Primary Aldosteronism in Diabetic Subjects with Resistant Hypertension

  1. Guillermo E. Umpierrez, M.D. (geumpie{at}emory.edu)1,
  2. Paul Cantey, M.D., M.P.H.1,
  3. Dawn Smiley, M.D.1,
  4. Andres Palacio, M.D.1,
  5. Diana Temponi, M.D.1,
  6. Karen Luster, M.D.1 and
  7. Arlene Chapman, M.D1
  1. 1Department of Medicine, Emory University School of Medicine, Atlanta, Georgia

    Abstract

    Background: Despite the high prevalence of hypertension in patients with type 2 diabetes, the prevalence of primary aldosteronism in this population has not been determined.

    Methods: One hundred subjects with type 2 diabetes and resistant hypertension, defined as a blood pressure > 140/90 mm Hg despite the use of ≥ 3 antihypertensive agents, were screened for primary aldosteronism. Screening was performed by measuring plasma aldosterone (PAC)/plasma renin activity (PRA) ratio. Subjects with a PAC/PRA ratio >30 ng·ml-1·h-1 underwent confirmatory salt load testing. Diagnostic criteria included a 24-hour urine aldosterone ≥12 mcg during the third day of oral salt load or a PAC ≥ 5 ng/dL after the 4-hour intravenous saline load.

    Results: Thirty four subjects had a PAC/PRA ratio >30 ng·ml-1·h-1. Fourteen subjects (14%, 95% CI: 7.2-20.8) had a confirmed diagnosis of primary aldosteronism. Ninety three patients were African Americans. There were no differences in age, glycemic control, and number of antihypertensive drugs between subjects with and without primary aldosteronism. Subjects with primary aldosteronism had lower serum potassium (3.7 ± 0.4 vs. 4.0 ± 0.4 mmol/L, p = 0.012), higher PAC (15.6 ± 8 vs. 9.1 ± 6 ng/dL, p = 0.0016), and higher PAC/PRA (98 ± 74 vs. 21 ± 30 ng·mL-1·h-1, p<0.001) than patients without primary aldosteronism.

    Conclusion: Primary aldosteronism is common in diabetic patients with resistant hypertension, with a prevalence of 14%. Our results indicate that diabetic subjects with poorly controlled hypertension on ≥3 antihypertensive drugs should be screened for primary aldosteronism.

    Footnotes

      • Received January 8, 2007.
      • Accepted March 30, 2007.