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评价两种免疫分析法在 Graves 病诊断中检测甲状腺刺激受体抗体的分析和临床性能。

Evaluation of analytic and clinical performance of two immunoassays for detecting thyroid-stimulating receptor antibody in the diagnosis of Graves' disease.

机构信息

Department of Laboratory Medicine, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Department of Nursing, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

出版信息

J Clin Lab Anal. 2021 Dec;35(12):e23950. doi: 10.1002/jcla.23950. Epub 2021 Nov 9.

Abstract

OBJECTIVE

To evaluate the analytical and clinical performance of two immunoassays for diagnosis of Graves' disease (GD), the Immulite thyroid-stimulating immunoglobulin (TSI), and Elecsys Anti-TSH receptor (TSHR) assay.

METHODS

Precision and analytical measurement range were assessed using pooled samples of patients. The comparison between the two methods was evaluated using 579 clinical samples, and receiver operating characteristic (ROC) curves were drawn using the final diagnosis as reference. Clinical sensitivity and specificity, accuracy, positive predictive value (PPV), and negative predictive value (NPV) were calculated for the two tests.

RESULTS

The repeatability and intermediate imprecision coefficient of variation (CV%) of the TSI assay were 3.8% and 4.1% at 0.95 IU/L, and 3.5% and3.6% at 19.5 IU/L, respectively. The assays were linear over a range 0.27-38.5 IU/L. There was a high correlation between the quantitative results of the two methods (correlation coefficient r = 0.930). The cut-off value obtained by ROC analysis for TSI assay was 0.7 IU/L with sensitivity of 93.7% and specificity of 85.1%. An overall qualitative agreement of 91.5% between two methods was observed. Among 44 patients with discordant qualitative results, the TSI assay provided more satisfactory results consistent with clinical diagnoses.

CONCLUSION

The TSI assay showed excellent analytical performance and provided a high PPV for GD.

摘要

目的

评估两种用于诊断格雷夫斯病(GD)的免疫测定法,即 Immulite 甲状腺刺激免疫球蛋白(TSI)和 Elecsys 抗 TSH 受体(TSHR)测定法的分析和临床性能。

方法

使用患者的混合样本评估精密度和分析测量范围。使用 579 份临床样本评估两种方法之间的比较,并使用最终诊断作为参考绘制接收者操作特征(ROC)曲线。计算两种检测方法的临床灵敏度、特异性、准确性、阳性预测值(PPV)和阴性预测值(NPV)。

结果

TSI 测定法的重复性和中间精密度变异系数(CV%)分别为 0.95 IU/L 时的 3.8%和 4.1%,19.5 IU/L 时的 3.5%和 3.6%。该测定法在 0.27-38.5 IU/L 范围内呈线性。两种方法的定量结果具有高度相关性(相关系数 r=0.930)。通过 ROC 分析获得的 TSI 测定法的截断值为 0.7 IU/L,其灵敏度为 93.7%,特异性为 85.1%。两种方法之间观察到总体定性一致性为 91.5%。在 44 例定性结果不一致的患者中,TSI 测定法提供了更多符合临床诊断的满意结果。

结论

TSI 测定法具有出色的分析性能,为 GD 提供了较高的 PPV。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/8649345/28044ca44276/JCLA-35-e23950-g005.jpg

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