Hepatitis B virus reactivation in patients with rheumatoid arthritis: Analysis of the National Database of Japan

Summary 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 util...

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Veröffentlicht in:Journal of viral hepatitis 2018-11, Vol.25 (11), p.1312-1320
Hauptverfasser: Fujita, M., Sugiyama, M., Sato, Y., Nagashima, K., Takahashi, S., Mizokami, M., Hata, A.
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container_end_page 1320
container_issue 11
container_start_page 1312
container_title Journal of viral hepatitis
container_volume 25
creator Fujita, M.
Sugiyama, M.
Sato, Y.
Nagashima, K.
Takahashi, S.
Mizokami, M.
Hata, A.
description Summary 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.
doi_str_mv 10.1111/jvh.12933
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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.</description><identifier>ISSN: 1352-0504</identifier><identifier>EISSN: 1365-2893</identifier><identifier>DOI: 10.1111/jvh.12933</identifier><identifier>PMID: 29770539</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Deoxyribonucleic acid ; DNA ; Glucocorticoids ; Health risk assessment ; Hepatitis ; Hepatitis B ; Hepatitis B surface antigen ; hepatitis B virus reactivation ; Immunosuppressive agents ; immunosuppressive therapy ; Methotrexate ; real‐world evidence ; Rheumatoid arthritis ; Risk factors ; Statistical analysis</subject><ispartof>Journal of viral hepatitis, 2018-11, Vol.25 (11), p.1312-1320</ispartof><rights>2018 John Wiley &amp; Sons Ltd</rights><rights>2018 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2018 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3533-3d5bc2deedfbc5277392e022a06bfa2c38d122343debcaa2084713de7778a9543</citedby><cites>FETCH-LOGICAL-c3533-3d5bc2deedfbc5277392e022a06bfa2c38d122343debcaa2084713de7778a9543</cites><orcidid>0000-0001-5308-4744 ; 0000-0003-4529-9045</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjvh.12933$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjvh.12933$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29770539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujita, M.</creatorcontrib><creatorcontrib>Sugiyama, M.</creatorcontrib><creatorcontrib>Sato, Y.</creatorcontrib><creatorcontrib>Nagashima, K.</creatorcontrib><creatorcontrib>Takahashi, S.</creatorcontrib><creatorcontrib>Mizokami, M.</creatorcontrib><creatorcontrib>Hata, A.</creatorcontrib><title>Hepatitis B virus reactivation in patients with rheumatoid arthritis: Analysis of the National Database of Japan</title><title>Journal of viral hepatitis</title><addtitle>J Viral Hepat</addtitle><description>Summary 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.</description><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Glucocorticoids</subject><subject>Health risk assessment</subject><subject>Hepatitis</subject><subject>Hepatitis B</subject><subject>Hepatitis B surface antigen</subject><subject>hepatitis B virus reactivation</subject><subject>Immunosuppressive agents</subject><subject>immunosuppressive therapy</subject><subject>Methotrexate</subject><subject>real‐world evidence</subject><subject>Rheumatoid arthritis</subject><subject>Risk factors</subject><subject>Statistical analysis</subject><issn>1352-0504</issn><issn>1365-2893</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kcFO3DAQhi1EVSj00BeoLHEph4A9juMNNwpttwjRS9trNEkmilfZJNjOon37OrvAAam-2OP55pPln7FPUlzIuC5Xm_ZCQq7UATuWKtMJLHJ1OJ81JEKL9Ih98H4lhFSg5Xt2BLkxQqv8mI1LGjHYYD3_yjfWTZ47wirYTbwdem57PvepD54_2dBy19K0xjDYmqMLrZtHr_h1j93WR8nQ8NASf9hNY8dvMWCJnubGHY7Yn7J3DXaePj7vJ-zP92-_b5bJ_a8fP2-u75NKaaUSVeuygpqobspKgzEqBxIAKLKyQajUopYAKlU1lRUiiEVqZCyMMQvMdapO2Je9d3TD40Q-FGvrK-o67GmYfAEiFSZL0x169gZdDZOLr4-UhDTLMw06Uud7qnKD946aYnR2jW5bSFHMMRQxhmIXQ2Q_Pxunck31K_ny7xG43ANPtqPt_03F3d_lXvkPhtuR0A</recordid><startdate>201811</startdate><enddate>201811</enddate><creator>Fujita, M.</creator><creator>Sugiyama, M.</creator><creator>Sato, Y.</creator><creator>Nagashima, K.</creator><creator>Takahashi, S.</creator><creator>Mizokami, M.</creator><creator>Hata, A.</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5308-4744</orcidid><orcidid>https://orcid.org/0000-0003-4529-9045</orcidid></search><sort><creationdate>201811</creationdate><title>Hepatitis B virus reactivation in patients with rheumatoid arthritis: Analysis of the National Database of Japan</title><author>Fujita, M. ; Sugiyama, M. ; Sato, Y. ; Nagashima, K. ; Takahashi, S. ; Mizokami, M. ; Hata, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3533-3d5bc2deedfbc5277392e022a06bfa2c38d122343debcaa2084713de7778a9543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Glucocorticoids</topic><topic>Health risk assessment</topic><topic>Hepatitis</topic><topic>Hepatitis B</topic><topic>Hepatitis B surface antigen</topic><topic>hepatitis B virus reactivation</topic><topic>Immunosuppressive agents</topic><topic>immunosuppressive therapy</topic><topic>Methotrexate</topic><topic>real‐world evidence</topic><topic>Rheumatoid arthritis</topic><topic>Risk factors</topic><topic>Statistical analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujita, M.</creatorcontrib><creatorcontrib>Sugiyama, M.</creatorcontrib><creatorcontrib>Sato, Y.</creatorcontrib><creatorcontrib>Nagashima, K.</creatorcontrib><creatorcontrib>Takahashi, S.</creatorcontrib><creatorcontrib>Mizokami, M.</creatorcontrib><creatorcontrib>Hata, A.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of viral hepatitis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujita, M.</au><au>Sugiyama, M.</au><au>Sato, Y.</au><au>Nagashima, K.</au><au>Takahashi, S.</au><au>Mizokami, M.</au><au>Hata, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis B virus reactivation in patients with rheumatoid arthritis: Analysis of the National Database of Japan</atitle><jtitle>Journal of viral hepatitis</jtitle><addtitle>J Viral Hepat</addtitle><date>2018-11</date><risdate>2018</risdate><volume>25</volume><issue>11</issue><spage>1312</spage><epage>1320</epage><pages>1312-1320</pages><issn>1352-0504</issn><eissn>1365-2893</eissn><abstract>Summary 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.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29770539</pmid><doi>10.1111/jvh.12933</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5308-4744</orcidid><orcidid>https://orcid.org/0000-0003-4529-9045</orcidid></addata></record>
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subjects Deoxyribonucleic acid
DNA
Glucocorticoids
Health risk assessment
Hepatitis
Hepatitis B
Hepatitis B surface antigen
hepatitis B virus reactivation
Immunosuppressive agents
immunosuppressive therapy
Methotrexate
real‐world evidence
Rheumatoid arthritis
Risk factors
Statistical analysis
title Hepatitis B virus reactivation in patients with rheumatoid arthritis: Analysis of the National Database of Japan
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