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. 2022 Jan 7;21:3. doi: 10.1186/s12944-021-01610-w

Table 5.

Cox regression analysis of PCSK9, NFS and the combination of NFS and PCSK9 with events in male and female

Variables Male Female
Multivariable model Multivariable model
Events/
Subjects
OR(95%CI) P Events/
Subjects
OR(95%CI) P
NFS per 1-SD increase 101/1215 1.528 (1.147,2.035) 0.004 57/793 1.033 (0.739,1.446) 0.848
PCSK9 per 1-SD increase 101/1215 1.344 (1.102,1.64) 0.004 57/793 1.042 (0.81,1.341) 0.747
PCSK9 + NFS
 Low PCSK9 + low NFS 7/210 1.0 2/87 1.0
 Low PCSK9 + intermediate-high NFS 20/265 1.907 (0.774,4.696) 0.161 8/107 2.32 (0.465,11.588) 0.310
 Intermediate PCSK9 + low NFS 10/162 1.729 (0.65,4.603) 0.273 5/96 2.216 (0.419,11.721) 0.350
 Intermediate PCSK9 + intermediate-high NFS 26/253 2.382 (0.985,5.764) 0.054 13/159 2.511 (0.524,12.024) 0.250
 High PCSK9 + low NFS 11/134 2.236 (0.855,5.846) 0.101 10/109 3.361 (0.708,15.95) 0.130
 High PCSK9 + intermediate-high NFS 27/191 3.377 (1.394,8.179) 0.007 19/235 2.178 (0.468,10.131) 0.320

PCSK9 proprotein convertase subtilisin/ kexin type 9, NFS non-alcoholic fatty liver disease fibrosis score, MACEs major adverse cardiovascular events, HR hazard ratio, CI confidence interval. Multivariable model was adjusted for body mass index, hypertension, family history of coronary artery disease, coronary artery disease, diabetes, smoking, drinking, triglyceride, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, fasting plasma glucose, hemoglobin A1c, antiplatelet drugs, antihypertensive drugs. P < 0.05 suggests significant difference