Table 1.
Study Title | Participants | Intervention | Duration | Comparison | Main Findings |
---|---|---|---|---|---|
1. HPS (Heart Protection Study) [70] | 20,536 patients (High-risk individuals) |
Simvastatin 40 mg/d | 5.3 years | Placebo | This randomized controlled trial assessed the impact on 11-year mortality and morbidity. Statin use reduces major vascular events. |
2. ASCOT-LLA (Anglo-Scandinavian Cardiac Outcomes TrialLipid-Lowering Arm) [71] | 10,305 patients (Hypertensive patients) | Atorvastatin 10 mg/d | Mean 3.3 years | Placebo | Atorvastatin reduces cardiovascular events in hypertensive patients. |
3. JUPITER (Justification for the Use of Statins in Prevention: An Intervention Trial Evaluating Rosuvastatin) [20] | 17,802 participants (High-risk individuals) | Rosuvastatin 20 mg/d | Average 2 years | Placebo | Rosuvastatin reduces cardiovascular events in individuals with elevated hs-CRP without a systematic rise in reported adverse events. |
4. PROVE-IT TIMI 22 (Pravastatin or Atorvastatin Evaluation and Infection Therapy-Thrombolysis in Myocardial Infarction 22) [72] | 4162 patients (post-ACS patients) | Pravastatin 40 mg/d vs. Atorvastatin 80 mg/d | Median 2 years | Intensive vs. moderate statin therapy | Intensive statin therapy (Atorvastatin) reduces cardiovascular events more than moderate therapy (Pravastatin). |
5. TNT (Treating to New Targets) [73] | 10,001 patients (stable coronary heart disease) | Atorvastatin 10 mg/d vs. 80 mg/d | Median 4.9 years | Standard vs. high-dose statin therapy | High-dose Atorvastatin is more effective in reducing cardiovascular events. |