Double blockade of renin-angiotensin-aldosteron system – is it always beneficial? Review article

Main Article Content

Anna Szyndler

Abstract

The wide indication spectrum for the angiotensin II converting enzyme inhibitors in the high risk patients therapy suggests that more selective blockers of angiotensin II (angiotensin II AT1 receptor blockers) will have similar if not better action profile. Because of those facts the interest in dual blockade of the RAS arises. It is thought that this may help to avoid the ACEI escape phenomenon. In this paper the potential benefits and indication for dual RAS blockade are revised.


Up till now there are no big clinical trials comparing the efficacy of dual blockade (ACEI + ARB) with other drug classes in hypertensive patients. In existing trials with nephropathy or heart failure patients the dual blockade was connected with lower blood pressure achieved. This finding may suggest lower complication risk that may be achieved with prescribing ACEI with ARB in hypertensive patients.


In congestive heart failure patients it have been observed that administrating dual blockade of RAS was connected with lower rates of combined endpoint of cardiovascular mortality and hospitalization rate. The improvement in quality of life was also observed. It is also noteworthy that this kind of therapy has higher adverse event rate (high potassium level).


Among patients with nephropathy receiving dual RAS blockade two fold decrease in incidence of primary end point (doubling of serum creatinine level or progression to ESRD) has been observed. This results were achieved independently of basic levels of proteinuria and nephropathy etiology.


To sum up it is thought that dual blockade of the RAA system in pre specified groups of patients may have a substantially beneficial clinical effect.

Downloads

Download data is not yet available.

Article Details

How to Cite
Szyndler , A. (2007). Double blockade of renin-angiotensin-aldosteron system – is it always beneficial?. Cardiology in Practice, 1(1), 35-40. Retrieved from https://www.journalsmededu.pl/index.php/kwp/article/view/1720
Section
Articles

References

1. Rocha e Silva M., Beraldo W.T., Rosenfeld G.: Bradykinin, a hypotensive and smooth muscle stimulating factor released from plasma globulin by snake venoms and by trypsin. Am J Physiol 1949, 156, 261-273.
2. Cushman D.W., Ondetti M.A.: Design of angiotensin converting encyme inhibitors. Nature Medicine (USA) 1999, 5, 1110-1112.
3. Blood Pressure Lowering Treatement Trialists’ Collaboration. Effects of different blood-pressure- lowering regimens on major cardiovascular events: results of prospectively-designed overviews of randomised trials. Lancet 2003, 362(9395), 1527-1535.
4. Gryglewski R.J.: Historia sartanów. In: Januszewicz A., Januszewicz W., Rużyłło W., editors. Antagoniści receptora angiotensyny II w leczeniu chorób układu sercowo-naczyniowego. Kraków: Medycyna Praktyczna 2006, 17-19.
5. Azizi M., Linhart A., Alexander J. et al.: Pilot study of combined blockade of the renin-angiotensin system in essential hypertensive patients. J Hypertens 2000, 18(8), 1139-1147.
6. Lithell H., Hansson L., Skogg I.: The Study on Cognition and Prognosis in the Elderly (SCOPE): principal results o a randomised double-blind intervention trial. J Hypertens 2003, 16, 127-137.
7. Dahlof B., Devereux R., Kjeldsen S.: Cardiovascular morbidity and mortality in the Losartan Intervention For Endpoint reduction in hypertension study (LIFE): a randomised trial against atenolol. Lancet 2002, 359, 995-1003.
8. European Society of Hypertension-European Society of Cardiology Guidelines Committee. 2003 European Society of Hypertension-European Society of Cardiology guidelines for the management of arterial hypertension. J Hypertens 2003, 21(6), 1011-1053.
9. Mogensen C.E., Neldam S., Tikkanen I. et al.: Randomised controlled trial of dual blockade of renin-angiotensin system in patients with hypertension, microalbuminuria, and non-insulin dependent diabetes: the candesartan and lisinopril microalbuminuria (CALM) study. BMJ 2000, 321(7274), 1440-1444.
10. HOPE (Heart Outcomes Prevention Evaluation) Study Investigators. Effects of and angiotensin-converting-enzyme inhibitor, ramipril, on cardiovascular events in high-risk patients. N Engl J Med 2000, 342, 145-153.
11. 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. JAMA 2002, 288, 2981-2997.
12. McMurray J.J., Ostergren J., Swedberg K.: Effects of candesartan in patients with chronic heart failure and reduced left-ventricular systolic function taking angiotensin-converting-enzyme inhibitors: the CHARM-Added trial. Lancet 2003, 362, 767-771.
13. Cohn J.N., Tognoni G. for the Valsartan Heart Failure Trial Investigators. A randomized trial of the angiotensin receptor blocker valsartan in chronic heart failure. N Engl J Med 2001, 345, 1667-1675.
14. Krum H., Carson P., Farsang C. et al.: Effect of valsartan added to background ACE inhibitor therapy in patients with heart failure: results form Val-HeFT. Eur J Heart Fail 2004, 6, 937-945.
15. Granger C.B., McMurray J.J., Yusuf S.: Effects of candesartan in patients with chronic heart failure and reduced left-ventricular systolic function intolerant to angiotensin-convertin-enzyme inhibitors: the CHARM-Alternative trial. Lancet 2003, (362), 772-776.
16. Maggioni A.P., Fabbri G.: VALIANT (VALsartan In Acute myocardial iNfarcTion) trial. Expert Opin Pharmacother 2005, 6(3), 507-512.
17. The Task Force for the Diagnosis and Treatment of Chronic Heart Failure of the European Society of Cardiology. Guidelines for the diagnosis and treatment of chronic heart failure:executive summary (update 2005). Eur Heart J 2005, 26, 1115-1140.
18. Lewis E.J., Hunsicker L.G., Bain R.P., Rohde R.: The effect if angiotensin-converting-enzyme inhibition on diabetic nephropathy. The Collaborative Study Group. N Engl J Med 1993, 329, 1456-1462.
19. Barnett A.H., Bain S.C., Bouter P. et al.: Angiotensin-receptor blocade versus converting-enzyme inhibition in type 2 diabetes and nephropathy. N Engl J Med 2004, 351, 1952-1961.
20. Ruggeneti P., Fassi A., Ilieva A.P. et al.: Preventing microalbuminuria in type 2 diabetes. N Engl J Med 2004, 351, 1941-1951.
21. Ruggeneti P., Perna A., Gherardi G. et al.: Renoprotective properties of ACE-Inhibition in non-diabetic nephropathies with non-nephrotic proteinuria. Lancet 1999, 354, 359-364.
22. Brenner B.M., Cooper M.E., de Zeeuw D. et al.: Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. N Engl J Med 2001, 345, 861-869.
23. Lewis E.J., Hunsicker L.G., Clarke W.R. et al.: Renoprotecive effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes. N Engl J Med 2001, 345, 851-860.
24. Nakao N., Yoshimura A., Morita H., Takada M., Kayano T., Ideura T.: Combination treatment of angiotensin-II receptor blocker and angiotensin-convertingenzyme inhibitor in non-diabetic renal disease (COOPERATE): a randomised controlled trial. Lancet 2003, 361, 117-124.
25. Kidney Disease Outcomes Quality Initiative (K/DOQI). K/DOQI clinical practice guidelines on hypertension and antihypertensive agents in chronic kidney disease. Am J Kidney Dis 2004, 43(5 supp. 1), S1-S290.