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甲状腺激素转运蛋白异常的诊断:概述

Diagnosis of thyroid hormone transport protein anomalies: an overview.

作者信息

Langsteger W

机构信息

Department of Internal Medicine, Hospital Barmherzige Brueder Eggenberg, Graz, Austria.

出版信息

Acta Med Austriaca. 1996;23(1-2):31-40.

PMID:8767512
Abstract

Inherited or acquired variations in the serum concentrations of TBG, TTR or albumin are rather common. Clinical studies have shown that most patients with transport protein variations were referred for thyroid testing because of incidentally detected "unusual" thyroid function tests. Although, usually no palpable thyroid abnormalities were found, the interpretation of these unexpected thyroid function tests resulted very often in inappropriate treatment with surgery, 131-iodine, antithyroid drugs as well as T4-replacement therapy. The clinical impact in the interpretation and diagnosis of thyroid hormone transport protein variations is to prevent these patients of unnecessary and sometimes also contraindicated treatment. If changes in thyroid hormone transport proteins in individuals with thyroid disorders or in individuals with the coexistence of two inherited defects are seen, difficulties in the interpretation of thyroid function tests will still occur.

摘要

血清甲状腺素结合球蛋白(TBG)、甲状腺素转运蛋白(TTR)或白蛋白浓度的遗传性或获得性变异相当常见。临床研究表明,大多数有转运蛋白变异的患者因偶然检测到“异常”的甲状腺功能检查结果而接受甲状腺检查。尽管通常未发现可触及的甲状腺异常,但对这些意外的甲状腺功能检查结果的解读往往导致不适当的手术、131碘、抗甲状腺药物以及甲状腺素替代治疗。甲状腺激素转运蛋白变异在甲状腺功能检查解读和诊断中的临床意义在于防止这些患者接受不必要且有时甚至是禁忌的治疗。如果在患有甲状腺疾病的个体或同时存在两种遗传缺陷的个体中发现甲状腺激素转运蛋白的变化,甲状腺功能检查结果的解读仍会存在困难。

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