Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures

Hepatitis B virus (HBV) infection is a serious global health problem, with 2 billion people infected worldwide, and 350 million suffering from chronic HBV infection. The 10th leading cause of death worldwide, HBV infections result in 500 000 to 1.2 million deaths per year caused by chronic hepatitis...

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Veröffentlicht in:Journal of viral hepatitis 2004-03, Vol.11 (2), p.97-107
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description Hepatitis B virus (HBV) infection is a serious global health problem, with 2 billion people infected worldwide, and 350 million suffering from chronic HBV infection. The 10th leading cause of death worldwide, HBV infections result in 500 000 to 1.2 million deaths per year caused by chronic hepatitis, cirrhosis, and hepatocellular carcinoma; the last accounts for 320 000 deaths per year [1, 2]. In Western countries, the disease is relatively rare and acquired primarily in adulthood, whereas in Asia and most of Africa, chronic HBV infection is common and usually acquired perinatally or in childhood. More efficacious treatments, mass immunization programs, and safe injection techniques are essential for eliminating HBV infection and reducing global HBV‐related morbidity and mortality. Safe and effective vaccines against HBV infection have been available since 1982. The implementation of mass immunization programs, which have been recommended by the World Health Organization since 1991, have dramatically decreased the incidence of HBV infection among infants, children, and adolescents in many countries [2]. However, not all countries have adopted these recommendations and there remains a large number of persons that were infected with HBV prior to the implementation of immunization programs. Antiviral treatment is the only way to reduce morbidity and mortality from chronic HBV infection. Conventional interferon alfa and lamivudine have been the primary treatments to date. Conventional interferon alfa produces a durable response in a moderate proportion of patients but has undesirable side‐effects and must be administered subcutaneously three times per week. Lamivudine also produces a response in a modest proportion of patients and causes few side‐effects [3]. However, prolonged treatment is often necessary to prevent relapse on cessation of therapy, and continuous treatment can lead to the development of lamivudine resistance [4]. Promising emerging new treatments include adefovir [5], entecavir [6] and peginterferon alfa‐2a (40 kDa) [7].
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However, not all countries have adopted these recommendations and there remains a large number of persons that were infected with HBV prior to the implementation of immunization programs. Antiviral treatment is the only way to reduce morbidity and mortality from chronic HBV infection. Conventional interferon alfa and lamivudine have been the primary treatments to date. Conventional interferon alfa produces a durable response in a moderate proportion of patients but has undesirable side‐effects and must be administered subcutaneously three times per week. Lamivudine also produces a response in a modest proportion of patients and causes few side‐effects [3]. However, prolonged treatment is often necessary to prevent relapse on cessation of therapy, and continuous treatment can lead to the development of lamivudine resistance [4]. Promising emerging new treatments include adefovir [5], entecavir [6] and peginterferon alfa‐2a (40 kDa) [7].</description><subject>adefovir</subject><subject>Antiviral Agents - pharmacology</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Carcinoma, Hepatocellular - epidemiology</subject><subject>Carcinoma, Hepatocellular - virology</subject><subject>cirrhosis</subject><subject>Hepatitis B - complications</subject><subject>Hepatitis B - epidemiology</subject><subject>Hepatitis B - prevention &amp; control</subject><subject>Hepatitis B - therapy</subject><subject>Hepatitis B e Antigens - blood</subject><subject>hepatitis B infection</subject><subject>hepatitis B vaccine</subject><subject>Hepatitis B Vaccines - therapeutic use</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B, Chronic - complications</subject><subject>Hepatitis B, Chronic - epidemiology</subject><subject>Hepatitis B, Chronic - prevention &amp; control</subject><subject>Hepatitis B, Chronic - therapy</subject><subject>hepatocellular carcinoma</subject><subject>Humans</subject><subject>interferon alfa</subject><subject>Interferon-alpha - pharmacology</subject><subject>Interferon-alpha - therapeutic use</subject><subject>lamivudine</subject><subject>Lamivudine - pharmacology</subject><subject>Lamivudine - therapeutic use</subject><subject>Liver Cirrhosis - epidemiology</subject><subject>Liver Cirrhosis - virology</subject><subject>peginterferon alfa-2a (40 kDa)</subject><subject>Polyethylene Glycols - pharmacology</subject><subject>Polyethylene Glycols - therapeutic use</subject><subject>Recombinant Proteins</subject><issn>1352-0504</issn><issn>1365-2893</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhS1ERUvhFZBXrCbBP4kdS2ygwAzVAJsW2FmOczPykL_aSZl5e5xmVJaw8rX9nWNZH0KYkpSSTLzZp5SLPGGF4ikjhKeEZIVMD0_QxePF03nOWUJykp2j5yHsCaGc5fQZOqeZUoJn_AKFDQxmdKML-D2-d34KGAZXQev6pt8dV7hyAUwAXE6-gm6FRw9mbKEbV9h0FbaT93HzMEMLfue6HR483MdD13cL03ej7xvcxqLJQ3iBzmrTBHh5Wi_R7aePN1ebZPtt_fnq3Tax8Q8yEUzI0kJtC1nXVJTGWMpJWcm8AKCqZsSWzNYKasm5EVVpWFkpQlUlpMgs55fo9dI7-P5ugjDq1gULTWM66KegJRVKyoL-E6RSMcJlFsFiAa3vQ_BQ68G71vijpkTPZvRezwL0LEDPZvSDGX2I0VenN6ayhepv8KQiAm8X4Ldr4Pjfxfr6-yYOMZ4scRdGODzGjf-lheQy1z--rvV28-Hnl61Ses3_AHFcrj4</recordid><startdate>200403</startdate><enddate>200403</enddate><creator>Lavanchy, D.