Department of Pediatrics, Chungnam National University Hospital, Daejeon, Korea.
Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
Gut Liver. 2021 Nov 15;15(6):851-857. doi: 10.5009/gnl20279.
BACKGROUND/AIMS: : Recently, the treatment of Crohn's disease (CD) has changed to a treat-to-target strategy, in which disease progression is prevented with early intervention. We analyzed the long-term evolution of nonstricturing, nonpenetrating (B1) disease at diagnosis and factors related to disease evolution in pediatric CD.
We retrospectively analyzed 402 patients between 2000 and 2013 who were younger than 18 years and had B1 disease at CD diagnosis. The median follow-up was 6.1 years (range, 1 to 13 years). The cumulative probabilities of developing stricturing (B2) or penetrating (B3) disease and associations between risk factors and disease behavior evolution were evaluated.
Among the 402 patients, 75 (18.7%) had B2 or B3 disease by the final follow-up. The cumulative probabilities of disease behavior evolution were 18.3%, 34.3%, and 50.9% at 5, 10, and 13 years, respectively. Patients whose disease progressed had an increased risk of intestinal resection (hazard ratio [HR], 3.61; 95% confidence interval [CI], 2.25 to 6.03; p<0.001). First-degree family history of inflammatory bowel disease (HR, 2.38; 95% CI, 1.07 to 5.28; p=0.032), isolated ileal involvement at diagnosis (HR, 7.55; 95% CI, 1.04 to 15.57; p=0.045), and positive anti-Saccharomyces cerevisiae antibody titers (HR, 2.10; 95% CI, 1.03 to 4.25; p=0.040) were associated with disease behavior evolution. Early treatment with biologics significantly reduced disease progression (HR, 0.46; 95% CI, 0.79 to 3.39; p=0.042).
This study suggests that early aggressive therapy should be considered in B1 behavior pediatric CD patients with risk factors of disease evolution to improve long-term outcomes.
背景/目的:最近,克罗恩病(CD)的治疗已转变为一种针对目标的治疗策略,即通过早期干预来预防疾病进展。我们分析了初诊时非狭窄非穿透(B1)疾病的长期演变以及儿科 CD 中与疾病演变相关的因素。
我们回顾性分析了 2000 年至 2013 年间 402 例年龄小于 18 岁且 CD 初诊时为 B1 疾病的患者。中位随访时间为 6.1 年(范围 1 至 13 年)。评估了发生狭窄(B2)或穿透(B3)疾病的累积概率以及危险因素与疾病行为演变之间的关系。
在 402 例患者中,最终随访时有 75 例(18.7%)发展为 B2 或 B3 疾病。疾病行为演变的累积概率分别为 5 年时 18.3%、10 年时 34.3%和 13 年时 50.9%。疾病进展的患者有更高的肠切除术风险(风险比[HR],3.61;95%置信区间[CI],2.25 至 6.03;p<0.001)。一级炎症性肠病家族史(HR,2.38;95%CI,1.07 至 5.28;p=0.032)、初诊时孤立性回肠受累(HR,7.55;95%CI,1.04 至 15.57;p=0.045)和抗酿酒酵母抗体滴度阳性(HR,2.10;95%CI,1.03 至 4.25;p=0.040)与疾病行为演变相关。早期使用生物制剂治疗可显著降低疾病进展的风险(HR,0.46;95%CI,0.79 至 3.39;p=0.042)。
本研究表明,对于有疾病进展危险因素的 B1 行为儿科 CD 患者,应考虑早期积极治疗,以改善长期结局。