Authors : Mustafa Guney; Ayfer Bakir; Harun Erdal; Armagan Gunal; Fatime Yildiz; Ali Korhan Sig; Muhammed Furkan Kurkcu; Mehmet Tevfik Yavuz; Mustafa Gulsen
Volume/Issue : Volume 6 - 2021, Issue 9 - September
Google Scholar : http://bitly.ws/gu88
Scribd : https://bit.ly/2ZlSnMZ
Introduction: The correlation between the
Hepatitis B virus (HBV) viral load and liver fibrosis is still
researched. Objective: This study aimed to investigate the
correlation of viral parameters and the different levels
and stages of liver disease in treatment-naïve patients with
chronic HBV. Methodology: A total of 128 treatmentnaïve chronic HBV patients who underwent liver biopsy
were assessed in this retrospective and cross-sectional
study. Simultaneously with biopsy, HBsAg (S/Co) was
measured with HBeAg (S/Co) chemiluminescent immune
assay (Abbott Diagnostics, Germany) and HBV viral load
was measured with PCR (Bosphore HBV Quantification
Kit v2, Turkey) test. The assessments of liver fibrosis were
based on the ISHAK staging system. Results: Out of 128
patients who were included in the study and whose ages
ranged from 18 to 73, 100 (78%) were male. A negative
but significant correlation was found between HBsAg
S/Co and HBV-DNA viral load levels in HBeAg negative
and positive patients (r= -0.277, p= 0.01 and r= -0.475, p=
0.001 respectively). Sensitivity, specificity and the area
under the curve (AUC) were 51.8%, 57.8% and 0.551
respectively at the viral load value of 5.1 (log) IU/ml for
the prediction of fibrosis score ≥ 2. Sensitivity, specificity
and AUC were 72.7%, 41.9% and 0.545 respectively at
the viral load value of 6.1 (log) IU/ml for the prediction of
fibrosis score ≥ 4. Conclusion: Different HBV-DNA levels
in treatment-naïve patients with chronic HBV can have
effects on the formation of fibrosis in liver tissues and
predict the severity of fibrosis. When the indirect serum
biomarkers and serum HBV-DNA levels are used together
in chronic HBV they may be more helpful in predicting of
fibrosis
Keywords : Chronic hepatitis B, viral load, liver fibrosis, liver inflammation