辛伐他汀
以兹提米比
冠状动脉疾病
PCSK9
内科学
医学
胆固醇
神经酰胺
内分泌学
等位基因
血脂谱
脂多糖学
他汀类
脂蛋白
胃肠病学
低密度脂蛋白受体
心脏病学
生物
基因
遗传学
细胞凋亡
作者
Kirill V. Tarasov,Kim Ekroos,Matti Suoniemi,Dimple Kauhanen,Tuulia Sylvänne,Reini Hurme,Ioanna Gouni‐Berthold,Heiner K. Berthold,Marcus E. Kleber,Reijo Laaksonen,Winfried März
摘要
Coronary artery disease (CAD) is among the leading causes of mortality and morbidity worldwide. Traditional risk markers explain only a proportion of total cardiovascular risk. Thus, development and improvement of early diagnostic strategies and targeted initiation of preventive measures would be of great benefit.We aimed to identify molecular lipids that are associated with fatal outcome of CAD patients. Furthermore, the effect of different lipid-lowering drugs on novel risk lipids was evaluated.Serum samples of 445 CAD subjects participating in a long-term follow-up of the Ludwigshafen Risk and Cardiovascular Health (LURIC) study were analyzed. In addition, samples obtained from a separate randomized parallel three-group study of subjects treated with simvastatin (n=24), ezetimibe (n=24), or their combination (n=24) were studied. Furthermore, samples from the LURIC participants with a loss-of-function mutation (R46L) in the PCSK9 gene (n=19) were analyzed and compared with major allele carriers (n=868).Distinct ceramide species were significantly associated with the fatal outcome of CAD patients. Simvastatin lowered plasma ceramides broadly by about 25%, but no changes in ceramides were observed in the ezetimibe group. PCSK9 deficiency was significantly associated (-13%) with lowered low-density lipoprotein cholesterol accompanied by a significant 20% reduction in CAD outcome risk-related ceramides.These data suggest that distinct ceramides associate significantly with CAD outcome independently of traditional risk factors and that the mechanism of lipid lowering is important.
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