全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Angiotensin-Converting Enzyme Inhibitors (ACEIs) and Angiotensin-Receptor Blockers (ARBs) in Patients at High Risk of Cardiovascular Events: A Meta-Analysis of 10 Randomised Placebo-Controlled Trials

DOI: 10.1155/2013/478597

Full-Text   Cite this paper   Add to My Lib

Abstract:

Context. Whether angiotensin converting-enzyme inhibitors (ACEI) and angiotensin-receptor blockers (ARB) are useful in high risk patients without heart failure is unclear. We perform a meta-analysis of prospective randomized placebo-controlled ACEI or ARB trials studying patients with a combination of risk factors to assess treatment impact on all cause mortality, cardiovascular mortality, nonfatal myocardial infarction (MI) and stroke. Method. A PubMed search was made for placebo-controlled trials recruiting at least 1,200 high risk patients randomized to either ACEI or ARB, with follow-up of at least 2 years. Meta-analysis was performed using the RevMan 5 program and Mantel-Haenszel analysis was done with a fixed effects model. Results. Ten trials recruiting 77,633 patients were reviewed. All cause mortality was significantly reduced by ACEI (RR 0.89; ), but not by ARB treatment (RR 1.00; ). Cardiovascular mortality and nonfatal MI were also reduced in the ACEI trials but not with ARB therapy. Stroke was significantly reduced in the ACEI trials (RR 0.75; ) and more modestly reduced in the ARB trials (RR 0.90; ). Conclusion. ACEI treatment reduced stroke, nonfatal MI, cardiovascular and total mortality in high risk patients, while ARB modestly reduced stroke with no effect on nonfatal MI, cardiovascular and total mortality. 1. Introduction Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin-receptor blockers (ARBs) have been shown to reduce cardiovascular outcomes in patients with heart failure or hypertension [1–3]. However, whether ACEI and ARB are useful in reducing cardiovascular events amongst patients at risk from a variety of clinical conditions but without left ventricular systolic dysfunction is more debatable. Several meta-analyses have addressed this issue, but these solely reviewed either ACEI or ARB alone or looked at patients with a single disease condition like hypertension or ischemic heart disease [4–10]. Both ACEI and ARB produce inhibition of the rennin-angiotensin system and have been shown to be equivalent in their blood pressure lowering effect [11]. We thus seek to answer the question of whether ACEI and ARB are useful and equivalent in their reduction of total mortality, cardiovascular mortality, nonfatal myocardial infarction (MI), and stroke in patients with normal systolic function and who are at high risk of cardiovascular events from a combination of various clinical conditions. 2. Methods This present meta-analysis seeks to address the question of whether ACEI and ARB should be routinely used in patients at

