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与游离前列腺特异抗原与总前列腺特异抗原比值解读相关的关键方面。

Critical aspects related to the interpretation of the free-to-total PSA-ratio.

作者信息

Wolff J M, Stocker G, Borchers H, Haubeck H, Greiling H, Jakse G

机构信息

Department of Urology, RWTH Aachen, Germany.

出版信息

Anticancer Res. 1999 Jul-Aug;19(4A):2633-6.

Abstract

INTRODUCTION

The number of assays available for the measurement of total and free PSA is increasing. As different methods can determine different PSA concentrations as well as different free-to-total PSA ratios in identical serum samples, the cut-offvalue for the ratio still needs to be determined.

METHODS

114 sera from patients with histologically confirmed benign prostatic hyperplasia (BPH; n = 58) and cancer of the prostate (CaP; n = 56) were analyzed with two different assays. Free PSA (free), total PSA (total) and the free-to-total- PSA ratio (ratio) were determined employing Enzym-Test PSA und freies PSA (Boehringer Mannheim, Germany) and Immulite PSA und freies PSA (DPC Biermann, Bad Nauheim, Germany)

RESULTS

The statistical results are tabulated below: [table: see text]

CONCLUSION

Direct comparison of the two assays revealed a high statistical correlation (r = 0.94-0.99) for free and total PSA. In contrast, the ratio of the two assays was not as reproducible (r = 0.81-0.83). This result indicates that the reference range for the ratio is dependent on the assay employed and an that uncritical use of an applied reference range can be counter-productive.

摘要

引言

可用于测量总前列腺特异性抗原(PSA)和游离PSA的检测方法数量正在增加。由于不同方法在相同血清样本中可测定出不同的PSA浓度以及不同的游离PSA与总PSA比值,该比值的临界值仍有待确定。

方法

采用两种不同检测方法分析了114份来自组织学确诊为良性前列腺增生(BPH;n = 58)和前列腺癌(CaP;n = 56)患者的血清。使用酶联免疫吸附试验法检测PSA和游离PSA(德国宝灵曼公司)以及免疫化学发光法检测PSA和游离PSA(德国拜耳公司,巴特瑙海姆)来测定游离PSA(free)、总PSA(total)以及游离PSA与总PSA的比值(ratio)。

结果

统计结果如下表所示:[表格:见原文]

结论

两种检测方法的直接比较显示,游离PSA和总PSA具有高度统计学相关性(r = 0.94 - 0.99)。相比之下,两种检测方法的比值重复性较差(r = 0.81 - 0.83)。这一结果表明,该比值的参考范围取决于所采用的检测方法,不加区分地使用既定参考范围可能会适得其反。

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