Evidence map›Paper›PMID 41745107›Full record

ArticleDiseases (Basel, Switzerland)2026

Burden and Clinical Impact of Hepatitis D Virus Co-Infection Among HBsAg-Positive Patients in Mauritania.

Mohamed Abdawa, Mohamed Hemeyine, Isabelle Chemin, Françoise Lunel-Fabiani, Mohamed Vall Mohamed Abdellahi

Abstract read
In one paragraph

Article in Diseases (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Mohamed AbdawaUnité d'Épidémiologie Moléculaire et Diversité des Micro-Organismes (EMDM), Université de Nouakchott, Nouakchott, Mauritania.ORCID 0009-0006-9774-4795
Mohamed HemeyineInstitut National d'Hépato-Virologie (INHV), Nouakchott, Mauritania.
Isabelle CheminInstitut National de la Santé et de la Recherche Médicale (INSERM) U1350, 151 Cours Albert Thomas, 69003 Lyon, France.ORCID 0000-0002-7188-5489
Françoise Lunel-FabianiHIFIH UFR Santé, Faculté de Médecine, University of Angers, 4 Rue de Larrey, 49933 Angers, France.
Mohamed Vall Mohamed AbdellahiUnité d'Épidémiologie Moléculaire et Diversité des Micro-Organismes (EMDM), Université de Nouakchott, Nouakchott, Mauritania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatitis B virus (HBV) infection remains highly endemic in sub-Saharan Africa, where hepatitis delta virus (HDV) co-infection substantially worsens liver disease outcomes. Mauritania has long been suspected to be a high-burden setting for HBV-HDV co-infection, yet contemporary data describing its clinical and virological impact remain limited.

methodsWe conducted a hospital-based cross-sectional study at the National Institute of Hepato-Virology (INHV) in Nouakchott, including 401 HBsAg-positive patients. Demographic, clinical, biological, and virological data were collected. HDV serology and RNA testing were performed when available. Liver disease severity, including cirrhosis and hepatocellular carcinoma (HCC), was assessed using clinical, biological, and imaging criteria.

resultsHDV antibodies were detected in 31.9% of HBsAg-positive patients, confirming Mauritania as a hyper-endemic area for HDV. HDV co-infection was strongly associated with advanced liver disease, with HDV antibodies present in 86.4% of cirrhotic patients and 82.4% of those with HCC. Patients with HDV infection frequently exhibited suppressed HBV DNA levels, reflecting viral interference. A substantial proportion of patients presented with decompensated cirrhosis or HCC at diagnosis, and nearly 70% were treatment-naïve. Overall, HDV co-infection emerged as the principal driver of severe liver disease in this cohort.

conclusionsHBV/HDV co-infection is highly prevalent in Mauritania and is associated with a wide clinical spectrum ranging from asymptomatic infection to decompensated cirrhosis and hepatocellular carcinoma. HDV co-infection is the principal driver of severe liver disease, often occurring despite low or undetectable HBV DNA levels. Systematic HDV screening among all HBsAg-positive individuals is urgently needed to improve risk stratification, guide therapeutic decisions, and reduce liver-related morbidity and mortality.

Indexed as

Africacirrhosishepatitis Bhepatitis D virushepatocellular carcinomaMauritania

Identifiers

PMID41745107
PMCPMC12940037

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