References

[1]  The SOLVD Investigators, “Effect of enalapril on survival in patients with reduced left ventricular ejection fractions and congestive heart failure,” The New England Journal of Medicine, vol. 325, no. 5, pp. 293–302, 1991.
[2]  C. B. Granger, J. J. V. McMurray, S. Yusuf et al., “Effects of candesartan in patients with chronic heart failure and reduced left-ventricular systolic function intolerant to angiotensin-converting-enzyme inhibitors: the CHARM-alternative trial,” The Lancet, vol. 362, no. 9386, pp. 772–776, 2003.
[3]  Blood Pressure Lowering Treatment Trialists’ Collaboration, “Effects of different blood-pressure-lowering regimens on major cardiovascular events: results of prospectively-designed overviews of randomised trials,” The Lancet, vol. 362, no. 9395, pp. 1527–1535, 2003.
[4]  M. H. Al-Mallah, I. M. Tleyjeh, A. A. Abdel-Latif, and W. D. Weaver, “Angiotensin-converting enzyme inhibitors in coronary artery disease and preserved left ventricular systolic function. A systematic review and meta-analysis of randomized controlled trials,” Journal of the American College of Cardiology, vol. 47, no. 8, pp. 1576–1583, 2006.
[5]  G. R. Dagenais, J. Pogue, K. Fox, M. L. Simoons, and S. Yusuf, “Angiotensin-converting-enzyme inhibitors in stable vascular disease without left ventricular systolic dysfunction or heart failure: a combined analysis of three trials,” The Lancet, vol. 368, no. 9535, pp. 581–588, 2006.
[6]  N. Danchin, M. Cucherat, C. Thuillez, E. Durand, Z. Kadri, and P. G. Steg, “Angiotensin-converting enzyme inhibitors in patients with coronary artery disease and absence of heart failure or left ventricular systolic dysfunction: an overview of long-term randomized controlled trials,” Archives of Internal Medicine, vol. 166, no. 7, pp. 787–796, 2006.
[7]  M. Volpe, G. Tocci, S. Sciarretta, P. Verdecchia, B. Trimarco, and G. Mancia, “Angiotensin II receptor blockers and myocardial infarction: an updated analysis of randomized clinical trials,” Journal of Hypertension, vol. 27, no. 5, pp. 941–946, 2009.
[8]  M. M. Al Khalaf, L. Thalib, and S. A. R. Doi, “Cardiovascular outcomes in high-risk patients without heart failure treated with ARBs: a systematic review and meta-analysis,” American Journal of Cardiovascular Drugs, vol. 9, no. 1, pp. 29–43, 2009.
[9]  L. C. van Vark, M. Bertrand, K. M. Akkerhius, et al., “Angiotensin-converting enzyme inhibitors reduce mortality in hypertension: a meta-analysis of randomized clinical trials of rennin-angiotensin-aldosterone system inhibitors involving 158,998 patients,” European Heart Journal, vol. 33, pp. 2088–2097, 2012.
[10]  W. L. Baker, C. I. Coleman, J. Kluger et al., “Systematic review: comparative effectiveness of angiotensin-converting enzyme inhibitors or angiotensin II-receptor blockers for ischemic heart disease,” Annals of Internal Medicine, vol. 151, no. 12, pp. 861–871, 2009.
[11]  The ONTARGET Investigators, “Telmisartan, ramipril or both in patients at high risk for vascular events,” The New England Journal of Medicine, vol. 358, pp. 1547–1559, 2008.
[12]  The Heart Outcomes Prevention Evaluation Study Investigators, “Effects of an angiotensin-converting-enzyme inhibitor, ramipril, on cardiovascular events in high-risk patients,” The New England Journal of Medicine, vol. 342, no. 3, pp. 145–153, 2000.
[13]  ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group, “Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT),” JAMA, vol. 288, pp. 2981–2997, 2002.
[14]  Review Manager (RevMan) [Computer program], Version 5.0. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2008.
[15]  PROGRESS Collaborative Group, “Randomised trial of a perindopril-based blood pressure lowering regimen among 6105 individuals with previous stroke or transient ischemic attack,” The Lancet, vol. 358, pp. 1033–1041, 2001.
[16]  B. Pitt, B. O'Neill, R. Feldman et al., “The Quinapril Ischemic Event Trial (QUIET): evaluation of chronic ACE inhibitor therapy in patients with ischemic heart disease and preserved left ventricular function,” American Journal of Cardiology, vol. 87, no. 9, pp. 1058–1063, 2001.
[17]  EURopean Trial on Reduction of Cardiac Events with Perindopril in Stable Coronary Artery Disease Investigators, “Efficacy of perindopril in reduction of cardiovascular events among patients with stable coronary artery disease: randomised, double-blind, placebo-controlled, multicentre trial (the EUROPA study),” The Lancet, vol. 362, no. 9386, pp. 782–788, 2003.
[18]  S. E. Nissen, E. M. Tuzcu, P. Libby et al., “Effect of antihypertensive agents on cardiovascular events in patients with coronary disease and normal blood pressure. The CAMELOT study: a randomized controlled trial,” Journal of the American Medical Association, vol. 292, no. 18, pp. 2217–2226, 2004.
