From the Guidelines
For a diabetic patient with elevated cholesterol (222 mg/dL), high triglycerides (199 mg/dL), and high LDL (137 mg/dL), rosuvastatin would be the preferred choice over atorvastatin, as it is more potent and achieves greater LDL reduction, which is beneficial for diabetic patients with high cardiovascular risk 1. The patient's lipid profile and high-risk factor of 4.9 indicate the need for aggressive lipid management to reduce the risk of cardiovascular events.
- Key considerations for the patient's treatment include:
- Starting with rosuvastatin 10-20 mg daily, taken at the same time each day regardless of meals
- Combining the medication with dietary modifications (reduced saturated fat and simple carbohydrates) and regular exercise
- Expecting follow-up bloodwork in 4-12 weeks to assess efficacy and tolerability
- Monitoring for muscle pain or weakness, which could indicate rare side effects
- According to the 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA guideline on the management of blood cholesterol, high-intensity statin therapy, such as rosuvastatin 20 mg, is recommended for patients with high cardiovascular risk, as it achieves an LDL-C lowering of ≥50% 1.
- If cost is a significant concern, atorvastatin (which is more widely available as a generic) could be considered as an alternative, starting at 20-40 mg daily to achieve similar LDL reduction, although it may not be as potent as rosuvastatin 1.
From the FDA Drug Label
Rosuvastatin was compared with the statins (atorvastatin, simvastatin, and pravastatin) in a multicenter, open-label, dose-ranging study of 2,240 patients with hyperlipidemia or mixed dyslipidemia. Table 11: Percent Change in LDL-C by Dose of Rosuvastatin, Atorvastatin, Simvastatin, and Pravastatin From Baseline to Week 6 (LS MEAN 1) in Adult Patients with Hyperlipidemia or Mixed Dyslipidemia (Sample Sizes Ranging from 156–167 Patients Per Group) Rosuvastatin-46 2-52 3-55 4--- Atorvastatin-37-43-48-51 In a study of adult patients with HeFH (baseline mean LDL of 291 mg/dL), patients were randomized to rosuvastatin 20 mg or atorvastatin 20 mg. Table 12: LDL-C Percent Change from Baseline 1LS Means are least square means adjusted for baseline LDL-C Rosuvastatin (n=435) LS Mean 1(95%CI) Atorvastatin (n=187) LS Mean 1(95% CI) Week 620 mg-47% (-49%, -46%)-38% (-40%, -36%)
Comparison of Rosuvastatin and Atorvastatin:
- Both rosuvastatin and atorvastatin reduce LDL-C levels.
- Rosuvastatin appears to be more effective in reducing LDL-C levels compared to atorvastatin, especially at higher doses.
- In patients with hyperlipidemia or mixed dyslipidemia, rosuvastatin reduced LDL-C by 46-55% compared to atorvastatin which reduced LDL-C by 37-51%.
- In patients with HeFH, rosuvastatin 20 mg reduced LDL-C by 47% compared to atorvastatin 20 mg which reduced LDL-C by 38%. 2
From the Research
Comparison of Rosuvastatin and Atorvastatin in Diabetic Patients with Lipid Profile Abnormalities
- The patient's lipid profile shows high levels of cholesterol (222), triglycerides (199), and LDL (137), with a low level of HDL (45) and a high risk factor (4.9) 3, 4.
- Studies have shown that type 2 diabetes mellitus is associated with a characteristic pattern of dyslipidemia, often termed diabetic dyslipidemia, which includes low HDL levels, elevated levels of small dense LDL particles, and elevated triglyceride levels 3.
- LDL lowering is the cornerstone of managing diabetic dyslipidemia, and statins are the mainstay of therapy 3, 5.
- Both rosuvastatin and atorvastatin are statins that can be used to lower LDL levels, but there is no direct comparison between the two in the provided studies.
- However, studies have shown that statins can reduce cardiovascular event rates in patients with diabetes, and that achieving LDL targets is important for reducing cardiovascular risk 4, 5, 6.
Treatment Options for Diabetic Dyslipidemia
- The cholesterol absorption inhibitor ezetimibe and PCSK9 inhibitors have also been shown to lower risk in patients with diabetes 3.
- Fibrates, which have low affinity for peroxisome proliferator-activated receptor alpha (PPARalpha), can improve most aspects of the atherogenic dyslipidemia of diabetes 4.
- Integrating potent PPARalpha and PPARgamma activity may deliver greater improvement of the diabetic dyslipidemic profile and its attendant risks than selective PPAR activation 4.
Management of High Cardiovascular Risk in Diabetic Patients
- The management of high cardiovascular risk in diabetic patients requires a comprehensive approach, including lifestyle modifications and pharmacological therapy 5.
- Statin therapy is a key component of this approach, and achieving LDL targets is important for reducing cardiovascular risk 5, 6.
- However, studies have shown that many patients with diabetes do not achieve their LDL targets, and that there is a need for improved management of diabetic dyslipidemia 5, 6.