Sheba Medical Center, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Sheba Medical Center, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Lancet Gastroenterol Hepatol. 2019 Jul;4(7):519-528. doi: 10.1016/S2468-1253(19)30088-3. Epub 2019 May 9.
The optimal monitoring strategy for predicting disease course in Crohn's disease remains undefined. We aimed to evaluate the accuracy, safety, and tolerability of an intensive monitoring strategy designed to predict the future course of Crohn's disease in patients with quiescent disease.
In a prospective observational cohort study, we recruited patients older than 18 years with quiescent (for 3-24 months) Crohn's disease involving the small bowel with confirmed small bowel patency from three tertiary medical centres in Israel. Enrolled patients underwent baseline magnetic resonance enterography (MRE) and patency capsule, clinical or biomarker assessment every 3 months, and video capsule endoscopy (VCE) at baseline and every 6 months for 2 years or until a clinical flare (the primary outcome, defined as an increase in the Crohn's disease activity index score by 70 points or more) or disease worsening necessitating treatment intensification. We assessed the ability of the different Crohn's disease monitoring methods used to predict the occurrence of a flare during the 24-month follow-up period.
Of 90 screened patients, 29 were excluded (17 because of non-patent small bowel). Of the 61 patients enrolled between July 3, 2013, and Feb 1, 2015, 17 (28%) had a flare during the 24-month follow-up. No clinicodemographic parameter predicted future flare. A baseline VCE Lewis score of 350 or more identified patients with future flare (area under the curve [AUC] 0·79, 95% CI 0·66-0·88; p<0·0001; hazard ratio 10·7, 3·8-30·3). C-reactive protein at baseline had an AUC of 0·73 (0·6-0·84; p=0·0013) for predicting flare. The AUC of baseline faecal calprotectin for the prediction of flare occurring within 2 years was 0·62 (0·49-0·74; p=0·17), but progressively improved for shorter timespans and reached an AUC of 0·81 (0·76-0·85) for the prediction of flare occurring within 3 months. Of four MRE-based indices, only MRE global score correlated with 2-year flare risk (AUC 0·71, 0·58-0·82; p=0·024). During follow-up, a Lewis score increase of 383 points or more from baseline predicted imminent disease exacerbation within 6 months (AUC 0·79, 0·65-0·89; p=0·011). The safety and tolerability of the 231 VCEs ingested was excellent, with none being retained.
In patients with quiescent Crohn's disease involving the small bowel, faecal calprotectin predicts short-term flare risk, whereas VCE predicts both short-term and long-term risk of disease exacerbation. If corroborated by additional studies, protocols incorporating VCE could expand the scope of available methods for monitoring disease activity and predicting outcomes in small bowel Crohn's disease.
The Leona M & Harry B Helmsley Charitable Trust.
预测克罗恩病病程的最佳监测策略仍未确定。我们旨在评估旨在预测处于缓解期的克罗恩病患者未来病程的强化监测策略的准确性、安全性和耐受性。
在一项前瞻性观察队列研究中,我们招募了来自以色列三个三级医疗中心的年龄在 18 岁以上、患有累及小肠的缓解期(3-24 个月)克罗恩病且小肠通畅得到证实的患者。入组患者在基线时接受磁共振肠造影(MRE)和通畅胶囊、临床或生物标志物评估每 3 个月进行一次,基线和每 6 个月进行一次视频胶囊内镜(VCE),随访 2 年或直至出现临床发作(主要结局,定义为克罗恩病活动指数评分增加 70 分或更多)或需要强化治疗的疾病恶化。我们评估了不同的克罗恩病监测方法在预测 24 个月随访期间发作的能力。
在筛选的 90 名患者中,有 29 名被排除(17 名因小肠非通畅)。2013 年 7 月 3 日至 2015 年 2 月 1 日期间入组的 61 名患者中,有 17 名(28%)在 24 个月随访期间出现发作。无临床或人口统计学参数可预测未来发作。基线 VCE 刘易斯评分≥350 可识别出未来有发作的患者(曲线下面积 [AUC] 0·79,95%CI 0·66-0·88;p<0·0001;风险比 10·7,3·8-30·3)。基线 C 反应蛋白 AUC 为 0·73(0·6-0·84;p=0·0013),用于预测发作。基线粪便钙卫蛋白用于预测 2 年内发作的 AUC 为 0·62(0·49-0·74;p=0·17),但对于较短的时间间隔预测能力逐渐提高,预测 3 个月内发作的 AUC 达到 0·81(0·76-0·85)。四种基于 MRE 的指数中,只有 MRE 总评分与 2 年内的发作风险相关(AUC 0·71,0·58-0·82;p=0·024)。在随访期间,基线时刘易斯评分增加 383 分或更多可预测 6 个月内即将发生疾病恶化(AUC 0·79,0·65-0·89;p=0·011)。摄入的 231 次 VCE 的安全性和耐受性非常好,没有出现滞留。
在处于缓解期的累及小肠的克罗恩病患者中,粪便钙卫蛋白预测短期发作风险,而 VCE 预测短期和长期疾病恶化风险。如果得到其他研究的证实,纳入 VCE 的方案可能会扩大监测疾病活动和预测小肠克罗恩病结局的现有方法的范围。
Leona M 和 Harry B Helmsley 慈善信托基金。