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两种测定分化型甲状腺癌患者血清甲状腺球蛋白浓度方法的比较评估

Comparative evaluation of two methods to assay thyroglobulin serum concentrations in patients with differentiated thyroid carcinomas.

作者信息

Ferrari L, Seregni E, Aliberti G, Martinetti A, Pallotti F, Villano C, Lucignani G, Bombardieri E

机构信息

Nuclear Medicine Division, Radioisotope Laboratory, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.

出版信息

Q J Nucl Med Mol Imaging. 2004 Sep;48(3):237-42.

Abstract

AIM

This study was aimed at the comparative assessment of the analytical and clinical performances of 2 tests for thyroglobulin (Tg) assays: the Dynotest Tg-Plus immunoradiometric assay (IRMA), a new method that might be of interest for its claimed superior sensitivity compared to other methods, and the HTGK-2 IRMA, one of the test currently used in clinical routine.

METHODS

The study was performed in serum samples from 157 patients with differentiated thyroid carcinoma (DTC). The clinical sensitivity of the test was evaluated in patients with and without thyroid stimulating hormone (TSH) suppression.

RESULTS

The lowest detectable Tg concentration values and the within-assay coefficient of variation (CV) were 0.4 and 0.8 microg/L and 5% and 3% for the Dynotest Tg-Plus assay and the HTGK-2 assay, respectively; the between-assay CV was 6% for both assays. The clinical results of the Dynotest Tg-Plus and those of the HTGK-2 kit were similar in both DTC patient populations, either under or off the TSH suppressive treatment. In spite of the manufacturer's statement that the calibrators of both assays had been standardized against the same common reference (standard CRM 457 of the Community Bureau of References), the Dynotest Tg-Plus test underrated by a factor of 0.5 the Tg values measured by means of HTGK-2 IRMA.

CONCLUSION

The sensitivity of the Dynotest Tg-Plus IRMA appears to be similar to that of the HTGK-2 assay.

摘要

目的

本研究旨在对两种甲状腺球蛋白(Tg)检测方法的分析性能和临床性能进行比较评估:Dynotest Tg-Plus免疫放射分析(IRMA),一种声称与其他方法相比具有更高灵敏度的新方法,以及HTGK-2 IRMA,临床常规中目前使用的检测方法之一。

方法

该研究在157例分化型甲状腺癌(DTC)患者的血清样本中进行。在有和没有促甲状腺激素(TSH)抑制的患者中评估检测的临床敏感性。

结果

Dynotest Tg-Plus检测和HTGK-2检测的最低可检测Tg浓度值和批内变异系数(CV)分别为0.4和0.8μg/L以及5%和3%;两种检测的批间CV均为6%。在TSH抑制治疗或未进行TSH抑制治疗的DTC患者群体中,Dynotest Tg-Plus和HTGK-2试剂盒的临床结果相似。尽管制造商声明两种检测的校准品已根据相同的通用参考标准(欧洲共同体标准物质局的标准CRM 457)进行了标准化,但Dynotest Tg-Plus检测测得的Tg值比通过HTGK-2 IRMA测得的值低0.5倍。

结论

Dynotest Tg-Plus IRMA的灵敏度似乎与HTGK-2检测相似。

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