Effects of sibutramine plus verapamil sustained release/trandolapril combination on blood pressure and metabolic variables in obese hypertensive patients

Expert Opin Pharmacother. 2008 Jul;9(10):1629-39. doi: 10.1517/14656566.9.10.1629.

Abstract

Objective: The management of obese hypertensive subjects may require the administration of anti-obesity and antihypertensive drugs. Sibutramine use has raised concerns regarding a potential increase in subjects' blood pressure and heart rate. The primary end-points of this study were an evaluation of the effect of sibutramine together with a verapamil sustained release/trandolapril combination tablet versus verapamil sustained release/trandolapril alone on the blood pressure and heart rate in obese hypertensive patients.

Research design/methods: Patients received a low-fat low-calorie diet and were randomly allocated to open-label verapamil sustained release/trandolapril 180/2 mg (n = 26) or sibutramine 10 mg together with verapamil sustained release/trandolapril 180/2 mg (n = 28) daily for 6 months.

Results: Significant reductions in the subjects' systolic blood pressure and diastolic blood pressure were observed in both groups (p < 0.01 versus baseline). At 6 months a greater fall in blood pressure was observed in the sibutramine/verapamil sustained release/trandolapril group compared with the verapamil sustained release/trandolapril group (systolic blood pressure 21.9 +/- 8.1 versus 15.9 +/- 12.3 mmHg and diastolic blood pressure 15.7 +/- 8.1 versus 9.1 +/- 9.9 mmHg) but this was only significant (p = 0.03) for diastolic blood pressure. The subjects' heart rate did not change significantly in any group. No significant sibutramine-associated attenuation of blood pressure reduction was observed during the study. The sibutramine/verapamil sustained release/trandolapril treatment resulted in significantly greater improvement in the subjects' anthropometric variables, homeostasis model assessment and lipid profiles compared with verapamil sustained release/trandolapril administration. The subjects' small dense low-density lipoprotein cholesterol, high-sensitivity C-reactive protein and visfatin plasma levels were only measured in the sibutramine/verapamil sustained release/trandolapril group (all decreased by p < 0.05 versus baseline).

Conclusions: The sibutramine/verapamil sustained release/trandolapril combination in obese hypertensive patients significantly reduced their blood pressure and improved their anthropometric and metabolic variables without affecting the heart rate.

Publication types

  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Antihypertensive Agents / administration & dosage
  • Antihypertensive Agents / therapeutic use*
  • Appetite Depressants / administration & dosage
  • Appetite Depressants / therapeutic use*
  • Blood Pressure / drug effects
  • Body Weights and Measures
  • C-Reactive Protein / analysis
  • Cyclobutanes / administration & dosage
  • Cyclobutanes / therapeutic use*
  • Delayed-Action Preparations
  • Diet
  • Drug Combinations
  • Drug Therapy, Combination
  • Female
  • Heart Rate / drug effects
  • Humans
  • Hypertension / complications
  • Hypertension / drug therapy*
  • Indoles / administration & dosage
  • Indoles / therapeutic use*
  • Lipids / blood
  • Male
  • Nicotinamide Phosphoribosyltransferase / drug effects
  • Obesity / complications
  • Obesity / drug therapy*
  • Verapamil / administration & dosage
  • Verapamil / therapeutic use*

Substances

  • Antihypertensive Agents
  • Appetite Depressants
  • Cyclobutanes
  • Delayed-Action Preparations
  • Drug Combinations
  • Indoles
  • Lipids
  • trandolapril
  • C-Reactive Protein
  • Verapamil
  • Nicotinamide Phosphoribosyltransferase
  • sibutramine