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These studies suggest that rosuvastatin is generally more effective than atorvastatin in improving lipid profiles, reducing coronary atherosclerosis, and achieving cholesterol goals, while both drugs show similar efficacy in lowering LDL-C and reno-protective effects.
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Statins, including atorvastatin (ATORVA) and rosuvastatin (ROSUVA), are widely prescribed for managing dyslipidemia and reducing cardiovascular risk. Both drugs are known for their lipid-lowering capabilities and potential benefits in various patient populations, including those with type 2 diabetes (T2D) and hypercholesterolemia.
Multiple studies have demonstrated that rosuvastatin is more effective than atorvastatin in improving lipid profiles. For instance, rosuvastatin significantly reduces LDL-C, total cholesterol, triglycerides, and atherogenic index more than atorvastatin in T2D patients with dyslipidemia. Additionally, rosuvastatin has been shown to increase HDL-C levels more effectively than atorvastatin .
In Japanese hypercholesterolemic patients with T2D, switching from atorvastatin to rosuvastatin resulted in a more significant reduction in small dense LDL-C levels, which are particularly atherogenic. This suggests that rosuvastatin may offer superior benefits in reducing specific harmful lipid fractions.
Rosuvastatin has been found to be more effective than atorvastatin in regressing coronary atherosclerotic plaques. A meta-analysis revealed that rosuvastatin administration led to a greater reduction in total atheroma volume and percent atheroma volume compared to atorvastatin. Similarly, another study showed that usual doses of rosuvastatin induced a more significant regression of coronary atherosclerosis than atorvastatin.
Both statins are effective in reducing inflammatory biomarkers and improving left ventricular (LV) function in T2D patients. However, rosuvastatin showed a more pronounced effect on reducing hs-CRP, sortilin, and leptin levels, while increasing adiponectin levels, which are associated with better cardiovascular outcomes.
The safety profiles of atorvastatin and rosuvastatin are generally comparable. A head-to-head trial comparing these statins found no significant differences in adverse event rates, including those related to liver and kidney function and skeletal muscle. However, both statins were associated with an increase in HbA1c levels, indicating a potential impact on glucose metabolism .
A meta-analysis comparing the effects of atorvastatin and rosuvastatin on renal function found no significant differences in glomerular filtration rate (GFR) between the two statins. However, rosuvastatin was associated with a higher risk of proteinuria at higher doses, although this effect was not significant at commonly used doses.
In obese hypertensive patients, both atorvastatin and rosuvastatin improved arterial stiffness parameters. However, rosuvastatin showed a more significant trend towards improvement in augmentation index (AIx) and pulse amplitude augmentation (PAA), indicating better vascular health outcomes.
In summary, while both atorvastatin and rosuvastatin are effective in managing dyslipidemia and reducing cardiovascular risk, rosuvastatin generally offers superior benefits in lipid profile improvement, atherosclerosis regression, and inflammatory biomarker modulation. However, the choice between these statins should be individualized based on patient-specific factors, including potential impacts on glucose metabolism and renal function.
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