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一种用于脂蛋白-X 定量的高通量 NMR 方法。

A High-Throughput NMR Method for Lipoprotein-X Quantification.

机构信息

Labcorp, Morrisville, NC 27560, USA.

Translational Vascular Medicine Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Molecules. 2024 Jan 23;29(3):564. doi: 10.3390/molecules29030564.

DOI:10.3390/molecules29030564
PMID:38338310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10856374/
Abstract

Lipoprotein X (LP-X) is an abnormal cholesterol-rich lipoprotein particle that accumulates in patients with cholestatic liver disease and familial lecithin-cholesterol acyltransferase deficiency (FLD). Because there are no high-throughput diagnostic tests for its detection, a proton nuclear magnetic resonance (NMR) spectroscopy-based method was developed for use on a clinical NMR analyzer commonly used for the quantification of lipoproteins and other cardiovascular biomarkers. The LP-X assay was linear from 89 to 1615 mg/dL (cholesterol units) and had a functional sensitivity of 44 mg/dL. The intra-assay coefficient of variation (CV) varied between 1.8 and 11.8%, depending on the value of LP-X, whereas the inter-assay CV varied between 1.5 and 15.4%. The assay showed no interference with bilirubin levels up to 317 mg/dL and was also unaffected by hemolysis for hemoglobin values up to 216 mg/dL. Samples were stable when stored for up to 6 days at 4 °C but were not stable when frozen. In a large general population cohort ( = 277,000), LP-X was detected in only 50 subjects. The majority of LP-X positive cases had liver disease (64%), and in seven cases, had genetic FLD (14%). In summary, we describe a new NMR-based assay for LP-X, which can be readily implemented for routine clinical laboratory testing.

摘要

脂蛋白 X (LP-X) 是一种异常的富含胆固醇的脂蛋白颗粒,在胆汁淤积性肝病和家族性卵磷脂胆固醇酰基转移酶缺乏症 (FLD) 患者中积聚。由于目前尚无用于检测其的高通量诊断测试,因此开发了一种基于质子磁共振(NMR)光谱的方法,可在临床 NMR 分析仪上使用,该分析仪通常用于定量脂蛋白和其他心血管生物标志物。LP-X 测定法在 89 至 1615 mg/dL(胆固醇单位)范围内呈线性,功能灵敏度为 44 mg/dL。批内变异系数(CV)在 1.8%至 11.8%之间变化,具体取决于 LP-X 的值,而批间 CV 在 1.5%至 15.4%之间变化。该测定法在胆红素水平高达 317 mg/dL 时无干扰,并且在血红蛋白值高达 216 mg/dL 时也不受溶血的影响。当在 4°C 下储存长达 6 天时,样品稳定,但冷冻时不稳定。在一个大型普通人群队列中(= 277,000),仅在 50 名受试者中检测到 LP-X。大多数 LP-X 阳性病例有肝病(64%),并且在七种情况下,有遗传性 FLD(14%)。总之,我们描述了一种新的基于 NMR 的 LP-X 测定法,该测定法可轻松用于常规临床实验室测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ef/10856374/4775335f9864/molecules-29-00564-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ef/10856374/8975420cbebc/molecules-29-00564-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ef/10856374/2b4fa3b46b7b/molecules-29-00564-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ef/10856374/4775335f9864/molecules-29-00564-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ef/10856374/8975420cbebc/molecules-29-00564-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ef/10856374/2b4fa3b46b7b/molecules-29-00564-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3ef/10856374/4775335f9864/molecules-29-00564-g003.jpg

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本文引用的文献

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Lipoprotein-X and Lipoprotein-Z Induced Hyperviscosity Syndrome in the Setting of Cholestatic Liver Failure.胆汁淤积性肝衰竭时脂蛋白-X和脂蛋白-Z所致的高黏滞综合征
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Very High Cholesterol Mimicking Homozygous Familial Hypercholesterolemia.酷似纯合子家族性高胆固醇血症的极高胆固醇血症
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A Simple Fluorescent Cholesterol Labeling Method to Cryoprotect and Detect Plasma Lipoprotein-X.
一种用于冷冻保护和检测血浆脂蛋白-X的简单荧光胆固醇标记方法。
Biology (Basel). 2022 Aug 22;11(8):1248. doi: 10.3390/biology11081248.
4
Characterization of LP-Z Lipoprotein Particles and Quantification in Subjects with Liver Disease Using a Newly Developed NMR-Based Assay.使用新开发的基于核磁共振的检测方法对LP-Z脂蛋白颗粒进行表征及对肝病患者进行定量分析。
J Clin Med. 2020 Sep 10;9(9):2915. doi: 10.3390/jcm9092915.
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Curr Opin Lipidol. 2020 Apr;31(2):71-79. doi: 10.1097/MOL.0000000000000673.
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Plasma lipoprotein-X quantification on filipin-stained gels: monitoring recombinant LCAT treatment ex vivo.载脂蛋白 X 脂蛋白在 filipin 染色凝胶上的定量:监测重组 LCAT 体外治疗。
J Lipid Res. 2019 May;60(5):1050-1057. doi: 10.1194/jlr.D090233. Epub 2019 Feb 26.
7
Lipoprotein-X in cholestatic patients causes xanthomas and promotes foam cell formation in human macrophages.胆汁淤积患者体内的脂蛋白-X会引发黄瘤,并促进人类巨噬细胞中泡沫细胞的形成。
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