Potential mechanisms of stroke benefit favoring losartan in the Losartan Intervention For Endpoint reduction in hypertension (LIFE) study.

Abstract

INTRODUCTION:

The Losartan Intervention For Endpoint reduction in hypertension (LIFE) study is the first, and, so far, the only endpoint trial in patients with hypertension and left ventricular hypertrophy (LVH) to show a divergent therapeutic outcome of one treatment modality over another with equivalent blood pressure control. The purpose of this article is to review post hoc sub-analyses of LIFE study data and other clinical studies that offer some insight into possible treatment-related differences contributing to the superior stroke outcome of losartan versus atenolol beyond blood pressure reduction.

METHODS:

Relevant randomized clinical trials and review articles were identified through a MEDLINE search of English-language articles published between 1990 and 2006 using the search terms losartan, atenolol, LIFE, hypertension, and LVH. Articles describing major clinical studies, new data, or mechanisms pertinent to the LIFE study were selected for review.

RESULTS:

Differences in blood pressure or in the distribution of add-on medications were not evident between study groups in the LIFE study. Thus, the observed outcomes benefits favoring losartan may involve other possible mechanisms, including differential effects of losartan and atenolol on LVH regression, left atrial diameter, atrial fibrillation, brain natriuretic peptide, vascular structure, thrombus formation/platelet aggregation, serum uric acid, albuminuria, new-onset diabetes, and lipid metabolism. Alternative explanations for the LIFE study findings have also been put forward, including the choice of atenolol as an appropriate active comparator and differential effects between treatment groups on central pulse pressure. Additional clinical trials are needed to determine if the beneficial effects of losartan seen in LIFE are shared by other inhibitors of the renin-angiotensin system.

CONCLUSION:

Sub-analyses of the LIFE study data suggest that losartan's stroke benefit may arise from a mosaic of mechanisms rather than a single action. Further studies are expected to continue to delineate the mechanisms of differential responses to treatments in LIFE.

• Authors: Richard B Devereux, Björn Dahlöf
• Journal: Current medical research and opinion (Curr Med Res Opin) Vol. 23 Issue 2 Pg. 443-57 (Feb 2007) ISSN: 1473-4877 [Electronic] England
• PMID: 17288698 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Review)

Chemical References

• Adrenergic beta-Antagonists
• Angiotensin II Type 1 Receptor Blockers
• Antihypertensive Agents
• Biomarkers
• Cardiovascular Agents
• N-terminal proatrial natriuretic peptide
• Peptide Fragments
• Platelet Aggregation Inhibitors
• Protein Precursors
• pro-brain natriuretic peptide (1-76)
• Natriuretic Peptide, Brain
• Atenolol
• Atrial Natriuretic Factor
• Losartan

Topics

• Adrenergic beta-Antagonists (pharmacology, therapeutic use)
• Angiotensin II Type 1 Receptor Blockers (pharmacology, therapeutic use)
• Antihypertensive Agents (pharmacology, therapeutic use)
• Atenolol (pharmacology, therapeutic use)
• Atrial Fibrillation (epidemiology, prevention & control)
• Atrial Natriuretic Factor (blood)
• Biomarkers
• Blood Pressure (drug effects)
• Cardiovascular Agents (therapeutic use)
• Cohort Studies
• Drug Utilization
• Endothelium, Vascular (physiopathology)
• Follow-Up Studies
• Heart Atria (pathology)
• Humans
• Hypertension (complications, drug therapy)
• Hypertrophy, Left Ventricular (complications, drug therapy)
• Losartan (pharmacology, therapeutic use)
• Models, Biological
• Myocardial Infarction (epidemiology, prevention & control)
• Natriuretic Peptide, Brain (blood)
• Peptide Fragments (blood)
• Platelet Aggregation (drug effects)
• Platelet Aggregation Inhibitors (pharmacology, therapeutic use)
• Protein Precursors (blood)
• Randomized Controlled Trials as Topic (statistics & numerical data)
• Research Design
• Risk
• Risk Factors
• Stroke (etiology, prevention & control)
• Thrombosis (prevention & control)
• Treatment Outcome