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Antihypertensive, antiproteinuric therapy and myocardial infarction and stroke prevention
Kenneth L Choi1, William J Elliott
1Department of Preventive Medicine, RUSH Medical College, 1700 West Van Buren Street, Suite 470, Chicago, IL 60612, USA.
Insights
Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin-receptor blockers (ARBs) benefit kidney health by reducing proteinuria. However, these drugs do not independently lower cardiovascular risks like heart attack or stroke.
Area of Science:
- Nephrology
- Cardiology
- Pharmacology
Background:
- Proteinuria indicates kidney damage and predicts cardiovascular events.
- Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin-receptor blockers (ARBs) reduce proteinuria and slow kidney disease progression, independent of blood pressure.
- Large trials like IDNT and RENAAL studied ARBs in type 2 diabetic patients with proteinuria.
Purpose of the Study:
- To evaluate the cardiovascular effects of ACEIs and ARBs beyond their blood pressure-lowering capabilities.
- To determine if ARBs offer independent protection against myocardial infarction and stroke in diabetic nephropathy.
Main Methods:
- Analysis of data from large, randomized, prospective trials (IDNT, RENAAL).
- Comparison of ARBs versus placebo in type 2 diabetic patients with proteinuria.
- Review of broader clinical trial data comparing ACEIs and ARBs with other antihypertensives.
Main Results:
- Neither the Irbesartan Diabetic Nephropathy Trial (IDNT) nor the Reduction in Endpoints in NIDDM with the Angiotensin Antagonist Losartan (RENAAL) study showed a reduction in myocardial infarction or stroke incidence with ARBs compared to placebo.
- A comprehensive review of clinical trials did not reveal significant blood pressure-independent cardiovascular benefits (stroke, myocardial infarction) for ACEIs or ARBs.
Conclusions:
- While ACEIs and ARBs are effective in reducing proteinuria and slowing renal impairment, they do not appear to offer independent cardiovascular protection against myocardial infarction or stroke.
- For cardiovascular outcomes, achieving blood pressure reduction is likely more critical than the specific mechanism initiated by ACEIs or ARBs.
Abstract:
Proteinuria is a graded marker for kidney damage, as well as the risk for future cardiovascular events. Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin-receptor blockers (ARBs) reduce urinary protein excretion and slow progression of renal impairment, independent of blood pressure lowering. Both the Irbesartan Diabetic Nephropathy Trial (IDNT) and the Reduction in Endpoints in NIDDM with the Angiotensin Antagonist Losartan (RENAAL) study were large, randomized, prospective studies in type 2 diabetic patients with proteinuria. There was no reduction in the incidence of myocardial infarction or stroke with the ARBs compared to placebo in either trial. A broader overview of clinical trials comparing ACEIs and ARBs with other antihypertensive drugs fails to show any substantive blood pressure-independent effects on stroke or myocardial infarction with these classes of drugs. Therefore, for cardiovascular end points (as opposed to renal end points), it may be more important that the blood pressure is reduced, rather than how the process is started.
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