Crockett Seth D, Gulati Ajay, Sandler Robert S, Kappelman Michael D
Division of Gastroenterology and Hepatology, Department of Medicine, University of North Carolina at Chapel Hill, CB#7080, Chapel Hill, North Carolina 27599, USA.
Am J Gastroenterol. 2009 Oct;104(10):2387-93. doi: 10.1038/ajg.2009.334.
Case reports have described a possible association between isotretinoin and inflammatory bowel disease (IBD). We critically appraised the literature on this association to assess whether it supports a causal relationship.
We systematically searched for case reports, case series, and clinical trials assessing this association. We then applied the Hill criteria to evaluate causality.
Twelve case reports and one case series reported an association between isotretinoin use and subsequent development of IBD. Cases occurred in seven countries over a 23-year period and differed with respect to reported isotretinoin dose, duration of treatment before development of disease, whether disease developed on or off medication, and clinical presentation of disease. No prospective or retrospective studies have examined the relationship between isotretinoin and IBD. An estimated 59 coincident cases of IBD would be expected in isotretinoin users each year, assuming no increased risk. Alternative explanations may account for the sequence of events seen in case reports. Strength, specificity, and consistency of the association are lacking.
Current evidence is insufficient to confirm or refute a causal association between isotretinoin and IBD. Additional prospective or well-designed retrospective (e.g., case-control) pharmacoepidemiological studies are needed to definitively establish causality.
病例报告描述了异维A酸与炎症性肠病(IBD)之间可能存在的关联。我们对有关该关联的文献进行了严格评估,以判断其是否支持因果关系。
我们系统检索了评估此关联的病例报告、病例系列和临床试验。然后应用希尔标准评估因果关系。
12篇病例报告和1篇病例系列报告了异维A酸使用与IBD后续发病之间的关联。在23年期间,7个国家出现了相关病例,报告的异维A酸剂量、发病前治疗持续时间、疾病在用药期间还是停药后发生以及疾病临床表现各不相同。尚无前瞻性或回顾性研究探讨异维A酸与IBD之间的关系。假设无风险增加,预计每年异维A酸使用者中会出现约59例IBD巧合病例。病例报告中所见事件顺序可能有其他解释。该关联缺乏强度、特异性和一致性。
目前的证据不足以证实或反驳异维A酸与IBD之间的因果关联。需要更多的前瞻性或设计良好的回顾性(如病例对照)药物流行病学研究来明确确定因果关系。