Division of Gastroenterology-Hepatology, Department of Internal Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.
School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University Medical Center, Maastricht, The Netherlands.
Am J Gastroenterol. 2018 Mar;113(3):384-395. doi: 10.1038/ajg.2017.482. Epub 2018 Jan 9.
Corticosteroid-free remission is an emerging treatment goal in the management of inflammatory bowel disease (IBD). In the population-based Inflammatory Bowel Disease South Limburg cohort, we studied temporal changes in corticosteroid use and assessed the corticosteroid-sparing effects of immunomodulators and biologicals in real life.
In total, 2,823 newly diagnosed patients with Crohn's disease (CD) or ulcerative colitis (UC) were included. Corticosteroid exposure and cumulative days of use were compared between patients diagnosed in 1991-1998 (CD: n=316, UC: n=539), 1999-2005 (CD: n=387, UC: n=527), and 2006-2011 (CD: n=459, UC: n=595). Second, the corticosteroid-sparing effects of immunomodulators and biologicals were assessed.
Over time, the corticosteroid exposure rate was stable (54.0% in CD and 31.4% in UC), even as the cumulative corticosteroid use in the first disease year (CD: 83 days (interquartile range (IQR) 35-189), UC: 62 days (IQR 0-137)). On the long-term, a gradual decrease in cumulative corticosteroid use was seen in CD (era '91-'98: 366 days (IQR 107-841), era '06-'11: 120 days (IQR 72-211), P<0.01), whereas in UC an initial decrease was observed (era '91-'98: 184 days (IQR 86-443), era '99-'05: 166 days (IQR 74-281), P=0.03), and stabilization thereafter. Immunomodulator and biological users had a lower risk of requiring corticosteroids than matched controls in CD only (33.6% vs. 49.9%, P<0.01, and 25.7% vs. 38.2%, P=0.04, respectively).
In a real-world setting, more recently diagnosed IBD patients used lower amounts of corticosteroids as of the second year of disease. For CD, a significant association was found with the use of immunomodulators and biologicals. These conclusions support the increasing use of these treatment modalities.
在炎症性肠病(IBD)的治疗中,无皮质类固醇缓解是一个新兴的治疗目标。在基于人群的炎症性肠病南林堡队列中,我们研究了皮质类固醇使用的时间变化,并评估了免疫调节剂和生物制剂在现实生活中的皮质类固醇节省作用。
共纳入 2823 例新诊断的克罗恩病(CD)或溃疡性结肠炎(UC)患者。比较了 1991-1998 年(CD:n=316,UC:n=539)、1999-2005 年(CD:n=387,UC:n=527)和 2006-2011 年(CD:n=459,UC:n=595)诊断的患者之间的皮质类固醇暴露情况和累积使用天数。其次,评估了免疫调节剂和生物制剂的皮质类固醇节省作用。
随着时间的推移,皮质类固醇的暴露率保持稳定(CD 为 54.0%,UC 为 31.4%),即使在疾病的第一年累积使用皮质类固醇(CD:83 天(四分位距(IQR)35-189),UC:62 天(IQR 0-137))。从长期来看,CD 中累积皮质类固醇的使用量逐渐减少('91-'98 时代:366 天(IQR 107-841),'06-'11 时代:120 天(IQR 72-211),P<0.01),而 UC 则观察到最初的减少('91-'98 时代:184 天(IQR 86-443),'99-'05 时代:166 天(IQR 74-281),P=0.03),此后趋于稳定。与匹配的对照组相比,仅在 CD 中,免疫调节剂和生物制剂的使用者需要皮质类固醇的风险较低(33.6%比 49.9%,P<0.01,和 25.7%比 38.2%,P=0.04)。
在现实环境中,最近诊断的 IBD 患者在疾病的第二年使用的皮质类固醇量较低。对于 CD,与免疫调节剂和生物制剂的使用存在显著相关性。这些结论支持越来越多地使用这些治疗方式。