Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois; Department of Gastroenterology, Alfred Hospital and Monash University, Melbourne, Australia; Department of Gastroenterology, The Royal Melbourne Hospital, Melbourne, Australia.
Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Clin Gastroenterol Hepatol. 2017 Oct;15(10):1557-1564.e1. doi: 10.1016/j.cgh.2017.02.016. Epub 2017 Feb 24.
BACKGROUND & AIMS: Mucosal healing, determined by histologic analysis, is a potential therapeutic target for patients with ulcerative colitis (UC). However, the histologic features of tissue normalization, as an outcome of treatment, have not been well described. We examined the prevalence and predictive values of normalization of the colonic mucosa, based on histologic analysis (histologic normalization) in patients with UC, and determined its association with risk of clinical relapse, compared with histologic disease quiescence and endoscopic mucosal healing.
We performed a retrospective study of 646 patients with confirmed UC who underwent colonoscopy at a tertiary medical center from August 2005 through October 2013. We reviewed reports from pathology analyses of random mucosal biopsies from each colon segment, and categorized them into 3 groups based on histology findings: (1) normalization (completely normal mucosa with no features of chronicity present), (2) quiescence (crypt atrophy or branching without signs of active inflammation including erosions, abscesses, or focal neutrophil infiltration), or (3) active disease (epithelial infiltration by neutrophils, crypt abscesses, erosions, or ulceration). Histology findings were compared with clinical and endoscopic findings. We assessed variables associated with histology findings and, in patients in clinical remission (Simple Clinical Colitis Activity Index score ≤2 and subscore of ≤1 for stool frequency or rectal bleeding), predictive values for clinical relapse at follow-up evaluations 6 months later or more were calculated.
Of the 646 patients included in the study, 60% had endoscopic mucosal healing, 40% had histologic quiescence, and 10% had histologic normalization. The level of agreement between mucosal and histologic activity was moderate (agreement for 68% of samples; κ = 0.50; P < .001). On multivariate analysis, only proctitis associated with histologic normalization (P = .002). Of 310 patients in clinical remission at initial review, 25% had a clinical relapse, after a median time of 16 months (interquartile range, 10-23 months). Histologic normalization was independently associated with increased odds of relapse-free survival compared with histologic quiescence (hazard ratio, 4.31; 95% confidence interval, 1.48-12.46; P = .007) and histologic activity (hazard ratio, 6.69; 95% confidence interval, 2.16-20.62; P = .001); mucosal healing was not associated with increased odds of relapse-free survival compared with no mucosal healing (hazard ratio, 1.02; 95% confidence interval, 0.56-1.85; P = .954).
Histologic normalization of colonic mucosa can be used as a clinical endpoint for patients with UC. We associated histologic normalization with increased odds of relapse-free survival compared with endoscopic healing or histologic quiescence. Further studies are needed to determine whether histologic normalization should be a goal of treatment for patients with UC.
组织学分析确定的黏膜愈合是溃疡性结肠炎(UC)患者的潜在治疗目标。然而,尚未充分描述组织正常化(治疗后的组织学结果)的特征。我们研究了溃疡性结肠炎患者的结肠黏膜组织学正常化(组织学正常化)的流行率和预测值,并与组织学疾病静止和内镜黏膜愈合相比,确定了其与临床复发风险的关系。
我们对 2005 年 8 月至 2013 年 10 月在一家三级医疗中心接受结肠镜检查的 646 例确诊 UC 患者进行了回顾性研究。我们回顾了每个结肠段随机黏膜活检的病理学分析报告,并根据组织学发现将其分为 3 组:(1)正常化(完全正常的黏膜,无慢性特征),(2)静止(隐窝萎缩或分支,无活动性炎症的迹象,包括糜烂、脓肿或局灶性中性粒细胞浸润),或(3)活跃疾病(中性粒细胞浸润上皮、隐窝脓肿、糜烂或溃疡)。将组织学发现与临床和内镜发现进行比较。我们评估了与组织学发现相关的变量,并在临床缓解(简单临床结肠炎活动指数评分≤2 且粪便频率或直肠出血的亚评分≤1)的患者中,计算了 6 个月后或更长时间的临床复发的预测值。
在纳入研究的 646 例患者中,60%的患者内镜下黏膜愈合,40%的患者组织学静止,10%的患者组织学正常化。黏膜和组织学活性之间的一致性程度中等(68%的样本一致;κ=0.50;P<0.001)。多变量分析显示,仅直肠炎与组织学正常化相关(P=0.002)。在最初评估时处于临床缓解的 310 例患者中,中位时间为 16 个月(四分位间距,10-23 个月)后有 25%发生临床复发。与组织学静止相比,组织学正常化与无复发生存的几率增加独立相关(风险比,4.31;95%置信区间,1.48-12.46;P=0.007)和组织学活动(风险比,6.69;95%置信区间,2.16-20.62;P=0.001);与无黏膜愈合相比,黏膜愈合与无复发生存的几率增加无关(风险比,1.02;95%置信区间,0.56-1.85;P=0.954)。
结直肠黏膜组织学正常化可作为 UC 患者的临床终点。我们将组织学正常化与内镜愈合或组织学静止相比,与无复发生存的几率增加相关。需要进一步的研究来确定组织学正常化是否应该成为 UC 患者的治疗目标。