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SAT-415 Clinical Performance of Thyroid-Stimulating Immunoglobulin for Graves′ Disease Diagnosis

机译:SAT-415甲状腺刺激免疫球蛋白的临床表现用于Graves疾病诊断

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INTRODUCTION The diagnosis of Graves′disease (GD) is likely when patient presents hyperthyroidism, symmetrical goiter and orbitopathy and further evaluation is unnecessary. Nevertheless patient with nodular thyroid or in the absence of clinical orbitopathy, measurement of TSH receptor antibodies (TRAb) is recommended to distinguish GD from toxic multinodular goiter, toxic adenoma and other etiologies. Radioiodine uptake (RAIU) also helps to diagnosis when TRAb is unavailable. Third generation TRAb assays measure all types of TSH receptor antibodies: stimulating, blocking and neutral with an excellent sensitivity and specificity for GD diagnosis. Recently, an automated bioassay for the thyroid stimulating immunoglobulin (TSI) was introduced to improve GD diagnosis. OBJECTIVE To analyze clinical performance of TSI and compare with TRAb assay for GD diagnosis. MATERIAL AND METHODS Serum samples of 117 patients with thyrotoxicosis due to GD, toxic multinodular goiter and toxic adenoma were runned simultaneously in two analytical system commercially available. TRAb was analyzed by Elecsys Anti-TSHR assay (Roche Diagnostics, Germany) in a Cobase411 analyzer (Roche Diagnostics, Germany) and results, according to the manufacturer interval reference, were negative if < 1.75 IU/L (analytical range: 0.3 to 40 IU/L). TSI was measured by Immulite TSI assay (Siemens Healthcare, UK) in Immulite XPi 2000 and results, according to the manufacturer interval reference, were negative if < 0.55 IU/L (analytical range: 0.1 to 40 IU/L). Clinical diagnoses of thyrotoxicosis were determined according to ATA guideline (2016). Statistical analyses were performed using SPSS and MedCalc softwares. Comparison were evaluated by regression equations and were considered significant when p values were < .05. RESULTS From 2017 to 2019 a total of 312 serum samples from 117 patients (96 females) were evaluated with mean age 49.5 ±15.8 years-old (18 to 90 yrs). We excluded 26 results above the analytical measurement range of both assays. A high degree correlation was observed with a slope of 0.647 and an intercept -.094 IU/L. Spearman correlation coefficient was 0.858 (p < 0.0001, 95% CI 0.825 to 0.886). TSI assay had higher sensibility and negative predictive value compared to TRAb (95.6% vs 88.5% and 83.6% vs 54.8%, respectively) but lower specificity and positive predictive value (90.3% vs 100% and 97.5% vs 100%, respectively). The results of TSI assay showed good agreement with those of the TRAb assay (k=0.74). A total of 31 samples were discordant, favoring to TSI assay in all but one case of GD according to clinical diagnosis (TRAb positive and TSI negative). CONCLUSION TSI assay showed an excellent performance for GD diagnosis with a better sensibility than TRAb assay.
机译:简介患者患者呈甲状腺功能亢进,对称甲状腺肿和胰腺炎以及进一步评估时,可能诊断坟墓(GD)的诊断很可能是不必要的。结节性甲状腺或在没有临床眼病的患者然而,TSH受体抗体(TRAb的)的测量建议从毒性多结节性甲状腺肿,有毒腺瘤和其他病因区分GD。放射碘摄取(RAIU)还有助于诊断TRAB不可用。第三代Trab测定测量所有类型的TSH受体抗体:刺激,阻断和中性,具有出色的敏感性和GD诊断的特异性。最近,引入了甲状腺刺激免疫球蛋白(TSI)的自动化生物测定以改善GD诊断。目的分析TSI的临床表现,与GD诊断进行比较。在可商购的两种分析系统中,在两种分析系统中同时绕过117例甲状腺毒性术患者的117例甲状腺毒性患者的血清样本。通过Elecsys Anti-Tshr Assay(Roche Diagnostics,Germany)在COBase411分析仪(Roche Diagnostics,Germany)和结果的情况下分析了TRAB,根据制造商间隔参考,如果<1.75 IU / L(分析范围:0.3至40 IU / L)。 TSI经IMMULITE TSI测定(西门子医疗,UK)在IMMULITE XPI 2000和结果测量,根据制造商的间隔基准,为阴性如果<0.55 IU / L(分析范围:0.1至40 IU / L)。根据ATA指南(2016年)确定甲状腺毒病的临床诊断。使用SPSS和MEDCALC软件进行统计分析。通过回归方程评估比较,当P值<05时,被认为是显着的。结果2017年至2019年,共有来自117名患者(96名女性)的312个血清样品,按平均年龄为49.5±15.8岁(18至90岁)。我们排除了26个结果,高于两种测定的分析测量范围。观察到高度相关性,斜率为0.647和截止-094 IU / L. Spearman相关系数为0.858(P <0.0001,95%CI 0.825至0.886)。与Trab相比,TSI测定具有更高的敏感性和负面预测值(分别为95.6%,分别为83.6%,分别为83.6%,阳性预测值降低(分别为90.3%,分别为97.5%97.5%,vs 100%)。 TSI检测结果与Trab测定的结果吻合良好(K = 0.74)。共有31种样品不和谐,在临床诊断(Trab阳性和TSI阴性)的所有GD中,所有案例都赞成TSI测定。结论TSI测定表明,GD诊断表现出优异的性能,具有比TRAB测定更好的敏感性。

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