Vital Signs: Decrease in Incidence of Diabetes-Related End-Stage Renal Disease among American Indians/Alaska Natives — United States, 1996–2013
Weekly / January 13, 2017 / 66(01);26-32
On January 10, 2017, this report was posted online as an MMWR Early Release.
Ann Bullock, MD1; Nilka Ríos Burrows, MPH2; Andrew S. Narva, MD3; Karen Sheff, MS1; Israel Hora, MS2; Akaki Lekiachvili, MD4; Hannah Cain5; David Espey, MD4 (View author affiliations)View suggested citation
• In the United States, American Indians/Alaska Natives (AI/AN) are more likely to have diagnosed diabetes than any other racial or ethnic group. In response to the epidemic of diabetes in AI/AN, the Indian Health Service (IHS) developed a comprehensive diabetes program, which includes clinical care improvements as well as public health and population management approaches.
• End-stage renal disease (ESRD) is a costly complication of diabetes. Incidence of ESRD related to diabetes (ESRD-D) among AI/AN decreased 54% during 1996–2013. By 2013, in adults with diabetes, ESRD-D incidence was the same in AI/AN as in whites.
• Since diabetes and its complications are public health problems, the response of IHS, a direct care agency organized around a public health model, might be useful to other health care systems.
• Additional information is available at https://www.cdc.gov/vitalsigns.
Background: American Indians and Alaska Natives (AI/AN) have the highest diabetes prevalence among any racial/ethnic group in the United States. Among AI/AN, diabetes accounts for 69% of new cases of end-stage renal disease (ESRD), defined as kidney failure treated with dialysis or transplantation. During 1982–1996, diabetes-related ESRD (ESRD-D) in AI/AN increased substantially and disproportionately compared with other racial/ethnic groups.
Methods: Data from the U.S. Renal Data System, the Indian Health Service (IHS), the National Health Interview Survey, and the U.S. Census were used to calculate ESRD-D incidence rates by race/ethnicity among U.S. adults aged ≥18 years during 1996–2013 and in the diabetic population during 2006–2013. Rates were age-adjusted based on the 2000 U.S. standard population. IHS clinical data from the Diabetes Cares and Outcomes Audit were analyzed for diabetes management measures in AI/AN.
Results: Among AI/AN adults, age-adjusted ESRD-D rates per 100,000 population decreased 54%, from 57.3 in 1996 to 26.5 in 2013. Although rates for adults in other racial/ethnic groups also decreased during this period, AI/AN had the steepest decline. Among AI/AN with diabetes, ESRD-D incidence decreased during 2006–2013 and, by 2013, was the same as that for whites. Measures related to the assessment and treatment of ESRD-D risk factors also showed more improvement during this period in AI/AN than in the general population.
Conclusion and implications for public health practice: Despite well-documented health and socioeconomic disparities among AI/AN, ESRD-D incidence rates among this population have decreased substantially since 1996. This decline followed implementation by the IHS of public health and population management approaches to diabetes accompanied by improvements in clinical care beginning in the mid-1980s. These approaches might be a useful model for diabetes management in other health care systems, especially those serving populations at high risk.
In the United States, diabetes is the leading cause of end-stage renal disease (ESRD), which is kidney failure treated with dialysis or transplantation (1). The prevalence of diabetes among American Indians/Alaska Natives (AI/AN) in the United States in 2012 (15.9%) was higher than that among non-Hispanic blacks (blacks) (13.2%), Hispanics (12.8%) or non-Hispanic whites (whites) (7.6%) during 2010–2012 (2). Diabetes accounts for 44% of new cases of ESRD (diabetes-associated ESRD [ESRD-D]) in the overall U.S. population and for 69% among AI/AN (1). Prevention or delay of ESRD-D involves control of blood pressure and blood glucose, early identification and monitoring of kidney disease, and use of angiotensin converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARB) in patients with albuminuria (3,4). This report presents trends in ESRD-D incidence for AI/AN compared with other racial/ethnic groups, and discusses the probable factors that influenced the improvements observed in this population during 1996–2013.
