Stimulating TSH receptor autoantibodies immunoassay: analytical evaluation and clinical performance in Graves’ disease

Annals of Clinical Biochemistry - Tập 55 Số 1 - Trang 172-177 - 2018
Chiara Autilio1, Renato Morelli1, Pietro Locantore2, Alfredo Pontecorvi2, Cecilia Zuppi1, Cinzia Carrozza1
1Department of Laboratory Medicine, Catholic University-Gemelli Hospital, Rome, Italy
2Units of Endocrinology, Catholic University – Gemelli Hospital, Rome, Italy

Tóm tắt

Background Thyroid-stimulating hormone (TSH) receptor (TSHR) autoantibodies (TRAbs) are a heterogeneous group of antibodies (Abs) with different functionalities. Among all TRAbs, only the stimulating ones (S-TRAbs) are considered as the pathogenetic marker of Graves’ disease (GD). To date, the methods available for TRAbs testing are based on immunoassays (IMAs) which detect total serum TRAbs or bioassays which are not suitable in clinical practice, even though they discern Abs functionality. The aim of our work was to evaluate the analytical and clinical performance of a very recent IMA (Immulite TSI method), supposed to test only the serum concentration of S-TRAbs, in comparison with a current method for total TRAbs (Roche/Elecsys IMA). Methods We evaluated serum samples of 145 subjects: 46 with untreated (GD), 36 with chronic autoimmune thyroiditis, 3 with atrophic thyroiditis, 10 with multinodular non-toxic goiter and 50 healthy subjects. Results The method showed an optimal analytical sensitivity and high precision levels (LoB: 0.04 UI/L, LoD:0.07 UI/L, LoQ:0.14 UI/L, intra-assay CV: 4.2–5.9%, inter-assay: 4.5–7.2%). By receiver operating characteristics curve analysis, we obtained a value of 0.57 (sensitivity: 98.0%, specificity: 99.9%) as the best cut-off to distinguish GD, apart from four cases. Passing Bablok regression and Bland Altman analysis pointed out a good correlation and agreement with Roche method (R2 = 0.98, slope = 1.03, bias = −2.70). Conclusions The new method presents very promising analytical characteristics and could be adopted in clinical practice for GD diagnosis. Moreover, the test allows to accurately detect very low values of analyte with a further clinical utility in detecting earlier possible relapses.

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Tài liệu tham khảo

10.1016/S1568-9972(03)00006-5

10.1530/EJE-11-0548

10.1016/j.autrev.2010.05.021

10.1210/jc.2012-4309

10.1055/s-0035-1559633

10.1159/000375445

10.1016/j.autrev.2012.07.003

10.1089/thy.2008.0119

10.1055/s-0035-1554662

10.1210/jc.2009-2470

10.1515/cclm-2016-0197

10.4158/EP.17.3.456

10.1089/105072503321086962

WHO. WHO guidelines on drawing blood: best practices in phlebotomy. Geneva: World Health Organization, 2010, www.euro.who.int.

CLSI EP17-A protocol. Protocols for determination of limits of detection and limits of quantification; approved guidelines. CLSI 2004; 24: 1–39.

CLSI EP5-A2 protocol. Evaluation of precision performance of quantitative measurement methods; approved guidelines (second edition). CLSI 2004; 24: 1–39.

10.1093/clinchem/39.4.561

Passing H, 1983, Clin Chem, 21, 709

10.1089/thy.1997.7.867

National Institute for Biological Standards and Controls (NIBSC): WHO International Standard or reference reagent. Thyroid stimulating antibody NIBSC 08/204. Instruction for use (version 2.0, dated 28.03.2013). NIBSC, Potters Bar, Hertfordshire, UK.

10.1515/CCLM.2001.007

10.1111/j.1749-6632.2009.04809.x