Division of Gastroenterology and Hepatology, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7080, USA.
Am J Gastroenterol. 2010 Sep;105(9):1986-93. doi: 10.1038/ajg.2010.124. Epub 2010 Mar 30.
Isotretinoin is commonly prescribed for the treatment of severe acne. Although cases of inflammatory bowel disease (IBD) have been reported in isotretinoin users, a causal association remains unproven.
We performed a case-control study using a large insurance claims database. Incident cases of IBD were identified and matched to three controls on the basis of age, gender, geographical region, health plan, and length of enrollment. Isotretinoin exposure was assessed in a 12-month period before case ascertainment. Conditional logistic regression was used to adjust for matching variables.
The study population comprised 8,189 cases (3,664 Crohn's disease (CD), 4,428 ulcerative colitis (UC), and 97 IBD unspecified) and 21,832 controls. A total of 60 subjects (24 cases and 36 controls) were exposed to isotretinoin. UC was strongly associated with previous isotretinoin exposure (odds ratio (OR) 4.36, 95% confidence interval (CI): 1.97, 9.66). However, there was no apparent association between isotretinoin and CD (OR 0.68, 95% CI: 0.28, 1.68). Increasing dose of isotretinoin was associated with elevated risk of UC (OR per 20 mg increase in dose: 1.50, 95% CI: 1.08, 2.09). Compared with non-users, the risk of UC was highest in those exposed to isotretinoin for more than 2 months (OR 5.63, 95% CI: 2.10, 15.03).
UC but not CD is associated with previous isotretinoin exposure. Higher dose of isotretinoin seems to augment this risk. Although the absolute risk of developing UC after taking isotretinoin is likely quite small, clinicians prescribing isotretinoin as well as prospective patients should be aware of this possible association.
异维 A 酸常用于治疗严重痤疮。虽然有报道称异维 A 酸使用者患有炎症性肠病(IBD),但两者之间的因果关系尚未得到证实。
我们使用大型保险索赔数据库进行了病例对照研究。根据年龄、性别、地理区域、健康计划和入组时间,确定了 IBD 病例,并与 3 名对照进行匹配。在病例确诊前的 12 个月内评估异维 A 酸暴露情况。采用条件逻辑回归来调整匹配变量。
研究人群包括 8189 例病例(3664 例克罗恩病(CD)、4428 例溃疡性结肠炎(UC)和 97 例 IBD 未特指)和 21832 例对照。共有 60 名受试者(24 例病例和 36 例对照)接受了异维 A 酸治疗。UC 与先前异维 A 酸暴露显著相关(比值比(OR)4.36,95%置信区间(CI):1.97,9.66)。然而,异维 A 酸与 CD 之间似乎没有明显关联(OR 0.68,95% CI:0.28,1.68)。异维 A 酸剂量增加与 UC 风险升高相关(剂量每增加 20mg,OR 为 1.50,95% CI:1.08,2.09)。与未使用者相比,暴露于异维 A 酸超过 2 个月的患者发生 UC 的风险最高(OR 5.63,95% CI:2.10,15.03)。
UC 而非 CD 与先前异维 A 酸暴露有关。较高剂量的异维 A 酸似乎会增加这种风险。尽管服用异维 A 酸后发生 UC 的绝对风险可能相当小,但开具异维 A 酸处方的临床医生和潜在患者都应该意识到这种可能的关联。