Medicare covers ESRD treatment for beneficiaries regardless of age and pays most of the cost of ESRD treatment in the United States (1). The U.S. Renal Data System (USRDS) is a surveillance system for ESRD based on clinical and claims data reports to the Centers for Medicare & Medicaid Services (CMS). Funded by the National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health, the USRDS collects, analyzes, and distributes demographic and clinical data on patients being treated for ESRD, including the primary diagnosis or cause of kidney failure. Because most ESRD patients become eligible for Medicare coverage after 90 days of ESRD treatment, only data on patients who have been treated for at least 90 days are included in the data set (1).
For each year studied, USRDS data were used to determine the number of adults aged ≥18 years in the United States who began treatment (dialysis or kidney transplantation) for ESRD-D. Data were analyzed for AI/AN, white, black, and Asian racial groups, which include persons of Hispanic and non-Hispanic origin. Data for persons of Hispanic origin were analyzed separately.
ESRD-D incidence was calculated using the number of newly treated ESRD-D cases and two population estimates for each racial and ethnic group: 1) total population from the U.S. Census during 1996–2013, and 2) population with diagnosed diabetes during 2006–2013.
The number of AI/AN with diagnosed diabetes was calculated using age- and sex-specific prevalence estimates from the Indian Health Service (IHS) National Data Warehouse during 2006–2013 and multiplying them by annual bridged single race population estimates for AI/AN from the U.S. Census; 2006 was the first year for which consistent prevalence data are available. The IHS National Data Warehouse includes patient registration and encounter data from IHS facilities, tribally operated health programs, and urban Indian (I/T/U) health systems.* These facilities serve approximately 2.2 million AI/AN persons who belong to 567 federally recognized tribes in 36 states.† Diabetes cases were identified using diagnosis codes 250.0–250.93 from the International Classification of Diseases, Ninth revision, Clinical Modification. Patients were considered to have diagnosed diabetes if they had at least two health care visits with a diabetes diagnosis code reported during the fiscal year (5). For the other racial and ethnic groups, estimates of the adult population with diagnosed diabetes (self-reported) were derived from the National Health Interview Survey.§
ESRD-D incidence rates were age-adjusted based on the 2000 U.S. standard population, and joinpoint regression was used to analyze trends (6,7). Each trend segment is described by an annual percentage change (APC) with a 95% confidence interval (CI), and the trend for the entire study period is described by the average annual percentage change (AAPC). The rate of change for linear trends was tested to determine whether it was significantly different from zero. Results were considered significant if the p value was <0.05.
Measures of care for AI/AN with diabetes were obtained from the IHS Diabetes Care and Outcomes Audit (Audit), including prescription of ACE inhibitors and ARBs; blood pressure; hemoglobin A1C to assess glucose control; and urine albumin-to-creatinine ratio testing for identifying and monitoring diabetic kidney disease. The Audit is an annual process for assessing diabetes care and health outcomes for AI/AN with diagnosed diabetes who receive care at I/T/U facilities, tracking performance on several dozen diabetes care measures and prevalence of several diabetes complications, including kidney disease.¶
Among AI/AN adults, age-adjusted ESRD-D incidence per 100,000 population increased, but not significantly, from 57.3 in 1996 to 63.5 in 1999 and then declined to 26.5 in 2013, a decrease of 54% (AAPC = −4.4% per year [95% CI = −5.7% to −3.0%], p<0.001) throughout the study period (Figure 1) (Table 1). Among other racial/ethnic groups, age-adjusted ESRD-D incidence among adults declined beginning in 1998 for Asians, 2001 for blacks, 2006 for whites, and 2000 for Hispanics.
Among AI/AN adults with diabetes, ESRD-D incidence declined during 2009–2013 (APC = −7.0% per year [−10.8% to −3.0%], p = 0.01) and, by 2013, was similar to that of whites with diabetes (152.7 versus 159.0 per 100,000 diabetic population, p = 0.84) (Figure 2) (Table 1). Among other racial/ethnic groups with diabetes, ESRD-D incidence declined in blacks and in whites during 2006–2013, and showed no consistent trend among Asians. Among Hispanics, ESRD-D incidence declined during 2006–2008, and then leveled off.
