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Rationale and design: the VALsartan In Diastolic Dysfunction (VALIDD) Trial: evolving the management of diastolic dysfunction in hypertension.

Authors :
Janardhanan R
Daley WL
Naqvi TZ
Mulvagh SL
Aurigemma G
Zile M
Arnold JM
Artis E
Purkayastha D
Thomas JD
Solomon SD
Source :
American heart journal [Am Heart J] 2006 Aug; Vol. 152 (2), pp. 246-52.
Publication Year :
2006

Abstract

Background: Although 50% of hypertensive patients in the community are estimated to have diastolic dysfunction, there is no specific guideline for diastolic dysfunction therapy at present despite the condition's clear association with increased cardiovascular risk. Although the efficacy of angiotensin II receptor blockers (ARBs) in hypertension and left ventricular hypertrophy regression has been established, the effect of angiotensin II receptor blockade on intrinsic parameters of diastolic function has not been evaluated in large-scale studies.<br />Methods: The VALIDD Trial is an investigator-initiated randomized, controlled, double-blind clinical trial on approximately 350 patients designed to explore whether antihypertensive therapy with the ARB valsartan, in addition to standard therapy, would improve intrinsic diastolic properties of the myocardium in patients with hypertension and evidence of diastolic dysfunction. The result of such therapy will be compared with placebo after 38 weeks of treatment. The primary efficacy variable is change in early diastolic lateral mitral annular relaxation velocity measured by tissue Doppler imaging on week 38.<br />Conclusions: We expect the VALIDD Trial to provide novel insights into the specific effects of ARBs on diastolic dysfunction, as assessed by tissue Doppler imaging, in hypertensive patients. The trial may provide clinically useful data on whether such therapy can directly improve diastolic function in patients with hypertension.

Details

Language :
English
ISSN :
1097-6744
Volume :
152
Issue :
2
Database :
MEDLINE
Journal :
American heart journal
Publication Type :
Academic Journal
Accession number :
16875904
Full Text :
https://doi.org/10.1016/j.ahj.2006.01.009