 612 - 620.
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JRSMHome page
J. Gray, C. Millett, C. O'Sullivan, R. Z Omar, and A. Majeed
Association of age, sex and deprivation with quality indicators for diabetes: population-based cross sectional survey in primary care
J R Soc Med, November 1, 2006; 99(11): 576 - 581.
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Diabetes CareHome page
A. H. Barnett, M. Dreyer, P. Lange, M. Serdarevic-Pehar, and on behalf of the Exubera Phase III Study Group
An Open, Randomized, Parallel-Group Study to Compare the Efficacy and Safety Profile of Inhaled Human Insulin (Exubera) With Glibenclamide as Adjunctive Therapy in Patients With Type 2 Diabetes Poorly Controlled on Metformin
Diabetes Care, August 1, 2006; 29(8): 1818 - 1825.
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Diabetes CareHome page
T. Fan, C. E. Koro, D. O. Fedder, and S. J. Bowlin
Ethnic Disparities and Trends in Glycemic Control Among Adults With Type 2 Diabetes in the U.S. From 1988 to 2002
Diabetes Care, August 1, 2006; 29(8): 1924 - 1925.
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British Journal of Diabetes & Vascular DiseaseHome page
R. E Pratley, A. Salsali, and G. Matfin
Review: Inhibition of dipeptidyl peptidase-4 with vildagliptin: a potential new treatment for type 2 diabetes
The British Journal of Diabetes & Vascular Disease, July 1, 2006; 6(4): 150 - 156.
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The Diabetes EducatorHome page
J. E. Gerich
Clinicians can help their patients control postprandial hyperglycemia as a means of reducing cardiovascular risk.
The Diabetes Educator, July 1, 2006; 32(4): 513 - 522.
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Diabetes Spectr.Home page
R. Hood, V. Valentine, S. Mac, and W. H Polonsky
Use of Exenatide in Patients With Type 2 Diabetes
Diabetes Spectr, July 1, 2006; 19(3): 181 - 186.
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