Kang Jian, Wang Jing, Su Juan, Wang Wei, Lu Yueyue, Tang Zhishun, Zou Liping, Yin Anning, Li Jiao, Ren Haixia, Zhou Qian, Wan Huipeng, An Ping
Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, China.
Hubei Provincial Clinical Research Center for Digestive Disease Minimally Invasive Incision, Renmin Hospital of Wuhan University, Wuhan, China.
United European Gastroenterol J. 2025 Jul;13(6):997-1011. doi: 10.1002/ueg2.70021. Epub 2025 Apr 17.
BACKGROUND & AIMS: Previous results showed that combined treatment of biologics and exclusive enteral nutrition (EEN) brought moderate-to-severe Crohn's disease patients significant improvements in clinical and endoscopic outcomes. Despite its essential role and favorable safety profile, EEN in the treatment of adult Crohn's disease is frequently underestimated because of lower compliance and several side effects, including EEN-related diarrhea (EEND).
In this prospective, single-center randomized clinical trial, 147 eligible patients with actively moderate-to-severe Crohn's disease treated with biologics and concomitant 16-week EEN were included. Sixty-one patients without EEND were enrolled in the ND group (without EEN-related diarrhea), and other patients with EEND who received pancreatic enzyme replacement therapy (PERT) (43 patients) or not (43 patients) were recruited in PERT and NPERT groups, respectively. The clinical outcomes, biologic outcomes, and endoscopic outcomes were evaluated. Quality of life (QoL) and psychological status were also assessed at baseline and endpoints (week 16).
Bowel movements (daily frequency decreased by 5.3 times) and stool consistency (reduced watery and loose stool) were greatly improved in PERT group at week 16. At week 16, patients in the ND and PERT groups achieved similar clinical responses (93% in ND group and 94.7% in PERT group, p = 0.731) and clinical remission (86.0% in ND group and 86.8% in PERT group, p = 0.90) while patients in the NPERT group had significantly lower proportions of these clinical outcomes (67.9% clinical response and 57.1% clinical remission). No significant difference was observed in endoscopic outcomes between each group (p = 0.904). QoL and mental status including anxiety and depression in PERT group had great improvement compared with the NPERT group.
Our prospective results provided invaluable evidence that PERT supplementation efficiently improved EEND in Crohn's disease patients with combined treatment of biologics and 16-week EEN, which had a promising effect in active Crohn's disease induction.
ChiCTR2200058343.
既往研究结果表明,生物制剂与全肠内营养(EEN)联合治疗能使中重度克罗恩病患者的临床和内镜检查结果得到显著改善。尽管EEN在成人克罗恩病治疗中起着至关重要的作用且安全性良好,但由于依从性较低以及包括EEN相关腹泻(EEND)在内的多种副作用,其在成人克罗恩病治疗中的作用常被低估。
在这项前瞻性单中心随机临床试验中,纳入了147例接受生物制剂治疗并同时接受16周EEN的中重度活动性克罗恩病合格患者。61例无EEND的患者被纳入ND组(无EEN相关腹泻),其他有EEND且接受胰酶替代疗法(PERT)的患者(43例)或未接受PERT的患者(43例)分别被纳入PERT组和NPERT组。评估临床结局、生物学结局和内镜检查结局。在基线和终点(第16周)时还评估了生活质量(QoL)和心理状态。
在第16周时,PERT组的排便情况(每日排便频率降低5.3次)和粪便稠度(减少水样便和稀便)有显著改善。在第16周时,ND组和PERT组患者的临床反应相似(ND组为93%,PERT组为94.7%,p = 0.731),临床缓解率也相似(ND组为86.0%,PERT组为86.8%,p = 0.90),而NPERT组患者的这些临床结局比例显著较低(临床反应为67.9%,临床缓解为57.1%)。各组间内镜检查结局无显著差异(p = 0.904)。与NPERT组相比,PERT组的QoL以及包括焦虑和抑郁在内的心理状态有显著改善。
我们的前瞻性研究结果提供了宝贵的证据,即补充PERT能有效改善接受生物制剂和16周EEN联合治疗的克罗恩病患者的EEND,这在诱导活动性克罗恩病缓解方面具有显著效果。
ChiCTR2200058343。