Literature DB >> 18843651

Blood pressure lowering efficacy of angiotensin converting enzyme (ACE) inhibitors for primary hypertension.

Balraj S Heran1, Michelle My Wong, Inderjit K Heran, James M Wright.   

Abstract

BACKGROUND: ACE inhibitors are widely prescribed for hypertension so it is essential to determine and compare their effects on blood pressure (BP), heart rate and withdrawals due to adverse effects (WDAE).
OBJECTIVES: To quantify the dose-related systolic and/or diastolic BP lowering efficacy of ACE inhibitors versus placebo in the treatment of primary hypertension. SEARCH STRATEGY: We searched CENTRAL (The Cochrane Library 2007, Issue 1), MEDLINE (1966 to February 2007), EMBASE (1988 to February 2007) and reference lists of articles. SELECTION CRITERIA: Double-blind, randomized, controlled trials evaluating the BP lowering efficacy of fixed-dose monotherapy with an ACE inhibitor compared with placebo for a duration of 3 to 12 weeks in patients with primary hypertension. DATA COLLECTION AND ANALYSIS: Two authors independently assessed the risk of bias and extracted data. Study authors were contacted for additional information. WDAE information was collected from the trials. MAIN
RESULTS: Ninety two trials evaluated the dose-related trough BP lowering efficacy of 14 different ACE inhibitors in 12 954 participants with a baseline BP of 157/101 mm Hg. The data do not suggest that any one ACE inhibitor is better or worse at lowering BP. A dose of 1/8 or 1/4 of the manufacturer's maximum recommended daily dose (Max) achieved a BP lowering effect that was 60 to 70% of the BP lowering effect of Max. A dose of 1/2 Max achieved a BP lowering effect that was 90% of Max. ACE inhibitor doses above Max did not significantly lower BP more than Max. Combining the effects of 1/2 Max and higher doses gives an estimate of the average trough BP lowering efficacy for ACE inhibitors as a class of drugs of -8 mm Hg for SBP and -5 mm Hg for DBP. ACE inhibitors reduced BP measured 1 to 12 hours after the dose by about 11/6 mm Hg. AUTHORS'
CONCLUSIONS: There are no clinically meaningful BP lowering differences between different ACE inhibitors. The BP lowering effect of ACE inhibitors is modest; the magnitude of trough BP lowering at one-half the manufacturers' maximum recommended dose and above is -8/-5 mm Hg. Furthermore, 60 to 70% of this trough BP lowering effect occurs with recommended starting doses. The review did not provide a good estimate of the incidence of harms associated with ACE inhibitors because of the short duration of the trials and the lack of reporting of adverse effects in many of the trials.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18843651      PMCID: PMC7156914          DOI: 10.1002/14651858.CD003823.pub2

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  145 in total

1.  Efficacy and tolerance of trandolapril (0.5-2 mg) administered for 4 weeks in patients with mild-to-moderate hypertension. Investigator Study Group.

Authors:  J H De Bruijn; B A Orofiamma; N C Pauly
Journal:  J Cardiovasc Pharmacol       Date:  1994       Impact factor: 3.105

2.  Angiotensin-converting enzyme inhibition in mild hypertension with concomitant diseases and therapies: an efficacy, safety, and compatibility study of novel design, the Perindopril Therapeutic Safety Study.

Authors:  K O Stumpe; A Overlack
Journal:  Am J Med       Date:  1992-04-27       Impact factor: 4.965

3.  Effect of spirapril and hydrochlorothiazide on platelet function and euglobulin clot lysis time in patients with mild hypertension.

Authors:  G Gleerup; J R Petersen; J Mehlsen; K Winther
Journal:  Angiology       Date:  1996-10       Impact factor: 3.619

4.  Are angiotensin converting enzyme inhibition and aldosterone antagonism equivalent in hypertensive patients over fifty?

Authors:  P F Plouin; C Battaglia; F Alhenc-Gélas; P Corvol
Journal:  Am J Hypertens       Date:  1991-04       Impact factor: 2.689

5.  Increased renal plasma flow in long-term enalapril treatment of hypertension.

Authors:  G Simon; S Morioka; D K Snyder; J N Cohn
Journal:  Clin Pharmacol Ther       Date:  1983-10       Impact factor: 6.875

6.  Captopril and nifedipine interactions in the treatment of essential hypertensives: a crossover study.

Authors:  A Salvetti; P F Innocenti; M Iardella; F Pambianco; G C Saba; M Rossetti; G F Botta
Journal:  J Hypertens Suppl       Date:  1987-12

7.  Cilazapril inhibits vascular responses to baroreflex-stimulated sympathetic neural activity in hypertensive patients.

