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血清和血浆(乙二胺四乙酸二钾)中嗜铬粒蛋白A(CgA)水平的比较以及健康男性的各自参考范围。

Comparison of chromogranin A (CgA) levels in serum and plasma (EDTA2K) and the respective reference ranges in healthy males.

作者信息

Glinicki Piotr, Jeske Wojciech, Kapuścińska Renata, Zgliczyński Wojciech

机构信息

Department of Endocrinology, The Centre of Postgraduate Medical Education, Warsaw, Poland.

出版信息

Endokrynol Pol. 2015;66(1):53-6. doi: 10.5603/EP.2015.0009.

DOI:10.5603/EP.2015.0009
PMID:25754282
Abstract

INTRODUCTION

Chromogranin A (CgA) is a major, nonspecific marker of neuroendocrine tumours (NET). There are a few routinely used assays for the measurement of CgA concentration in serum or plasma. These assays differ in analytical techniques (radioimmunoassay, ELISA, CLIA, TRACE), have different calibrators, and use different antibodies which recognise different epitopes of CgA molecule. Our study was designed to confirm the noted earlier differences in CgA levels measured in serum and plasma, and to establish respective reference ranges in a group of healthy males.

MATERIAL AND METHODS

In 145 male blood donors (age 19-61 years, mean = 35.7), blood was collected into two tubes: one with EDTA2K (plasma) and one with clot activator (serum). Chromogranin A was measured by immunoradiometric kit (CIS bio, France).

RESULTS

In blood donors, the median (and the range) of CgA concentration were as follows for serum samples - 42.0 ng/mL (16-108 ng/mL) and for plasma (EDTA2K) samples - 58.0 ng/mL (23-153 ng/mL). The differences between serum and plasma ranged 15-75% (median 26%). Plasma CgA levels were significantly higher in relation to serum CgA levels (p < 0.0001). Correlation of CgA in serum and plasma was r = 0.8493; p < 0.01. The reference ranges for CgA measured in serum and plasma in males, expressed as 2.5 to 97.5 percentiles, were: 21.0-108.0 ng/mL and 31.0-153.0 ng/mL respectively.

CONCLUSIONS

  1. Significant differences in the concentrations of CgA measured in plasma and in serum demand the application of separate reference ranges adjusted to the type of investigated material. 2. Each laboratory should recommend only one sort of sample material for CgA assay.
摘要

引言

嗜铬粒蛋白A(CgA)是神经内分泌肿瘤(NET)的一种主要非特异性标志物。有几种常规方法可用于测定血清或血浆中CgA的浓度。这些检测方法在分析技术(放射免疫测定、酶联免疫吸附测定、化学发光免疫分析、微量分析)上有所不同,校准物不同,且使用识别CgA分子不同表位的不同抗体。我们的研究旨在证实先前所述的血清和血浆中CgA水平的差异,并确定一组健康男性的各自参考范围。

材料与方法

在145名男性献血者(年龄19 - 61岁,平均35.7岁)中,血液被采集到两支试管中:一支含有乙二胺四乙酸二钾(血浆),另一支含有促凝剂(血清)。使用免疫放射分析试剂盒(CIS bio,法国)测定嗜铬粒蛋白A。

结果

在献血者中,血清样本的CgA浓度中位数(及范围)如下 - 42.0 ng/mL(16 - 108 ng/mL),血浆(乙二胺四乙酸二钾)样本的CgA浓度中位数(及范围)如下 - 58.0 ng/mL(23 - 153 ng/mL)。血清和血浆之间的差异范围为15 - 75%(中位数26%)。血浆CgA水平相对于血清CgA水平显著更高(p < 0.0001)。血清和血浆中CgA的相关性为r = 0.8493;p < 0.01。男性血清和血浆中CgA的参考范围,以第2.5至97.5百分位数表示,分别为:21.0 - 108.0 ng/mL和31.0 - 153.0 ng/mL。

结论

  1. 血浆和血清中测得的CgA浓度存在显著差异,需要应用根据所研究材料类型调整的单独参考范围。2. 每个实验室应为CgA检测仅推荐一种样本材料。

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