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. 2017 Apr 24;38(32):2459–2472. doi: 10.1093/eurheartj/ehx144

Table 2.

Expected proportional risk reduction based on pre-treatment low-density lipoprotein cholesterol (LDL-C), absolute magnitude of LDL-C reduction, and total duration of therapy

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.