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Risk stratification and clinical course of hepatitis B virus reactivation in rheumatoid arthritis patients with resolved infection: final report of a multicenter prospective observational study at Japanese Red Cross Hospital

BACKGROUND: The prophylaxis for hepatitis B virus (HBV) reactivation assumes that hepatic injury after reactivation is often rapidly progressive and can evoke fulminant hepatitis. The incidence and prognosis of reactivation in patients with rheumatoid arthritis (RA) may be different from those recei...

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Autores principales: Fukuda, Wataru, Hanyu, Tadamasa, Katayama, Masaki, Mizuki, Shinichi, Okada, Akitomo, Miyata, Masayuki, Handa, Yuichi, Hayashi, Masatoshi, Koyama, Yoshinobu, Arii, Kaoru, Kitaori, Toshiyuki, Hagiyama, Hiroyuki, Urushidani, Yoshinori, Yamasaki, Takahito, Ikeno, Yoshihiko, Suzuki, Takeshi, Omoto, Atsushi, Sugitani, Toshifumi, Morita, Satoshi, Inokuma, Shigeko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883521/
https://www.ncbi.nlm.nih.gov/pubmed/31779676
http://dx.doi.org/10.1186/s13075-019-2053-1
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author Fukuda, Wataru
Hanyu, Tadamasa
Katayama, Masaki
Mizuki, Shinichi
Okada, Akitomo
Miyata, Masayuki
Handa, Yuichi
Hayashi, Masatoshi
Koyama, Yoshinobu
Arii, Kaoru
Kitaori, Toshiyuki
Hagiyama, Hiroyuki
Urushidani, Yoshinori
Yamasaki, Takahito
Ikeno, Yoshihiko
Suzuki, Takeshi
Omoto, Atsushi
Sugitani, Toshifumi
Morita, Satoshi
Inokuma, Shigeko
author_facet Fukuda, Wataru
Hanyu, Tadamasa
Katayama, Masaki
Mizuki, Shinichi
Okada, Akitomo
Miyata, Masayuki
Handa, Yuichi
Hayashi, Masatoshi
Koyama, Yoshinobu
Arii, Kaoru
Kitaori, Toshiyuki
Hagiyama, Hiroyuki
Urushidani, Yoshinori
Yamasaki, Takahito
Ikeno, Yoshihiko
Suzuki, Takeshi
Omoto, Atsushi
Sugitani, Toshifumi
Morita, Satoshi
Inokuma, Shigeko
author_sort Fukuda, Wataru
collection PubMed
description BACKGROUND: The prophylaxis for hepatitis B virus (HBV) reactivation assumes that hepatic injury after reactivation is often rapidly progressive and can evoke fulminant hepatitis. The incidence and prognosis of reactivation in patients with rheumatoid arthritis (RA) may be different from those receiving organ transplantation and cancer chemotherapy. This study aimed to investigate the incidence, risk factors, and clinical course of HBV reactivation and develop a scoring system for risk stratification in RA patients with resolved infection. METHODS: HBV DNA was measured using real-time polymerase chain reaction, and patient data were collected for 4 years in RA patients with resolved HBV infection who were treated with steroids or synthetic or biologic immunosuppressive drugs. RESULTS: Among 1127 patients, HBV DNA was detected in 57 patients (1.65/100 person-years); none of the reactivated patients exhibited worsening of hepatic function. Multivariate logistical analysis revealed that age > 70 years and HB core antibody (HBcAb) positivity alone were independent risk factors for HBV reactivation. HBV DNA ≥ 2.1 log copies/mL was observed in 15 patients (0.43/100 person-years); seven patients were treated with nucleic acid analogs (NAAs), whereas the remaining eight were observed without treatment. Among reactivated cases, 15 cases changed to HBV DNA-negative status spontaneously, whereas 24 cases remained HBV DNA positive < 2.1 log copies/mL during the observation period. We designed the following scoring system: HBV reactivation risk score = 1 × (age > 70 years) + 2 × (HBcAb positivity alone) + 1 × (treatment other than methotrexate monotherapy). This revealed that patients with the highest score had an odds ratio of 13.01 for HBV reactivation, compared to those with the lowest score. CONCLUSIONS: Rapid progression and poor outcomes after HBV reactivation were not frequent in RA patients with resolved infection. Our new risk scoring system might be useful for screening and optimization of prophylactic treatment by distinguishing patients with significantly lower reactivation risk.
