Benefits and Side Effects of Blood Pressure Lowering Treatment: What Was Wrong with Doxazosin in the ALLHAT?

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dc.contributor.author Gavras, Irene en_US
dc.contributor.author Gavras, Haralambos en_US
dc.date.accessioned 2011-12-29T21:02:26Z
dc.date.available 2011-12-29T21:02:26Z
dc.date.copyright 2001 en_US
dc.date.issued 2001-11-3 en_US
dc.identifier.citation Gavras, Irene, Haralambos Gavras. "Benefits and side effects of blood pressure lowering treatment: what was wrong with doxazosin in the ALLHAT?" Current Controlled Trials in Cardiovascular Medicine 2(6): 257-259. (2001) en_US
dc.identifier.issn 1468-6694 en_US
dc.identifier.uri http://hdl.handle.net/2144/2537
dc.description.abstract The lowering of high blood pressure is supposed to protect target organs from hypertensive damage. The Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial was designed to compare the cardioprotective properties of three antihypertensives from different classes (lisinopril, amlodipine and doxazosin) with chlorthalidone. Despite effective blood pressure lowering and a favorable metabolic profile, the doxazosin arm of the trial had a significantly higher relative risk of cardiovascular disease and heart failure compared with the chlorthalidone arm. This article speculates on possible causes for this unexpected result and suggests that the culprit may be accentuation of the vascular effects of vasopressin, which are maximized under α-adrenergic blockade. These findings may have implications for the large number of older men who receive monotherapy with α-blockers for treatment of prostatic symptoms. en_US
dc.language.iso en en_US
dc.publisher BioMed Central en_US
dc.rights Copyright 2001 BioMed Central Ltd en_US
dc.subject α1-adrenoceptor blockade en_US
dc.subject Coronary constriction en_US
dc.subject Ischemic heart disease en_US
dc.subject Vasopressin en_US
dc.title Benefits and Side Effects of Blood Pressure Lowering Treatment: What Was Wrong with Doxazosin in the ALLHAT? en_US
dc.type article en_US
dc.identifier.doi 10.1186/cvm-2-6-257 en_US
dc.identifier.pubmedid 11806808 en_US
dc.identifier.pmcid 64825 en_US

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