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Commensurate incidence and outcomes of liver enzyme elevation between anti-tumor necrosis factor users with or without prior hepatitis B virus infections

机译:抗肿瘤坏死因子患者肝酶升高的发病率和结果,或没有现有乙型肝炎病毒感染

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摘要

Potential hepatoxicity is an important clinical concern when administering immunosuppressive therapies to patients infected by hepatitis B virus (HBV). Tumor necrosis factor inhibitors (anti-TNF) increase the likelihood of hepatitis consequent to HBV reactivation, but reported risks and outcomes vary. We determined the risks of liver enzyme elevation in anti-rheumatic drug users from an HBV-endemic region with differing HBV serostatus.We established retrospective cohorts with rheumatoid arthritis, ankylosing spondylitis, or psoriasis/psoriatic arthritis who: 1) received anti-TNF agents from 1 January 2004 to 30 June 2013; 2) received care from 1 June 2011 to 30 June 2013 but only ever used conventional disease-modifying anti-rheumatic drugs (DMARDs). Serology results defined three subgroups: HBV surface antigen positive (HBsAg+), HBsAg negative/HBV core antibody positive (HBsAg-/HBcAb+), or uninfected. We compared incidences of serum alanine aminotransferase (ALT) exceeding twice the upper reference limit between HBV serostatus subgroups in each treatment cohort.Among 783 patients treated with anti-TNF (n = 472) or DMARDs only (n = 311), HBsAg-/HBcAb+ anti-TNF users had incidence of ALT elevation commensurate with uninfected counterparts (6.1 vs. 6.0/100 person-years), compared to 19.6/100 person-years in HBsAg+ patients (standardized rate ratio 3.3, 95% CI 1.3-8.2); none effected had severe or fatal hepatitis and ALT levels in all HBsAg-/HBcAb+ patients remained stable, mostly normalizing spontaneously, or after moderating treatment. Patterns of of ALT elevation associated with differing HBV serostatus in the DMARD cohort, resembled those in anti-TNF users.In this large HBV-endemic cohort, the absolute incidence of ALT elevation in anti-TNF users was more than three-fold higher in HBsAg+ patients than in uninfected counterparts; however, no such association was evident in patients with HBsAg-/HBcAb+ serotype, whose risk and outcomes of liver enzyme elevation were similar to uninfected patients, suggesting that anti-TNF use by HBsAg-/HBcAb+ patients is probably safe.
机译:潜在的肝毒性是对由乙型肝炎病毒(HBV)感染的患者施用免疫抑制疗法时的重要临床关注。肿瘤坏死因子抑制剂(抗TNF)增加了肝炎对HBV再活化的可能性,但报告的风险和结果不同。我们确定了来自HBV-流行区域的肝酶升高的风险,具有不同的HBV Serostatume。我们建立了类风湿性关节炎,强直性脊柱炎或牛皮癣/银屑病关节炎的回顾队列:1)接受抗TNF药剂2004年1月1日至2013年6月30日; 2)从2011年6月1日至2013年6月30日收到护理,但只使用常规疾病改性抗风湿药物(DMARDS)。血清学结果定义了三个亚组:HBV表面抗原阳性(HBsAg +),HBsAg阴性/ HBV核心抗体阳性(HBsAg- / Hbcab +),或未感染。我们比较了血清丙氨酸氨基转移酶(ALT)的血清丙氨酸氨基转移酶(ALT)的发生率超过每种治疗的核血清783患者的HBV Serostarus亚组的上参考限制两倍(n = 472)或DMARDS(n = 311),HBsAg- / Hbcab +抗TNF用户的发病率与未感染的同行(6.1与6.0 / 100人)相应的Alt抬高的发病率为19.6 / 100人群,患者(标准化率比3.3,95%CI 1.3-8.2) ;没有影响患有严重或致命的肝炎和所有HBsAg-/ Hbcab +患者的ALT水平保持稳定,大部分自发地归一成,或者在调节治疗后。与DMARD队列中不同HBV Serostatus相关的Alt升降的模式类似于抗TNF用户中的那些。在这种大型HBV-特点队列中,抗TNF用户的ALT升高的绝对发病率超过三倍以上HBsAg +患者比未感染的同行;然而,HBsAg-/ Hbcab +血清型患者没有明显的这种关联,其风险和肝脏酶升高的结​​果与未感染的患者类似,表明HBsAg- / Hbcab +患者的抗TNF使用可能是安全的。

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