北美极早发炎症性肠病的自然史:一项回顾性队列研究。
Natural History of Very Early Onset Inflammatory Bowel Disease in North America: A Retrospective Cohort Study.
机构信息
University of Massachusetts Medical School (UMMS), Worcester, MA, United States.
Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
出版信息
Inflamm Bowel Dis. 2021 Feb 16;27(3):295-302. doi: 10.1093/ibd/izaa080.
BACKGROUND
The incidence of very early onset inflammatory bowel disease (VEOIBD) is increasing, yet the phenotype and natural history of VEOIBD are not well described.
METHODS
We performed a retrospective cohort study of patients diagnosed with VEOIBD (6 years of age and younger) between 2008 and 2013 at 25 North American centers. Eligible patients at each center were randomly selected for chart review. We abstracted data at diagnosis and at 1, 3, and 5 years after diagnosis. We compared the clinical features and outcomes with VEOIBD diagnosed younger than 3 years of age with children diagnosed with VEOIBD at age 3 to 6 years.
RESULTS
The study population included 269 children (105 [39%] Crohn's disease, 106 [39%] ulcerative colitis, and 58 [22%] IBD unclassified). The median age of diagnosis was 4.2 years (interquartile range 2.9-5.2). Most (94%) Crohn's disease patients had inflammatory disease behavior (B1). Isolated colitis (L2) was the most common disease location (70% of children diagnosed younger than 3 years vs 43% of children diagnosed 3 years and older; P = 0.10). By the end of follow-up, stricturing/penetrating occurred in 7 (6.6%) children. The risk of any bowel surgery in Crohn's disease was 3% by 1 year, 12% by 3 years, and 15% by 5 years and did not differ by age at diagnosis. Most ulcerative colitis patients had pancolitis (57% of children diagnosed younger than 3 years vs 45% of children diagnosed 3 years and older; P = 0.18). The risk of colectomy in ulcerative colitis/IBD unclassified was 0% by 1 year, 3% by 3 years, and 14% by 5 years and did not differ by age of diagnosis.
CONCLUSIONS
Very early onset inflammatory bowel disease has a distinct phenotype with predominantly colonic involvement and infrequent stricturing/penetrating disease. The cumulative risk of bowel surgery in children with VEOIBD was approximately 14%-15% by 5 years. These data can be used to provide anticipatory guidance in this emerging patient population.
背景
非常早发性炎症性肠病(VEOIBD)的发病率正在增加,但 VEOIBD 的表型和自然史尚未得到很好的描述。
方法
我们对 2008 年至 2013 年间在北美 25 个中心诊断为 VEOIBD(6 岁及以下)的患者进行了回顾性队列研究。每个中心符合条件的患者均随机选择进行病历回顾。我们在诊断时以及诊断后 1、3 和 5 年采集数据。我们比较了 3 岁以下和 3 至 6 岁诊断为 VEOIBD 的儿童的临床特征和结局。
结果
该研究人群包括 269 名儿童(105 名[39%]克罗恩病、106 名[39%]溃疡性结肠炎和 58 名[22%]IBD 未分类)。诊断中位年龄为 4.2 岁(四分位间距 2.9-5.2)。大多数(94%)克罗恩病患者存在炎症性疾病行为(B1)。孤立性结肠炎(L2)是最常见的疾病部位(3 岁以下诊断的儿童中有 70%,3 岁及以上诊断的儿童中有 43%;P=0.10)。随访结束时,7 名(6.6%)儿童发生狭窄/穿透。克罗恩病患儿在 1 年内任何肠道手术的风险为 3%,3 年内为 12%,5 年内为 15%,且与诊断年龄无关。大多数溃疡性结肠炎患儿有全结肠炎(3 岁以下诊断的儿童中有 57%,3 岁及以上诊断的儿童中有 45%;P=0.18)。溃疡性结肠炎/IBD 未分类患儿在 1 年内接受结肠切除术的风险为 0%,3 年内为 3%,5 年内为 14%,且与诊断年龄无关。
结论
非常早发性炎症性肠病具有独特的表型,以结肠受累为主,狭窄/穿透性疾病少见。患有 VEOIBD 的儿童在 5 年内进行肠道手术的累积风险约为 14%-15%。这些数据可用于为这一新兴患者群体提供预期指导。
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