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Cardiovascular risk reduction in hypertensive black patients with left ventricular hypertrophy: the LIFE study
Stevo Julius1, Michael H Alderman, Gareth Beevers
1Department of Internal Medicine, Division of Hypertension, University of Michigan Medical Center, 3918 Taubman Center, Ann Arbor, MI 48109-0356, USA. sjulius@umich.edu
Insights
Black patients with hypertension and left ventricular hypertrophy (LVH) may not benefit as much from losartan compared to atenolol. This subanalysis suggests losartan may not be a preferred first-line treatment for this demographic.
Area of Science:
- Cardiology
- Pharmacology
- Hypertension Research
Background:
- The Losartan Intervention For Endpoint reduction in hypertension (LIFE) study investigated losartan vs. atenolol in 9,193 hypertensive patients with left ventricular hypertrophy (LVH).
- Overall, losartan reduced the primary composite endpoint (cardiovascular death, stroke, myocardial infarction) by 13% (p=0.021) with comparable blood pressure (BP) reduction to atenolol.
- A potential interaction between ethnic background and treatment efficacy was suggested (p=0.057).
Purpose of the Study:
- To conduct a subanalysis of the LIFE study focusing on the effects of losartan and atenolol on cardiovascular events specifically in black patients.
- To explore potential differences in treatment response between black and non-black hypertensive patients with LVH.
Main Methods:
- Exploratory analyses categorized LIFE study participants into black (n=533) and non-black (n=8,660) groups.
- Further stratification was performed for U.S. patients: African American (n=523) and non-black (n=1,184).
Main Results:
- A significant interaction between race (black/non-black) and treatment was observed (p=0.005).
- The hazard ratio for the primary endpoint favored atenolol in black patients (HR=1.666, p=0.033) but favored losartan in non-black patients (HR=0.829, p=0.003).
- In black patients, BP reduction was similar between groups, though losartan showed greater regression of electrocardiographic-LVH.
Conclusions:
- The subanalysis generates a hypothesis that black patients with hypertension and LVH may not achieve similar cardiovascular outcome benefits with losartan-based treatment compared to non-black patients.
- Findings do not support the use of losartan as a first-line treatment for cardiovascular outcomes in this specific patient population.
- The subanalysis is limited by a relatively small number of cardiovascular events in the black patient subgroup.
Objectives:
We report on a subanalysis of the effects of losartan and atenolol on cardiovascular events in black patients in the Losartan Intervention For Endpoint reduction in hypertension (LIFE) study.
Background:
The LIFE study compared losartan-based to atenolol-based therapy in 9,193 hypertensive patients with left ventricular hypertrophy (LVH). Overall, the risk of the primary composite end point (cardiovascular death, stroke, myocardial infarction) was reduced by 13% (p = 0.021) with losartan, with similar blood pressure (BP) reduction in both treatment groups. There was a suggestion of interaction between ethnic background and treatment (p = 0.057).
Methods:
Exploratory analyses were performed that placed LIFE study patients into black (n = 533) and non-black (n = 8,660) categories, overall, and in the U.S. (African American [n = 523]; non-black [n = 1,184]).
Results:
A significant interaction existed between the dichotomized groups (black/non-black) and treatment (p = 0.005); a test for qualitative interaction was also significant (p = 0.016). The hazard ratio (losartan relative to atenolol) for the primary end point favored atenolol in black patients (1.666 [95% confidence interval (CI) 1.043 to 2.661]; p = 0.033) and favored losartan in non-blacks (0.829 [95% CI 0.733 to 0.938]; p = 0.003). In black patients, BP reduction was similar in both groups, and regression of electrocardiographic-LVH was greater with losartan.
Conclusions:
Results of the subanalysis are sufficient to generate the hypothesis that black patients with hypertension and LVH might not respond as favorably to losartan-based treatment as non-black patients with respect to cardiovascular outcomes, and do not support a recommendation for losartan as a first-line treatment for this purpose. The subanalysis is limited by the relatively small number of events.
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