TY - JOUR
T1 - Hepatitis B virus reactivation in patients with rheumatoid arthritis
T2 - Analysis of the National Database of Japan
AU - Fujita, M.
AU - Sugiyama, M.
AU - Sato, Y.
AU - Nagashima, K.
AU - Takahashi, S.
AU - Mizokami, M.
AU - Hata, A.
N1 - Funding Information:
We greatly appreciate the valuable help and support of the staff members of MHLW in Japan, particularly Kensuke Yoshimura, M.D., M.P.H. and the staff of Nissay Information Technology Co., LTD, particularly, Kunihiko Tanno, Hiroki Morimoto and Yayoi Ishikawa. We would like to thank Editage (www.editage.jp) for English language editing. This study was supported by a grant from the Japan Agency for Medical Research and Development Program for Basic and Clinical Research on Hepatitis (JP17fk0210302).
Publisher Copyright:
© 2018 John Wiley & Sons Ltd
PY - 2018/11
Y1 - 2018/11
N2 - This study aimed to determine the incidence and risk factors for hepatitis B virus (HBV) reactivation in patients with rheumatoid arthritis (RA) undergoing immunosuppressive therapy. The National Database of Japan, in which insurance claim data have been comprehensively accumulated, was utilized. The subjects were 76 641 RA patients who were plausibly initiated on immunosuppressive therapy from April 2013 to March 2014. Laboratory tests of the hepatitis B surface antigen, anti-hepatitis B virus surface antibody, and anti-hepatitis B virus core antibody were performed in 28.23%, 12.52% and 14.63% of patients, respectively, when the therapy was initiated. We found that HBV reactivation and fulminant hepatitis occurred in both the patients with and without HBV DNA monitoring, indicating insufficient monitoring in Japan during the study. The cumulative incidence of HBV reactivation over 24 months was 1.57% (95% confidence interval [CI] = 1.28%-1.92%) in the monitoring group, which consisted of those with resolved HBV infection. Glucocorticoid administration was a potent risk factor for HBV reactivation (hazard ratio [HR] = 1.70, 95% CI = 1.26-2.29, P =.001 in all subjects, and HR = 1.82, 95% CI = 1.18-2.81, P =.007 in the nonmonitoring group), although it was not statistically significant in the monitoring group (HR = 1.49, 95% CI = 0.99-2.26 and P =.057). No significant risk difference was observed between single administration of methotrexate and biological drugs.
AB - This study aimed to determine the incidence and risk factors for hepatitis B virus (HBV) reactivation in patients with rheumatoid arthritis (RA) undergoing immunosuppressive therapy. The National Database of Japan, in which insurance claim data have been comprehensively accumulated, was utilized. The subjects were 76 641 RA patients who were plausibly initiated on immunosuppressive therapy from April 2013 to March 2014. Laboratory tests of the hepatitis B surface antigen, anti-hepatitis B virus surface antibody, and anti-hepatitis B virus core antibody were performed in 28.23%, 12.52% and 14.63% of patients, respectively, when the therapy was initiated. We found that HBV reactivation and fulminant hepatitis occurred in both the patients with and without HBV DNA monitoring, indicating insufficient monitoring in Japan during the study. The cumulative incidence of HBV reactivation over 24 months was 1.57% (95% confidence interval [CI] = 1.28%-1.92%) in the monitoring group, which consisted of those with resolved HBV infection. Glucocorticoid administration was a potent risk factor for HBV reactivation (hazard ratio [HR] = 1.70, 95% CI = 1.26-2.29, P =.001 in all subjects, and HR = 1.82, 95% CI = 1.18-2.81, P =.007 in the nonmonitoring group), although it was not statistically significant in the monitoring group (HR = 1.49, 95% CI = 0.99-2.26 and P =.057). No significant risk difference was observed between single administration of methotrexate and biological drugs.
KW - hepatitis B virus reactivation
KW - immunosuppressive therapy
KW - real-world evidence
KW - rheumatoid arthritis
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U2 - 10.1111/jvh.12933
DO - 10.1111/jvh.12933
M3 - Article
C2 - 29770539
AN - SCOPUS:85055463217
SN - 1352-0504
VL - 25
SP - 1312
EP - 1320
JO - Journal of Viral Hepatitis
JF - Journal of Viral Hepatitis
IS - 11
ER -