American Journal of Kidney Diseases
Volume 51, Issue 1 , Pages 21-28, January 2008

Metabolic Syndrome and the Development of CKD in American Indians: The Strong Heart Study

  • Jaime Lucove, MSPH

      Affiliations

    • Department of Epidemiology, University of North Carolina-Chapel Hill, NC
    • Corresponding Author InformationAddress correspondence to Jaime C. Lucove, MSPH, Research Scientist, Allscripts, 27 East Delaware Ave, Pennington, NJ.
  • ,
  • Suma Vupputuri, PhD

      Affiliations

    • Department of Epidemiology, University of North Carolina-Chapel Hill, NC
    • University of North Carolina Kidney Center, Chapel Hill, NC
  • ,
  • Gerardo Heiss, MD, PhD

      Affiliations

    • Department of Epidemiology, University of North Carolina-Chapel Hill, NC
  • ,
  • Kari North, PhD

      Affiliations

    • Department of Epidemiology, University of North Carolina-Chapel Hill, NC
  • ,
  • Marie Russell, MD

      Affiliations

    • Medstar Research Institute, Phoenix, AZ.

Received 23 January 2007; accepted 27 September 2007. published online 03 December 2007.

Background

Metabolic impairments that precede type 2 diabetes, such as metabolic syndrome, may contribute to the development of chronic kidney disease (CKD). This study documents the prevalence and incidence of CKD and the prospective association between metabolic syndrome and CKD in American Indians without diabetes in the Strong Heart Study.

Study Design

Prospective cohort study.

Setting & Participants

American Indians aged 45 to 74 years from 3 geographic regions were recruited by using tribal records and were assessed every 3 years from 1989 to 1999 as part of the Strong Heart Study. Participants with type 2 diabetes, on dialysis therapy, or who received a kidney transplant at baseline examination were excluded.

Predictor

Metabolic syndrome, defined using Adult Treatment Panel III criteria.

Outcomes & Measurements

CKD was measured by using estimated glomerular filtration rate (eGFR) and urinary albumin-creatinine ratio (ACR) dichotomized at conventional cutoff values. The association between metabolic syndrome and incident CKD was evaluated by using multivariable Cox proportional hazards models and binomial regression, with statistical adjustment for confounders (age, sex, study center, education, and smoking).

Results

Metabolic syndrome was present in 896 (37.7%) and absent in 1,484 participants (62.3%) at baseline. The prevalence of ACR of 30 mg/g or greater at baseline examination was 12.1%, with 290 new cases and an incidence of 233/10,000 person-years. The prevalence of eGFR less than 60 mL/min/1.73 m2 was 7.8%, with 189 new cases and an incidence of 138/10,000 person-years. The prevalence of CKD was 17.8%, with 388 new cases and an incidence of 342/10,000 person-years. The adjusted hazard ratio for CKD associated with metabolic syndrome was 1.3 (95% confidence interval [CI], 1.1 to 1.6). Equivalent hazard ratios for ACR greater than 30 mg/g and eGFR less than 60 mL/min/1.73 m2 were 1.4 (95% CI, 1.0 to 1.9) and 1.3 (95% CI, 1.0 to 1.6), respectively. The relationship between metabolic syndrome and kidney outcomes was stronger in those who developed diabetes during follow-up.

Limitations

Intraindividual variability in serum creatinine and ACR measures may have resulted in some misclassification of participants by outcome status.

Conclusions

Metabolic syndrome is associated with an increased risk of developing CKD in American Indians without diabetes. The mechanism through which metabolic syndrome may cause CKD in this population likely is the development of diabetes.

Index Words: Metabolic syndrome, glomerular filtration rate, albuminuria, chronic kidney disease, American Indians

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 Originally published online as doi:10.1053/j.ajkd.2007.09.014 on November 28, 2007.This work was performed at the University of North Carolina-Chapel Hill and all Strong Heart Study Centers: Medstar Research Institute, Aberdeen Area Indian Health Service, Aberdeen Area Tribal Chairmen’s Health Board, Center for American Indian Health Research, and University of Oklahoma Health Sciences Center.

PII: S0272-6386(07)01309-1

doi:10.1053/j.ajkd.2007.09.014

American Journal of Kidney Diseases
Volume 51, Issue 1 , Pages 21-28, January 2008