Hepatitis Delta and Liver Disease Among People Living With Hepatitis B With or Without HIV Co-Infection in Senegal
- PMID: 39967446
- PMCID: PMC11836594
- DOI: 10.1111/liv.70026
Hepatitis Delta and Liver Disease Among People Living With Hepatitis B With or Without HIV Co-Infection in Senegal
Abstract
Background and aims: The prevalence of hepatitis delta virus (HDV) infection among persons living with hepatitis B virus (HBV) and its impact on liver-related complications in West Africa are ill-defined. Wetested a large urban HBV cohort in Senegal for the presence of HDV/HBV co-infection and evaluated its association with liver fibrosis.
Methods: We included persons with positive hepatitis B surface antigen (HBsAg) enrolled in the SEN-B cohort since 2019. Anti-HDV antibodies (HDVAb) were tested using the Anti-HD Diasorin LiaisonXL test, HDV RNA was measured with RT-qPCR and genotyping was determined through sequencing. We used multivariable logistic regression to evaluate the association between HDVAb positivity and liver fibrosis, defined as a liver stiffness measurement > 7.0 kPa.
Results: We analysed 914 individuals with a median age of 32 years (interquartile range [IQR] 26-41), of whom 487 (53.3%) were men and 117 (12.8%) had HIV co-infection. Thirteen participants (1.4%, 95% CI 0.8-2.4) had a positive HDVAb test, of whom 8/13 (61.5%) showed detectable HDV RNA. HDV genotype 5 was found in 75.0% of cases. In multivariable analyses, HDVAb positivity (aOR 11.7, 95% CI 3.1-45.7), male sex (aOR 5.4, 95% CI 3.1-10.3), ALT > 40 IU/L (aOR 4.4, 95% CI 2.4-8.2) and HBeAg positivity (aOR 4.6, 95% CI 1.8-11.9) were independently associated with liver fibrosis.
Conclusion: The prevalence of HDV infection was low in persons living with HBV in Dakar, but those affected had a very high risk of presenting with liver cirrhosis. Efforts to improve HDV screening and management are urgently needed in Senegal.
Keywords: Senegal; hepatitis B; hepatitis D; liver fibrosis; prevalence.
© 2025 The Author(s). Liver International published by John Wiley & Sons Ltd.
Conflict of interest statement
G.W. received research grants from Roche Diagnostics and Gilead Sciences and served on advisory boards for ViiV, Gilead Sciences and MSD. All other authors declare no conflicts of interest. The funders had no role in the design of the study; in the collection, analyses or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
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References
-
- WHO , Global Hepatitis Report 2024: Action for Access in Low‐ and Middle‐Income Countries (World Health Organization, 2024), Licence: CC BY‐NC‐SA 3.0 IGO, accessed Aug 26, 2024, https://www.who.int/publications/i/item/9789240091672.
-
- Le Gal F., Brichler S., Drugan T., et al., “Genetic Diversity and Worldwide Distribution of the Deltavirus Genus: A Study of 2,152 Clinical Strains,” Hepatology 66, no. 6 (2017): 1826–1841. - PubMed
-
- Devarbhavi H., Asrani S. K., Arab J. P., Nartey Y. A., Pose E., and Kamath P. S., “Global Burden of Liver Disease: 2023 Update,” Journal of Hepatology 79, no. 2 (2023): 516–537. - PubMed
-
- Béguelin C., Atkinson A., Boyd A., et al., “Hepatitis Delta Infection Among Persons Living With HIV in Europe,” Liver International 43, no. 4 (2023): 819–828. - PubMed
-
- Roulot D., Brichler S., Layese R., et al., “Origin, HDV Genotype and Persistent Viremia Determine Outcome and Treatment Response in Patients With Chronic Hepatitis Delta,” Journal of Hepatology 73, no. 5 (2020): 1046–1062. - PubMed
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