Comparison of the efficacy and safety of irbesartan and olmesartan in patients with hypertension (EARTH study)

Clin Exp Hypertens. 2012;34(5):342-9. doi: 10.3109/10641963.2012.683912. Epub 2012 May 8.

Abstract

Fifty-four patients were randomly divided into irbesartan and olmesartan groups. Blood pressure (BP) was significantly decreased in all patients at 12 weeks. In particular, BP in patients who initially received irbesartan showed significant reductions. The equality of variance of BP in the irbesartan group was significantly smaller than that in the olmesartan group at 12 weeks. Blood concentrations of adiponectin were significantly increased in the irbesartan group at 12 weeks. Log [pentraxin-3] in the irbesartan group were significantly decreased. In conclusion, the ability of irbesartan to reduce BP is comparable to that of olmesartan with equivalent safety.

Publication types

  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Aged, 80 and over
  • Angiotensin II Type 1 Receptor Blockers / adverse effects
  • Angiotensin II Type 1 Receptor Blockers / therapeutic use*
  • Antihypertensive Agents / adverse effects
  • Antihypertensive Agents / therapeutic use*
  • Biphenyl Compounds / adverse effects
  • Biphenyl Compounds / therapeutic use*
  • Blood Pressure / drug effects
  • Female
  • Humans
  • Hypertension / drug therapy*
  • Imidazoles / adverse effects
  • Imidazoles / therapeutic use*
  • Irbesartan
  • Male
  • Middle Aged
  • Tetrazoles / adverse effects
  • Tetrazoles / therapeutic use*

Substances

  • Angiotensin II Type 1 Receptor Blockers
  • Antihypertensive Agents
  • Biphenyl Compounds
  • Imidazoles
  • Tetrazoles
  • olmesartan
  • Irbesartan