Table 1.
Reference | Study Setting | Participants and Follow-Up | Treatment | Main Result |
---|---|---|---|---|
232 | SHEP | 4736 people, ~72 years at baseline, followed up to 4.5 years | Diuretic ± β-blocker ± hypertensive drug or placebo | No significant effect of treatment on AD risk |
233, 234 | MRC trial | 2584 people, ~69 years at baseline, followed up to 3.9 years | Diuretic or β-blocker or placebo | No significant effect of treatment on AD risk |
235, 236 | SCOPE | 4964 people, ~76 years at baseline, followed up to 4.5 years | ATI receptor agonist or placebo (candesartan ± hydrochlorothiazide versus placebo) | Significantly less cognitive decline in the treated group |
237 | PROGRESS | 6105 people, ~64 years at baseline, followed up to 4.5 years | ACE inhibitor ± diuretic or placebo (perindopril ± indapamide versus placebo) | Decreased the rates of dementia in actively treated patients |
238–240 | Syst-Eur study | 2418 people, ~68 years at baseline, followed up to 2 years | Calcium channel blocker ± ACE inhibitor ± diuretic or placebo (nitrendipine ± enalapril ± hydrochlorothiazide versus placebo | Decreased the risk of dementia by 55% |
NOTE: This table is a summary of randomized, double-blind, placebo-controlled studies describing the association between hypertension and antihypertensive therapy in relation to AD and has been adapted from Takeda et al.1 and Poon.241
Abbreviations: ACE, angiotensin converting enzyme; AD, Alzheimer's disease; ATI, angiotensin II type 1; MRC, Medical Research Council; PROGRESS, Perindopril Protection Against Recurrent Stroke Study; SCOPE, Study on Cognition and Prognosis in the Elderly; SHEP, Systolic Hypertension in the Elderly Program; Syst-Eur, Systolic Hypertension in Europe.