Mixed hypercholesterolemia, LDL-C levels of >4.14 mmol/L, and TG > 2.54 mmol/L
BPF: 1000 mg Patients: 15
Group A Rosuvastatin: 10 mg Patients: 16 Group B Rosuvastatin: 20 mg Patients: 16 Group C BPF: 1000 mg + Rosuvastatin: 10 mg Patients: 15 Group D Placebo Patients: 15
4
NR
I:
C: Group A
Group B
Group C
Group D
NR
I-C(A): NR () I-C(B): NR () I-C(C): NR () I-C(D): NR ()
Prospective, open label, parallel-group, placebo-controlled study (Level 3)
Group A (A1, A2, APLacebo) Hypercholesterolemia, HC cLDL levels ≥ 3.36 mmol/L Group B (B1, B2, BPLacebo) Hyperlipidemia (hypercholesterolemia and hypertriglyceridemia, HC/HT) Group C (C1, C2, CPLacebo) Hyperlipidemia and glycemia over 110 mg/dL, HC/HT/HG Group D or “poststatin.” Simvastatin therapy stopped due to muscular pain and a significant elevation of serum creatine-phosphokinase (CPK)
Group A1 BPF: 500 mg Patients: 35 Group A2 BPF: 1000 mg Patients: 37 Group B1 BPF: 500 mg Patients: 14 Group B2 BPF: 1000 mg Patients: 14 Group C1 BPF: 500 mg Patients: 20 Group C2 BPF: 1000 mg Patients: 19 Group D: BPF: 1500 mg Patients: 32
Placebo (APL + BPL + CPL) Patients: 59
4
NR
NR
NR
I(C1)-C: NR () I(C2)-C: NR () I(C2)-I(C1): NR ()
Randomized, double-blind, placebo-controlled study (Level 2)
MDΔ: mean difference Δ change. I: intervention; C: control. : value; NS: not significant (); NR: not recorded; NE: not expected. As suggested by Centre for Evidence-Based Medicine [29].