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. 2020 Jun 18;22(8):38. doi: 10.1007/s11883-020-00858-4

Table 1.

Lipid-lowering treatments and outcomes of the homozygous FH patients from the Italian and Chinese centers [18]

Variable Italy (n = 18) China (n = 44) P value
Age started pharmacotherapy treatment (years) 5.6 ± 3.4 10.7 6 4.6 < 0.001
Lipid-lowering drugs (%) 94.4 95.5 0.866
Statins (%) 88.9 95.5 0.339
Ezetimibe (%) 77.8 81.8 0.715
Resins (%) 66.7 0 < 0.001
Fibrates (%) 16.7 0 0.022
Probucol (%) 0 77.3 < 0.001
PCSK9 inhibitors (%) 0 0
Lomitapide (%) 61.1 0 < 0.001
Age started lomitapide (years) 23.5 ± 4.1
Lipoprotein apheresis (%) 100 0 < 0.001
Age started apheresis (years) 8.9 ± 5.5
Treated LDL cholesterol (mmol/L) 6.6 ± 2.7* 13.1 ± 2.7 < 0.001
ΔLDL cholesterol (mmol/L) 12.5 ± 5.0 2.6 ± 3.6 < 0.001
Treatment duration (years) 17.4 ± 8.8 5.5 ± 4.8 < 0.001
LDL cholesterol life (years) 258.9 ± 98.7 227.3 ± 112.8

0.305

0.792

Mean LDL cholesterol exposure/year (mmol/L) 12.4 ± 3.0 14.6 ± 3.0

0.011

< 0.001

CVD event, n (%) 4 (22.2) 20 (45.5) 0.088
Age at CVD event (years) 19.0 ± 9.6 16.1 ± 5.8 0.421
Death, n (%) 3 (16.7) 14 (31.8) 0.225
Age at death (years) 20.3 ± 10.7 17.9 ± 6.2 0.586

Continuous variables are expressed as mean 6 standard deviation, and categorical variables are expressed as proportions (Permission will be needed from Elsevier to reproduce this.)

CVD cardiovascular disease, LDL low-density lipoprotein, PCSK9 proprotein convertase subtilisin/kexin type 9

*Time-average LDL cholesterol calculated using Kroon’s equation [14]

†Censored at age 30 years

Adjusted for (baseline) untreated LDL cholesterol