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血液甲状腺球蛋白信使核糖核酸检测的低特异性使其无法用于分化型甲状腺癌患者的随访。

Low specificity of blood thyroglobulin messenger ribonucleic acid assay prevents its use in the follow-up of differentiated thyroid cancer patients.

作者信息

Elisei Rossella, Vivaldi Agnese, Agate Laura, Molinaro Eleonora, Nencetti Chiara, Grasso Lucia, Pinchera Aldo, Pacini Furio

机构信息

Department of Endocrinology and Metabolism, University of Pisa, 56124 Pisa, Italy.

出版信息

J Clin Endocrinol Metab. 2004 Jan;89(1):33-9. doi: 10.1210/jc.2003-031341.

Abstract

Thyroglobulin (Tg) is a glycoprotein specifically synthesized by follicular thyroid epithelium. After thyroidectomy and remnant (131)I ablation, serum Tg is a specific and sensitive marker for the presence of thyroid cancer tissue, and its measurement is fundamental in the follow-up of patients affected by differentiated thyroid carcinomas (DTCs), being even more sensitive than diagnostic whole-body scan. Unfortunately, serum Tg measurement becomes useless in approximately 15-25% of DTC cases who are positive for anti-Tg antibodies that interfere with the Tg measurement. In these cases, Tg mRNA measurement has been proposed as an alternative to serum Tg determination. The aim of this study was to verify the sensitivity and specificity of Tg mRNA measurement, performed by quantitative real-time RT-PCR, in a series of 100 subjects (80 DTC patients and 20 controls). From our data, the sensitivity and the specificity of the blood Tg mRNA measurement are 82.3 and 24.2%, respectively, with a positive predictive value and a negative predictive value of 65.6 and 43.7%, respectively. The comparison of the Tg mRNA with the serum Tg, measured by both chemiluminescent and ultrasensitive ELISA methods, confirmed the low specificity of the Tg mRNA assay. The hypothesis that Tg mRNA detectable levels could be predictive of future recurrences is not supported by the long follow-up (median, 7 yr; range, 3-29 yr) of our disease-free patients, who did not develop any recurrences in their clinical history. Moreover, nine disease-free patients, who showed positive levels of Tg mRNA (11.8-336 pg equivalents/ micro g RNA), were confirmed to be serum Tg free, both in basal conditions and after recombinant human TSH stimulation, 4 yr after the Tg mRNA detection. In conclusion, we demonstrated that the Tg mRNA assay is of poor utility in the follow-up of DTC patients. On the contrary, serum Tg measurement is a very sensitive and specific thyroid tumor marker, and we recommend that the follow-up of patients affected by DTC must be performed using serum Tg rather than blood Tg mRNA measurement.

摘要

甲状腺球蛋白(Tg)是一种由甲状腺滤泡上皮细胞特异性合成的糖蛋白。甲状腺切除术后及残余甲状腺(131)I消融后,血清Tg是甲状腺癌组织存在的特异性和敏感标志物,其检测在分化型甲状腺癌(DTC)患者的随访中至关重要,甚至比诊断性全身扫描更敏感。不幸的是,在约15%-25%抗Tg抗体阳性的DTC病例中,血清Tg检测变得毫无用处,因为这些抗体会干扰Tg检测。在这些情况下,有人提出检测Tg mRNA作为血清Tg测定的替代方法。本研究的目的是通过定量实时逆转录聚合酶链反应(RT-PCR),验证在100名受试者(80例DTC患者和20名对照)中检测Tg mRNA的敏感性和特异性。根据我们的数据,血液中Tg mRNA检测的敏感性和特异性分别为82.3%和24.2%,阳性预测值和阴性预测值分别为65.6%和43.7%。通过化学发光法和超敏酶联免疫吸附测定(ELISA)法将Tg mRNA与血清Tg进行比较,证实了Tg mRNA检测的低特异性。我们对无病患者进行了长期随访(中位时间7年;范围3-29年),期间他们在临床过程中未出现任何复发,这一结果不支持Tg mRNA可检测水平能够预测未来复发这一假设。此外,9名无病患者在检测到Tg mRNA后4年,无论是基础状态还是重组人促甲状腺激素刺激后,均被证实血清Tg阴性,但他们的Tg mRNA水平呈阳性(11.8-336 pg当量/μg RNA)。总之,我们证明了Tg mRNA检测在DTC患者随访中的应用价值不大。相反,血清Tg检测是一种非常敏感和特异的甲状腺肿瘤标志物,我们建议对DTC患者进行随访时应采用血清Tg检测,而非血液Tg mRNA检测。

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