Morise Anthony P, Tennant Jennifer, Holmes Sari D, Tacker Danyel H
Section of Cardiology, West Virginia University Heart and Vascular Institute, Morgantown, WV, USA.
Department of Pathology, Anatomy, and Laboratory Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
J Lipids. 2018 Jul 19;2018:9194736. doi: 10.1155/2018/9194736. eCollection 2018.
Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have demonstrated significant effects on low-density lipoprotein (LDL) cholesterol and nonhigh density lipoprotein (HDL) cholesterol. To date, there have been limited reports on the effect of PCSK9 inhibitors on remnant cholesterol.
Assess the effect of PCSK9 inhibitors on nonfasting remnant cholesterol in a real world population. Identify whether pretreatment triglyceride levels are associated with PCSK9 inhibition success as indicated by changes in remnant cholesterol levels.
Patients in our adult lipid clinic ( = 109) receiving PCSK9 inhibition for atherosclerotic cardiovascular disease or familial hypercholesterolemia who had available pre- and post-PCSK9 inhibition standard nonfasting lipid data were, retrospectively, selected for data analysis. Remnant cholesterol was the difference between non-HDL and LDL cholesterol. LDL cholesterol was measured directly and calculated from Friedewald and Martin/Hopkins methods. Data were analyzed using repeated measures ANOVA and multivariable linear regression for differential effects on remnant and LDL cholesterol based upon pretreatment nonfasting triglyceride levels.
Remnant cholesterol as well as total, LDL, non-HDL cholesterol, and triglycerides decreased significantly (<0.001) after PCSK9 inhibition. Patients with higher pretreatment triglyceride levels showed greater decrease in remnant cholesterol after PCSK9 inhibition (<0.001) than those with lower pretreatment triglycerides.
In patients receiving PCSK9 inhibitors, remnant cholesterol as determined from nonfasting blood was reduced in proportion to pretreatment triglycerides.
前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)抑制剂已被证明对低密度脂蛋白(LDL)胆固醇和非高密度脂蛋白(HDL)胆固醇有显著影响。迄今为止,关于PCSK9抑制剂对残留胆固醇影响的报道有限。
评估PCSK9抑制剂对现实世界人群中非空腹残留胆固醇的影响。确定治疗前甘油三酯水平是否与残留胆固醇水平变化所表明的PCSK9抑制成功相关。
回顾性选择我们成人脂质诊所中接受PCSK9抑制治疗以治疗动脉粥样硬化性心血管疾病或家族性高胆固醇血症且有PCSK9抑制前后标准非空腹血脂数据的患者(n = 109)进行数据分析。残留胆固醇是非HDL胆固醇与LDL胆固醇之间的差值。LDL胆固醇通过Friedewald法和Martin/Hopkins法测量。基于治疗前非空腹甘油三酯水平,使用重复测量方差分析和多变量线性回归分析对残留胆固醇和LDL胆固醇的差异影响。
PCSK9抑制后,残留胆固醇以及总胆固醇、LDL胆固醇、非HDL胆固醇和甘油三酯均显著降低(P<0.001)。治疗前甘油三酯水平较高的患者在PCSK9抑制后残留胆固醇的降低幅度(P<0.001)大于治疗前甘油三酯水平较低的患者。
在接受PCSK9抑制剂治疗的患者中,非空腹血液中测定的残留胆固醇与治疗前甘油三酯成比例降低。