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接受抗肿瘤坏死因子α治疗的患者患结核病风险增加。

Increased risk of tuberculosis in patients treated with antitumor necrosis factor alpha.

作者信息

Elbek Osman, Uyar Meral, Aydin Neriman, Börekçi Sermin, Bayram Nazan, Bayram Hasan, Dikensoy Oner

机构信息

Department of Pulmonary Diseases, Faculty of Medicine, University of Gaziantep, Gaziantep 27035, Turkey.

出版信息

Clin Rheumatol. 2009 Apr;28(4):421-6. doi: 10.1007/s10067-008-1067-x. Epub 2008 Dec 4.

Abstract

Drugs which antagonize tumor necrosis factor alpha (TNF-alpha) are known to increase the risk of tuberculosis. We aimed to evaluate the risk of tuberculosis in patients treated with anti-TNF-alpha, in Turkey. Two hundred and forty patients receiving anti-TNF-alpha, from December 2005 to December 2007, were included in the study. All participants provided a history and underwent a physical examination, a chest X-ray, and a tuberculin skin test. Isoniazid treatment was initiated in those patients with a latent infection, and they were followed up at 2-month intervals. A Bacillus Calmette-Guerin (BCG) scar was present in 184 patients (77.6%). The mean tuberculin skin test induration of patients on admission was 10.7+/-7.0 mm. Male gender and the presence of a BCG scar were predictors of a higher tuberculin skin test result (P<0.05), while there was no significant effect of age on the tuberculin skin test (P>0.05). Of the 240 subjects, 229 (95.4%) received methotrexate or corticosteroid treatment prior to anti-TNF-alpha therapy. Isoniazid treatment preceded anti-TNF-alpha administration in 185 (77.1%) of the 240 patients. Two patients developed tuberculosis (incidence 833/100,000). There was no correlation between initial and 12-month tuberculin skin test results (P>0.05). Tuberculin skin test conversion was detected in five subjects during the 12-month follow-up; however, none developed active tuberculosis. One patient developed a drug reaction secondary to etanercept, and another demonstrated hepatotoxicity due to isoniazid. This study shows that anti-TNF-alpha therapy increases the risk of tuberculosis, despite treatment of latent infection.

摘要

已知拮抗肿瘤坏死因子α(TNF-α)的药物会增加患结核病的风险。我们旨在评估土耳其接受抗TNF-α治疗的患者患结核病的风险。纳入了2005年12月至2007年12月期间接受抗TNF-α治疗的240例患者。所有参与者均提供了病史,并接受了体格检查、胸部X光检查和结核菌素皮肤试验。对那些潜伏感染的患者开始使用异烟肼治疗,并每2个月进行一次随访。184例患者(77.6%)有卡介苗(BCG)瘢痕。入院时患者结核菌素皮肤试验硬结的平均值为10.7±7.0毫米。男性和存在BCG瘢痕是结核菌素皮肤试验结果较高的预测因素(P<0.05),而年龄对结核菌素皮肤试验无显著影响(P>0.05)。在240名受试者中,229名(95.4%)在抗TNF-α治疗前接受了甲氨蝶呤或皮质类固醇治疗。240例患者中有185例(77.1%)在抗TNF-α给药前接受了异烟肼治疗。2例患者发生了结核病(发病率833/100,000)。初始和12个月时的结核菌素皮肤试验结果之间无相关性(P>0.05)。在12个月的随访期间,5名受试者检测到结核菌素皮肤试验结果转换;然而,没有人发生活动性结核病。1例患者发生了依那西普继发的药物反应,另1例因异烟肼出现肝毒性。这项研究表明,尽管对潜伏感染进行了治疗,但抗TNF-α治疗仍会增加患结核病的风险。

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