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. 2016 Jun 10;5(6):e003323. doi: 10.1161/JAHA.116.003323

Table 1.

Subject Characteristics at Main Baseline (Day −29)

Treatment Group Alirocumab 150 mg Q4W+Placebo (n=24) Alirocumab 150 mg Q4W+Ezetimibe (n=24) Alirocumab 150 mg Q4W+Fenofibrate (n=24)
Age, y 48.5 (12.8) 49.5 (10.7) 54.6 (7.6)
Male, n (%) 11 (45.8) 11 (45.8) 10 (41.7)
Race, n (%)
Caucasian/white 23 (95.8) 21 (87.5) 24 (100)
Black 1 (4.2) 3 (12.5) 0
Body mass index, kg/m2 23.9 (2.0) 25.5 (2.7) 24.7 (2.5)
Calculated LDL‐C, mg/dL 183.3 (38.7) 181.7 (37.1) 180.6 (31.3)
Total cholesterol, mg/dL 264.5 (43.7) 260.6 (40.6) 263.7 (40.6)
Apolipoprotein B, g/L 1.28 (0.21) 1.28 (0.22) 1.28 (0.17)
Non–HDL‐C, mg/dL 198.4 (40.6) 200.3 (39.8) 199.5 (31.7)
HDL‐C, mg/dL 65.7 (12.4) 60.3 (13.1) 64.2 (15.5)
Apolipoprotein A1, g/L 1.58 (0.16) 1.55 (0.21) 1.57 (0.20)
Triglycerides (mg/dL), median (range) 78.8 (44.3–177.1) 95.7 (35.4–168.3) 94.8 (53.1–194.9)
Lipoprotein(a) (g/L), median (range) 0.27 (0.0–1.6) 0.33 (0.0–1.6) 0.17 (0.0–1.5)
Free PCSK9, ng/mL 146.5 (54.3) 150.7 (48.5) 152.1 (54.1)

Values are mean (SD) unless otherwise stated. HDL‐C indicates high‐density lipoprotein cholesterol; LDL‐C, low‐density lipoprotein cholesterol; PCSK9, proprotein convertase subtilisin/kexin type 9; Q4W, every 4 weeks.