4.7 Article

Prevalence and Prognostic Significance of Apparent Treatment Resistant Hypertension in Chronic Kidney Disease Report From the Chronic Renal Insufficiency Cohort Study

Journal

HYPERTENSION
Volume 67, Issue 2, Pages 387-396

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/HYPERTENSIONAHA.115.06487

Keywords

antihypertensive agents; hypertension; hypertension resistant to conventional therapy; myocardial infarction; renal insufficiency; chronic

Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases [U01DK060990, U01DK060984, U01DK061022, U01DK061021, U01DK061028, U01DK060980, U01DK060963, U01DK060902]
  2. Perelman School of Medicine at the University of Pennsylvania Clinical and Translational Science Award National Institutes of Health (NIH)/National Center for Advancing Translational Sciences (NCATS) [UL1TR000003]
  3. Johns Hopkins University [UL1 TR-000424]
  4. University of Maryland GCRC [M01 RR-16500]
  5. Clinical and Translational Science Collaborative of Cleveland from the NCATS component of the National Institutes of Health [UL1TR000439]
  6. NIH roadmap for Medical Research
  7. Michigan Institute for Clinical and Health Research [UL1TR000433]
  8. University of Illinois at Chicago Clinical and Translational Science Award [UL1RR029879]
  9. Tulane University Translational Research in Hypertension and Renal Biology [P30GM103337]
  10. Kaiser Permanente NIH/National Center for Research Resources UCSF-CTSI [UL1 RR-024131]

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The association between apparent treatment resistant hypertension (ATRH) and clinical outcomes is not well studied in chronic kidney disease. We analyzed data on 3367 hypertensive participants in the Chronic Renal Insufficiency Cohort (CRIC) to determine prevalence, associations, and clinical outcomes of ATRH in nondialysis chronic kidney disease patients. ATRH was defined as blood pressure 140/90 mm Hg on 3 antihypertensives, or use of 4 antihypertensives with blood pressure at goal at baseline visit. Prevalence of ATRH was 40.4%. Older age, male sex, black race, diabetes mellitus, and higher body mass index were independently associated with higher odds of having ATRH. Participants with ATRH had a higher risk of clinical events than participants without ATRHcomposite of myocardial infarction, stroke, peripheral arterial disease, congestive heart failure (CHF), and all-cause mortality (hazard ratio [95% confidence interval], 1.38 [1.22-1.56]); renal events (1.28 [1.11-1.46]); CHF (1.66 [1.38-2.00]); and all-cause mortality (1.24 [1.06-1.45]). The subset of participants with ATRH and blood pressure at goal on 4 medications also had higher risk for composite of myocardial infarction, stroke, peripheral arterial disease, CHF, and all-cause mortality (hazard ratio [95% confidence interval], (1.30 [1.12-1.51]) and CHF (1.59 [1.28-1.99]) than those without ATRH. ATRH was associated with significantly higher risk for CHF and renal events only among those with estimated glomerular filtration rate 30 mL/min per 1.73 m(2). Our findings show that ATRH is common and associated with high risk of adverse outcomes in a cohort of patients with chronic kidney disease. This underscores the need for early identification and management of patients with ATRH and chronic kidney disease.

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