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2020 Guidelines of the Polish Society of Laboratory Diagnostics (PSLD) and the Polish Lipid Association (PoLA) on laboratory diagnostics of lipid metabolism disorders

机译:波兰实验室诊断学会(PSLD)和波兰脂质协会(PoLA)关于脂质代谢紊乱的实验室诊断的2020年指南

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摘要

The lipid profile, which is routinely done to assess a cardiovascular risk, involves the measurement/calculation of serum/plasma levels of total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), triglycerides (TG) and non-HDL cholesterol (non-HDL-C), although LDL-C measurement still plays a key role in the diagnosis, prediction and the monitoring of both the course and treatment of lipid disorders [ – ]. The results of the measurements indirectly and approximately reflect the blood content of individual lipoproteins. Quantitative measurement of atherogenic lipoproteins, i.e. LDL, lipoprotein(a) [Lp(a)], chylomicron (CM) remnants and very low-density lipoprotein (VLDL) remnants, is of special importance in laboratory assessment of lipid metabolism and the risk of atherosclerosis progression [ , ]. This is why lipid profile, which usually applies only to the LDL level, should be supplemented with the measurement of Lp(a) as well as CM and VLDL remnants, if possible.
机译:常规进行的脂质分布评估是评估心血管疾病的风险,涉及测量/计算总胆固醇(TC),高密度脂蛋白胆固醇(HDL-C),低密度脂蛋白胆固醇(LDL- C),甘油三酸酯(TG)和非HDL胆固醇(non-HDL-C),尽管LDL-C的测量在脂类疾病的病程和治疗的诊断,预测和监测中仍然发挥着关键作用[–] 。测量结果间接且大致反映了单个脂蛋白的血液含量。定量测量动脉粥样硬化性脂蛋白,例如LDL,脂蛋白(a)[Lp(a)],乳糜微粒(CM)残留物和极低密度脂蛋白(VLDL)残留物,在实验室评估脂代谢和患病风险中特别重要动脉粥样硬化进展[,]。这就是为什么如果可能的话,通常仅适用于LDL水平的脂质概况应补充Lp(a)以及CM和VLDL残留物的测量值。

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