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第三代促甲状腺激素检测在甲状腺功能测试中的应用

Utility of third generation thyrotropin assays in thyroid function testing.

作者信息

Saller B, Broda N, Heydarian R, Görges R, Mann K

机构信息

Department of Internal Medicine, University of Essen, Germany.

出版信息

Exp Clin Endocrinol Diabetes. 1998;106 Suppl 4:S29-33. doi: 10.1055/s-0029-1212053.

Abstract

Determination of thyrotropin (TSH) by sensitive immunometric assays is currently judged as the most sensitive and also most cost-effective first-line approach to thyroid function testing. Further improvement of assay sensitivity has led to the description of third generation TSH assays with a functional sensitivity in the range of 0.01 to 0.02 mU/l. In the present study, we analyzed interassay precision profiles of a commercially available third generation assay (ACS:180 TSH-3) and documented the critical role of the time span used for the assessment of a method's functional sensitivity. By using a standardized approach with five serum pools measured in 30 different runs across a 6-week period, functional sensitivity was calculated as 0.015 mU/l. The TSH concentrations measured by two different third generation assays (ACS: 180 TSH-3 and Elecsys TSH) in samples from healthy blood donors were highly correlated (r = 0.76, n = 252). In some samples, however, discordant results were obtained. Euthyroid reference intervals were determined as 0.30-3.68 mU/l for the ACS:180 TSH-3 assay and as 0.36-3.64 mU/l for the Elecsys TSH assay. Reevaluation of reference intervals including only TPOAb or TgAb negative samples resulted in almost the same reference ranges. Measuring TSH concentrations in various patient populations, third generation assay turned out to be advantageous in the following clinical situations. (a) In patients with mildly suppressed but well detectable TSH concentrations due to functional thyroid autonomy (0.03-0.3 mU/l), overt hyperthyroidism can be excluded by third generation TSH measurement alone without the need of additional thyroid hormone measurements; (b) in patients receiving long term suppressive T4 treatment after thyroidectomy for differentiated thyroid cancer, measurement of basal TSH by third generation assays allow accurate monitoring of hormone therapy without the need for TRH testing; (c) in most patients with severe nonthyroidal illnesses and decreased TSH levels, TSH concentrations measured by third generation assays are only moderately suppressed and can be clearly discriminated from undetectable levels in overt hyperthyroidism. In conclusion, the use of third generation TSH assays is recommended in specialized clinical laboratories frequently analyzing samples taken in one of those clinical situations.

摘要

目前,采用灵敏免疫测定法测定促甲状腺激素(TSH)被认为是甲状腺功能检测最灵敏且最具成本效益的一线方法。检测灵敏度的进一步提高促使了第三代TSH检测方法的出现,其功能灵敏度范围为0.01至0.02 mU/l。在本研究中,我们分析了一种市售第三代检测方法(ACS:180 TSH-3)的批间精密度概况,并记录了评估方法功能灵敏度所用时间跨度的关键作用。通过采用标准化方法,在6周内对5个血清池进行30次不同检测,计算出功能灵敏度为0.015 mU/l。在健康献血者样本中,两种不同的第三代检测方法(ACS:180 TSH-3和Elecsys TSH)测得的TSH浓度高度相关(r = 0.76,n = 252)。然而,在一些样本中得到了不一致的结果。ACS:180 TSH-3检测方法的甲状腺功能正常参考区间确定为0.30 - 3.68 mU/l,Elecsys TSH检测方法的参考区间为0.36 - 3.64 mU/l。仅对TPOAb或TgAb阴性样本重新评估参考区间,结果几乎相同。在各类患者群体中测量TSH浓度时,第三代检测方法在以下临床情况中显示出优势。(a)对于因功能性甲状腺自主性导致TSH浓度轻度降低但仍可检测到(0.03 - 0.3 mU/l)的患者,仅通过第三代TSH检测即可排除明显甲亢,无需额外检测甲状腺激素;(b)对于分化型甲状腺癌甲状腺切除术后接受长期抑制性T4治疗的患者,采用第三代检测方法测量基础TSH可准确监测激素治疗,无需进行TRH检测;(c)在大多数患有严重非甲状腺疾病且TSH水平降低的患者中,第三代检测方法测得的TSH浓度仅轻度受抑制,可与明显甲亢时无法检测到的水平明显区分。总之,对于经常分析处于上述临床情况之一的样本的专业临床实验室,建议使用第三代TSH检测方法。

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