Discrepancies in Lipemia Interference Between Endogenous Lipemic Samples and Smoflipid®-Supplemented Samples.

Carla Fernández-Prendes, Maria-José Castro-Castro, Laura Jiménez-Añón, Cristian Morales-Indiano, María Martínez-Bujidos
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Abstract

Background: Manufacturers evaluate lipemia-induced interference using Intralipid®, but it does not contain all lipoprotein types. The aim of this study was to evaluate lipemiainduced interference in biochemical parameters from endogenous lipemic samples and SMOFlipid® supplemented samples, in order to assess if SMOFlipid® can be used in lipemic interference studies.

Methods: Serum pools were supplemented with SMOFlipid® to achieve 800 mg/dL and 1500 mg/dL triglyceride concentration, and analyzed for 25 biochemical parameters both before and after the supplementation. In another independent phase, lipemic serum pools were prepared choosing patient samples of 800 mg/dL and 1500 mg/dL triglyceride concentration. These lipemic serum pools were ultracentrifugated in order to remove lipids. Biochemical parameters were analyzed before and after ultracentrifugation. The bias between SMOFlipid®-supplemented samples and endogenous lipemic samples were compared. The bias between the lipemic and non-lipemic samples were compared with the reference change value.

Results: At 800 mg/dL triglyceride concentration, we found that total protein and transferrin had been affected only in endogenous lipemic serum samples. Magnesium and creatinine had been affected only in SMOFlipid®-supplemented samples. At 1500 mg/dL triglyceride concentration, we found that total protein, amylase, ferritin and glucose had lipemic interference only in endogenous lipemic samples, and chloride only in SMOFlipid®-supplemented samples.

Conclusions: The use of SMOFlipid®-supplemented samples does not provide suitable data to estimate lipemia-induced interference. Thus, interference studies should be performed using a wide variety of lipemic patient samples that represent the heterogeneity of the lipoprotein particles size.

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内源性脂血症样品与smof脂®补充样品之间的脂血症干扰差异
背景:制造商使用Intralipid®评估血脂诱导干扰,但它不包含所有类型的脂蛋白。本研究的目的是评估内源性脂质血症样品和添加smof脂质®样品中脂质诱导的生化参数干扰,以评估smof脂质®是否可用于脂质血症干扰研究。方法:在血清池中添加smof脂®,使其甘油三酯浓度达到800 mg/dL和1500 mg/dL,分析添加前后25项生化指标。在另一个独立的阶段,选择甘油三酯浓度为800 mg/dL和1500 mg/dL的患者样品制备血脂血清池。这些血脂血清池进行超离心以去除脂质。分析超离心前后的生化参数。比较了SMOFlipid®补充样品和内源性脂血症样品之间的偏倚。将血脂和非血脂样本的偏差与参考变化值进行比较。结果:当甘油三酯浓度为800 mg/dL时,我们发现总蛋白和转铁蛋白仅在内源性血脂血清样本中受到影响。镁和肌酐仅在添加了smof脂的样品中受到影响。当甘油三酯浓度为1500 mg/dL时,我们发现总蛋白、淀粉酶、铁蛋白和葡萄糖仅在内源性脂血症样品中有脂血症干扰,而氯化物仅在添加了smoflide®的样品中有。结论:使用SMOFlipid®补充样品不能提供适当的数据来评估血脂诱导的干扰。因此,干扰研究应该使用各种各样的血脂患者样本来进行,这些样本代表了脂蛋白颗粒大小的异质性。
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