Role of hepatitis C virus core antigen assay in hepatitis C care in developing country

Abstract

Background The World Health Organization (WHO) aims to achieve global hepatitis C elimination by 2030, defined as diagnosis of 90% of infected individuals and treating 80% of them. Current guidelines for the screening and diagnosis of hepatitis C infection denote using a relatively cheap screen with anti-hepatitis C virus (HCV) antibody immunoassay, followed by the much costlier molecular test for HCV RNA levels using polymerase chain reaction (PCR) assay to confirm active HCV infection. Simplification of the HCV evaluation algorithm to reduce the number of required tests could considerably expand the provision of HCV treatment especially in a developing country. This study investigates the performance of hepatitis C Core Antigen (HCV Ag) test by comparing HCV Ag results versus the results obtained with HCV ribonucleic acid (RNA) PCR which is considered the gold standard for the diagnosis of HCV infection. Results Among the 109 anti-HCV positive sera, 96 were positive for both HCV Ag (> 3 fmol/L) and HCV RNA (> 15 IU/mL); 8 were negative for both tests, while the remaining 5 were positive for HCV RNA only. Considering the HCV RNA as gold standard; the sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of HCV Ag test were found to be 95.05%, 100%, 100%, and 61.54%, respectively. HCV genotype was performed for 59 patients. The most common HCV genotype was genotype 1 (72.9%). Genotype 2 (15.3%) and genotype 3 (11.9%) were detected in the others samples. A high level of correlation was seen between HCV RNA and HCV Ag (r = 0.958, p < 0.001). The correlation for the samples that were genotyped 1 was significant (r = 0.966, p < 0.001). Conclusion In our study, it was found that there was strong correlation between HCV RNA levels and HCV Ag levels. So, it can be used for a one-step HCV antigen test to diagnose active HCV infection.

Comparing RT-qPCR and Hepatitis C Virus Antigen Detection Assay for Detecting Active Infection in Blood Donors in Fars Province, Iran

“…However, it cannot be routinely used by low-income countries to screen blood donors due to the high technical skills needed, costs, and long turnaround times. Nevertheless, RNA levels and HCVcAg were found to be strongly correlated (18). Overall, the detection of HCVcAg can provide a valuable alternative to molecular testing and is of particular importance during the window period of HCV infection and before antibodies appear.…”

The Study of Performance of a Nanoribbon Biosensor, Sensitized with Aptamers and Antibodies, upon Detection of Core Antigen of Hepatitis C Virus

“…The primary sequence of HCVcoreAg is highly conserved among all the different genotypes of the virus [10]. HCVcoreAg appears in blood 10-15 days after infection with HCV (1-2 days later than HCV RNA), thus not hindering early diagnosis of the disease [10,11]. This is why HCVcoreAg represents a promising protein marker for the early revelation of HCV.…”

Performance of a Nanoribbon Biosensor Sensitized with Aptamers and Antibodies upon Detection of HCVcoreAg<strong> </strong>

“…The primary sequence of HCVcoreAg is highly conserved among all the different genotypes of the virus [31]. HCVcoreAg appears in blood 10-15 days after infection with HCV (1-2 days later than HCV RNA), thus not hindering early diagnosis of the disease [10,11]. This is why HCVcoreAg represents a promising protein marker for early revelation of HCV.…”