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Lipids and Lipoproteins: Analysis and Assessment in Models of Atherosclerosis

机译:脂质和脂蛋白:动脉粥样硬化模型的分析和评估

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Lipids and lipoproteins play a central role in the pathogenesis of atherosclerosis and its clinical sequale, coronary heart disease, stroke, and peripheral vascular disease. Since lipids are insoluble in water the bulk of the lipids in the blood are transported as part of a complex with specific proteins, called lipoproteins. Knowledge of an individual's lipoprotein profile is essential to the evaluation of risk of developing atherosclerosis, and of efficacy of treatment. In addition, some lipoproteins [LDL, VLDL, Lp(a)] promote the development of atherosclerosis, while others (HDL), are protective. Although a number of risk factors have been identified (hypertension, smoking, diabetes, etc.), hypercholesterolemia is the only risk factor that by itself will produce atherosclerosis in animal models and man. In human beings this is seen most clearly in the disease, Familial Hypercholesterolemia. In 1985, the National Cholesterol Education Program (NCEP) established plasma total cholesterol concentrations of 200-240 mg/dl (5.17-6.21 mmol/l), as the level above which a medical decision is made. They also established that medical decisions would be based on specific LDL-Cholesterol (LDLC) concentrations. For this to be effective, a national cholesterolstandardization program was established to monitor accuracy and precision of lipid and lipoprotein measurements. Cholesterol was the first clinical analyte for which national performance standards were established. For more information on the CDC-Lipidand lipoprotein standardization programs see (www.cdc.aov/nceh/dls/crmln/crmln.htm). Only commercial labs and chemistry analyzers that meet this level of performance should be used for cholesterol, triglyceride, LDLC, HDLC and other lipid and lipoproteinmeasurements. The same standards should apply for these measurements in animals. Caution is needed, however, for the measurement of lipoproteins using antibody-based methods [e.g. direct HDL, LDL, Lp(a)] for animals in which verification of specificityof the antibody has not been established for that animal species.
机译:脂质和脂蛋白在动脉粥样硬化和临床序列,冠心病,中风和外周血血管疾病的发病机制中起着核心作用。由于脂质不溶于水,因此血液中的大部分脂质作为与特定蛋白质的复合物的一部分运输,称为脂蛋白。知识对个体的脂蛋白概况对于评估动脉粥样硬化和治疗疗效的风险至关重要。此外,一些脂蛋白[LDL,VLDL,LP(a)]促进动脉粥样硬化的发育,而其他脂蛋白粥样硬化的发育是保护性的。虽然已经确定了许多风险因素(高血压,吸烟,糖尿病等),但高胆固醇血症是唯一的危险因素,其本身将在动物模型和人类中产生动脉粥样硬化。在人类中,这在疾病中最清楚地看到家族性高胆固醇血症。 1985年,国家胆固醇教育计划(NCEP)建立了200-240 mg / DL(5.17-6.21mmol / L)的血浆总胆固醇浓度,作为上述水平的水平。他们还确定医学决策将基于特定的LDL-胆固醇(LDLC)浓度。为此有效,建立了国家胆固醇标准化计划,以监测脂质和脂蛋白测量的准确性和精度。胆固醇是第一个建立国家绩效标准的临床分析物。有关CDC-脂质和脂蛋白标准化计划的更多信息,请参阅(www.cdc.aov / nceh / dls / crmln / crmln.htm)。只有符合这种性能水平的商业实验室和化学分析仪应用于胆固醇,甘油三酯,LDLC,HDLC和其他脂质和脂蛋白水溶液。相同的标准应该在动物中申请这些测量。然而,需要使用基于抗体的方法测量脂蛋白的注意力[例如用于动物的直接HDL,LDL,LP(A)],其中尚未为该动物物种建立抗体特异性的验证。

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