The Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Mod Rheumatol. 2013 Jul;23(4):694-704. doi: 10.1007/s10165-012-0709-7. Epub 2012 Jul 18.
Though concern of hepatitis B virus (HBV) reactivation by antirheumatic agents has limited therapeutic opportunities in HBV-infected rheumatoid arthritis (RA) patients, the relative risks (RR) among such agents have not been clarified.
We compared the reporting of antirheumatic-agent-associated hepatitis B.
We assessed 92 hepatitis B cases and 98,069 controls from a population of 98,161 RA patients registered into the US Food and Drug Administration's (FDA's) adverse event database between 2004 and 2010.
A reporting odds ratio (ROR), a signal suggesting a risk for hepatitis B among antirheumatic agents, was measured.
Treatment with corticosteroids [ROR 2.3 (95% confidence interval 1.3-4.0)], methotrexate [4.9 (3.9-6.0)], rituximab [7.2 (5.3-9.9)], tacrolimus [4.2 (1.5-11.9)], or reporting from Japan [2.2 (1.1-4.2)] were associated with higher signal, whereas adalimumab had a lower ROR [0.2 (0.1-0.4)].
There are known limitations of spontaneous reporting, such as underreporting, the Weber effect, reporting bias, indication bias, and limited clinical information such as HBV status.
Adalimumab's low reporting rate is most likely be due to notoriety. However, the possibility that adalimumab might suppress reactivation of HBV cannot be denied. Until the possibility is clarified in well-designed clinical studies, physicians should use adalimumab cautiously in patients with HBV.
尽管抗风湿药物(antirheumatic agents)会导致乙型肝炎病毒(hepatitis B virus,HBV)再激活,从而限制了乙型肝炎病毒感染的类风湿关节炎(rheumatoid arthritis,RA)患者的治疗选择,但这些药物之间的相对风险(relative risk,RR)尚未明确。
我们比较了抗风湿药物相关乙型肝炎的报告情况。
我们评估了 92 例乙型肝炎病例和 98161 例 RA 患者中的 98069 例对照者,这些患者的数据来自于 2004 年至 2010 年期间美国食品和药物管理局(Food and Drug Administration,FDA)不良事件数据库中的人群。
报告比值比(odds ratio,OR),一种提示抗风湿药物与乙型肝炎相关风险的信号,被用来测量。
皮质类固醇(corticosteroids)[比值比(odds ratio,OR)2.3(95%置信区间 1.3-4.0)]、甲氨蝶呤(methotrexate)[4.9(3.9-6.0)]、利妥昔单抗(rituximab)[7.2(5.3-9.9)]、他克莫司(tacrolimus)[4.2(1.5-11.9)]或来自日本的报告[2.2(1.1-4.2)]与更高的信号相关,而阿达木单抗(adalimumab)的 OR 较低[0.2(0.1-0.4)]。
自发报告存在已知的局限性,例如漏报、韦伯效应、报告偏倚、指示偏倚以及有限的临床信息,如乙型肝炎病毒(hepatitis B virus,HBV)状态。
阿达木单抗(adalimumab)的低报告率很可能归因于其恶名。然而,不能否认阿达木单抗(adalimumab)可能抑制 HBV 再激活的可能性。在精心设计的临床研究中明确这种可能性之前,医生应谨慎使用阿达木单抗(adalimumab)治疗乙型肝炎病毒(hepatitis B virus,HBV)患者。