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血清甲状腺球蛋白测量的欧洲实验室间比对

European interlaboratory comparison of serum thyroglobulin measurement.

作者信息

Feldt-Rasmussen U, Schlumberger M

机构信息

Department of Medicine E, Frederiksberg Hospital, Copenhagen, Denmark.

出版信息

J Endocrinol Invest. 1988 Mar;11(3):175-81. doi: 10.1007/BF03350129.

Abstract

A European interlaboratory comparison of serum thyroglobulin measurements was performed after an initiative from the European Organization of Research and Therapy of Cancer. Fifty-two laboratories were addressed and 45 of these (83%) participated in the study by measuring serum thyroglobulin and its autoantibody in 5 thyroglobulin containing sera. Thyroglobulin antibodies were added to two of the sera. Two commercial kits were used by a large number of the laboratories (11 and 8, respectively). Each kit showed a reasonably low interlaboratory coefficient of variation at concentrations above 25 micrograms/l, but with discrepancy between the methods. The remaining miscellaneous methods (24) showed a variation above 65% in all samples. In all laboratories the addition of thyroglobulin antibodies resulted in false thyroglobulin measurements with either elevated or depressed levels. It is concluded that a reference calibrator for serum thyroglobulin is strongly needed as the first essential step towards interlaboratory standardization of serum thyroglobulin, thereby opening a possibility for multicentre studies of its value in the post-therapy follow-up of patients with differentiated thyroid carcinoma.

摘要

在欧洲癌症研究与治疗组织的倡导下,开展了一项欧洲血清甲状腺球蛋白测量的实验室间比对。共联系了52个实验室,其中45个(83%)参与了该研究,对5份含甲状腺球蛋白的血清样本测量了血清甲状腺球蛋白及其自身抗体。向其中两份血清中添加了甲状腺球蛋白抗体。大量实验室(分别为11个和8个)使用了两种商业试剂盒。每种试剂盒在浓度高于25微克/升时,实验室间变异系数都相当低,但不同方法之间存在差异。其余的各种方法(24种)在所有样本中的变异率均高于65%。在所有实验室中,添加甲状腺球蛋白抗体均导致甲状腺球蛋白测量值出现错误,水平要么升高要么降低。结论是,强烈需要血清甲状腺球蛋白的参考校准物,这是血清甲状腺球蛋白实验室间标准化的首要关键步骤,从而为多中心研究其在分化型甲状腺癌患者治疗后随访中的价值开辟了可能性。

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