Prevalence and burden of hepatitis D virus infection in the global population: a systematic review and meta-analysis

ObjectiveHepatitis D virus (HDV) is a defective virus that completes its life cycle only with hepatitis B virus (HBV). The HBV with HDV super-infection has been considered as one of the most severe forms of the chronic viral hepatitis. However, there is a scarcity of data on the global burden of HDV...

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Published inGut Vol. 68; no. 3; pp. 512 - 521
Main Authors Chen, Hai-Yan, Shen, Dan-Ting, Ji, Dong-Ze, Han, Pei-Chun, Zhang, Wei-Ming, Ma, Jian-Feng, Chen, Wen-Sen, Goyal, Hemant, Pan, Shiyang, Xu, Hua-Guo
Format Journal Article
LanguageEnglish
Published England BMJ Publishing Group LTD 01.03.2019
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Abstract ObjectiveHepatitis D virus (HDV) is a defective virus that completes its life cycle only with hepatitis B virus (HBV). The HBV with HDV super-infection has been considered as one of the most severe forms of the chronic viral hepatitis. However, there is a scarcity of data on the global burden of HDV infection.DesignWe searched PubMed, Embase, Cochrane Library and China Knowledge Resource Integrated databases from 1 January 1977 to 31 December 2016. We included studies with a minimum sample size of 50 patients. Our study analysed data from a total of 40 million individuals to estimate the prevalence of HDV by using Der-Simonian Laird random-effects model. The data were further categorised according to risk factors.ResultsFrom a total of 2717 initially identified studies, only 182 articles from 61 countries and regions met the final inclusion criteria. The overall prevalence of HDV was 0.98% (95% CI 0.61 to 1.42). In HBsAg-positive population, HDV pooled prevalence was 14.57% (95% CI 12.93 to 16.27): Seroprevalence was 10.58% (95% CI 9.14 to 12.11) in mixed population without risk factors of intravenous drug use (IVDU) and high-risk sexual behaviour (HRSB). It was 37.57% (95% CI 29.30 to 46.20) in the IVDU population and 17.01% (95% CI 10.69 to 24.34) in HRSB population.ConclusionWe found that approximately 10.58% HBsAg carriers (without IVDU and HRSB) were coinfected with HDV, which is twofold of what has been estimated before. We also noted a substantially higher HDV prevalence in the IVDU and HRSB population. Our study highlights the need for increased focus on the routine HDV screening and rigorous implementation of HBV vaccine programme.
AbstractList ObjectiveHepatitis D virus (HDV) is a defective virus that completes its life cycle only with hepatitis B virus (HBV). The HBV with HDV super-infection has been considered as one of the most severe forms of the chronic viral hepatitis. However, there is a scarcity of data on the global burden of HDV infection.DesignWe searched PubMed, Embase, Cochrane Library and China Knowledge Resource Integrated databases from 1 January 1977 to 31 December 2016. We included studies with a minimum sample size of 50 patients. Our study analysed data from a total of 40 million individuals to estimate the prevalence of HDV by using Der-Simonian Laird random-effects model. The data were further categorised according to risk factors.ResultsFrom a total of 2717 initially identified studies, only 182 articles from 61 countries and regions met the final inclusion criteria. The overall prevalence of HDV was 0.98% (95% CI 0.61 to 1.42). In HBsAg-positive population, HDV pooled prevalence was 14.57% (95% CI 12.93 to 16.27): Seroprevalence was 10.58% (95% CI 9.14 to 12.11) in mixed population without risk factors of intravenous drug use (IVDU) and high-risk sexual behaviour (HRSB). It was 37.57% (95% CI 29.30 to 46.20) in the IVDU population and 17.01% (95% CI 10.69 to 24.34) in HRSB population.ConclusionWe found that approximately 10.58% HBsAg carriers (without IVDU and HRSB) were coinfected with HDV, which is twofold of what has been estimated before. We also noted a substantially higher HDV prevalence in the IVDU and HRSB population. Our study highlights the need for increased focus on the routine HDV screening and rigorous implementation of HBV vaccine programme.
