Application Study of Neutralization Confirmatory Testing for Low Positive Hepatitis B Surface Antigen.

IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY Clinical laboratory Pub Date : 2024-09-01 DOI:10.7754/Clin.Lab.2024.240337
Hui Han, Yan-Hua Huang, Qian Dong, Jian-Qiang Lu, Kang Chen
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Abstract

Background: The high sensitivity of HBsAg quantitative tests has led to some challenges in the qualitative interpretation of weakly positive specimens. This study aimed to explore the clinical utility of neutralization confirma-tory testing for specimens with low positive hepatitis B surface antigen (HBsAg).

Methods: A retrospective analysis was conducted on outpatient and inpatient cases, from January 2021 to January 2022, at the Zhongshan City People's Hospital, Zhongshan. Confirmatory testing as well as enzyme-linked immunosorbent assay (ELISA) was applied to reanalyze 382 samples with low positive HBsAg detected by chemilumi-nescence microparticle immunoassay (CMIA). A retrospective analysis of hepatitis B serum markers, including e-antigen, e-antibody, and core antibody patterns, was also performed.

Results: When the HBsAg value ranged from 0.05 - 0.09 IU/mL, the positivity rate of the confirmatory testing was 34.5%. The HBsAg true positivity levels were all between 0.07 and 0.09. In the range of 0.10 - 0.49, the positivity rate of confirmatory testing was 96.1%. The three methods exhibited a high consistency, when testing samples with relatively high HBsAg values. A receiver operating characteristic (ROC) analysis showed that the optimal sensitivity and specificity were achieved at 0.14 IU/mL. For the HBV e-antigen-positive and negative groups, the positivity rate of confirmatory testing was 100% and 93.8%, with no statistical difference between them.

Conclusions: For specimens with weakly positive, low-value HBsAg, particularly when the hepatitis B surface an-tigen level is less than 0.14 IU/mL, neutralization confirmatory testing can serve as a means for further confirmation.

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乙型肝炎表面抗原低阳性中和确证检验的应用研究。
背景:HBsAg定量检测的高灵敏度导致了对弱阳性标本定性解读的一些挑战。本研究旨在探讨乙肝表面抗原(HBsAg)低阳标本中和确证试验的临床实用性:方法:对中山市人民医院 2021 年 1 月至 2022 年 1 月的门诊和住院病例进行回顾性分析。对化学发光微粒子免疫分析法(CMIA)检测出的382份HBsAg低阳性样本进行了确证检测和酶联免疫吸附试验(ELISA)。此外,还对乙肝血清标志物(包括 e 抗原、e 抗体和核心抗体模式)进行了回顾性分析:当 HBsAg 值介于 0.05 - 0.09 IU/mL 之间时,确证检测的阳性率为 34.5%。HBsAg 真阳性水平均在 0.07 至 0.09 之间。在 0.10 - 0.49 的范围内,确证检测的阳性率为 96.1%。在检测 HBsAg 值相对较高的样本时,这三种方法表现出很高的一致性。接受者操作特征(ROC)分析表明,0.14 IU/mL时灵敏度和特异性最佳。对于 HBV e 抗原阳性组和阴性组,确证检测的阳性率分别为 100%和 93.8%,两者之间没有统计学差异:结论:对于HBsAg弱阳性、低值的标本,尤其是当乙肝表面抗原水平低于0.14 IU/mL时,中和确证试验可作为进一步确证的手段。
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来源期刊
Clinical laboratory
Clinical laboratory 医学-医学实验技术
CiteScore
1.50
自引率
0.00%
发文量
494
审稿时长
3 months
期刊介绍: Clinical Laboratory is an international fully peer-reviewed journal covering all aspects of laboratory medicine and transfusion medicine. In addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies. The journal publishes original articles, review articles, posters, short reports, case studies and letters to the editor dealing with 1) the scientific background, implementation and diagnostic significance of laboratory methods employed in hospitals, blood banks and physicians'' offices and with 2) scientific, administrative and clinical aspects of transfusion medicine and 3) in addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies.
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