Authors:  P G Fernandez; P Bolli; C Lee; S Vasdev
Journal:  Can J Cardiol       Date:  1990 Jan-Feb       Impact factor: 5.223

8.  Nitrendipine and enalapril combination therapy in mild to moderate hypertension: assessment of dose-response relationship by a clinical trial of factorial design.

Authors:  A Roca-Cusachs; F Torres; M Horas; J Ríos; G Calvo; J Delgadillo; M Terán
Journal:  J Cardiovasc Pharmacol       Date:  2001-12       Impact factor: 3.105

9.  Ketanserin and captopril interaction in the treatment of essential hypertensives.

Authors:  G Lavezzaro; P E Ladetto; M Valente; D Stramignoni; C Zanna; G Assogna; A Salvetti
Journal:  Cardiovasc Drugs Ther       Date:  1990-01       Impact factor: 3.727

10.  Treatment of hypertension with enalapril and hydrochlorothiazide or enalapril and atenolol: contrasts in hypotensive interactions.

Authors:  L M Wing; J P Chalmers; M J West; A J Bune; A E Russell; J M Elliott; M J Morris
Journal:  J Hypertens Suppl       Date:  1987-12
View more
  43 in total

1.  A randomized trial of dietary sodium restriction in CKD.

Authors:  Emma J McMahon; Judith D Bauer; Carmel M Hawley; Nicole M Isbel; Michael Stowasser; David W Johnson; Katrina L Campbell
Journal:  J Am Soc Nephrol       Date:  2013-11-07       Impact factor: 10.121

Review 2.  Blood pressure-lowering efficacy of loop diuretics for primary hypertension.

Authors:  Vijaya M Musini; Pouria Rezapour; James M Wright; Ken Bassett; Ciprian D Jauca
Journal:  Cochrane Database Syst Rev       Date:  2015-05-22

Review 3.  Efficacy and toxicity of antihypertensive pharmacotherapy relative to effective dose 50.

Authors:  Simon B Dimmitt; Hans G Stampfer; Jennifer H Martin; Robin E Ferner
Journal:  Br J Clin Pharmacol       Date:  2019-08-19       Impact factor: 4.335

Review 4.  Why maximum tolerated dose?

Authors:  Hans G Stampfer; Genevieve M Gabb; Simon B Dimmitt
Journal:  Br J Clin Pharmacol       Date:  2019-07-22       Impact factor: 4.335

Review 5.  Exercise-based cardiac rehabilitation for coronary heart disease.

Authors:  Balraj S Heran; Jenny Mh Chen; Shah Ebrahim; Tiffany Moxham; Neil Oldridge; Karen Rees; David R Thompson; Rod S Taylor
Journal:  Cochrane Database Syst Rev       Date:  2011-07-06

Review 6.  Eplerenone for hypertension.

Authors:  Tina Sc Tam; May Hy Wu; Sarah C Masson; Matthew P Tsang; Sarah N Stabler; Angus Kinkade; Anthony Tung; Aaron M Tejani
Journal:  Cochrane Database Syst Rev       Date:  2017-02-28

7.  High sodium intake is associated with important risk factors in a large cohort of chronic kidney disease patients.

Authors:  F B Nerbass; R Pecoits-Filho; N J McIntyre; C W McIntyre; M W Taal
Journal:  Eur J Clin Nutr       Date:  2014-10-08       Impact factor: 4.016

8.  Early Time-Restricted Feeding Improves Insulin Sensitivity, Blood Pressure, and Oxidative Stress Even without Weight Loss in Men with Prediabetes.

Authors:  Elizabeth F Sutton; Robbie Beyl; Kate S Early; William T Cefalu; Eric Ravussin; Courtney M Peterson
Journal:  Cell Metab       Date:  2018-05-10       Impact factor: 27.287

Review 9.  Exercise-based cardiac rehabilitation for coronary heart disease.

Authors:  Lindsey Anderson; David R Thompson; Neil Oldridge; Ann-Dorthe Zwisler; Karen Rees; Nicole Martin; Rod S Taylor
Journal:  Cochrane Database Syst Rev       Date:  2016-01-05

Review 10.  Opportunities and limitations of genetic analysis of hypertensive rat strains.

Authors:  Juan M Saavedra
Journal:  J Hypertens       Date:  2009-06       Impact factor: 4.844

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.