Data from the Audit show that prescription of ACE inhibitors and ARBs for AI/AN patients with diabetes increased substantially, from 42% in 1997 to 74% in 2002, and then remained steady, ranging from 68% to 73% each year through 2015 (Figure 3). Among AI/AN patients with diabetes and hypertension or chronic kidney disease (CKD), prescription of ACE inhibitors and ARBs was >77% for each year studied. Furthermore in 2014, among AI/AN with diabetes, 76% were prescribed ACE inhibitors or ARBs, compared with 56% of adults with diabetes in the general U.S. population during 2009–2014, assessed using National Health and Nutrition Examination Survey data (8).** Average blood pressure levels in AI/AN with diabetes have been well controlled since 1997, the first year such data were available. In 2015, average blood pressure among >101,000 AI/AN in the Audit with diabetes and hypertension was 133/76 mmHg, below the target of <140/90.†† Average hemoglobin A1C levels in AI/AN with diabetes decreased 10% from 1996 to 2014, from 9.0% to 8.1% (9). Finally, urine albumin-to-creatinine ratio testing was performed in 50% of AI/AN aged ≥65 years with diabetes in 2013, increasing to 62% by 2016. In the general Medicare diabetes population aged ≥65 years, the rate of urine albumin testing was 40% in 2013 (1).
Among AI/AN adults, age-adjusted ESRD-D incidence decreased 54% during 1996–2013; by 2013, among adults with diabetes, the ESRD-D rate was the same in AI/AN as in whites. This decline is especially remarkable given the well-documented health and socioeconomic disparities in the AI/AN population, including poverty, limited health care resources, and disproportionate burden of many health problems (10). The findings in this report are consistent with other studies among AI/AN nationwide and among Pima Indians in the Southwest, which concluded that improvements in blood pressure, blood glucose, and the use of ACE inhibitors and ARBs played a significant role in the decline of ESRD-D in these populations (11,12).
The decrease of ESRD-D in AI/AN with diabetes was likely the result of improvements in both process and outcome measures presented in this report. Prescription of ACE inhibitors and ARBs in AI/AN with diabetes increased 76% from 1997 to 2002. In 2014, prescription of these medications among AI/AN with diabetes was 36% higher than for the overall U.S. population with diabetes (8). Similarly, among persons with diabetes aged ≥65 years, the rate of urine albumin-to-creatinine ratio testing is 55% higher in AI/AN compared with Medicare beneficiaries (1). Outcome measures are also positive, including blood pressure control in AI/AN with diabetes and hypertension and improved glycemic control overall. Establishing and sustaining these favorable trends in diabetes management and prevention of ESRD-D are related to population and team-based approaches to diabetes management undertaken by the IHS.
Starting in the mid-1980s, IHS implemented systematic approaches to diabetes care that have contributed to the outcomes presented here (13,14). These approaches were informed by public health and population management principles, which focus not just on short-term outcomes for individual patients who seek care, but also long-term outcomes, costs, disparities, and wellness of the entire community (15). These approaches include multidisciplinary team-based, coordinated clinical care and education, community outreach, and tracking of clinical process and outcomes data at the local, regional, and national levels (9).
This IHS system of diabetes care enabled I/T/U sites to successfully and consistently deliver evidence-based interventions that reduce ESRD-D risk factors. In 1986, IHS developed its first Diabetes Standards of Care to disseminate evidence-based recommendations aimed at improving diabetes care for AI/AN (13). These standards were revised in the early 1990s to include assessment and treatment of CKD (16). IHS was one of the first systems to establish routine reporting of the estimated glomerular filtration rate, yearly monitoring of urine albumin excretion, and prescription of ACE inhibitors and ARBs (14). Both of these classes of therapeutic agents have been shown to prevent or delay the development of ESRD-D in patients with albuminuria, independent of their effects in reducing blood pressure (4,17).
