The global prevalence of hepatitis D virus infection: Systematic review and meta-analysis.


Journal

Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886

Informations de publication

Date de publication:
09 2020
Historique:
received: 19 12 2019
revised: 01 04 2020
accepted: 06 04 2020
pubmed: 27 4 2020
medline: 9 11 2021
entrez: 27 4 2020
Statut: ppublish

Résumé

There are uncertainties about the epidemic patterns of HDV infection and its contribution to the burden of liver disease. We estimated the global prevalence of HDV infection and explored its contribution to the development of cirrhosis and hepatocellular carcinoma (HCC) among HBsAg-positive people. We searched Pubmed, EMBASE and Scopus for studies reporting on total or IgG anti-HDV among HBsAg-positive people. Anti-HDV prevalence was estimated using a binomial mixed model, weighting for study quality and population size. The population attributable fraction (PAF) of HDV to cirrhosis and HCC among HBsAg-positive people was estimated using random effects models. We included 282 studies, comprising 376 population samples from 95 countries, which together tested 120,293 HBsAg-positive people for anti-HDV. The estimated anti-HDV prevalence was 4.5% (95% CI 3.6-5.7) among all HBsAg-positive people and 16.4% (14.6-18.6) among those attending hepatology clinics. Worldwide, 0.16% (0.11-0.25) of the general population, totalling 12.0 (8.7-18.7) million people, were estimated to be anti-HDV positive. Prevalence among HBsAg-positive people was highest in Mongolia, the Republic of Moldova and countries in Western and Middle Africa, and was higher in injecting drug users, haemodialysis recipients, men who have sex with men, commercial sex workers, and those with HCV or HIV. Among HBsAg-positive people, preliminary PAF estimates of HDV were 18% (10-26) for cirrhosis and 20% (8-33) for HCC. An estimated 12 million people worldwide have experienced HDV infection, with higher prevalence in certain geographic areas and populations. HDV is a significant contributor to HBV-associated liver disease. More quality data are needed to improve the precision of burden estimates. We combined all available studies to estimate how many people with hepatitis B also have hepatitis D, a viral infection that only affects people with hepatitis B. About 1 in 22 people with hepatitis B also have hepatitis D, increasing to 1 in 6 when considering people with liver disease. Hepatitis D may cause about 1 in 6 of the cases of cirrhosis and 1 in 5 of the cases of liver cancer that occur in people with hepatitis B. Hepatitis D is an important contributor to the global burden of liver disease.

Sections du résumé

BACKGROUND AND AIMS
There are uncertainties about the epidemic patterns of HDV infection and its contribution to the burden of liver disease. We estimated the global prevalence of HDV infection and explored its contribution to the development of cirrhosis and hepatocellular carcinoma (HCC) among HBsAg-positive people.
METHODS
We searched Pubmed, EMBASE and Scopus for studies reporting on total or IgG anti-HDV among HBsAg-positive people. Anti-HDV prevalence was estimated using a binomial mixed model, weighting for study quality and population size. The population attributable fraction (PAF) of HDV to cirrhosis and HCC among HBsAg-positive people was estimated using random effects models.
RESULTS
We included 282 studies, comprising 376 population samples from 95 countries, which together tested 120,293 HBsAg-positive people for anti-HDV. The estimated anti-HDV prevalence was 4.5% (95% CI 3.6-5.7) among all HBsAg-positive people and 16.4% (14.6-18.6) among those attending hepatology clinics. Worldwide, 0.16% (0.11-0.25) of the general population, totalling 12.0 (8.7-18.7) million people, were estimated to be anti-HDV positive. Prevalence among HBsAg-positive people was highest in Mongolia, the Republic of Moldova and countries in Western and Middle Africa, and was higher in injecting drug users, haemodialysis recipients, men who have sex with men, commercial sex workers, and those with HCV or HIV. Among HBsAg-positive people, preliminary PAF estimates of HDV were 18% (10-26) for cirrhosis and 20% (8-33) for HCC.
CONCLUSIONS
An estimated 12 million people worldwide have experienced HDV infection, with higher prevalence in certain geographic areas and populations. HDV is a significant contributor to HBV-associated liver disease. More quality data are needed to improve the precision of burden estimates.
LAY SUMMARY
We combined all available studies to estimate how many people with hepatitis B also have hepatitis D, a viral infection that only affects people with hepatitis B. About 1 in 22 people with hepatitis B also have hepatitis D, increasing to 1 in 6 when considering people with liver disease. Hepatitis D may cause about 1 in 6 of the cases of cirrhosis and 1 in 5 of the cases of liver cancer that occur in people with hepatitis B. Hepatitis D is an important contributor to the global burden of liver disease.