</creator><general>Blackwell Science Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200403</creationdate><title>Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures</title><author>Lavanchy, D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3657-6267bcefc87ff16baac130bd758ee19f20cb2cf9ef733a6dba2bd9019d6764c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>adefovir</topic><topic>Antiviral Agents - pharmacology</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Carcinoma, Hepatocellular - epidemiology</topic><topic>Carcinoma, Hepatocellular - virology</topic><topic>cirrhosis</topic><topic>Hepatitis B - complications</topic><topic>Hepatitis B - epidemiology</topic><topic>Hepatitis B - prevention &amp; control</topic><topic>Hepatitis B - therapy</topic><topic>Hepatitis B e Antigens - blood</topic><topic>hepatitis B infection</topic><topic>hepatitis B vaccine</topic><topic>Hepatitis B Vaccines - therapeutic use</topic><topic>Hepatitis B virus</topic><topic>Hepatitis B, Chronic - complications</topic><topic>Hepatitis B, Chronic - epidemiology</topic><topic>Hepatitis B, Chronic - prevention &amp; control</topic><topic>Hepatitis B, Chronic - therapy</topic><topic>hepatocellular carcinoma</topic><topic>Humans</topic><topic>interferon alfa</topic><topic>Interferon-alpha - pharmacology</topic><topic>Interferon-alpha - therapeutic use</topic><topic>lamivudine</topic><topic>Lamivudine - pharmacology</topic><topic>Lamivudine - therapeutic use</topic><topic>Liver Cirrhosis - epidemiology</topic><topic>Liver Cirrhosis - virology</topic><topic>peginterferon alfa-2a (40 kDa)</topic><topic>Polyethylene Glycols - pharmacology</topic><topic>Polyethylene Glycols - therapeutic use</topic><topic>Recombinant Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lavanchy, D.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of viral hepatitis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lavanchy, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures</atitle><jtitle>Journal of viral hepatitis</jtitle><addtitle>J Viral Hepat</addtitle><date>2004-03</date><risdate>2004</risdate><volume>11</volume><issue>2</issue><spage>97</spage><epage>107</epage><pages>97-107</pages><issn>1352-0504</issn><eissn>1365-2893</eissn><abstract>Hepatitis B virus (HBV) infection is a serious global health problem, with 2 billion people infected worldwide, and 350 million suffering from chronic HBV infection. 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However, not all countries have adopted these recommendations and there remains a large number of persons that were infected with HBV prior to the implementation of immunization programs. Antiviral treatment is the only way to reduce morbidity and mortality from chronic HBV infection. Conventional interferon alfa and lamivudine have been the primary treatments to date. Conventional interferon alfa produces a durable response in a moderate proportion of patients but has undesirable side‐effects and must be administered subcutaneously three times per week. Lamivudine also produces a response in a modest proportion of patients and causes few side‐effects [3]. However, prolonged treatment is often necessary to prevent relapse on cessation of therapy, and continuous treatment can lead to the development of lamivudine resistance [4]. 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subjects adefovir
Antiviral Agents - pharmacology
Antiviral Agents - therapeutic use
Carcinoma, Hepatocellular - epidemiology
Carcinoma, Hepatocellular - virology
cirrhosis
Hepatitis B - complications
Hepatitis B - epidemiology
Hepatitis B - prevention & control
Hepatitis B - therapy
Hepatitis B e Antigens - blood
hepatitis B infection
hepatitis B vaccine
Hepatitis B Vaccines - therapeutic use
Hepatitis B virus
Hepatitis B, Chronic - complications
Hepatitis B, Chronic - epidemiology
Hepatitis B, Chronic - prevention & control
Hepatitis B, Chronic - therapy
hepatocellular carcinoma
Humans
interferon alfa
Interferon-alpha - pharmacology
Interferon-alpha - therapeutic use
lamivudine
Lamivudine - pharmacology
Lamivudine - therapeutic use
Liver Cirrhosis - epidemiology
Liver Cirrhosis - virology
peginterferon alfa-2a (40 kDa)
Polyethylene Glycols - pharmacology
Polyethylene Glycols - therapeutic use
Recombinant Proteins
title Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures
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