Comparison of angiotensin II receptor antagonists

被引:22
作者
Kirch, W [1 ]
Horn, B [1 ]
Schweizer, J [1 ]
机构
[1] Tech Univ Dresden, Inst Clin Pharmacol, Fac Med, D-01307 Dresden, Germany
关键词
angiotensin II receptor antagonists; hypertension;
D O I
10.1046/j.1365-2362.2001.00871.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nonpeptide orally active angiotensin II type 1 (AT(1)) receptor antagonists are the most specific means presently available to block the renin-angiotensin enzymatic cascade. Six of these drugs have already been licensed in Europe and in the United States for the treatment of high blood pressure, and additional candidates are in the pipeline. The World Health Organisation has also recently endorsed their use for this condition. Inasmuch as AT(1) receptor antagonists have proven themselves the equals of angiotensin converting enzyme inhibitors with respect to antihypertensive efficacy, but demonstrated better safety profiles, this class of drugs may be considered to be a qualitative improvement in the treatment of essential hypertension. Interestingly, the six agents now on the market diverge considerably with respect to their pharmacokinetic and pharmacodynamic properties, although it is not certain whether such differences are clinically relevant. A considerable number of large multicentre trials are in progress to ascertain the possible longer-term organoprotective effects of these substances on cardiovascular morbidity and mortality. Because of their noteworthy safety record to date, and simple once-a-day dosage regimen, AT(1) receptor antagonists have the potential to improve compliance in patients with chronic hypertension.
引用
收藏
页码:698 / 706
页数:9
相关论文
共 59 条
[1]  
Andersson OK, 1997, J HUM HYPERTENS, V11, pS63
[2]  
Andersson Ove K., 1998, Blood Pressure, V7, P53
[3]   The ELITE study - What are its implications for the drug treatment of heart failure? [J].
Aronow, WS .
DRUGS & AGING, 1998, 12 (06) :423-428
[4]  
Belz G G, 2000, J Renin Angiotensin Aldosterone Syst, V1, P336, DOI 10.3317/jraas.2000.063
[5]   Time course and extent of angiotensin II antagonism after irbesartan, losartan, and valsartan in humans assessed by angiotensin II dose response and radioligand receptor assay [J].
Belz, GG ;
Butzer, R ;
Kober, S ;
Mang, C ;
Mutschler, E .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1999, 66 (04) :367-373
[6]  
BELZ GG, 1999, J HYPERTENS S3, V17
[7]  
*BOEHR ING, 1998, FACH
[8]   SHORT-TERM AND SUSTAINED RENAL EFFECTS OF ANGIOTENSIN-II RECEPTOR BLOCKADE IN HEALTHY-SUBJECTS [J].
BURNIER, M ;
HAGMAN, M ;
NUSSBERGER, J ;
BIOLLAZ, J ;
ARMAGNAC, C ;
BROUARD, R ;
WAEBER, B ;
BRUNNER, HR .
HYPERTENSION, 1995, 25 (04) :602-609
[9]   Angiotensin II receptor antagonists [J].
Burnier, M ;
Brunner, HR .
LANCET, 2000, 355 (9204) :637-645
[10]   Pharmacokinetics and pharmacodynamics of candesartan cilexetil in patients with normal to severely impaired renal function [J].
Buter, H ;
Navis, GY ;
Woittiez, AJJ ;
de Zeeuw, D ;
de Jong, PE .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1999, 54 (12) :953-958