Identifiants

pubmed: 32335166
pii: S0168-8278(20)30220-8
doi: 10.1016/j.jhep.2020.04.008
pmc: PMC7438974
pii:
doi:

Substances chimiques

Hepatitis Antibodies 0
Hepatitis B Surface Antigens 0
Immunoglobulin G 0
RNA, Viral 0

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

523-532

Subventions

Organisme : World Health Organization
ID : 001
Pays : International
Organisme : Wellcome Trust
ID : 109130/Z/15/Z
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest AMG reports personal payments and consulting honoraria from Roche Pharma Research & Early Development, Gilead, Janssen, and ViiV, and research funding from Roche Pharma Research & Early Development, Gilead, Janssen and ViiV, outside of the submitted work. Other authors do not declare any conflicts of interest. Please refer to the accompanying ICMJE disclosure forms for further details.

Références

J Hepatol. 2015 Sep;63(3):586-92
pubmed: 25962883
Lancet. 2011 Jul 2;378(9785):73-85
pubmed: 21511329
Lancet Gastroenterol Hepatol. 2018 Jun;3(6):383-403
pubmed: 29599078
Hepatology. 2016 Nov;64(5):1483-1494
pubmed: 27530084
Am J Epidemiol. 1974 May;99(5):325-32
pubmed: 4825599
Gut. 2019 Mar;68(3):381-382
pubmed: 30368454
Int J Evid Based Healthc. 2015 Sep;13(3):147-53
pubmed: 26317388
Stat Med. 2001 Dec 30;20(24):3875-89
pubmed: 11782040
J Viral Hepat. 2019 Jun;26(6):618-626
pubmed: 30771261
BMC Med. 2014 Sep 18;12:145
pubmed: 25242656
Lancet Gastroenterol Hepatol. 2017 Dec;2(12):877-889
pubmed: 28964701
JAMA Oncol. 2017 Dec 1;3(12):1683-1691
pubmed: 28983565
Lancet. 2015 Oct 17;386(10003):1546-55
pubmed: 26231459
Hepatology. 2017 Dec;66(6):1739-1749
pubmed: 27880976
Gut. 2020 Feb;69(2):396-397
pubmed: 30567743
Stat Med. 2001 Jun 30;20(12):1771-82
pubmed: 11406840
Gut. 2000 Mar;46(3):420-6
pubmed: 10673308
J Viral Hepat. 2018 Nov;25(11):1384-1394
pubmed: 29888837
Gastroenterology. 2019 Jan;156(2):461-476.e1
pubmed: 30342879
J Clin Microbiol. 2014 May;52(5):1694-7
pubmed: 24523467
Virol J. 2017 Sep 13;14(1):177
pubmed: 28903779
Lancet Glob Health. 2017 Oct;5(10):e992-e1003
pubmed: 28911765

Auteurs

Alexander J Stockdale (AJ)

Institute of Infection and Global Health, University of Liverpool, Liverpool, United Kingdom; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.

Benno Kreuels (B)

College of Medicine, Blantyre, Malawi; University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

Marc Y R Henrion (MYR)

Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi; Liverpool School of Tropical Medicine, Liverpool, United Kingdom.

Emanuele Giorgi (E)

Centre for Health Informatics, Computing, and Statistics, University of Lancaster, Lancaster, United Kingdom.

Irene Kyomuhangi (I)

Centre for Health Informatics, Computing, and Statistics, University of Lancaster, Lancaster, United Kingdom.

Catherine de Martel (C)

International Agency for Research on Cancer, Lyon, France.

Yvan Hutin (Y)

World Health Organization, Geneva, Switzerland.

Anna Maria Geretti (AM)

Institute of Infection and Global Health, University of Liverpool, Liverpool, United Kingdom. Electronic address: geretti@liverpool.ac.uk.

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Classifications MeSH