[19]  The PEACE Trial Investigators, “Angiotensin-converting enzyme inhibition in stable Coronary Artery Disease,” The New England Journal of Medicine, vol. 351, pp. 2058–2068, 2004.
[20]  S. Mochizuki, B. Dahl?f, M. Shimizu et al., “Valsartan in a Japanese population with hypertension and other cardiovascular disease (Jikei Heart Study): a randomised, open-label, blinded endpoint morbidity-mortality study,” The Lancet, vol. 369, no. 9571, pp. 1431–1439, 2007.
[21]  The Telmisartan Randomised Assessment Study in ACE Intolerant Subjects with Cardiovascular Disease (TRANSCEND) Investigators, “Effects of the angiotensin-receptor blocker telmisartan on cardiovascular events in high-risk patients intolerant to angiotensin-converting enzyme inhibitors: a randomized controlled trial,” The Lancet, vol. 372, pp. 1174–1183, 2008.
[22]  S. Yusuf, H. C. Diener, R. L. Sacco, et al., “Telmisartan to prevent recurrent stroke and cardiovascular events,” The New England Journal of Medicine, vol. 359, pp. 1225–1237, 2008.
[23]  The NAVIGATOR Study Group, “Effect of valsartan on the incidence of diabetes and cardiovascular events,” The New England Journal of Medicine, vol. 362, pp. 1463–1476, 2010.
[24]  P. Svensson, U. de Faire, P. Sleight, S. Yusuf, and J. Ostergren, “Comparative effects of ramipril on ambulatory and office blood pressures: a HOPE Substudy,” Hypertension, vol. 38, no. 6, pp. E28–E32, 2001.
[25]  G. D. Moutsatsos, “More hype than HOPE,” Hypertension, vol. 41, no. 4, pp. e4–e5, 2003.
[26]  N. Freemantle, J. Cleland, P. Young, J. Mason, and J. Harrison, “β blockade after myocardial infarction: systematic review and meta regression analysis,” British Medical Journal, vol. 318, no. 7200, pp. 1730–1737, 1999.
[27]  Scandinavian Simvastatin Survival Study Group, “Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: the Scandinavian Simvastatin Survival Study (4S),” The Lancet, vol. 344, no. 8934, pp. 1383–1389, 1994.
[28]  Heart Protection Study Collaborative Group, “MRC/BHF Heart Protection Study of cholesterol lowering with simvastatin in 5963 people with diabetes: a randomized placebo controlled trial,” The Lancet, vol. 361, pp. 2005–2016, 2003.
[29]  A. N. DeMaria, “Lies, damned lies, and statistics,” Journal of the American College of Cardiology, vol. 52, no. 17, pp. 1430–1431, 2008.
[30]  I. Boutron, S. Dutton, P. Ravaud, and D. G. Altman, “Reporting and interpretation of randomized controlled trials with statistically nonsignificant results for primary outcomes,” Journal of the American Medical Association, vol. 303, no. 20, pp. 2058–2064, 2010.
[31]  J. N. Cohn and G. Tognoni, “A randomized trial of the angiotensin-receptor blocker valsartan in chronic heart failure,” The New England Journal of Medicine, vol. 345, no. 23, pp. 1667–1675, 2001.
[32]  UK Prospective Diabetes Study Group, “Efficacy of atenolol and captopril in reducing risk of macrovascular and microvascular complications in type 2 diabetes: UKPDS 39,” British Medical Journal, vol. 317, no. 7160, pp. 713–720, 1998.
[33]  L. Hansson, L. H. Lindholm, L. Niskanen et al., “Effect of angiotensin-converting-enzyme inhibition compared with conventional therapy on cardiovascular morbidity and mortality in hypertension: the Captopril Prevention Project (CAPPP) randomised trial,” The Lancet, vol. 353, no. 9153, pp. 611–616, 1999.
[34]  L. Hansson, L. H. Lindholm, T. Ekbom et al., “Randomised trial of old and new antihypertensive drugs in elderly patients: cardiovascular mortality and morbidity the Swedish trial in old patients with hypertension-2 study,” The Lancet, vol. 354, no. 9192, pp. 1751–1756, 1999.
[35]  B. Dahl?f, R. B. Devereux, S. E. Kjeldsen et al., “Cardiovascular morbidity and mortality in the Losartan Intervention For Endpoint reduction in hypertension study (LIFE): a randomised trial against atenolol,” The Lancet, vol. 359, no. 9311, pp. 995–1003, 2002.
[36]  S. Julius, S. E. Kjeldsen, M. Weber et al., “Outcomes in hypertensive patients at high cardiovascular risk treated with regimens based on valsartan or amlodipine: the VALUE randomised trial,” The Lancet, vol. 363, no. 9426, pp. 2022–2031, 2004.
[37]  Y. Yui, T. Sumiyoshi, K. Kodama et al., “Comparison of nifedipine retard with angiotensin converting enzyme inhibitors in Japanese hypertensive patients with coronary artery disease: the Japan Multicenter Investigation for Cardiovascular Diseases-B (JMIC-B) randomized trial,” Hypertension Research, vol. 27, no. 3, pp. 181–191, 2004.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133