Jun Yu Kyung, Yoon Hyuk, Koh Seong-Joon, Kim A Hyeon, Kim Kwang Woo, Park Jun Won, Lee Hyun Jung, Kang Hyoun Woo, Im Jong Pil, Park Young Soo, Kim Joo Sung
Division of Gastroenterology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Seoul National University College of Medicine, Seoul, Korea.
Intest Res. 2023 Apr;21(2):244-251. doi: 10.5217/ir.2022.00057. Epub 2022 Aug 8.
BACKGROUND/AIMS: Patients with inflammatory bowel disease (IBD) are diagnosed with ankylosing spondylitis (AS) often. However, the disease course of patients with both IBD and AS is not well understood. This study aims to evaluate the effect of concomitant AS on IBD outcomes.
Among the 4,722 patients with IBD who were treated in 3 academic hospitals from 2004 to 2021, 55 were also diagnosed with AS (IBD-AS group). Based on patients' electronic medical records, the outcomes of IBD in IBD-AS group and IBD group without AS (IBD-only group) were appraised.
The proportion of patients treated with biologics or small molecule therapies was significantly higher in IBD-AS group than the proportion in IBD-only group (27.3% vs. 12.7%, P= 0.036). Patients with both ulcerative colitis and AS had a significantly higher risk of biologics or small molecule therapies than patients with only ulcerative colitis (P< 0.001). For univariable logistic regression, biologics or small molecule therapies were associated with concomitant AS (odds ratio, 4.099; 95% confidence interval, 1.863-9.021; P< 0.001) and Crohn's disease (odds ratio, 3.552; 95% confidence interval, 1.590-7.934; P= 0.002).
Concomitant AS is associated with the high possibility of biologics or small molecule therapies for IBD. IBD patients who also had AS may need more careful examination and active treatment to alleviate the severity of IBD.
背景/目的:炎症性肠病(IBD)患者常被诊断出患有强直性脊柱炎(AS)。然而,IBD和AS患者的疾病进程尚未得到充分了解。本研究旨在评估AS合并症对IBD结局的影响。
在2004年至2021年期间于3家学术医院接受治疗的4722例IBD患者中,有55例也被诊断出患有AS(IBD-AS组)。基于患者的电子病历,对IBD-AS组和无AS的IBD组(仅IBD组)的IBD结局进行评估。
IBD-AS组接受生物制剂或小分子疗法治疗的患者比例显著高于仅IBD组(27.3%对12.7%,P = 0.036)。溃疡性结肠炎合并AS的患者接受生物制剂或小分子疗法的风险显著高于仅患有溃疡性结肠炎的患者(P < 0.001)。单因素逻辑回归分析显示,生物制剂或小分子疗法与AS合并症(优势比,4.099;95%置信区间,1.863 - 9.021;P < 0.001)和克罗恩病(优势比,3.552;95%置信区间,1.590 - 7.934;P = 0.002)相关。
AS合并症与IBD患者接受生物制剂或小分子疗法的可能性较高有关。同时患有AS的IBD患者可能需要更仔细的检查和积极的治疗,以减轻IBD的严重程度。