PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 29, 2003Circulation258 citations

Regression of Electrocardiographic Left Ventricular Hypertrophy by Losartan Versus Atenolol

View Full Paper
POPeter M. OkinRDRichard B. DevereuxSJSverker Jern

Key Result

Losartan-based therapy resulted in greater regression of ECG left ventricular hypertrophy by Cornell product (-200 vs -69 mm.ms, P<0.001) than atenolol-based therapy at 6 months.

Study Design

Type

RCT (n=9,193)

Blinding

Blinded

Structured PICO

Does losartan-based therapy improve regression of ECG LVH compared to atenolol-based therapy in hypertensive patients with ECG LVH?

P
Population
9,193 hypertensive patients with ECG LVH by Sokolow-Lyon voltage or Cornell voltage-duration product criteria enrolled in the LIFE Study.
I
Intervention
Blinded losartan-based therapy evaluated at 6 months and annually up to 5 years.
C
Comparator
Blinded atenolol-based therapy evaluated at 6 months and annually up to 5 years.
O
Outcome
Regression of ECG LVH by Cornell voltage-duration product and Sokolow-Lyon voltage criteria.surrogate

Losartan-based therapy is superior to atenolol-based therapy for regressing electrocardiographic left ventricular hypertrophy in hypertensive patients, independent of blood pressure reduction.

Main Result

Absolute Event Rate: -200% vs -69%

p-value: p=<0.001

Abstract

BACKGROUND: Electrocardiographic left ventricular hypertrophy (LVH) predicts cardiovascular morbidity and mortality, and regression of ECG LVH may predict improved prognosis in hypertensive patients. However, uncertainty persists as to how best to regress ECG LVH. METHODS AND RESULTS: Regression of ECG LVH with losartan versus atenolol therapy was assessed in 9193 hypertensive patients with ECG LVH by Sokolow-Lyon voltage or Cornell voltage-duration product criteria enrolled in the Losartan Intervention For Endpoint Reduction in Hypertension (LIFE) Study. Patients had ECGs at study baseline and after 6 months, 1, 2, 3, 4, and 5 years of blinded losartan-based or atenolol-based therapy. After 6 months' follow-up, adjusting for baseline ECG LVH levels, baseline and in-treatment systolic and diastolic pressures, and for diuretic therapy, losartan-based therapy was associated with greater regression of both Cornell product (adjusted means, -200 versus -69 mm. ms, P<0.001) and Sokolow-Lyon voltage (-2.5 versus -0.7 mm, P<0.001) than was atenolol-based therapy. Greater regression of ECG LVH persisted at each subsequent annual evaluation in the losartan-treated group, with between 140 and 164 mm. ms greater mean reductions in Cornell product and from 1.7 to 2.2 mm greater mean reductions in Sokolow-Lyon voltage (all P<0.001). The effect of losartan was consistent across subgroups defined by gender, age, ethnicity, and diabetes. CONCLUSIONS: After adjusting for baseline and in-treatment blood pressure and baseline severity of ECG LVH, losartan-based antihypertensive therapy resulted in greater regression of ECG LVH by Cornell voltage-duration product and Sokolow-Lyon voltage criteria than did atenolol-based therapy. These findings support the value of angiotensin receptor blockade with losartan for reversing ECG LVH.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Okin et al. (2003) conducted an RCT in Hypertension with ECG left ventricular hypertrophy (n=9,193). Losartan-based therapy vs. Atenolol-based therapy was evaluated on Regression of ECG left ventricular hypertrophy by Cornell voltage-duration product at 6 months (p=<0.001). Losartan-based therapy resulted in greater regression of ECG left ventricular hypertrophy by Cornell product (-200 vs -69 mm.ms, P<0.001) than atenolol-based therapy at 6 months.

synapsesocial.com/papers/6a0f408504e2b0ba896cbe84https://doi.org/10.1161/01.cir.0000083724.28630.c3
Ask AI
Helpful
Bookmark
Share
View Full Paper