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肿瘤坏死因子-α抑制剂相关的溃疡性结肠炎

Tumor necrosis factor-alpha inhibitor associated ulcerative colitis.

作者信息

Prescott Kara, Costner Melissa, Cohen Stanley, Kazi Salahuddin

机构信息

Internal Medicine Department, Rheumatic Diseases Division, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

出版信息

Am J Med Sci. 2007 Mar;333(3):137-9. doi: 10.1097/MAJ.0b013e3180312362.

DOI:10.1097/MAJ.0b013e3180312362
PMID:17496730
Abstract

BACKGROUND

Flares or onset of inflammatory bowel disease in association with immunosuppression has been reported in the literature.

METHODS

We studied 4 cases of patients with rheumatic disease who developed or had a flare of ulcerative colitis either after initiation of or while taking a tumor necrosis factor-alpha inhibitor.

RESULTS

We identified 4 patients, three male and one female. Two of the male patients had a seronegative spondyloarthropathy and one had rheumatoid arthritis. The female patient had amyopathic dermatomyositis. Two of the 4 patients had ulcerative colitis prior to tumor necrosis factor-alpha treatment. Both of these patients had quiescent ulcerative colitis that flared after they began taking etanercept. Two patients developed de novo ulcerative colitis while taking a tumor necrosis factor-alpha inhibitor.

CONCLUSIONS

The data presented in these 4 cases supports a temporal relationship between initiating a tumor necrosis factor-alpha inhibitor and onset or flare of ulcerative colitis. These observations raise the possibility that tumor necrosis factor-alpha inhibitor therapy, which has been used as treatment for inflammatory bowel disease, may rarely be a factor in the development of disease.

摘要

背景

文献中已报道炎症性肠病的发作或 flare 与免疫抑制相关。

方法

我们研究了 4 例风湿性疾病患者,他们在开始使用或正在服用肿瘤坏死因子-α抑制剂后发生或出现了溃疡性结肠炎 flare。

结果

我们确定了 4 例患者,3 名男性和 1 名女性。2 名男性患者患有血清阴性脊柱关节病,1 名患有类风湿性关节炎。女性患者患有无肌病性皮肌炎。4 例患者中有 2 例在肿瘤坏死因子-α治疗前患有溃疡性结肠炎。这两名患者在开始服用依那西普后,静止期的溃疡性结肠炎均出现 flare。2 例患者在服用肿瘤坏死因子-α抑制剂时新发溃疡性结肠炎。

结论

这 4 例病例中的数据支持开始使用肿瘤坏死因子-α抑制剂与溃疡性结肠炎的发作或 flare 之间存在时间关系。这些观察结果增加了一种可能性,即一直被用作炎症性肠病治疗方法的肿瘤坏死因子-α抑制剂治疗可能很少是疾病发展的一个因素。

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