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不同检测系统在中国人群抗磷脂抗体检测中的比较。

Comparison of Different Test Systems for the Detection of Antiphospholipid Antibodies in a Chinese Cohort.

机构信息

Department of Rheumatology, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, Key Laboratory of Rheumatology & Clinical Immunology, Ministry of Education, Beijing, China.

National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Beijing, China.

出版信息

Front Immunol. 2021 Jul 2;12:648881. doi: 10.3389/fimmu.2021.648881. eCollection 2021.

Abstract

BACKGROUND

Diagnosis of antiphospholipid syndrome (APS) is based on the positivity of laboratory criteria antiphospholipid antibodies (aPLs). Test results for aPLs could be contradictory among different detection methods as well as commercial manufacturers. This study aimed to assess and compare the diagnostic and analytic performances of four commercial assays prevalently used in China.

METHODS

A total of 313 patients including 100 patients diagnosed with primary APS, 52 with APS secondary to SLE, 71 with SLE, and 90 health controls were recruited. Serum IgG, IgM, and IgA for aCL, and a2GPI antibodies were detected with two ELISA and two CLIA systems, and test system with the best diagnostic value was explored of its correlation with key clinical features.

RESULTS

CLIA by YHLO Biotech Co. was considered as the system with the best predictive power, where 58.55 and 57.89% of APS patients were positive for aCL or a2GPI for at least one antibody (IgG or IgM or IgA). Overall, CLIA showed better performance characteristics than traditional ELISA test systems.

CONCLUSION

CLIA was considered as a better platform for aPL detection in APS diagnosis. A combination of other detection platforms could assist in differential diagnosis as well as in identifying high-risk patients.

摘要

背景

抗磷脂综合征(APS)的诊断基于实验室标准抗磷脂抗体(aPLs)的阳性。不同检测方法和商业制造商的 aPL 检测结果可能存在差异。本研究旨在评估和比较在中国广泛使用的四种商业检测方法的诊断和分析性能。

方法

共纳入 313 例患者,包括 100 例原发性 APS 患者、52 例狼疮相关 APS 患者、71 例系统性红斑狼疮(SLE)患者和 90 例健康对照者。采用两种 ELISA 和两种 CLIA 系统检测血清 IgG、IgM 和 IgA 型抗心磷脂抗体和抗β2-糖蛋白 I 抗体,并探索具有最佳诊断价值的检测系统与关键临床特征的相关性。

结果

YHLO 生物科技公司的 CLIA 被认为是预测能力最佳的系统,至少有一种抗体(IgG 或 IgM 或 IgA)阳性的 APS 患者中,58.55%和 57.89%为抗心磷脂抗体或抗β2-糖蛋白 I 抗体阳性。总体而言,CLIA 的性能特征优于传统 ELISA 检测系统。

结论

CLIA 被认为是 APS 诊断中 aPL 检测的较好平台。结合其他检测平台有助于鉴别诊断和识别高危患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ef3/8283786/dce762a50962/fimmu-12-648881-g001.jpg

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