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. 2022 Mar 12;4(6):558–567. doi: 10.1016/j.cjco.2022.03.003

Table 3.

Low-density lipoprotein cholesterol (LDL-C) concentrations and measurement characteristics at baseline and post-evolocumab therapy initiation

Outcome Value
Baseline LDL-C concentration, mmol/L (N = 119)
 Mean ± SD 3.7 ± 1.7
 Median (IQR) 3.5 (2.5–4.6)
Average number of LDL-C tests post-evolocumab initiation (N = 131)
 Mean ± SD 2 ± 1
Frequency of LDL-C measurements (N = 131)
0 11 (8.4)
 1 31 (23.7)
 2 48 (36.6)
 > 2 41 (31.3)
Time from evolocumab therapy initiation to LDL-C measurement, d, median (IQR; N = 120)
 First measurement 55 (33-106)
 Last measurement 247 (162-315)
Overall LDL-C concentration post-evolocumab therapy (N = 120)
 Mean ± SD, mmol/L 1.6 ± 1.0
 Median (IQR) 1.20 (0.75–2.14)
Incidence of LDL-C < 1.8 mmol/L (N = 120) 93 (77.5)
 In FH patients (N = 66) 47 (71.2)
 In non-FH patients (N = 54) 46 (85.2)
Incidence of LDL-C reduction ≥ 50% (N = 109) 78 (71.6)

Values are n (%), unless otherwise indicated.

FH, familial hypercholesterolemia; HDL, high-density lipoprotein; IQR, interquartile range; SD, standard deviation; TC, total cholesterol; TG, triglyceride.

The last LDL-C concentration measured within 6 months prior to initiation of evolocumab therapy in 119 patients with available data was regarded as the baseline LDL-C concentration. Twelve patients did not have a baseline LDL-C concentration reported.

Eleven patients did not have an LDL-C measurement post-evolocumab therapy initiation, of which 3 patients had other lipid measures taken (total cholesterol, HDL, non-HDL, and triglyceride; data not reported), and 8 patients had no lipid tests.