Baker Emma H, Duggal Ajay, Dong Yanbin, Ireson Nicola J, Wood Monique, Markandu Nirmala D, MacGregor Graham A
Department of Physiological Medicine, St George's Hospital Medical School, Cranmer Terrace, London, United Kingdom.
Hypertension. 2002 Jul;40(1):13-7. doi: 10.1161/01.hyp.0000022570.02119.75.
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 In an open, controlled study, 14 black hypertensive individuals with the T594M polymorphism were withdrawn from their usual medication and treated with amiloride.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 When amiloride was withdrawn for 2 weeks, there was a large increase in blood pressure of 17/8+/-4/2 mm Hg (systolic, P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.
上皮钠通道的T594M多态性在约5%的非洲裔人群中被发现,且与高血压显著相关。尽管T594M多态性可能通过影响通道增加肾脏对钠的重吸收,但尚不清楚这种多态性是否会导致高血压。氨氯吡脒能特异性抑制过度活跃的钠通道,并有效控制利德尔综合征患者的血压,该综合征中的高血压是由上皮钠通道的单独突变引起的。本研究的目的是确定氨氯吡脒对具有T594M多态性的个体降低血压是否有效。在一项开放、对照研究中,14名具有T594M多态性的黑人高血压个体停用其常用药物,改用氨氯吡脒治疗。在进入研究时,平均服用2种药物的个体血压为142/89±3/3 mmHg。单独使用氨氯吡脒(每日两次,每次10 mg)可有效将血压控制在相同水平(140/91±4/2 mmHg)。当停用氨氯吡脒2周时,血压大幅升高17/8±4/2 mmHg(收缩压,P<0.05;舒张压,P<0.01)。重新开始使用氨氯吡脒后,血压再次被控制在140/88±6/2 mmHg。这些结果表明,每日两次、每次10 mg的氨氯吡脒对具有T594M多态性的非洲裔高血压个体控制血压有效。我们的研究支持T594M多态性导致血压升高这一概念,并建议应考虑在受影响个体中使用氨氯吡脒。