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Blood pressure control and cardiovascular outcomes in normal-weight, overweight, and obese hypertensive patients treated with three different antihypertensives in ALLHAT.

AbstractOBJECTIVE:
Epidemiologically, there is a strong relationship between BMI and blood pressure (BP) levels. We prospectively examined randomization to first-step chlorthalidone, a thiazide-type diuretic; amlodipine, a calcium-channel blocker; and lisinopril, an angiotensin-converting enzyme inhibitor, on BP control and cardiovascular outcomes in a hypertensive cohort stratified by baseline BMI [kg/m(2); normal weight (BMI <25), overweight (BMI = 25-29.9), and obese (BMI >30)].
METHODS:
In a randomized, double-blind, practice-based Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial, 33,357 hypertensive participants, aged at least 55 years, were followed for an average of 4.9 years, for a primary outcome of fatal coronary heart disease or nonfatal myocardial infarction, and secondary outcomes of stroke, heart failure, combined cardiovascular disease, mortality, and renal failure.
RESULTS:
Of participants, 37.9% were overweight and 42.1% were obese at randomization. For each medication, BP control (<140/90 mmHg) was equivalent in each BMI stratum. At the fifth year, 66.1, 66.5, and 65.1% of normal-weight, overweight, and obese participants, respectively, were controlled. Those randomized to chlorthalidone had highest BP control (67.2, 68.3, and 68.4%, respectively) and to lisinopril the lowest (60.4, 63.2, and 59.6%, respectively) in each BMI stratum. A significant interaction (P = 0.004) suggests a lower coronary heart disease risk in the obese for lisinopril versus chlorthalidone (hazard ratio 0.85, 95% confidence interval 0.74-0.98) and a significant interaction (P = 0.011) suggests a higher risk of end-stage renal disease for amlodipine versus chlorthalidone in obese participants (hazard ratio 1.49, 95% confidence interval 1.06-2.08). However, these results were not consistent among other outcomes.
CONCLUSION:
BMI status does not modify the effects of antihypertensive medications on BP control or cardiovascular disease outcomes.
AuthorsEfrain Reisin, John W Graves, José-Miguel Yamal, Joshua I Barzilay, Sara L Pressel, Paula T Einhorn, Richard A Dart, Tamrat M Retta, Mohammad G Saklayen, Barry R Davis, ALLHAT Collaborative Research Group
JournalJournal of hypertension (J Hypertens) Vol. 32 Issue 7 Pg. 1503-13; discussion 1513 (Jul 2014) ISSN: 1473-5598 [Electronic] Netherlands
PMID24842697 (Publication Type: Journal Article, Randomized Controlled Trial, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Angiotensin-Converting Enzyme Inhibitors
  • Antihypertensive Agents
  • Calcium Channel Blockers
  • Diuretics
  • Amlodipine
  • Lisinopril
  • Chlorthalidone
Topics
  • Aged
  • Aged, 80 and over
  • Amlodipine (therapeutic use)
  • Angiotensin-Converting Enzyme Inhibitors (therapeutic use)
  • Antihypertensive Agents (therapeutic use)
  • Blood Pressure (drug effects)
  • Body Mass Index
  • Calcium Channel Blockers (therapeutic use)
  • Cardiovascular Diseases (prevention & control)
  • Chlorthalidone (therapeutic use)
  • Cohort Studies
  • Diuretics (therapeutic use)
  • Double-Blind Method
  • Female
  • Humans
  • Hypertension (complications, drug therapy, physiopathology)
  • Lisinopril (therapeutic use)
  • Male
  • Middle Aged
  • Obesity (complications, pathology, physiopathology)
  • Overweight (complications, pathology, physiopathology)
  • Prospective Studies

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