Atorvastatin (Lipitor) was best, followed in no particular order by fluvastatin (Lescol), pravastatin (Pravachol), and rosuvastatin (Crestor). Simvastatin (Zocor) had the lowest benefit.
Notably, statin intake correlated with a significant reduction in cancer incidence (odds ratio [OR], .72; 95% confidence interval [CI], .70–.74). For statin-taking patients, we calculated a higher cancer survival probability versus subjects not taking any statins (Cox proportional-hazards model; hazards ratio [HR], .64; 95% CI, .48–.86). We found no difference for low-dose (20 mg: HR, 1.1; 95% CI, 0.89–1.37) versus high-dose (80 mg: HR, 1.11; 95% CI, .83–1.48) treatments; similarly, low-dose (10–20 mg: HR, .80; 95% CI, .59–1.09) and high-dose atorvastatin regimes (80 mg: HR, .72; 95% CI, .51–1.02) were comparable. When considering each statin separately, we found a strong cancer-preventive effect for atorvastatin (OR, .41; 95% CI, .38–.43) and significant effects for fluvastatin (OR, .7; 95% CI, .57–.85), pravastatin (OR, .63; 95% CI, .56–.71) and rosuvastatin (OR, .43; 95% CI, .36–.51); simvastatin showed only a weak cancer-preventive effect (OR, .9; 95% CI, .87–.94), and lovastatin effects were not readily assessed (relatively few patients; broad confidence intervals; Table S2).
We also considered the clinical data as a 1:1 matched-study design, using propensity score-matched sub-cohorts to better control for confounding associations that might stem from different distributions of age and gender between the whole dataset and the subset of cancer patients. We discovered further evidence supporting the cancer-preventive effect of statins (Figure 4 and Figure S4): (i) all statins considered together had an OR of .5 (95% CI, .48–.51), with (ii) atorvastatin .30 (95% CI, .28–.32), fluvastatin .65 (95% CI, .47–.88), lovastatin .51 (95% CI, .38–.7), pravastatin .47 (95% CI, .42–.54), rosuvastatin .32 (95% CI, .26–.38), and simvastatin .63 (95% CI, .61–.66).
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...except, of course, for the side-effects.
Statins do more harm than good.
For later
Big mistake to be pursuing chemical modification of blood cholesterol on the basis of the fraudulent lipid hypothesis.
HUGE mistake, wrong direction.
Thanks for posting...