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Effects of losartan and captopril on left ventricular systolic and diastolic function after acute myocardial infarction: Results of the Optimal Trial in Myocardial Infarction with Angiotensin II antagonist losartan (optimaal) echocardiographic substudy - 26/08/11

Doi : 10.1016/j.ahj.2003.10.031 
Jacob E Møller, MD, PhD a, , Ulf Dahlström, MD, PhD b, Ole Gøtzsche, MD, DmSC c, Avijit Lahiri, MBBS, MSc d, Knud Skagen, MD, DmSC e, Gert Steen Andersen, MD f, Kenneth Egstrup, MD, DmSC h

OPTIMAAL Study Group

a Department of Cardiology, Odense University Hospital, Odense, Denmark 
b Department of Medicine, Linköbing Hospital, Linköbing, Sweden 
c Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark 
d Department of Cardiovascular Medicine, Northwick Park Hospital, Harrow, United Kingdom 
e Department of Cardiology, Herlev Hospital, Copenhagen, Denmark 
f MERCK, Copenhagen, Denmark 
h Department of Medicine, Svendborg Hospital, Svendborg, Denmark 

*Reprint requests: Jacob E. Møller, MD, PhD, Department of Cardiology, Odense University Hospital, DK – 5000 Odense C, Denmark.

Abstract

Background

Angiotensin-converting enzyme inhibitors have been shown to attenuate adverse remodeling after acute myocardial infarction (AMI), and the same has been suggested for angiotensin II type 1 receptor antagonists in animal models. Therefore the aim of the study was to compare the effects of losartan and captopril on regional systolic, diastolic, and overall left ventricular (LV) function after AMI.

Methods

Two hundred twenty-five patients aged ≥50 years with documented AMI and heart failure and/or LV dysfunction were randomly assigned treatment with either losartan (50 mg/d) or captopril (50 mg 3 times/d). Echocardiography was performed at randomization and after 3 months; echocardiograms were analyzed blinded at the core laboratory. Main outcome measures were changes in wall motion score index (WMSI), E-wave deceleration time (E-DT), and Tei index of overall LV function.

Results

WMSI decreased in both groups (losartan 1.58 ± 0.23 to 1.52 ± 0.26, P = .009, captopril 1.60 ± 0.24 to 1.48 ± 0.22, P < .001), although the decrease was greater in patients allocated to captopril (captopril −0.12 ± 0.17 vs losartan −0.05 ± 0.19, P = .007). In both groups E-DT increased, although the increase was significant only in patients treated with captoril (193 ± 61 ms to 208 ± 70 ms, P = .05). The change in E-DT was not different between treatment groups (captopril 14 ± 74 ms vs losartan 7 ± 80 ms, P = .52). Tei index decreased in both groups (losartan 0.59 ± 0.13 to 0.55 ± 0.15, P = .04, captopril 0.62 ± 0.15 to 0.55 ± 0.13, P < .001). However, the reduction was significantly greater in patients treated with captopril (captopril −0.08 ± 0.14 vs losartan −0.03 ± 0.14, P = .01).

Conclusion

Losartan and captopril improve systolic and overall LV function after AMI, but the benefit is greater for patients treated with captopril.

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Mappa


 The study was a substudy of the OPTIMAAL Study supported by MERCK. Dr G. S. Andersen is an MERCK employee and Dr J. E. Møller was supported by a grant from the Danish Heart Foundation.


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Vol 147 - N° 3

P. 494-501 - Marzo 2004 Ritorno al numero
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