Eliminating Hepatitis C Virus Among Human Immunodeficiency Virus-Infected Men Who Have Sex With Men in Berlin: A Modeling Analysis.


Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
08 10 2019
Historique:
received: 26 02 2019
accepted: 11 07 2019
pubmed: 14 7 2019
medline: 21 5 2020
entrez: 14 7 2019
Statut: ppublish

Résumé

Despite high hepatitis C virus (HCV) treatment rates, HCV incidence among human immunodeficiency virus (HIV)-infected men who have sex with men (HIV-infected MSM) in Germany rose before HCV direct-acting antivirals (DAAs). We model what intervention can achieve the World Health Organization (WHO) elimination target of an 80% reduction in HCV incidence by 2030 among HIV-infected MSM in Berlin. An HCV transmission model among HIV-diagnosed MSM was calibrated to Berlin (rising HCV incidence and high rates of HCV testing and treatment). We modeled the HCV incidence among HIV-diagnosed MSM in Berlin until 2030 (relative to 2015 WHO baseline) under scenarios of DAA scale-up with or without behavior change (among HIV-diagnosed MSM and/or all MSM). Continuing current treatment rates will marginally reduce the HCV incidence among HIV-diagnosed MSM in Berlin by 2030. Scaling up DAA treatment rates, beginning in 2018, to 100% of newly diagnosed HCV infections within 3 months of diagnosis and 25% each year of previously diagnosed and untreated HCV infections could reduce the HCV incidence by 61% (95% confidence interval, 55.4%-66.7%) by 2030. The WHO target would likely be achieved by combining DAA scale-up with a 40% reduction in HCV transmission among HIV-diagnosed MSM and a 20% reduction among HIV-undiagnosed or HIV-uninfected MSM. HCV elimination among HIV-infected MSM in Berlin likely requires combining DAA scale-up with moderately effective behavioral interventions to reduce risk among all MSM.

Sections du résumé

BACKGROUND
Despite high hepatitis C virus (HCV) treatment rates, HCV incidence among human immunodeficiency virus (HIV)-infected men who have sex with men (HIV-infected MSM) in Germany rose before HCV direct-acting antivirals (DAAs). We model what intervention can achieve the World Health Organization (WHO) elimination target of an 80% reduction in HCV incidence by 2030 among HIV-infected MSM in Berlin.
METHODS
An HCV transmission model among HIV-diagnosed MSM was calibrated to Berlin (rising HCV incidence and high rates of HCV testing and treatment). We modeled the HCV incidence among HIV-diagnosed MSM in Berlin until 2030 (relative to 2015 WHO baseline) under scenarios of DAA scale-up with or without behavior change (among HIV-diagnosed MSM and/or all MSM).
RESULTS
Continuing current treatment rates will marginally reduce the HCV incidence among HIV-diagnosed MSM in Berlin by 2030. Scaling up DAA treatment rates, beginning in 2018, to 100% of newly diagnosed HCV infections within 3 months of diagnosis and 25% each year of previously diagnosed and untreated HCV infections could reduce the HCV incidence by 61% (95% confidence interval, 55.4%-66.7%) by 2030. The WHO target would likely be achieved by combining DAA scale-up with a 40% reduction in HCV transmission among HIV-diagnosed MSM and a 20% reduction among HIV-undiagnosed or HIV-uninfected MSM.
DISCUSSION
HCV elimination among HIV-infected MSM in Berlin likely requires combining DAA scale-up with moderately effective behavioral interventions to reduce risk among all MSM.

Identifiants

pubmed: 31301142
pii: 5532024
doi: 10.1093/infdis/jiz367
pmc: PMC7360352
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1635-1644

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI036214
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA037773
Pays : United States

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

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Auteurs

Natasha K Martin (NK)

Division of Infectious Diseases and Global Public Health, University of California San Diego.

Klaus Jansen (K)

Robert-Koch Institut, Berlin, Germany.

Matthias An der Heiden (M)

Robert-Koch Institut, Berlin, Germany.

Christoph Boesecke (C)

Department of Medicine, University of Bonn, Germany.

Anders Boyd (A)

INSERM, Paris, Institut Pierre Louis d'Epidémiologie et de Santé Publique, France.
Department of Infectious Diseases, Research and Prevention, Public Health Service of Amsterdam, Netherlands.

Knud Schewe (K)

Infektionsmedizinisches Centrum Hamburg, Germany.

Axel Baumgarten (A)

Center for Infectiology, Berlin, Germany.

Thomas Lutz (T)

Infektiologikum, Frankfurt, Germany.

Stefan Christensen (S)

Centrum für Innere Medizin, Muenster, Germany.

Alexander Thielen (A)

Insitute for Immunology and Genetics, Kaiserslautern, Germany.

Stefan Mauss (S)

Center for HIV and Hepatogastroenterology, Duesseldorf, Germany.

Jürgen K Rockstroh (JK)

Department of Medicine, University of Bonn, Germany.

Britt Skaathun (B)

Division of Infectious Diseases and Global Public Health, University of California San Diego.

Patrick Ingiliz (P)

Center for Infectiology, Berlin, Germany.
Department of Hepatology and Gastroenterology, Charité University Medical Center Berlin, Germany.

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