# Prevalence and Risk Factors of Hepatocellular Carcinoma in Patients Co-infected With Hepatitis B Virus (HBV) and Hepatitis C Virus (HCV): A Cross-Sectional Retrospective Study

**Authors:** Saleem Iqbal, Zarak Qureshi, Hafiz Muhammad Mudasir, Asif Khan, Amir Sohail, Jamil Ahmad, Fatima Tu Zuhra, Muhammad Younas Ali, Moosa Ali, Zubair Ahmad, Kainat Khan

PMC · DOI: 10.7759/cureus.85985 · 2025-06-14

## TL;DR

This study found that 21% of patients co-infected with hepatitis B and C viruses developed liver cancer, with risk factors including older age, cirrhosis, and longer infection duration.

## Contribution

The study identifies independent risk factors for hepatocellular carcinoma in HBV-HCV co-infected patients using a cross-sectional retrospective analysis.

## Key findings

- 20.98% of HBV-HCV co-infected patients were diagnosed with hepatocellular carcinoma.
- Age >45 years, cirrhosis, and elevated alpha-fetoprotein levels were significant independent predictors of HCC.
- Comorbidities and infection duration ≥5 years were also independently associated with HCC development.

## Abstract

Background

A serious consequence of long-term hepatitis B virus (HBV) and hepatitis C virus (HCV) infections is hepatocellular carcinoma (HCC), particularly in co-infected individuals, who are at a significantly higher risk of malignant transformation.

Objective

The main objective of this study is to determine the frequency and identify associated risk factors of HCC in patients co-infected with HBV and HCV through a retrospective cross-sectional analysis.

Methodology

This retrospective cross-sectional study was conducted at Hayatabad Medical Complex, Peshawar, Pakistan, using medical records of HBV-HCV co-infected patients from January 2023 to December 2024. A total of 348 patients aged ≥18 years, with complete clinical, biochemical, and radiological/histopathological data, were included. Data were analyzed using IBM SPSS Statistics for Windows, Version 25 (Released 2017; IBM Corp., Armonk, NY, USA), evaluating demographics, comorbidities, alpha-fetoprotein (AFP) levels, liver function tests, and HCC diagnosis. Chi-square and logistic regression analyses were used to identify significant risk factors, with p-values <0.05 considered statistically significant.

Results

Out of 348 HBV-HCV co-infected patients, 73 (20.98%) were diagnosed with HCC. The majority of patients were aged between 31 and 60 years, with a mean age of 47.8 ± 12.6 years. Males comprised 58.91% (n = 205) of the cohort. Among the HCC patients, age >45 years was significantly associated with HCC occurrence (71.23% vs. 47.27%, p = 0.002). Cirrhosis was found in 68.49% of HCC patients versus 35.64% without HCC (p < 0.001). Infection duration ≥5 years was observed in 72.60% of HCC cases compared to 60.36% of non-HCC cases (p = 0.054). Elevated AFP >20 ng/mL was significantly associated with HCC (61.64% vs. 24.36%, p < 0.001), as was elevated alanine aminotransferase (ALT) (76.71% vs. 57.82%, p = 0.006). Comorbidities were more common in HCC patients (39.73%) compared to non-HCC patients (21.82%, p = 0.004). Logistic regression analysis identified several independent predictors of HCC: age >45 years (adjusted odds ratio (AOR): 2.45; 95% CI: 1.38-4.36; p = 0.002), cirrhosis (AOR: 3.87; 95% CI: 2.15-6.96; p < 0.001), infection duration ≥5 years (AOR: 1.62; 95% CI: 1.01-2.59; p = 0.046), AFP >20 ng/mL (AOR: 3.09; 95% CI: 1.74-5.48; p < 0.001), and presence of comorbidities (AOR: 1.85; 95% CI: 1.09-3.15; p = 0.022).

Conclusion

Among HBV-HCV co-infected patients, a high proportion of HCC was observed. Significant risk factors independently associated with HCC included age over 45 years, presence of cirrhosis, longer infection duration, elevated AFP levels, and comorbidities. These findings underscore the importance of early risk stratification and regular surveillance in co-infected individuals to enable timely diagnosis and intervention.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** long-term (MESH:D000088562), HBV-HCV co-infected (MESH:D006525), Infection (MESH:D007239), HCC (MESH:D006528), Cirrhosis (MESH:D005355)
- **Species:** HCV [taxon 11103], Hepatitis B virus (no rank) [taxon 10407], Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12257254/full.md

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Source: https://tomesphere.com/paper/PMC12257254