No effect of PCSK9 inhibitors on D-dimer and fibrinogen levels in patients with familial hypercholesterolemia

被引:13
作者
Schol-Gelok, Suzanne [1 ,2 ]
Galema-Boers, J. M. H. [2 ]
van Gelder, Teun [1 ,2 ]
Kruip, Marieke J. H. A. [3 ]
van Lennep, Jeanine E. Roeters [2 ]
Versmissen, Jorie [2 ]
机构
[1] Erasmus MC, Dept Hosp Pharm & Internal Med, S Gravendijkwal 230, NL-3015CE Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Internal Med, Vasc & Metab Dis Sect, S Gravendijkwal 230, NL-3015CE Rotterdam, Netherlands
[3] Erasmus MC, Dept Hematol, S Gravendijkwal 230, NL-3015CE Rotterdam, Netherlands
关键词
Cardiovascular pharmacology; PCSK9; inhibitor; Lipids; Coagulation; STATINS; CHOLESTEROL; THERAPY; SMOKING;
D O I
10.1016/j.biopha.2018.09.164
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Statins are generally believed to have cardiovascular protective effects independent of low-density lipoprotein-cholesterol (LDL-C) lowering, such as antithrombotic effects characterized by a decrease in D-dimer levels. For the recently introduced Proprotein convertase subtilisin/kexin 9 (PCSK9) inhibitors antithrombotic effects are yet unknown. We determined the effect of starting PCSK9 inhibitors on D-dimer and fibrinogen levels as most robust markers for thrombogenicity in statin-intolerant patients with familial hypercholesterolemia. We determined D-dimer and fibrinogen levels before and after start of evolocumab (n = 19) or alirocumab (n = 11). Baseline median D-dimer levels were 0.34 mg/L (IQR 0.24-0.59 mg/L) and baseline median fibrinogen levels 3.2 g/L (IQR 2.88-3.63 g/L). At follow-up D-dimer levels (median 0.31 mg/L (IQR 0.25-0.59 mg/L); p = 0.37), and fibrinogen levels (median 3.4 g/L (IQR 2.98-3.62 g/L); p = 0.38) did not change significantly. We therefore conclude PCSK9 inhibitors do not seem to have a profound antithrombotic effect, although a more subtle effect can not been excluded.
引用
收藏
页码:1412 / 1414
页数:3
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