Hepatitis D virus (HDV) is a defective virus that completes its life cycle only with hepatitis B virus (HBV). The HBV with HDV super-infection has been considered as one of the most severe forms of the chronic viral hepatitis. However, there is a scarcity of data on the global burden of HDV infection.OBJECTIVEHepatitis D virus (HDV) is a defective virus that completes its life cycle only with hepatitis B virus (HBV). The HBV with HDV super-infection has been considered as one of the most severe forms of the chronic viral hepatitis. However, there is a scarcity of data on the global burden of HDV infection.We searched PubMed, Embase, Cochrane Library and China Knowledge Resource Integrated databases from 1 January 1977 to 31 December 2016. We included studies with a minimum sample size of 50 patients. Our study analysed data from a total of 40 million individuals to estimate the prevalence of HDV by using Der-Simonian Laird random-effects model. The data were further categorised according to risk factors.DESIGNWe searched PubMed, Embase, Cochrane Library and China Knowledge Resource Integrated databases from 1 January 1977 to 31 December 2016. We included studies with a minimum sample size of 50 patients. Our study analysed data from a total of 40 million individuals to estimate the prevalence of HDV by using Der-Simonian Laird random-effects model. The data were further categorised according to risk factors.From a total of 2717 initially identified studies, only 182 articles from 61 countries and regions met the final inclusion criteria. The overall prevalence of HDV was 0.98% (95% CI 0.61 to 1.42). In HBsAg-positive population, HDV pooled prevalence was 14.57% (95% CI 12.93 to 16.27): Seroprevalence was 10.58% (95% CI 9.14 to 12.11) in mixed population without risk factors of intravenous drug use (IVDU) and high-risk sexual behaviour (HRSB). It was 37.57% (95% CI 29.30 to 46.20) in the IVDU population and 17.01% (95% CI 10.69 to 24.34) in HRSB population.RESULTSFrom a total of 2717 initially identified studies, only 182 articles from 61 countries and regions met the final inclusion criteria. The overall prevalence of HDV was 0.98% (95% CI 0.61 to 1.42). In HBsAg-positive population, HDV pooled prevalence was 14.57% (95% CI 12.93 to 16.27): Seroprevalence was 10.58% (95% CI 9.14 to 12.11) in mixed population without risk factors of intravenous drug use (IVDU) and high-risk sexual behaviour (HRSB). It was 37.57% (95% CI 29.30 to 46.20) in the IVDU population and 17.01% (95% CI 10.69 to 24.34) in HRSB population.We found that approximately 10.58% HBsAg carriers (without IVDU and HRSB) were coinfected with HDV, which is twofold of what has been estimated before. We also noted a substantially higher HDV prevalence in the IVDU and HRSB population. Our study highlights the need for increased focus on the routine HDV screening and rigorous implementation of HBV vaccine programme.CONCLUSIONWe found that approximately 10.58% HBsAg carriers (without IVDU and HRSB) were coinfected with HDV, which is twofold of what has been estimated before. We also noted a substantially higher HDV prevalence in the IVDU and HRSB population. Our study highlights the need for increased focus on the routine HDV screening and rigorous implementation of HBV vaccine programme.
Hepatitis D virus (HDV) is a defective virus that completes its life cycle only with hepatitis B virus (HBV). The HBV with HDV super-infection has been considered as one of the most severe forms of the chronic viral hepatitis. However, there is a scarcity of data on the global burden of HDV infection. We searched PubMed, Embase, Cochrane Library and China Knowledge Resource Integrated databases from 1 January 1977 to 31 December 2016. We included studies with a minimum sample size of 50 patients. Our study analysed data from a total of 40 million individuals to estimate the prevalence of HDV by using Der-Simonian Laird random-effects model. The data were further categorised according to risk factors. From a total of 2717 initially identified studies, only 182 articles from 61 countries and regions met the final inclusion criteria. The overall prevalence of HDV was 0.98% (95% CI 0.61 to 1.42). In HBsAg-positive population, HDV pooled prevalence was 14.57% (95% CI 12.93 to 16.27): Seroprevalence was 10.58% (95% CI 9.14 to 12.11) in mixed population without risk factors of intravenous drug use (IVDU) and high-risk sexual behaviour (HRSB). It was 37.57% (95% CI 29.30 to 46.20) in the IVDU population and 17.01% (95% CI 10.69 to 24.34) in HRSB population. We found that approximately 10.58% HBsAg carriers (without IVDU and HRSB) were coinfected with HDV, which is twofold of what has been estimated before. We also noted a substantially higher HDV prevalence in the IVDU and HRSB population. Our study highlights the need for increased focus on the routine HDV screening and rigorous implementation of HBV vaccine programme.
