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高胆固醇血症和血脂异常:临床医生面临的问题

Hypercholesterolemia and Dyslipidemia: Issues for the Clinician.

作者信息

Superko H. Robert, Chronos Nicolas A.

机构信息

American Cardiovascular Research Institute, 5665 Peachtree Dunwoody Road, Suite 225, Atlanta, GA 30342, USA.

出版信息

Curr Treat Options Cardiovasc Med. 2003 Feb;5(1):35-50. doi: 10.1007/s11936-003-0013-0.

Abstract

The current state of the art in the diagnosis and treatment of lipoprotein disorders has progressed beyond the standard "lipid profile," which includes total low-density lipoprotein (LDL), and high-density lipoprotein (HDL) cholesterol, along with fasting triglycerides. Incorporating aspects of the atherogenic lipoprotein profile (ALP) (ALP and LDL subclass distribution), HDL subclass distribution, apolipoprotein E isoforms, lipoprotein (a), homocysteine, and high-sensitivity C-reactive protein provides the clinician with the tools to create a more detailed, accurate, and personalized diagnosis of disorders contributing to coronary artery disease in their patients. Sophisticated laboratory tests are available to clinicians through technology transfer programs as exemplified by the Lawrence Berkeley National Laboratory/Berkeley HeartLab, Berkeley, CA, collaboration and allow clinicians access to research quality laboratory tools. This has significant clinical relevance because the presence of these disorders guides treatment that is specific to the disorder(s). Appropriate treatment has been shown to have significantly greater clinical benefit in patient subgroups exhibiting the disorder the therapy is most likely to correct. A single drug or lifestyle therapy plan is no longer appropriate for all patients. The treatment must match the individual disorder(s).

摘要

脂蛋白紊乱的诊断和治疗的当前技术水平已经超越了标准的“血脂谱”,后者包括总低密度脂蛋白(LDL)、高密度脂蛋白(HDL)胆固醇以及空腹甘油三酯。纳入致动脉粥样硬化脂蛋白谱(ALP)(ALP和LDL亚类分布)、HDL亚类分布、载脂蛋白E异构体、脂蛋白(a)、同型半胱氨酸和高敏C反应蛋白等方面,为临床医生提供了工具,以便对其患者中导致冠状动脉疾病的紊乱进行更详细、准确和个性化的诊断。通过技术转让项目,临床医生可以获得先进的实验室检测方法,例如加利福尼亚州伯克利市劳伦斯伯克利国家实验室/伯克利心脏实验室的合作项目,这使临床医生能够使用具有研究质量的实验室工具。这具有重大的临床意义,因为这些紊乱的存在指导了针对特定紊乱的治疗。已证明,在表现出该疗法最有可能纠正的紊乱的患者亚组中,适当的治疗具有显著更大的临床益处。单一药物或生活方式治疗方案不再适用于所有患者。治疗必须与个体紊乱相匹配。

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