Parameter | Subjects without AVD | Subjects with AVD |
---|
| Guidelines | Treatment group | Guidelines | Treatment group |
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| CCS* | EU†high risk | E + A10 | A20 | CCS* | EU† very high risk | E + A10 | A20 |
---|
| n = 66‡ | n = 67‡ | | n = 449‡ | n = 448‡ |
---|
LDL-C | (mmol/L) | ≤2.0 or | <2.5 | 3.25 (0.55) | 3.11 (0.53) | ≤2.0 or | <1.8 | 2.58 (0.70) | 2.56 (0.49) |
↓50% | ↓50% | or ↓50% |
Non-HDL-C | (mmol/L) | ≤2.6 | <3.3 | 4.04 (0.64) | 3.84 (0.65) | ≤2.6 | <2.6 | 3.21 (0.76) | 3.21 (0.61) |
Apo B | (g/L) | ≤0.8 | <1.0 | 1.2 (0.2) | 1.1 (0.2) | ≤0.8 | <0.8 | 1.0 (0.2) | 1.0 (0.2) |
- Baseline lipid and lipoprotein levels were determined for parameters common to CCS2012 and EU2012 targets.
- A 10/20, atorvastatin 10 or 20 mg; Apo, apolipoprotein; AVD, atherosclerotic vascular disease; CCS, Canadian Cardiovascular Society guidelines (2012); E, ezetimibe 10 mg; EU, European Guidelines (2012); LDL-C, low-density lipoprotein cholesterol; non-HDL-C, non-high-density lipoprotein cholesterol.
- *Canadian guidelines specify that treatment targets should not change based on risk assessment.
- †European guidelines state that total cholesterol should be considered a treatment target if other analyses are not available.
- ‡n may vary slightly between measured parameters due to differences in available data.