Table 2.
Baseline | Absolute reduction | Duration of treatment exposure | Guideline | ||||
---|---|---|---|---|---|---|---|
LDL-C (mmol/L) | LDL-C (mmol/L) | [expected proportional risk reduction (%)] |
recommended treatment51,52 | ||||
5 years | 10 years | 20 years | 30 years | 40 years | |||
7 | 3.5 | 58 | 68 | 81 | 89 | 93 | Yes (due to markedly elevated LDL-C) |
7 | 3.0 | 53 | 62 | 76 | 85 | 90 | |
7 | 2.5 | 46 | 56 | 70 | 79 | 86 | |
7 | 2.0 | 39 | 48 | 61 | 71 | 79 | |
7 | 1.5 | 31 | 39 | 51 | 61 | 69 | |
5 | 2.5 | 46 | 56 | 70 | 79 | 86 | Yes (due to markedly elevated LDL-C) |
5 | 2.0 | 39 | 48 | 61 | 71 | 79 | |
5 | 1.5 | 31 | 39 | 51 | 61 | 69 | |
5 | 1.0 | 22 | 28 | 38 | 46 | 54 | |
3 | 1.5 | 31 | 39 | 51 | 61 | 69 | Depends on risk of ASCVD |
3 | 1.0 | 22 | 28 | 38 | 46 | 54 | |
3 | 0.5 | 12 | 15 | 21 | 27 | 32 | |
2 | 1.0 | 22 | 28 | 38 | 46 | 54 | Depends on risk of ASCVD |
2 | 0.5 | 12 | 15 | 21 | 27 | 32 |
Recommendations for treatment: expected clinical benefit per unit reduction in LDL-C expressed as the expected proportional risk reduction (%). The proportional reduction in short-term risk is based on an expected 22% reduction in risk per millimole per litre reduction in LDL-C over 5 years as estimated from randomized trials and is calculated as [(1−0.78 (absolute reduction in LDL-C in mmol/L)) × 100]. The proportional reduction in long-term risk is based on an expected 54% reduction in risk per millimole per litre reduction in LDL-C over 40 years of exposure as estimated from Mendelian randomization studies and is calculated as [(1−0.46 (absolute reduction in LDL-C in mmol/L)) × 100]. The expected proportional risk reduction per mmol/L reduction in LDL-C for any specific treatment duration is calculated as: [(1−e(−0.249 + (number of years of treatment − 5) × (−0.0152))) × 100].
ASCVD, atherosclerotic cardiovascular disease.