Comparison of the Clinical Features of Hepatitis A in People Living with HIV between Pandemics in 1999-2000 and 2017-2018 in the Metropolitan Area of Japan.


Journal

Japanese journal of infectious diseases
ISSN: 1884-2836
Titre abrégé: Jpn J Infect Dis
Pays: Japan
ID NLM: 100893704

Informations de publication

Date de publication:
24 Mar 2020
Historique:
pubmed: 2 11 2019
medline: 21 10 2020
entrez: 1 11 2019
Statut: ppublish

Résumé

Since 2017, hepatitis A virus (HAV) infection has been an epidemic among men who have sex with men (MSM) in Japan. We have come across 11 MSM patients with hepatitis A who were also infected with HIV. In 1999-2000, we came across 5 HIV-infected patients with hepatitis A. Since the conditions of current HIV-infected patients have changed owing to the recent progress in anti-HIV therapies, we compared clinical features of hepatitis A between patients in 2017-2018 and those in 1999-2000. By comparing the background characteristics of the patients, we found that the CD4/CD8 ratio was significantly higher in the 2017-2018 group. After the onset of hepatitis, peak levels of hepatic transaminases were found to be higher in the 2017-2018 group, suggesting severe hepatocellular damage. In contrast, neither the peak level of total bilirubin nor the nadir of prothrombin time was significantly different among the 2 groups. We also analyzed the HAV genome derived from some of the recently infected patients, and found that the HAV strains were almost the same among these patients; slight differences were observed from the previously identified strain. Thus, we concluded that the recovery of immunity by recent anti-HIV therapies may result in more severe hepatocellular damages and differences in clinical features.

Identifiants

pubmed: 31666497
doi: 10.7883/yoken.JJID.2019.275
doi:

Substances chimiques

Anti-Retroviral Agents 0
Hepatitis A Antibodies 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

89-95

Auteurs

Michiko Koga (M)

Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, The University of Tokyo.

Lay Ahyoung Lim (LA)

Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of The Institute of Medical Science, The University of Tokyo.

Masato Ogishi (M)

Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, The University of Tokyo.

Hidenori Satoh (H)

Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of The Institute of Medical Science, The University of Tokyo.

Tadashi Kikuchi (T)

Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of The Institute of Medical Science, The University of Tokyo.

Eisuke Adachi (E)

Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of The Institute of Medical Science, The University of Tokyo.

Ryuichi Sugiyama (R)

Department of Virology II, National Institute of Infectious Diseases.

Tomoko Kiyohara (T)

Department of Virology II, National Institute of Infectious Diseases.

Ryosuke Suzuki (R)

Department of Virology II, National Institute of Infectious Diseases.

Masamichi Muramatsu (M)

Department of Virology II, National Institute of Infectious Diseases.

Tomohiko Koibuchi (T)

Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of The Institute of Medical Science, The University of Tokyo.

Takeya Tsutsumi (T)

Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, The University of Tokyo.

Hiroshi Yotsuyanagi (H)

Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, The University of Tokyo.
Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of The Institute of Medical Science, The University of Tokyo.

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