As data collection and analysis are fundamental components of an effective diabetes care system, IHS first implemented the Diabetes Care and Outcomes Audit in 1986 at several sites, and in 1997, developed a centralized, national database (18). Successful implementation of evidence-based clinical interventions as documented by the Audit might explain in part the decline in ESRD-D incidence in AI/AN adults with diabetes. IHS has made other improvements in diabetes care by developing clinical education programs and tools; culturally relevant patient education materials; and population-based management tools in the IHS electronic health record (9,14,19). I/T/U case managers help coordinate in-house care as well as referrals for specialty services, to facilitate greater care continuity than in more fragmented systems.§§ I/T/U facilities also support diabetes care and education by using public health nurses and community health workers to provide outreach and education to the community.¶¶,***
In 1997, Congress established the Special Diabetes Program for Indians (SDPI) (9). The SDPI provides much-needed funding to 301 I/T/U sites to implement interventions which reduce risk factors for diabetes and its complications, including ESRD-D (Table 2) (9).††† In addition, SDPI funds have been used by IHS to improve its national program for disseminating evidence-based interventions and providing training, tools for data collection and analysis, and support to diabetes programs in AI/AN communities across the country. Because of SDPI, the partnership of IHS and I/T/U programs is stronger, and together they provide a comprehensive public health–oriented national program that has demonstrated success in addressing the diabetes epidemic and reducing complications such as ESRD-D (9).
The findings in this report are subject to at least five limitations. First, the data are for persons receiving ESRD treatment as reported to CMS and do not include patients who refused treatment, those who died before receiving treatment, or those whose treatment was not reported to CMS. Second, primary diagnosis was obtained from the CMS Medical Evidence Report and was based on a physician’s assessment of the patient, which could be influenced by the physician’s awareness of diabetes prevalence among AI/AN. Third, differential classification of AI/AN race in the USRDS, U.S. Census, and IHS data systems could result in over- or underestimation of the actual incidence of ESRD-D in this population. Fourth, IHS data on diabetes prevalence might not be representative of the total AI/AN population and might result in over- or underestimation of the number of AI/AN with diabetes in the United States and, therefore, the incidence of ESRD-D. Although these biases might have affected incidence estimates, trends in incidence would not be affected if the biases remained consistent over time. Finally, the data on diabetes measures reflect care provided to AI/AN who access the I/T/U system and cannot be generalized to AI/AN who do not.
ESRD-D is a disabling and costly condition associated with high mortality.§§§ The Medicare expenditure per person per year for hemodialysis patients was $84,550 in 2013, and the per person per year cost for ESRD-D was $82,141 (1). In 2013, total Medicare spending for ESRD-D was $14 billion, about half (45%) of the $31 billion Medicare spending for ESRD overall (1). A decrease in ESRD-D incidence in the general U.S. population comparable to that experienced in the AI/AN population could result in fewer cases of newly treated ESRD-D and contribute to leveling or lowering of total Medicare expenditures for ESRD. Integrating public health, clinical, and community-based approaches to deliver evidence-based interventions aimed at reducing ESRD-D risk factors can sustain and improve trends in ESRD-D incidence.
Corresponding author: Nilka Ríos Burrows, MPH, NRios@cdc.gov, 770-488-1057.
1Division of Diabetes Treatment and Prevention, Indian Health Service, Rockville, Maryland; 2Division of Diabetes Translation, CDC; 3National Institute of Diabetes Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland; 4National Center for Chronic Disease Prevention and Health Promotion, CDC; 5Office for State, Tribal, Local & Territorial Support, CDC.
† IHS. The 2016 Indian Health Service and Tribal Health Care Facilities’ Needs Assessment Report to Congress. https://www.ihs.gov/newsroom/includes/themes/newihstheme/display_objects/documents/RepCong_2016/IHSRTC_on_FacilitiesNeedsAssessmentReport.pdfCdc-pdfExternal.
