Murphy Andrew J, Tall Alan R
Haematopoiesis and Leukocyte Biology, Baker IDI Heart and Diabetes Institute, Melbourne, Victoria 3004, Australia Department of Immunology, Monash University, Melbourne, Victoria 3165, Australia
Division of Molecular Medicine, Department of Medicine, Columbia University, New York, NY 10032, USA.
Eur Heart J. 2016 Apr 7;37(14):1113-21. doi: 10.1093/eurheartj/ehv718. Epub 2016 Feb 10.
Atherosclerosis, the major underlying cause of cardiovascular disease, is characterized by a lipid-driven infiltration of inflammatory cells in large and medium arteries. Increased production and activation of monocytes, neutrophils, and platelets, driven by hypercholesterolaemia and defective high-density lipoproteins-mediated cholesterol efflux, tissue necrosis and cytokine production after myocardial infarction, or metabolic abnormalities associated with diabetes, contribute to atherogenesis and athero-thrombosis. This suggests that in addition to traditional approaches of low-density lipoproteins lowering and anti-platelet drugs, therapies directed at abnormal haematopoiesis, including anti-inflammatory agents, drugs that suppress myelopoiesis, and excessive platelet production, rHDL infusions and anti-obesity and anti-diabetic agents, may help to prevent athero-thrombosis.
动脉粥样硬化是心血管疾病的主要潜在病因,其特征是脂质驱动炎症细胞浸润大中动脉。高胆固醇血症和高密度脂蛋白介导的胆固醇流出缺陷、心肌梗死后的组织坏死和细胞因子产生,或与糖尿病相关的代谢异常,导致单核细胞、中性粒细胞和血小板的产生和激活增加,促进动脉粥样硬化和动脉粥样硬化血栓形成。这表明,除了降低低密度脂蛋白和使用抗血小板药物的传统方法外,针对异常造血的治疗,包括抗炎药、抑制骨髓生成的药物、抑制血小板过度生成的药物、重组高密度脂蛋白输注以及抗肥胖和抗糖尿病药物,可能有助于预防动脉粥样硬化血栓形成。