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  4. Performance of Hepatitis C Virus (HCV) Core Antigen Assay in the Diagnosis of Recently Acquired HCV Infection among High-Risk Populations
 
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Performance of Hepatitis C Virus (HCV) Core Antigen Assay in the Diagnosis of Recently Acquired HCV Infection among High-Risk Populations

Journal
Microbiology Spectrum
Journal Volume
10
Journal Issue
3
Date Issued
2022
Author(s)
HSIN-YUN SUN  
Wang, Chih-Wen
WANG-DA LIU  
Wei, Yu-Ju
KUAN-YIN LIN  
YU-SHAN HUANG  
Su, Li-Hsin
Chen, Yi-Ting
Liu, Wen-Chun
Su, Yi-Chin
Chen, Yea-Wen
YU-CHUNG CHUANG  
Lu, Po-Liang
CHIEN-CHING HUNG  
Yu, Ming-Lung
DOI
10.1128/spectrum.00345-22
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85133214234&doi=10.1128%2fspectrum.00345-22&partnerID=40&md5=e16dab0d848f6b7ce76dad1a91552670
https://scholars.lib.ntu.edu.tw/handle/123456789/620501
Abstract
How the hepatitis C virus (HCV) core antigen (HCVcAg) assay performs in detecting recently acquired HCV infection among people living with HIV (PLWH) and HIV-negative men who have sex with men (MSM) is rarely assessed in the Asia-Pacific region. High-risk participants, including PLWH with sexually transmitted infections (STIs), HCV clearance by antivirals or spontaneously, or elevated aminotransferases, HIV-negative MSM with STIs or on HIV preexposure prophylaxis, and low-risk PLWH were enrolled. Blood samples were subjected to 3-stage pooled-plasma HCV RNA testing every 3 to 6 months until detection of HCV viremia or completion of the 1-year follow-up. The samples at enrollment and all of the archived samples preceding the detection of HCV RNA during follow-up were tested for HCVcAg. During June 2019 and February 2021, 1,639 blood samples from 744 high-risk and 727 low-risk PLWH and 86 HIV-negative participants were tested for both HCV RNA and HCVcAg. Of 62 samples positive for HCV RNA, 54 (87.1%) were positive for HCVcAg. Of 1,577 samples negative for HCV RNA, 1,568 (99.4%) were negative for HCVcAg. The mean HCV RNA load of the 8 individual samples positive for HCV RNA but negative for HCVcAg was 3.2 (range, 2.5 to 3.9) log10 IU/mL, and that of the remaining 54 samples with concordant results was 6.2 (range, 1.3 to 8.5) log10 IU/mL. The positive predictive value (PPV) and negative predictive value (NPV) of HCVcAg were 85.7% and 99.5%, respectively. In at-risk populations, HCVcAg has a high specificity and NPV but lower sensitivity and PPV, particularly in individuals with low HCV RNA loads. IMPORTANCE The HCV core antigen assay has a high specificity of 99.4% and negative predictive value of 99.5% but a lower sensitivity of 87.1% and positive predictive value of 85.7% in the diagnosis of recently acquired HCV infection in high-risk populations. Our findings are informative for many countries confronted with limited resources to timely identify acute HCV infections and provide effective direct-acting antivirals to halt onward transmission.
SDGs

[SDGs]SDG3

[SDGs]SDG5

Publisher
American Society for Microbiology
Type
journal article

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