Table 4.
Study | Design | Findings related to statin exposure |
---|---|---|
Animal studies | ||
Chade et al.20,21 | Porcine unilateral RVD model | Renoprotective effects: reduced renal fibrosis and remodelling; increased renal blood flow and glomerular filtration rate |
Zhu et al.22 | Porcine unilateral RVD model | Cardioprotective effects: left ventricular hypertrophy prevented; myocardial perfusion increased; reduced microvascular remodelling |
Laina et al.23 | Rodent bilateral RVD model | Renoprotective effects: improved glomerular filtration rate, free water clearance, and fractional sodium excretion |
Lavi et al.24 | Porcine unilateral RVD model | Renoprotective effects: improved endothelial function, reduced renal oxidative stress, inflammation and fibrosis; attenuated endothelial progenitor cell apoptosis |
| ||
Human studies | ||
Khong et al.29 | Case report (n = 1) | Marked regression of renal artery stenosis over 3 years following institution of statin therapy (and despite continued heavy smoking) |
Basta et al.28 | Case report (n = 1) | Marked regression of renal artery stenosis, including spontaneous remission of hypertension and renin levels |
Bates et al.11 | Cohort study (n = 748) | Reduced mortality over 11 year follow-up with statins (HR 0.71; 95% CI 0.53–0.95) |
Davies et al.25 | Cohort study (n = 447) | Reduced restenosis after renal artery stenting as well as greater freedom from recurrent symptoms (hypertension and worsening renal failure) with statins; risk ratios not provided |
Silva et al.26 | Cohort study (n = 104) | Reduced all-cause mortality (HR 0.13; 95% CI 0.04–0.44) and renal mortality (HR 0.21; 95% CI 0.07–0.64) |
Cheung et al.27 | Cohort study (n = 79) | Reduced angiographic progression of RVD with statins (HR 0.28; 95% CI 0.10–0.77); increased likelihood of regression with statins (HR 4.88; 95% CI 1.32–19.4) |
Multivariable-adjusted results were provided in the table above (wherever possible).