Key result
Atorvastatin significantly improved 5-year survival (HR 3.48) and reduced levels of inflammatory cytokines and uric acid in patients with dilated cardiomyopathy.
Why the study?
Does atorvastatin improve inflammatory parameters, left ventricular function, and survival in patients with dilated cardiomyopathy?
RCT (n=68)
Open-label
Randomized
No
Does atorvastatin improve inflammatory parameters, left ventricular function, and survival in patients with dilated cardiomyopathy?
Effect estimate: HR 3.48 (95% CI 1.42-8.56)
p-value: p=0.005
Atorvastatin therapy in patients with dilated cardiomyopathy significantly reduced inflammatory cytokines, improved left ventricular ejection fraction, and increased 5-year survival.
Supports atorvastatin in DCM with LVEF ≤40%; extends anti-inflammatory effects to survival in RCT.
BACKGROUND: We assessed the influence of atorvastatin on selected indicators of an inflammatory condition, left ventricular function, hospitalizations and mortality in patients with dilated cardiomyopathy (DCM). METHODS: We included 68 DCM patients with left ventricular ejection fraction (LVEF) ≤40% treated optimally in a prospective, randomized study. They were observed for 5 years. Patients were divided into two groups: patients who were commenced on atorvastatin 40 mg daily for two months followed by an individually matched dose of 10 or 20 mg/day (group A), and patients who were treated according to current recommendations without statin therapy (group B). RESULTS: After 5-year follow-up we assessed 45 patients of mean age 59 ± 11 years - 22 patients in group A (77% male) and 23 patients in group B (82% male). Interleukin-6, tumor necrosis factor alpha, and uric acid concentrations were significantly lower in the statin group than in group B (14.96 ± 4.76 vs. 19.02 ± 3.94 pg/ml, p = 0.012; 19.10 ± 6.39 vs. 27.53 ± 7.39 pg/ml, p = 0.001, and 5.28 ± 0.48 vs. 6.53 ± 0.46 mg/dl, p = 0.001, respectively). In patients on statin therapy a reduction of N-terminal pro-brain natriuretic peptide concentration (from 1425.28 ± 1264.48 to 1098.01 ± 1483.86 pg/ml, p = 0.045), decrease in left ventricular diastolic (from 7.15 ± 0.90 to 6.67 ± 0.88 cm, p = 0.001) and systolic diameters (from 5.87 ± 0.92 to 5.17 ± 0.97, p = 0.001) in comparison to initial values were observed. We also showed the significant increase of LVEF in patients after statin therapy (from 32.0 ± 6.4 to 38.8 ± 8.8%, p = 0.016). Based on a comparison of curves using the log-rank test, the probability of survival to 5 years was significantly higher in patients receiving statins (p = 0.005). CONCLUSIONS: Atorvastatin in a small dose significantly reduce levels of inflammatory cytokines and uric acid, improve hemodynamic parameters and improve 5-year survival in patients with DCM.
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Bielecka‐Dąbrowa et al. (2013) conducted an RCT in Dilated cardiomyopathy (n=68). Atorvastatin vs. Standard therapy without statin was evaluated on 5-year survival (HR 3.48, 95% CI 1.42-8.56, p=0.005). Atorvastatin significantly improved 5-year survival (HR 3.48) and reduced levels of inflammatory cytokines and uric acid in patients with dilated cardiomyopathy.
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