Table 1.
Study | Target population | Dates of recruitment | Mean follow-up (years) | Statin | Number of participants | Proportion of women (%) | Mean age (range, years) | Diabetes (%) | History of CVD (%) | Duration of post-trial follow-up | Difference in proportion taking statins post-trial (%) |
Primary prevention/primary care population | |||||||||||
ALLHAT-LLT | Treated for high BP with high cholesterol | 1994–1998 | 4.8 | Pravastatin 40 mg | 10 355 | 49 | 66 (55-NA) | 35 | 11 | 4 | NA |
ASCOT-LLA | High BP and no history of CHD, with 3+ other CVD risk factors |
1998–2000 | 3.2 | Atorvostatin 10 mg | 10 305 | 19 | 63 (40–79) | 25 | 14 | 8.3 | 4 |
WOS-COPS | Men with high cholesterol and no history of myocardial infarction | 1989–1991 | 4.8 | Pravastatin 40 mg | 6595 | 0 | 55 (45–64) | 1 | 8 | 15.1 | 4 |
Secondary prevention/clinical population | |||||||||||
ALERT | Renal or combined renal and pancreas transplant recipients at high risk of CVD |
1996–1997 | 5.1 | Fluvastatin 40 mg | 2102 | 34 | 50 (30–75) | 19 | 19 | 1.6 | 0 |
SSSS | History of angina or myocardial infarction | 1988–1989 | 5.2 | Simvastatin 20–40 mg | 4444 | 19 | 60+ (35-70) | 5 | 100 | 5 | 4 |
PROSPER | ≥70 years with history of CVD or at high risk of CVD | 1997–1999 | 3.2 | Pravastatin 40 mg | 5804 | 52 | 75 (70–82) | 11 | 44 | 5.4 | NA |
HPS | Coronary disease, other occlusive arterial disease, diabetes or treated for high BP | 1994–1997 | 5.0 | Simvastatin 40 mg | 20 536 | 25 | 64 (40–80) | 29 | 85 | 5.7 | 0 |
LIPID | Myocardial infarction or hospitalisation for unstable angina | 1990–1992 | 5.6 | Pravastatin 40 mg | 9014 | 17 | 62 (31–75) | 9 | >99 | 10 | 1 |
Order of trials within primary prevention and secondary prevention order is from shortest post-trial follow-up to longest.
BP, blood pressure; CVD, cardiovascular disease; NA, not available.