Key result
Loading doses of atorvastatin (80 mg) or rosuvastatin (40 mg) did not significantly alter platelet reactivity compared to no loading dose in patients with chronic stable angina on DAPT.
Why the study?
Does a loading dose of atorvastatin or rosuvastatin reduce platelet reactivity in patients with chronic stable angina on chronic DAPT before elective PCI?
RCT (n=145)
Randomized into 3 treatment groups
Does a loading dose of atorvastatin or rosuvastatin reduce platelet reactivity in patients with chronic stable angina on chronic DAPT before elective PCI?
A loading dose of atorvastatin or rosuvastatin does not acutely alter platelet reactivity in stable angina patients on chronic DAPT before PCI, though chronic statin use is associated with lower baseline reactivity.
Loading statin doses confer no acute platelet reactivity benefit before elective PCI; challenges assumptions of rapid antiplatelet effects in stable patients on DAPT.
BACKGROUND: The acute effects of statin loading dose (LD) on platelet reactivity in patients with chronic stable angina (CSA) are not completely clear. HYPOTHESIS: We hypothesized that LDs of atorvastatin and rosuvastatin have different pharmacodynamic acute effects on platelet aggregability in CSA patients with baseline normal platelet reactivity while on dual antiplatelet therapy (DAPT). METHODS: From September 2011 to February 2014, all consecutive CSA patients on chronic DAPT (aspirin and clopidogrel) were evaluated before elective percutaneous coronary intervention (PCI). An initial assessment of platelet reactivity in response to thrombin receptor agonist, ADP, and ASP (respectively, indicative of the response to clopidogrel and aspirin) was performed with impedance aggregometry. Patients with high platelet reactivity to ADP test (area under the curve >47) were excluded. The remaining patients were randomized into 3 treatment groups: Group A, atorvastatin LD 80 mg; Group B, rosuvastatin LD 40 mg; and Group C, no statin LD (control group). A second assessment of platelet reactivity was performed ≥12 hours after statin LD. RESULTS: 682 patients were screened and 145 were randomized into the 3 groups. At baseline and after statin LD, no significant difference was found in platelet reactivity in response to 3 different agonists between the 3 groups. Subgroup analysis showed that platelet reactivity to ADP test was significantly lower in patients chronically treated with low-dose statins (n = 94) compared with statin-naïve patients (n = 51; 15.32 ± 1.50 vs 18.59 ± 1.30; P = 0.007). CONCLUSIONS: Loading dose of atorvastatin (80 mg) or rosuvastatin (40 mg) did not induce significant variation in platelet reactivity in CSA patients with baseline reduced platelet reactivity as in chronic DAPT. Our data confirm that chronic concomitant treatment with low-dose statins and clopidogrel resulted in significantly lower platelet reactivity compared with clopidogrel alone.
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Godino et al. (2017) conducted an RCT in Chronic stable angina (n=145). Atorvastatin or rosuvastatin vs. No statin loading dose was evaluated on Platelet reactivity in response to thrombin receptor agonist, ADP, and ASP. Loading doses of atorvastatin (80 mg) or rosuvastatin (40 mg) did not significantly alter platelet reactivity compared to no loading dose in patients with chronic stable angina on DAPT.
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