§ CDC. U.S. Diabetes Surveillance System. http://www.cdc.gov/diabetes/data.
** American Community Survey 1-Year Estimates, 2015. United States Census Bureau. https://www.census.gov/programs-surveys/acs/External.
†† American Diabetes Association. Standards of Medical Care in Diabetes—2017. Diabetes Care 2017 Jan; 40 (Supplement 1): S1–S135.
§§ IHS: Special Diabetes Program for Indians—2011 report to Congress, 2011. https://www.ihs.gov/newsroom/includes/themes/newihstheme/display_objects/documents/RepCong_2012/2011RTC_Layout_10102012_508c.pdfCdc-pdfExternal.
¶¶ IHS. Public Health Nursing. http://www.ihs.gov/dper/index.cfm/planning/rrm/public-health-nursingExternal.
*** IHS. Community Health Representatives. https://www.ihs.gov/chrExternal.
††† IHS Division of Diabetes Treatment and Prevention. Special Diabetes Program for Indians FY 2016 Community-Directed Grant Programs 2016. https://www.ihs.gov/sdpi/includes/themes/newihstheme/display_objects/documents/factsheets/SDPI_FY2016_CD_GrantPrograms.pdfCdc-pdfExternal.
§§§ Morbidity and Mortality in Patients with Chronic Kidney Disease. USRDS Coordinating Center. https://www.usrds.org/2015/view/v1_03.aspx?zoom_highlight=mortalityExternal.
- United States Renal Data System. USRDS annual data report: Epidemiology of kidney disease in the United States. Bethesda, MD: National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, United States Renal. Data Syst 2015;2015. https://www.usrds.org/2015/view/Default.aspxExternal.
- CDC. National diabetes statistics report: estimates of diabetes and its burden in the United States, 2014. Atlanta, GA: US Department of Health and Human Services, CDC; 2014. https://www.cdc.gov/diabetes/data/statistics/2014StatisticsReport.html
- Zoungas S, de Galan BE, Ninomiya T, et al. ; ADVANCE Collaborative Group. Combined effects of routine blood pressure lowering and intensive glucose control on macrovascular and microvascular outcomes in patients with type 2 diabetes: new results from the ADVANCE trial. Diabetes Care 2009;32:2068–74. CrossRefExternal PubMedExternal
- Brenner BM, Cooper ME, de Zeeuw D, et al. ; RENAAL Study Investigators. Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. N Engl J Med 2001;345:861–9. CrossRefExternal PubMedExternal
- Wilson C, Susan L, Lynch A, Saria R, Peterson D. Patients with diagnosed diabetes mellitus can be accurately identified in an Indian Health Service patient registration database. Public Health Rep 2001;116:45–50. PubMedExternal
- Kim HJ, Fay MP, Feuer EJ, Midthune DN. Permutation tests for joinpoint regression with applications to cancer rates. Stat Med 2000;19:335–51. CrossRefExternal PubMedExternal
- National Cancer Institute. Joinpoint Regression Program, Version 22.214.171.124—April 2016. Bethesda, MD: National Institute of Health, National Cancer Institute, Statistical Methodology and Applications Branch, Surveillance Research Program; 2016. https://surveillance.cancer.gov/joinpointExternal
- Afkarian M, Zelnick LR, Hall YN, et al. Clinical manifestations of kidney disease among US adults with diabetes, 1988–2014. JAMA 2016;316:602–10. CrossRefExternal PubMedExternal
- Indian Health Service. Special Diabetes Program for Indians—2014 report to Congress. Rockville, Maryland: Indian Health Service; 2014. https://www.ihs.gov/newsroom/includes/themes/newihstheme/display_objects/documents/RepCong_2016/SDPI_2014_Report_to_Congress.pdfCdc-pdfExternal
- Indian Health Service. Indian Health Service Year 2016 Profile. Rockville, Maryland: Indian Health Service; 2016. https://www.ihs.gov/newsroom/index.cfm/factsheets/ihsprofile/External
- Burrows NR, Li Y, Williams DE. Racial and ethnic differences in trends of end-stage renal disease: United States, 1995 to 2005. Adv Chronic Kidney Dis 2008;15:147–52. CrossRefExternal PubMedExternal
- Pavkov ME, Knowler WC, Hanson RL, Nelson RG. Diabetic nephropathy in American Indians, with a special emphasis on the Pima Indians. Curr Diab Rep 2008;8:486–93. CrossRefExternal PubMedExternal
- Acton K, Valway S, Helgerson S, et al. Improving diabetes care for American Indians. Diabetes Care 1993;16:372–5. CrossRefExternal PubMedExternal
- Narva AS. Reducing the burden of chronic kidney disease among American Indians. Adv Chronic Kidney Dis 2008;15:168–73. CrossRefExternal PubMedExternal
- Frieden TR. A framework for public health action: the health impact pyramid. Am J Public Health 2010;100:590–5. CrossRefExternal PubMedExternal
- Narva AS. Caring for the patient with progressive renal disease. IHS Prim Care Provid 1990;15:101–4.
