Summary of clinical trials demonstrating the value of lowering blood pressure in hypertensive subjects aged 60–79 years
Trial | Entry criteria | n | Age | Treatment | Results/update |
---|---|---|---|---|---|
ANBP 2, Second Australian National Blood Pressure Study Group9,10; EWPHE, European Working Party on High Blood Pressure in the Elderly11; MRC, Medical Research Council trial of treatment of hypertension in older adults12; SCOPE, Study on Cognition and Prognosis in the Elderly13,14; SHELL, Systolic Hypertension in the Elderly Long-term Lacidipine trial15,16; SHEP, Systolic Hypertension in the Elderly Program17; STOP-Hypertension 2, Swedish Trial in Old Patients with Hypertension18,19; Syst-Eur, Systolic Hypertension in Europe20,21; Syst-China, Systolic Hypertension in China.22,23 | |||||
ANBP 2 | SBP⩾160 mm Hg | 6083 | 65–84 years | ACE inhibitor or diuretic | Similar reduction in BP in both groups. ACE inhibitor |
DBP⩾90 mm Hg | based regimen | reduced cardiovascular events or death (p = 0.05) | |||
EWPHE | SBP 160–239 mm Hg | 840 | ⩾60 years | Hydrochlorothiazide and | No significant reduction in total mortality. Significant |
DBP 90–119 mm Hg | (mean 72 years) | triamterene with possible addition of | reduction in cardiovascular mortality (p<0.05) and | ||
methyldopa or matching placebo | non-fatal cerebrovascular events (p<0.05) | ||||
MRC | SBP 160–209 mm Hg | 4396 | 65–74 years | Diuretic, β-blocker or placebo | Diuretic reduced stroke (p = 0.04), coronary events |
DBP<115 mm Hg | (p = 0.001) and cardiovascular events (p = 0.001) | ||||
compared with placebo | |||||
SCOPE | SBP 160–179 mm Hg | 4964 | 70–89 years | Candesartan, cilexetil or placebo | Candesartan reduced non-fatal stroke (p = 0.04) and |
and/or DBP 90– | all stroke events (p = 0.056). Cognitive decline | ||||
99 mm Hg, Mini | and development of dementia was similar in | ||||
Mental State | both groups | ||||
Examination⩾24 | |||||
SHELL | SBP⩾160 mm Hg | 1882 | ⩾60 years | Lacidipine or chlorthalidone | Both treatments reduced SBP and DBP (p<0.001). |
DBP⩽95 mm Hg | Total mortality and cardiovascular events were | ||||
similar in both groups | |||||
SHEP | SBP 160–219 mm Hg | 4736 | ⩾60 years | Chlorthalidone titrated or | Stroke was reduced (p = 0.001) and major |
DBP<90 mm Hg | (mean 72 years) | changed to atenolol or placebo | cardiovascular events were reduced in the | ||
active treatment group | |||||
STOP- | SBP⩾180 mm Hg | 6614 | 70–84 years | β-Blockers and/or diuretics | No difference was found in the prevention of |
Hyperten- | and/or | compared with ACE-inhibitors or | cardiovascular mortality or major events between | ||
sion 2 | DBP⩾105 mm Hg | calcium antagonists | the groups | ||
Syst-Eur | DBP<95 mm Hg | 4695 | ⩾60 years | Nitrendipine plus enalapril and/or | Active treatment reduced all strokes (p = 0.003) and |
SBP 160–219 mm Hg | (mean 70 years) | hydrochlorothiazide as necessary | non-fatal strokes (p = 0.007). Fatal and non-fatal | ||
and matching placebos | cardiac endpoints also decreased (p = 0.03) | ||||
Syst-China | SBP 160–219 mm Hg | 2394 | ⩾60 years | Nitrendipine plus captopril, | Active treatment reduced stroke (p = 0.01), stroke |
DBP<95 mm Hg | (mean 66.5 years) | and/or hydrochlorothiazide if | mortality (p = 0.02), all-cause mortality (p = 0.003), | ||
necessary and matching | cardiovascular mortality (p = 0.03) and all fatal and | ||||
placebos | non-fatal cardiovascular endpoints (p = 0.004) |