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Published on: July 16, 2012
The correlation of HCV RNA and HCV core antigen in different genotypes of HCV
Yu Xiang1, Xiao-Fei Lai1, Pu Chen1
1Department of Clinical Laboratory, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Insights
Hepatitis C virus (HCV) core antigen (HCV cAg) shows a positive correlation with HCV RNA levels in genotype 1b infections. Chemiluminescent microparticle immunoassay (CMIA) detection of HCV cAg facilitates earlier diagnosis and treatment for HCV patients.
Area of Science:
- Virology
- Hepatology
- Infectious Diseases
Background:
- Hepatitis C virus (HCV) infection remains a significant global health concern.
- Accurate and early diagnosis of HCV infection is crucial for effective treatment and management.
- Understanding the correlation between HCV RNA and HCV core antigen (HCV cAg) across different genotypes is important for diagnostic strategies.
Purpose of the Study:
- To investigate the correlation between HCV RNA and HCV cAg levels in patients with various HCV genotypes.
- To compare the diagnostic performance of chemiluminescent microparticle immunoassay (CMIA) and enzyme-linked immunosorbent assay (ELISA) for HCV cAg detection.
- To evaluate HCV cAg as a potential early diagnostic marker for HCV infection, particularly in genotype 1b.
Main Methods:
- A cohort of 106 patients diagnosed with HCV infection was analyzed.
- HCV genotypes were identified using PCR fluorescent probe technology.
- HCV cAg expression was quantified using CMIA and qualitatively assessed via ELISA.
Main Results:
- HCV genotype 1b was the predominant subtype (43.4%).
- CMIA demonstrated a significantly higher positive rate (100%) for HCV cAg compared to ELISA (56%).
- A positive correlation was observed between HCV RNA and HCV cAg in genotype 1b infections (r=0.894, P=0.04).
Conclusions:
- HCV genotype 1b is the most prevalent subtype in the studied population.
- CMIA offers superior sensitivity for HCV cAg detection, aiding in earlier diagnosis.
- HCV cAg serves as a valuable early indicator for diagnosing HCV infection, especially in genotype 1b, correlating with viral load.
Background:
To analyze the correlation of HCV RNA and HCV core antigen (HCV cAg) in different genotypes of HCV.
Methods:
One hundred and six patients who were diagnosed with HCV infection by HCV RNA test were included in the study. HCV genotypes were detected by PCR fluorescent probe. Detected HCV cAg's expression in serum quantitatively and qualitatively with chemiluminescent micro-particle immuno assay (CMIA) and enzyme-linked immunosorbent assay (ELISA), respectively, and compared positive rates. Analyzed the correlation of HCV RNA and HCV cAg in different genotypes.
Results:
Distribution of HCV genotypes in 106 HCV infected patients were as follows: 1b genotype 46 (43.4%); 2a genotype 7 (6.6%); 3a genotype 18 (17.0%); 3b genotype 3 (2.8%); 6a genotype 9 (8.5%); 1b/3b mixed type 13 (12.3%); and unidentified type 10 (9.4%). Positive rates of HCV cAg detected by CMIA and ELISA were 100% and 56%, respectively, with statistical significance (χ2 = 60.38, P = 0.000). HCV cAg in 1b genotype group was higher than that in 3b and 1b/3b genotype groups, with statistical significance (U = 3.0, P = 0.006, U = 165, P = 0.014). HCV RNA and HCV cAg in genotype 1b demonstrated a positive correlation (r = 0.894, P = 0.04).
Conclusion:
Major genetic subtype of HCV genotype was 1b. Compared with ELISA, detection of HCV cAg by CMIA increased the positive rate and facilitated early diagnosis and treatment of HCV-infected patients. With the increase in HCV RNA load and the expression of HCV cAg, HCV cAg could be an early indicator for the diagnosis of HCV infection in 1b genotype.
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