Table 4.
Agent | Study | Key findings |
---|---|---|
Losartan | LIFE | Overall stroke: significant stroke reduction vs. atenolol (25%; P=0.0010),29 with significant reductions in a subset without clinical vascular disease (34%; P<0.001)111 and in ischemic (27%; P=0.001), atherothrombotic (27%; P=0.002), and fatal (35%; P=0.032) stroke in a subanalysis of specific subtypes34 Secondary prevention: significant reduction (n=26 vs. n=46; P=0.017) in subtype-focused analysis34 |
| ||
Valsartan | Jikei Heart Study | Overall stroke: significant reduction vs. non-ARB regimens (40%; P=0.028) in stroke or transient ischemic attack in patients with hypertension, coronary heart disease, and/ or heart failure51 |
KYOTO HEART Study | Overall stroke: significant reduction vs. non-ARB regimens (45%; P=0.015) in stroke or transient ischemic attack in patients with hypertension at high risk for cardiovascular events52 | |
| ||
Candesartan | SCOPE | Overall stroke: significant reduction vs. placebo (28%; P=0.04) in nonfatal stroke in elderly hypertensive patients,65 with significant all-stroke reduction in a subset with isolated systolic hypertension66 |
E-COST | Primary prevention: no significant stroke reduction vs. conventional antihypertensive treatment, with a 29% increased risk with candesartan in patients without history of stroke or MI64 Secondary prevention: significant stroke reduction for candesartan vs. conventional antihypertensive treatment in patients with past stroke or MI (61%; P<0.01)64 |
|
| ||
Telmisartan | PRoFESS | Secondary prevention: no significant recurrent stroke reduction (primary endpoint) vs. placebo when initiated within 90 days after ischemic stroke93 |
TRANSCEND | Overall stroke: no significant stroke reduction vs. placebo in ACEI-intolerant patients with cardiovascular disease or diabetes/end-organ damage92 | |
| ||
Eprosartan | MOSES | Secondary prevention: significant reduction vs. nitrendipine (25%; P=0.026) in fatal/ nonfatal cerebrovascular events104 |
ACEI=angiotensin-converting enzyme inhibitor; ARB=angiotensin II receptor blockers; MI=myocardial infarction.
In which the overall study population included >100 patients.