Prevalence, Risk Factors and Vaccine Response against Hepatitis B in People Aged 50 Years or Older

Author:

da Cunha Rosa Luana Rocha1,Brandão Leyla Gabriela Verner Amaral1,Moura Winny Éveny Alves1ORCID,Campos Lays Rosa1,Pessoni Grécia Carolina2,de Oliveira Roque e Lima Juliana1,de Moraes José Cássio3,dos Santos Carneiro Megmar Aparecida4,Teles Sheila Araújo1ORCID,Caetano Karlla Antonieta Amorim1ORCID

Affiliation:

1. Faculty of Nursing, Federal University of Goias, Goiânia 74605-080, GO, Brazil

2. Municipal Health Secretariat, Goiânia 74884-900, GO, Brazil

3. Faculty of Medical Sciences of Santa Casa de São Paulo, São Paulo 01224-001, SP, Brazil

4. Institute of Tropical Pathology and Public Health, Federal University of Goias, Goiânia 74690-900, GO, Brazil

Abstract

Universal immunization against hepatitis B has contributed to reducing incidence of the disease, but older individuals remain susceptible to acquiring the hepatitis B virus worldwide. Thus, this study aimed to investigate the epidemiology of HBV infection in individuals aged 50 years and over in central Brazil and to evaluate the immunogenicity of the monovalent vaccine against hepatitis B in this age group using two vaccine regimens. Method: Initially, a cross-sectional and analytical study was carried out to investigate the epidemiology of hepatitis B. Then, individuals without proof of vaccination for hepatitis B were recruited for a phase IV randomized and controlled clinical trial using two vaccine regimens: Intervention Regimen (IR) (three doses of 40 μg at months 0, 1 and 6) vs. Comparison Regimen (CR) (three doses of 20 μg at months 0, 1 and 6). Results: The overall prevalence of exposure to HBV was 16.6% (95% CI: 14.0%–9.5%). In the clinical trial, statistical differences in protective titers were observed (p = 0.007; IR 96% vs. CR 86%) and the geometric mean of anti-HBs titers was higher in individuals who received the IR (518.2 mIU/mL vs. 260.2 mIU/mL). In addition, the proportion of high responders was higher among those who received the IR (65.3%). Conclusion: reinforced doses should be used in individuals aged 50 years or older to overcome the lower efficacy of the vaccine against hepatitis B.

Funder

National Council for Scientific and Technological Development

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

Reference48 articles.

1. World Health Organization (2017). Global Hepatitis Report 2017, World Health Organization. Available online: https://www.who.int/publications/i/item/9789241565455.

2. Global, regional, and national burden of hepatitis B, 1990–2019: A systematic analysis for the Global Burden of Disease Study 2019;Sheena;Lancet Gastroenterol. Hepatol.,2022

3. Hepatitis B vaccine: Demonstration of efficacy in a controlled clinical trial in a high-risk population in the United States;Szmuness;N. Engl. J. Med.,1980

4. World Health Organization (2016). Global Health Sector Strategy on Viral Hepatitis 2016–2021, World Health Organization. Available online: https://apps.who.int/iris/bitstream/handle/10665/246177/WHO-HIV-2016.06-eng.pdf.

5. The epidemiology of hepatitis B and hepatitis C infections in China from 2004 to 2014: An observational population-based study;Liu;J. Viral Hepat.,2018

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