Kim Kwang Yeon, Lee Eun Joo, Kim Ju Whi, Moon Jin Soo, Jang Ju Young, Yang Hye Ran, Ko Jae Sung
Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.
Pediatr Gastroenterol Hepatol Nutr. 2018 Jan;21(1):34-42. doi: 10.5223/pghn.2018.21.1.34. Epub 2018 Jan 12.
Monogenic inflammatory bowel disease (IBD) patients do not respond to conventional therapy and are associated with a higher morbidity. We summarized the clinical characteristics of monogenic IBD patients and compared their clinical outcomes to that of non-monogenic IBD patients.
We performed a retrospective cohort study of all children <18 years old who were diagnosed with IBD between 2005 and 2016. A total of 230 children were enrolled. Monogenic IBD was defined as a presentation age less than 6 years old with confirmation of a genetic disorder. We subdivided the groups into monogenic IBD (n=18), non-monogenic very early-onset IBD (defined as patients with a presentation age <6 years old without a confirmed genetic disorder, n=12), non-monogenic IBD (defined as all patients under 18 years old excluding monogenic IBD, n=212), and severe IBD (defined as patients treated with an anti-tumor necrosis factor excluding monogenic IBD, n=92). We compared demographic data, initial pediatric Crohn disease activity index/pediatric ulcerative colitis activity index (PCDAI/PUCAI) score, frequency of hospitalizations, surgical experiences, and height and weight under 3rd percentile among the patients enrolled.
The initial PCDAI/PUCAI score (<0.05), incidence of surgery per year (<0.05), and hospitalization per year (<0.05) were higher in the monogenic IBD group than in the other IBD groups. Additionally, the proportion of children whose weight and height were less than the 3rd percentile (<0.05 and <0.05, respectively) was also higher in the monogenic IBD group.
Monogenic IBD showed more severe clinical manifestations than the other groups.
单基因炎症性肠病(IBD)患者对传统治疗无反应,且发病率较高。我们总结了单基因IBD患者的临床特征,并将其临床结局与非单基因IBD患者进行比较。
我们对2005年至2016年间诊断为IBD的所有18岁以下儿童进行了一项回顾性队列研究。共纳入230名儿童。单基因IBD定义为发病年龄小于6岁且确诊为遗传性疾病。我们将这些组分为单基因IBD(n = 18)、非单基因极早发型IBD(定义为发病年龄<6岁但未确诊遗传性疾病的患者,n = 12)、非单基因IBD(定义为18岁以下除单基因IBD外的所有患者,n = 212)和重度IBD(定义为接受抗肿瘤坏死因子治疗的除单基因IBD外的患者,n = 92)。我们比较了纳入患者的人口统计学数据、初始儿童克罗恩病活动指数/儿童溃疡性结肠炎活动指数(PCDAI/PUCAI)评分、住院频率、手术经历以及身高和体重低于第3百分位数的情况。
单基因IBD组的初始PCDAI/PUCAI评分(<0.05)、每年手术发生率(<0.05)和每年住院率(<0.05)均高于其他IBD组。此外,单基因IBD组中体重和身高低于第3百分位数的儿童比例也更高(分别为<0.05和<0.05)。
单基因IBD的临床表现比其他组更严重。