Author Shen, Dan-Ting
Ji, Dong-Ze
Ma, Jian-Feng
Goyal, Hemant
Pan, Shiyang
Han, Pei-Chun
Zhang, Wei-Ming
Chen, Hai-Yan
Xu, Hua-Guo
Chen, Wen-Sen
Author_xml – sequence: 1
  givenname: Hai-Yan
  surname: Chen
  fullname: Chen, Hai-Yan
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Laboratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
– sequence: 2
  givenname: Dan-Ting
  surname: Shen
  fullname: Shen, Dan-Ting
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Laboratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
– sequence: 3
  givenname: Dong-Ze
  surname: Ji
  fullname: Ji, Dong-Ze
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
– sequence: 4
  givenname: Pei-Chun
  surname: Han
  fullname: Han, Pei-Chun
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Laboratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
– sequence: 5
  givenname: Wei-Ming
  surname: Zhang
  fullname: Zhang, Wei-Ming
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
– sequence: 6
  givenname: Jian-Feng
  surname: Ma
  fullname: Ma, Jian-Feng
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Laboratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
– sequence: 7
  givenname: Wen-Sen
  surname: Chen
  fullname: Chen, Wen-Sen
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Infection Control and Hospital Epidemiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
– sequence: 8
  givenname: Hemant
  surname: Goyal
  fullname: Goyal, Hemant
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Internal Medicine, Mercer University School of Medicine, Macon, Georgia, USA
– sequence: 9
  givenname: Shiyang
  surname: Pan
  fullname: Pan, Shiyang
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Laboratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
– sequence: 10
  givenname: Hua-Guo
  orcidid: 0000-0001-7170-9445
  surname: Xu
  fullname: Xu, Hua-Guo
  email: sypan@njmu.edu.cn, huaguoxu@njmu.edu.cn
  organization: Department of Laboratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30228220$$D View this record in MEDLINE/PubMed
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Snippet ObjectiveHepatitis D virus (HDV) is a defective virus that completes its life cycle only with hepatitis B virus (HBV). The HBV with HDV super-infection has...
Hepatitis D virus (HDV) is a defective virus that completes its life cycle only with hepatitis B virus (HBV). The HBV with HDV super-infection has been...
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SubjectTerms Coinfection - epidemiology
Data processing
Epidemiology
Global Health - statistics & numerical data
Hepatitis
Hepatitis B
Hepatitis B surface antigen
Hepatitis B Surface Antigens - blood
Hepatitis B, Chronic - epidemiology
Hepatitis D - epidemiology
Hepatitis D - transmission
Hepatitis delta virus
Hepatology
Humans
Infections
Intravenous administration
Life cycles
Liver cancer
Meta-analysis
Mortality
Population
Population studies
Prevalence
Risk Factors
Risk-Taking
Serology
Sexual Behavior
Studies
Substance Abuse, Intravenous - complications
Substance Abuse, Intravenous - epidemiology
Superinfection
Systematic review
Title Prevalence and burden of hepatitis D virus infection in the global population: a systematic review and meta-analysis
URI https://gut.bmj.com/content/68/3/512.full
https://www.ncbi.nlm.nih.gov/pubmed/30228220
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https://www.proquest.com/docview/2179215610
Volume 68
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