Abstract

BackgroundCo-infection between hepatitis B virus (HBV) and hepatitis delta virus (HDV) causes the severest chronic hepatitis and is associated with a high risk of cirrhosis and hepatocellular carcinoma (HCC). The Global Health Sector Strategy on Viral Hepatitis called for the elimination of hepatitis (− 65% mortality and − 90% incidence) by 2030. Our aims were to summarize key points of knowledge and to identify the gaps that need to be addressed to mount a public health response to HDV.MethodsWe performed a current literature review in terms of epidemiology by WHO regions, genotypes distribution and their pathogenicity, factors associated with HDV infection, mortality due to HDV infection, testing strategies and treatment.ResultsPrevalence of infection and genotypes are heterogeneous distributed, with highest prevalence in foci around the Mediterranean, in the Middle East, and in Central, Northern Asia and Eastern Asia. Persons who inject drugs (PWID) and migrants from highly endemic areas are highly affected. While antibody detection tests are available, HDV RNA tests of current infection are not standardized nor widely available. The few therapeutic options, including lofartinib, are not widely available; however several new and promising agents have entered clinical trials.ConclusionHDV infection is an poorly known cause of chronic liver disease. To mount a public health response, we need a better description of the HDV epidemic, standardized testing strategies and better treatment options.

Highlights

  • Co-infection between hepatitis B virus (HBV) and hepatitis delta virus (HDV) causes the severest chronic hepatitis and is associated with a high risk of cirrhosis and hepatocellular carcinoma (HCC)

  • We performed a current literature review in terms of epidemiology by World Health Organization (WHO) regions, genotypes distribution and their pathogenicity, factors associated with HDV infection, mortality due to HDV infection, testing strategies and treatment

  • While certain countries and risk/ethnic groups have very high HDV prevalence, there is a lot of heterogeneity and many data gaps

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Summary

Introduction

Co-infection between hepatitis B virus (HBV) and hepatitis delta virus (HDV) causes the severest chronic hepatitis and is associated with a high risk of cirrhosis and hepatocellular carcinoma (HCC). Our aims were to summarize key points of knowledge and to identify the gaps that need to be addressed to mount a public health response to HDV. Of the viruses causing hepatitis, Hepatitis delta Virus (HDV) is unique in that it needs the helper function of Hepatitis B Virus (HBV) to infect hepatocytes [1]. WHO does not have estimates of prevalence or mortality for HDV. Most published reviews quote 5% as an estimate of the prevalence of HDV coinfection among persons with HBV infection (about 13 million persons worldwide) [3], mostly in high endemicity foci or among immigrants from highly endemic regions [4].

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