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使用含磁性抗体的微胶囊测量游离甲状腺素。

Measuring free thyroxin by using magnetic antibody-containing microcapsules.

作者信息

Wallace A M, Aitken S, Duffy F A, Fraser W D, Beastall G H

机构信息

Institute of Biochemistry, Royal Infirmary, Glasgow, Scotland, U.K.

出版信息

Clin Chem. 1990 Apr;36(4):614-9.

PMID:2108822
Abstract

We describe a novel magnetic-separation microencapsulated antibody displacement assay for free thyroxin. The method is rapid (results available in just over an hour), with a detection limit of 3 pmol/L, and an interassay precision of less than 10% over the range 8-75 pmol/L. Results are not influenced by changes in the concentration of thyroxin-binding globulin or albumin, nor by the presence of circulating anti-thyroxin antibodies or physiological concentrations of nonesterified (free) fatty acids. A reference interval of 8.4-18.4 pmol/L was established for a large euthyroid adult population. Patients with various nonthyroidal illnesses exhibited a similar reference interval (6.2-17.4 pmol/L). Results from pregnant women, at all stages of gestation, were within the nonpregnant euthyroid reference interval. Complete discrimination was obtained between the euthyroid reference interval and values from patients with untreated thyrotoxicosis (24-75 pmol/L). Excellent, though incomplete, discrimination was obtained for patients with untreated hypothyroidism (less than 3.0-9.0 pmol/L). Results for a group of patients defined as having compensated euthyroidism (5.0-15 pmol/L) showed considerable overlap with the euthyroid reference interval. Patients taking thyroxin, who were clinically euthyroid and whose serum concentration of thyrotropin was within its euthyroid reference interval, had free thyroxin concentrations in the range 13.4-24.2 pmol/L. We discuss the validity of this assay in clinical practice.

摘要

我们描述了一种用于游离甲状腺素的新型磁分离微囊化抗体置换测定法。该方法快速(仅需一个多小时即可获得结果),检测限为3 pmol/L,在8 - 75 pmol/L范围内批间精密度小于10%。结果不受甲状腺素结合球蛋白或白蛋白浓度变化的影响,也不受循环抗甲状腺素抗体或生理浓度的非酯化(游离)脂肪酸的影响。为一大群甲状腺功能正常的成年人建立了8.4 - 18.4 pmol/L的参考区间。患有各种非甲状腺疾病的患者表现出类似的参考区间(6.2 - 17.4 pmol/L)。妊娠各阶段孕妇的结果均在非妊娠甲状腺功能正常的参考区间内。甲状腺功能正常的参考区间与未经治疗的甲状腺毒症患者的值(24 - 75 pmol/L)之间实现了完全区分。对于未经治疗的甲状腺功能减退患者(低于3.0 - 9.0 pmol/L),虽有区分但不完全。一组被定义为代偿性甲状腺功能正常(5.0 - 15 pmol/L)的患者结果与甲状腺功能正常的参考区间有相当大的重叠。临床甲状腺功能正常且血清促甲状腺激素浓度在其甲状腺功能正常参考区间内的服用甲状腺素的患者,游离甲状腺素浓度在13.4 - 24.2 pmol/L范围内。我们讨论了该测定法在临床实践中的有效性。

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