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[运用6种不同方法对9家法国医院实验室血浆总同型半胱氨酸测定结果的比较]

[Comparison of plasma total homocysteine determinations in 9 French hospital laboratories by using 6 different methods].

作者信息

Ducros V, Candito M, Caussé E, Couderc R, Demuth K, Diop M E, Drai J, Gerhardt M F, Quillard M, Read M H, Sauvant M P

机构信息

Département de biologie intégrée, CHU Grenoble.

出版信息

Ann Biol Clin (Paris). 2002 Jul-Aug;60(4):421-8.

Abstract

A lot of methods are now available for total plasma homocysteine (tHcy) determination. Commercial kits using immunoassay, easier to use, begin to supplant in-house laboratory methods. Our aim is to evaluate the interchangeability of tHcy measurements in 9 French hospital laboratories. Six different method types were used: 2 gas chromatography-mass spectrometry (GC-MS), 2 HPLC with fluorescence detection subdivided in one in-house method and one commercial kit (Bio-Rad ), 3 fluorescence polarization immunoassays (FPIA), 1 enzyme immunoassay, 1 amino acid analyser, 1 capillary electrophoresis coupled with laser-induced fluorescence detection (EC-LIF). Each laboratory analysed 41 patient's plasma samples in which 8 samples contained added homocystine. Results were analysed for imprecision, recovery, and methodological differences. The mean among-laboratory imprecision (CV) ranged from 12.5 to 18% in function of plasma sample type and was identical to the mean among-method variation. In terms of recovery, we obtained underestimated results with immunoassays. The bias relative to the GC-MS method was less than 12.5% except for two laboratories, one using FPIA assay and the other EC-LIF. In conclusion, the interchangeability of tHcy results between laboratories is not satisfactory and does not allow us to evaluate cardiovascular risk linked to moderate increases of tHcy.

摘要

目前有许多方法可用于测定血浆总同型半胱氨酸(tHcy)。使用免疫测定法的商业试剂盒使用起来更方便,开始取代内部实验室方法。我们的目的是评估法国9家医院实验室中tHcy测量结果的可互换性。使用了六种不同的方法类型:2种气相色谱 - 质谱法(GC - MS),2种带荧光检测的高效液相色谱法,其中一种为内部方法,另一种为商业试剂盒(伯乐公司),3种荧光偏振免疫分析法(FPIA),1种酶免疫分析法,1种氨基酸分析仪,1种毛细管电泳 - 激光诱导荧光检测法(EC - LIF)。每个实验室分析了41份患者血浆样本,其中8份样本添加了同型胱氨酸。对结果进行了不精密度、回收率和方法学差异分析。实验室间平均不精密度(CV)根据血浆样本类型在12.5%至18%之间,与方法间平均变异相同。在回收率方面,免疫测定法得到的结果偏低。除了两个实验室,一个使用FPIA测定法,另一个使用EC - LIF测定法外,相对于GC - MS方法的偏差小于12.5%。总之,实验室间tHcy结果的可互换性并不令人满意,无法让我们评估与tHcy适度升高相关的心血管风险。

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