- Patel A, MacMahon S, Chalmers J, et al. ; ADVANCE Collaborative Group. Effects of a fixed combination of perindopril and indapamide on macrovascular and microvascular outcomes in patients with type 2 diabetes mellitus (the ADVANCE trial): a randomised controlled trial. Lancet 2007;370:829–40. CrossRefExternal PubMedExternal
- Acton KJ, Shields R, Rith-Najarian S, et al. Applying the diabetes quality improvement project indicators in the Indian Health Service primary care setting. Diabetes Care 2001;24:22–6. CrossRefExternal PubMedExternal
- Sequist TD, Cullen T, Acton KJ. Indian health service innovations have helped reduce health disparities affecting American Indian and Alaska native people. Health Aff (Millwood) 2011;30:1965–73. CrossRefExternal PubMedExternal
TABLE 1. Age-adjusted incidence rates* and trend analysis of diabetes-related end-stage renal disease among adults aged ≥18 years in the general population (1996–2013) and in the diabetic population (2006–2013), by race and ethnicity† — United States
|General population||Rate||% change||Overall trend||Trend segment 1§||Trend segment 2/3§|
|1996||2013||AAPC (95% CI)||p value||Period||APC (95% CI)||p value||Period||APC (95% CI)||p value|
|AI/AN||57.3||26.5||−54||−4.4 (−5.7 to −3.0)||<0.001||1996–1999||3.3 (−4.7 to 12.0)||0.40||1999–2013||−6.0 (−6.7 to −5.2)||<0.001|
|Asians||23.1||22.2||−4||−0.2 (−1.0 to 0.6)||0.62||1996–1998||5.4 (−2.2 to 13.6)||0.15||1998–2013||−0.9 (−1.2 to −0.6)||<0.001|
|Blacks||52.2||42.7||−18||−1.3 (−1.8. to −0.7)||<0.001||1996–2001||1.7 (0.5 to 2.9)||0.01||2001–2009||−1.3 (−2.0 to −0.6)||0.002|
|2009–2013||−4.8 (−6.4 to −3.2)||<0.001|
|Whites||12.1||15.5||+28||1.4 (0.9 to 1.8)||<0.001||1996–2000||5.8 (4.5 to 7.1)||<0.001||2000–2006||0.7 (−0.1 to 1.6)||0.09|
|2006–2013||−0.6 (−1.1 to −0.1)||0.03|
|Hispanics||40.1||34.2||−15||−0.6 (−1.3 to 0.1)||0.08||1996–2000||4.4 (1.6 to 7.3)||0.005||2000–2013||−2.1 (−2.5 to −1.6)||<0.001|
|Diabetic population||Rate||% change||Overall trend||Trend segment 1§||Trend segment 2/3§|
|2006||2013||AAPC (95% CI)||p value||Period||APC (95% CI)||p value||Period||APC (95% CI)||p value|
|AI/AN||210.7||152.7||−28||−4.9 (−7.0 to −2.7)||<0.001||2006–2009||−2.0 (−8.2 to 4.7)||0.41||2009–2013||−7.0 (−10.8 to −3.0)||0.01|
|Asians||219.0||227.4||+4||−0.8 (−5.9 to 4.6)||0.72||2006–2013||−0.8¶ (−5.9 to 4.6)||0.72||—||—||—|
|Blacks||379.8||329.6||−13||−2.8 (−4.7 to −1.0)||0.01||2006–2013||−2.8¶ (−4.7 to -1.0)||0.01||—||—||—|
|Whites||185.8||159.0||−14||−2.0 (−3.9 to −0.0)||0.05||2006–2013||−2.0¶ (−3.9 to −0.0)||0.05||—||—||—|
|Hispanics||287.6||223.0||−22||−0.1 (−0.1 to −0.1)||<0.001||2006–2008||−0.3 (−0.5 to −0.1)||0.01||2008–2013||−0.0 (−0.0 to 0.0)||0.79|
TABLE 2. Percentage of Special Diabetes Program for Indians programs reporting diabetes services — United States
|Intervention||1997 %||2013 %|
|Diabetes clinical teams||30||96|
