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michigan hypertension core curriculum - State of Michigan

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(mean age, 54 years). Overall, ACE inhibitors were found to have a modest collective effect in reducing<br />

BP. The mean reduction in SBP ranged between 6 mm Hg and 9 mm Hg, and the mean reduction<br />

in DBP was 4-5 mm Hg. 11 It was notable that all the ACE inhibitors studied were homogeneous in<br />

their efficacy and that lower doses were generally as effective in reducing BP as the manufacturer’s<br />

maximum recommended doses. This observation can be most readily explained by the fact that ACE<br />

inhibitors have relatively flat-dose-response curves.<br />

ACE inhibitors are notable for a low incidence <strong>of</strong> side effects and ease <strong>of</strong> dosing. For this<br />

reason they are very popular antihypertensive agents in clinical practice, though, as noted under the<br />

diuretic section above, national guidelines continue to endorse the use <strong>of</strong> thiazide diuretics as first<br />

line agents for the treatment <strong>of</strong> uncomplicated <strong>hypertension</strong>. They have traditionally been perceived<br />

to be more effective in Caucasians and younger patients, though more recent data suggests they are<br />

effective in African American patients, as well, with perhaps higher dosing. Race, however, should<br />

never be sole criterion upon which an ACE inhibitor or any other antihypertensive agent is either<br />

chosen or avoided. 12<br />

The ACE inhibitors have pleiotropic effects on the renal and cardiovascular systems making<br />

them ideal antihypertensive agents for specific medical populations. There is some evidence that they<br />

have a beneficial effect on glucose metabolism (improve glucose tolerance without affecting fasting<br />

glucose levels) and appear to delay the onset <strong>of</strong> type 2 diabetes. These agents reduce preload<br />

and afterload, down-regulate sympathetic activity by blocking the facilitating effects <strong>of</strong> angiotensin II<br />

on sympathetic nerves, and promote renal excretion <strong>of</strong> sodium and water by blocking the effects <strong>of</strong><br />

angiotensin II in the proximal tubule and by antagonizing angiotensin II-mediated aldosterone secretion.<br />

ACE inhibitors also inhibit cardiac and vascular remodeling associated with chronic <strong>hypertension</strong> and<br />

heart failure. All <strong>of</strong> these qualities make ACE inhibitors excellent antihypertensives for the treatment<br />

<strong>of</strong> patients with heart failure and following myocardial infarction for which they have been shown<br />

to reduce mortality in multiple clinical trials. Finally, there is abundant evidence from many clinical<br />

trials demonstrating that the ACE inhibitors are effective in reducing proteinuria and decreasing the<br />

rate <strong>of</strong> decline in kidney function in patients with chronic kidney disease. While strict control <strong>of</strong> BP<br />

appears to be the most important in regards to preservation <strong>of</strong> kidney function, it also appears that the<br />

ACE inhibitors have a beneficial effect on renal function – especially amongst those individuals with<br />

NKFM & MDCH 193

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