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. 2021 Sep 24;10(19):4363. doi: 10.3390/jcm10194363

Table 1.

Baseline characteristics of the study population.

FH (n = 260)
Demographic Characteristics Age, years 49.4 ± 6.22
Men, n (%) 129 (49.6)
ASCVD, n (%) 80 (30.8)
Body mass index, kg/m2 25.3 ± 2.24
FH Genotype
Pathogenic variants, n (%) 267 (100.0)
LDLR, n (%) 261 (97.7)
ApoB, n (%) 4 (1.5)
PCSK9, n (%) 1 (0.4)
ApoE, n (%) 1 (0.4)
FH Phenotype
Heterozygous, n (%) 254 (97.7)
Double heterozygous, n (%) 3 (1.1)
Compound heterozygous, n (%) 2 (0.8)
Homozygous, n (%) 1 (0.4)
Pretreated Lipid Profile TC, mg/dL 362.38 ± 19.48
HDL-C, mg/dL 51.38 ± 10.5
TG, mg/dL 96.5 (71.5–115.5)
LDL-C, mg/dL 257.53 ± 18.15
Non-HDL-C, mg/dL 301.51 ± 19.12
Risk Factors Type 2 diabetes, n (%) 6 (2.3)
Hypertension, n (%) 72 (27.7)
Smokers, n (%) 59 (22.7)
≥2 risk factors, n (%) 34 (13.1)
Treatments
High-intensity statin, n (%) 191 (73.5)
Moderate-intensity statin, n (%) 64 (24.6)
Low-intensity statin, n (%) -
Statin intolerant, n (%) 5 (1.9)
Ezetimibe, n (%) 225 (86.5)
PCSK9 inhibitor, n (%) 62 (23.8)
Statin plus ezetimibe, n (%) 195 (75.0)
Statin plus ezetimibe plus PCSK9 inhibitor, n (%) 57 (21.9)
Antiplatelet therapy, n (%) 80 (30.8)

Data are presented as mean ± standard deviation, percentages or median (interquartile range). FH = familial hypercholesterolemia, ASCVD = atherosclerotic cardiovascular disease, LDLR = low-density lipoprotein receptor, ApoB = apolipoprotein B, PCSK9 = proprotein convertase subtilisin-kexin type 9, ApoE = apolipoprotein E, TC = total cholesterol, HDL-C = high-density lipoprotein cholesterol, TG = triglycerides, LDL-C = low-density lipoprotein cholesterol.