AI Article Synopsis

  • The benefits of blood pressure control on reducing risks of heart failure and stroke are well documented.
  • Candesartan cilexetil, an angiotensin II receptor blocker, is effective for treating hypertension and helps lower various cardiovascular risks.
  • Clinical studies show that candesartan is more effective than losartan and comparable to other leading treatments, featuring strong efficacy, long-lasting effects, and a tolerability profile similar to a placebo.

Article Abstract

The advantages of blood pressure (BP) control on the risks of heart failure and stroke are well established. The renin-angiotensin system plays an important role in volume homeostasis and BP regulation and is a target for several groups of antihypertensive drugs. Angiotensin II receptor blockers represent a major class of antihypertensive compounds. Candesartan cilexetil is an angiotensin II type 1 (AT[1]) receptor antagonist (angiotensin receptor blocker [ARB]) that inhibits the actions of angiotensin II on the renin-angiotensin-aldosterone system. Oral candesartan 8-32 mg once daily is recommended for the treatment of adult patients with hypertension. Clinical trials have demonstrated that candesartan cilexetil is an effective agent in reducing the risk of cardiovascular mortality, stroke, heart failure, arterial stiffness, renal failure, retinopathy, and migraine in different populations of adult patients including patients with coexisting type 2 diabetes, metabolic syndrome, or kidney impairment. Clinical evidence confirmed that candesartan cilexetil provides better antihypertensive efficacy than losartan and is at least as effective as telmisartan and valsartan. Candesartan cilexetil, one of the current market leaders in BP treatment, is a highly selective compound with high potency, a long duration of action, and a tolerability profile similar to placebo. The most important and recent data from clinical trials regarding candesartan cilexetil will be reviewed in this article.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253768PMC
http://dx.doi.org/10.2147/VHRM.S22591DOI Listing

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