O'Keefe James H, DiNicolantonio James J, Lavie Carl J
Mid America Heart Institute at Saint Luke's Hospital and University of Missouri-Kansas City, Kansas City, Missouri.
Mid America Heart Institute at Saint Luke's Hospital and University of Missouri-Kansas City, Kansas City, Missouri.
Am J Cardiol. 2017 Feb 15;119(4):565-571. doi: 10.1016/j.amjcard.2016.11.001. Epub 2016 Nov 23.
Multiple lines of evidence suggest that the physiologically normal levels of low-density lipoprotein cholesterol (LDL-C) and the thresholds for development of atherosclerosis and adverse coronary events are in the 30- to 70-mg/dl range. More patients have been studied in randomized controlled trials assessing the effects of statins on outcomes than any other drug class in the history of medicine. This cumulative body of evidence documents that atherosclerosis progression is halted and coronary heart disease events are minimized when statin therapy with or without ezetimibe, and possibly proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors, is used to drive down the LDL-C to a range of about 30 to 50 mg/dl. Thus far, these agents appear to be safe even when LDL-C is lowered to about 50 mg/dl, although more robust outcome and safety data are required, particularly for the PCSK9 inhibitors and very low LDL-C levels (e.g., down to 25 mg/dl). In conclusion, the current national guidelines specifying only the use of a high-potency statin without specific LDL-C goals may lead to substantial undertreatment of high-risk patients, leaving them vulnerable to future adverse cardiovascular events.
多条证据表明,低密度脂蛋白胆固醇(LDL-C)的生理正常水平以及动脉粥样硬化发展和不良冠状动脉事件的阈值在30至70mg/dl范围内。在评估他汀类药物对结局影响的随机对照试验中,接受研究的患者比医学史上任何其他药物类别的患者都多。这一累积的证据表明,使用他汀类药物(无论是否联合依折麦布,可能还联合前蛋白转化酶枯草溶菌素9型(PCSK9)抑制剂)将LDL-C降至约30至50mg/dl范围时,动脉粥样硬化进展会停止,冠心病事件会减至最少。迄今为止,即使LDL-C降至约50mg/dl,这些药物似乎也是安全的,不过还需要更有力的结局和安全性数据,尤其是关于PCSK9抑制剂和极低LDL-C水平(例如降至25mg/dl)的数据。总之,当前仅规定使用高强度他汀类药物而无特定LDL-C目标的国家指南可能导致高危患者的治疗不足,使他们易发生未来的不良心血管事件。