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spelling pubmed-68835212019-12-03 Risk stratification and clinical course of hepatitis B virus reactivation in rheumatoid arthritis patients with resolved infection: final report of a multicenter prospective observational study at Japanese Red Cross Hospital Fukuda, Wataru Hanyu, Tadamasa Katayama, Masaki Mizuki, Shinichi Okada, Akitomo Miyata, Masayuki Handa, Yuichi Hayashi, Masatoshi Koyama, Yoshinobu Arii, Kaoru Kitaori, Toshiyuki Hagiyama, Hiroyuki Urushidani, Yoshinori Yamasaki, Takahito Ikeno, Yoshihiko Suzuki, Takeshi Omoto, Atsushi Sugitani, Toshifumi Morita, Satoshi Inokuma, Shigeko Arthritis Res Ther Research Article BACKGROUND: The prophylaxis for hepatitis B virus (HBV) reactivation assumes that hepatic injury after reactivation is often rapidly progressive and can evoke fulminant hepatitis. The incidence and prognosis of reactivation in patients with rheumatoid arthritis (RA) may be different from those receiving organ transplantation and cancer chemotherapy. This study aimed to investigate the incidence, risk factors, and clinical course of HBV reactivation and develop a scoring system for risk stratification in RA patients with resolved infection. METHODS: HBV DNA was measured using real-time polymerase chain reaction, and patient data were collected for 4 years in RA patients with resolved HBV infection who were treated with steroids or synthetic or biologic immunosuppressive drugs. RESULTS: Among 1127 patients, HBV DNA was detected in 57 patients (1.65/100 person-years); none of the reactivated patients exhibited worsening of hepatic function. Multivariate logistical analysis revealed that age > 70 years and HB core antibody (HBcAb) positivity alone were independent risk factors for HBV reactivation. HBV DNA ≥ 2.1 log copies/mL was observed in 15 patients (0.43/100 person-years); seven patients were treated with nucleic acid analogs (NAAs), whereas the remaining eight were observed without treatment. Among reactivated cases, 15 cases changed to HBV DNA-negative status spontaneously, whereas 24 cases remained HBV DNA positive < 2.1 log copies/mL during the observation period. We designed the following scoring system: HBV reactivation risk score = 1 × (age > 70 years) + 2 × (HBcAb positivity alone) + 1 × (treatment other than methotrexate monotherapy). This revealed that patients with the highest score had an odds ratio of 13.01 for HBV reactivation, compared to those with the lowest score. CONCLUSIONS: Rapid progression and poor outcomes after HBV reactivation were not frequent in RA patients with resolved infection. Our new risk scoring system might be useful for screening and optimization of prophylactic treatment by distinguishing patients with significantly lower reactivation risk. BioMed Central 2019-11-28 2019 /pmc/articles/PMC6883521/ /pubmed/31779676 http://dx.doi.org/10.1186/s13075-019-2053-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Fukuda, Wataru
Hanyu, Tadamasa
Katayama, Masaki
Mizuki, Shinichi
Okada, Akitomo
Miyata, Masayuki
Handa, Yuichi
Hayashi, Masatoshi
Koyama, Yoshinobu
Arii, Kaoru
Kitaori, Toshiyuki
Hagiyama, Hiroyuki
Urushidani, Yoshinori
Yamasaki, Takahito
Ikeno, Yoshihiko
Suzuki, Takeshi
Omoto, Atsushi
Sugitani, Toshifumi
Morita, Satoshi
Inokuma, Shigeko
Risk stratification and clinical course of hepatitis B virus reactivation in rheumatoid arthritis patients with resolved infection: final report of a multicenter prospective observational study at Japanese Red Cross Hospital
title Risk stratification and clinical course of hepatitis B virus reactivation in rheumatoid arthritis patients with resolved infection: final report of a multicenter prospective observational study at Japanese Red Cross Hospital
title_full Risk stratification and clinical course of hepatitis B virus reactivation in rheumatoid arthritis patients with resolved infection: final report of a multicenter prospective observational study at Japanese Red Cross Hospital
title_fullStr Risk stratification and clinical course of hepatitis B virus reactivation in rheumatoid arthritis patients with resolved infection: final report of a multicenter prospective observational study at Japanese Red Cross Hospital
title_full_unstemmed Risk stratification and clinical course of hepatitis B virus reactivation in rheumatoid arthritis patients with resolved infection: final report of a multicenter prospective observational study at Japanese Red Cross Hospital
title_short Risk stratification and clinical course of hepatitis B virus reactivation in rheumatoid arthritis patients with resolved infection: final report of a multicenter prospective observational study at Japanese Red Cross Hospital
title_sort risk stratification and clinical course of hepatitis b virus reactivation in rheumatoid arthritis patients with resolved infection: final report of a multicenter prospective observational study at japanese red cross hospital
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883521/
https://www.ncbi.nlm.nih.gov/pubmed/31779676
http://dx.doi.org/10.1186/s13075-019-2053-1
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