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

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 r...

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Published in:The American heart journal 2006-08, Vol.152 (2), p.246-252
Main Authors: Janardhanan, Rajesh, Daley, William L., Naqvi, Tasneem Z., Mulvagh, Sharon L., Aurigemma, Gerard, Zile, Michael, Arnold, J. Malcolm O., Artis, Eunice, Purkayastha, Das, Thomas, James D., Solomon, Scott D.
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cited_by cdi_FETCH-LOGICAL-c409t-cdb29c27732d646d700b75b7ced39bc62689952e19c87c5085bdb11c52f5a053
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container_title The American heart journal
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creator Janardhanan, Rajesh
Daley, William L.
Naqvi, Tasneem Z.
Mulvagh, Sharon L.
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Zile, Michael
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Artis, Eunice
Purkayastha, Das
Thomas, James D.
Solomon, Scott D.
description 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. 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. 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.
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Malcolm O.</au><au>Artis, Eunice</au><au>Purkayastha, Das</au><au>Thomas, James D.</au><au>Solomon, Scott D.</au><aucorp>for the VALIDD Investigators</aucorp><aucorp>VALIDD Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rationale and design: The VALsartan In Diastolic Dysfunction (VALIDD) Trial: Evolving the management of diastolic dysfunction in hypertension</atitle><jtitle>The American heart journal</jtitle><addtitle>Am Heart J</addtitle><date>2006-08-01</date><risdate>2006</risdate><volume>152</volume><issue>2</issue><spage>246</spage><epage>252</epage><pages>246-252</pages><issn>0002-8703</issn><eissn>1097-6744</eissn><coden>AHJOA2</coden><abstract>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. 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. 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subjects Angiotensin II Type 1 Receptor Blockers - administration & dosage
Angiotensin II Type 1 Receptor Blockers - pharmacology
Angiotensin II Type 1 Receptor Blockers - therapeutic use
Arterial hypertension. Arterial hypotension
Biological and medical sciences
Blood and lymphatic vessels
Blood pressure
Cardiology. Vascular system
Clinical manifestations. Epidemiology. Investigative techniques. Etiology
Comorbidity
Diastole - drug effects
Double-Blind Method
Drug dosages
Drug therapy
Echocardiography, Doppler
Heart failure
Humans
Hypertension
Hypertension - epidemiology
Hypotheses
Medical sciences
Randomized Controlled Trials as Topic
Research Design
Substance abuse treatment
Tetrazoles - administration & dosage
Tetrazoles - pharmacology
Tetrazoles - therapeutic use
Valine - administration & dosage
Valine - analogs & derivatives
Valine - pharmacology
Valine - therapeutic use
Valsartan
Ventricular Dysfunction - drug therapy
Ventricular Dysfunction - epidemiology
title Rationale and design: The VALsartan In Diastolic Dysfunction (VALIDD) Trial: Evolving the management of diastolic dysfunction in hypertension
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