Literature DB >> 12105131

Amiloride, a specific drug for hypertension in black people with T594M variant?

Emma H Baker1, Ajay Duggal, Yanbin Dong, Nicola J Ireson, Monique Wood, Nirmala D Markandu, Graham A MacGregor.   

Abstract

The T594M polymorphism of the epithelial sodium channel is found in approximately 5% of people of African origin and is significantly associated with high blood pressure. Although the T594M polymorphism could increase renal sodium absorption through affected channels, it is not known whether this polymorphism causes hypertension. Amiloride specifically inhibits overactive sodium channels and effectively controls blood pressure in Liddle's syndrome, in which hypertension is caused by separate epithelial sodium channel mutations. The aim of this study was to determine whether amiloride was effective in lowering blood pressure in individuals with the T594M polymorphism. In an open, controlled study, 14 black hypertensive individuals with the T594M polymorphism were withdrawn from their usual medication and treated with amiloride. On entry to the study, individuals taking a mean of 2 drugs had blood pressure of 142/89+/-3/3 mm Hg. Amiloride alone (10 mg BID) controlled blood pressure effectively to the same level (140/91+/-4/2 mm Hg). When amiloride was withdrawn for 2 weeks, there was a large increase in blood pressure of 17/8+/-4/2 mm Hg (systolic, P<0.05; diastolic, P<0.01). On restarting amiloride, blood pressure was again controlled to 140/88+/-6/2 mm Hg. These results demonstrate that 10 mg BID amiloride is effective in controlling blood pressure in hypertensive individuals of African origin who have the T594M polymorphism. Our study supports the concept that the T594M polymorphism contributes to the elevation of blood pressure and suggests that consideration should be given to the use of amiloride in affected individuals.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12105131     DOI: 10.1161/01.hyp.0000022570.02119.75

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  21 in total

Review 1.  Racial and ethnic differences in response to medicines: towards individualized pharmaceutical treatment.

Authors:  Valentine J Burroughs; Randall W Maxey; Richard A Levy
Journal:  J Natl Med Assoc       Date:  2002-10       Impact factor: 1.798

Review 2.  Epithelial Na(+) channel regulation by cytoplasmic and extracellular factors.

Authors:  Ossama B Kashlan; Thomas R Kleyman
Journal:  Exp Cell Res       Date:  2012-03-03       Impact factor: 3.905

Review 3.  Role of epithelial sodium channels and their regulators in hypertension.

Authors:  Rama Soundararajan; David Pearce; Rebecca P Hughey; Thomas R Kleyman
Journal:  J Biol Chem       Date:  2010-07-12       Impact factor: 5.157

4.  Deletion of α-subunit exon 11 of the epithelial Na+ channel reveals a regulatory module.

Authors:  Jingxin Chen; Thomas R Kleyman; Shaohu Sheng
Journal:  Am J Physiol Renal Physiol       Date:  2014-01-08

Review 5.  Personalizing the diuretic treatment of hypertension: the need for more clinical and research attention.

Authors:  Samuel J Mann; Michael E Ernst
Journal:  Curr Hypertens Rep       Date:  2015-04       Impact factor: 5.369

6.  Management of resistant hypertension.

Authors:  J David Spence
Journal:  CMAJ       Date:  2015-03-03       Impact factor: 8.262

7.  Gain-of-function variant of the human epithelial sodium channel.

Authors:  Jingxin Chen; Thomas R Kleyman; Shaohu Sheng
Journal:  Am J Physiol Renal Physiol       Date:  2012-11-07

Review 8.  Intensive management of risk factors for accelerated atherosclerosis: the role of multiple interventions.

Authors:  J David Spence
Journal:  Curr Neurol Neurosci Rep       Date:  2007-01       Impact factor: 5.081

Review 9.  Epithelial sodium channel, salt intake, and hypertension.

Authors:  Edith Hummler
Journal:  Curr Hypertens Rep       Date:  2003-02       Impact factor: 5.369

10.  Physiologic tailoring of treatment in resistant hypertension.

Authors:  J David Spence
Journal:  Curr Cardiol Rev       Date:  2010-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.