|Diabetes patient registries||34||98|
|Nutrition services for adults||39||93|
|Access to registered dietitians||37||79|
|Access to physical activity specialists||8||74|
|Access to culturally tailored diabetes education materials||36||97|
FIGURE 1. Incidence* of diabetes-related end-stage renal disease among adults aged ≥18 years, by race and ethnicity — United States, 1996–2013
Source: Data from the U.S. Renal Data System and the U.S. Census.
Abbreviation: AI/AN=American Indians and Alaska Natives.
* Rate per 100,000 population and age-adjusted based on the 2000 U.S. standard population. Racial groups include persons of Hispanic and non-Hispanic origin; Hispanics may be of any race.
FIGURE 2. Incidence* of diabetes-related end-stage renal disease among adults aged ≥18 years with diabetes, by race and ethnicity — United States, 2006–2013
Sources: U.S. Renal Data System, U.S. Diabetes Surveillance System, and data from the Indian Health Service applied to the U.S. Census population.
Abbreviation: AI/AN=American Indians and Alaska Natives.
* Rate per 100,000 diabetic population and age-adjusted based on the 2000 U.S. standard population. Racial groups include persons of Hispanic and non-Hispanic origin; Hispanics may be of any race.
Source: Indian Health Service Diabetes Care and Outcomes Audit.
Abbreviations: ACE = angiotensin converting enzyme; AI/AN = American Indians and Alaska Natives; ARB = angiotensin receptor blocker; CKD = chronic kidney disease.
Suggested citation for this article: Bullock A, Burrows NR, Narva AS, et al. Vital Signs: Decrease in Incidence of Diabetes-Related End-Stage Renal Disease among American Indians/Alaska Natives — United States, 1996–2013. MMWR Morb Mortal Wkly Rep 2017;66:26-32. DOI: http://dx.doi.org/10.15585/mmwr.mm6601e1External.
MMWR and Morbidity and Mortality Weekly Report are service marks of the U.S. Department of Health and Human Services.
Use of trade names and commercial sources is for identification only and does not imply endorsement by the U.S. Department of Health and Human Services.
References to non-CDC sites on the Internet are provided as a service to MMWR readers and do not constitute or imply endorsement of these organizations or their programs by CDC or the U.S. Department of Health and Human Services. CDC is not responsible for the content of pages found at these sites. URL addresses listed in MMWR were current as of the date of publication.
All HTML versions of MMWR articles are generated from final proofs through an automated process. This conversion might result in character translation or format errors in the HTML version. Users are referred to the electronic PDF version (https://www.cdc.gov/mmwr) and/or the original MMWR paper copy for printable versions of official text, figures, and tables.
Questions or messages regarding errors in formatting should be addressed to firstname.lastname@example.org.