Division of Rheumatology, Department of Internal Medicine, Hanyang University College of Medicine, Guri, Republic of Korea.
J Rheumatol. 2010 Feb;37(2):346-50. doi: 10.3899/jrheum.090436. Epub 2009 Dec 15.
To assess the safety of anti-tumor necrosis factor (TNF-alpha) therapy in patients with rheumatic diseases in terms of the reactivation of potential hepatitis B virus (HBV) occult infection.
Patients who had taken anti-TNF-alpha for the treatment of rheumatic diseases from January 2002 to May 2008 were included in the study. In this patient group, we retrospectively investigated a series of serum aminotransferase levels, HBV serologic status, the type of anti-TNF-alpha therapy, duration of the anti-TNF-alpha treatment, and concurrent use of hepatotoxic drugs.
A total of 266 cases were documented using 3 serologic markers for HBV infection: HBV surface antigen (HBsAg), HBV surface antibody (HBsAb), and HBV core IgG Ab (HBcAb). Of these, 8 cases had chronic hepatitis B (HBsAg+), 170 cases were HBcAb-negative, and 88 cases were identified as having potential HBV occult infections represented by HBsAg-negative and HBcAb-positive, irrespective of the status of the HBsAb. The frequency of clinically significant (> 2 times normal value) and persistent increase (> 2 consecutive tests) of aminotransferase levels was significantly higher in the group with a potential HBV occult infection compared to the HBcAb-negative group. In the multiple logistic regression analysis controlling for various potential confounding factors such as prophylactic anti-tuberculosis medication, methotrexate, nonsteroidal antiinflammatory drugs, and the type of anti-TNF-alpha therapy, only potential HBV occult infection was a significant risk factor for abnormal liver function test (LFT).
All rheumatic patients who plan to take anti-TNF-alpha treatment should undergo a test for HBV serology, including HBcAb, and have a close followup with an LFT test during therapy. Further prospective studies for hepatitis B viral load using HBV-polymerase chain reaction in patients who are HbcAb positive are needed to identify whether the abnormal LFT comes from the reactivation of occult HBV infection.
评估抗肿瘤坏死因子(TNF-α)治疗对风湿性疾病患者的安全性,特别是针对潜在乙型肝炎病毒(HBV)隐匿性感染的再激活。
纳入 2002 年 1 月至 2008 年 5 月期间接受 TNF-α 治疗的风湿性疾病患者。在该患者组中,我们回顾性调查了一系列血清转氨酶水平、HBV 血清学状态、TNF-α 治疗类型、TNF-α 治疗持续时间以及同时使用肝毒性药物的情况。
使用 HBV 感染的 3 项血清学标志物(HBV 表面抗原[HBsAg]、HBV 表面抗体[HBsAb]和 HBV 核心 IgG Ab[HBcAb])记录了 266 例病例。其中,8 例为慢性乙型肝炎(HBsAg+),170 例为 HBcAb 阴性,88 例被确定为 HBV 隐匿性感染,表现为 HBsAg 阴性和 HBcAb 阳性,而不管 HBsAb 的状态如何。与 HBcAb 阴性组相比,隐匿性 HBV 感染组中临床显著(>2 倍正常值)和持续升高(>2 次连续检测)的转氨酶频率明显更高。在控制各种潜在混杂因素(如预防性抗结核药物、甲氨蝶呤、非甾体抗炎药和 TNF-α 治疗类型)的多变量逻辑回归分析中,仅潜在 HBV 隐匿性感染是肝功能试验(LFT)异常的显著危险因素。
所有计划接受 TNF-α 治疗的风湿性疾病患者均应进行 HBV 血清学检测,包括 HBcAb,并在治疗期间密切随访 LFT。需要进一步前瞻性研究 HBV 聚合酶链反应在 HBcAb 阳性患者中的乙型肝炎病毒载量,以确定异常 LFT 是否来自隐匿性 HBV 感染的再激活。