Table 2.
Total Sample | Myalgic Sample | |||
---|---|---|---|---|
ATOR (n=203) | PL (n=217) | ATOR (n=19) | PL (n=10) | |
Δ Total-C (mg/dL) | −65.3(−70.1,−60.5)* | 2.7(−0.2,5.6) | −73.9(−88.0,−59.8)* | 12.2(0.0,24.4) |
Δ LDL-C (mg/dL) | −59.0(−63.4,−54.6)* | 0.9 (−1.8,3.6) | −70.6(−83.5,−57.7)* | 10.1(−1.4,21.6) |
Δ HDL-C (mg/dL) | −0.8(−2.0,0.4) | 0.4(−0.7,1.5) | 0.2(−4.3,4.7) | −3.4(−9.1,2.3) |
Δ TRIG (mg/dL) | −28.3(−34.4,−22.3)* | 3.5(−3.1,10.1) | −18.2(−28.0,−8.4)* | 16.5(−12.3,45.3) |
Data are presented as point estimates and 95% confidence intervals for atorvastatin (ATOR) vs. placebo (PL)
subjects in the entire sample and only in subjects classified as myalgic. Δ = absolute change from pre-to-post
study; C = cholesterol; LDL = low-density lipoprotein; HDL = high-density lipoprotein; TRIG = triglycerides.
indicates significant change from baseline at p < 0.01; there were no differences between myalgic and nonmyalgic subjects within a treatment group.