*CHU Lille, Hepato-Gastroenterology Department, Claude Huriez Hospital, University of Lille 2, Lille, France; †CHU Lille, Dermatology Department, Claude Huriez Hospital, University of Lille 2, Lille, France; and ‡CHU Lille, Pharmacy Department, Claude Huriez Hospital, University of Lille 2, Lille, France.
Inflamm Bowel Dis. 2017 Oct;23(10):1853-1859. doi: 10.1097/MIB.0000000000001179.
Infliximab (IFX) is effective in inducing and maintaining remission in patients with luminal and anoperineal Crohn's disease (CD). However, treatment failure within 12 months after initiating IFX is observed in a significant proportion of patients. The aim of the present study was to determine whether the body mass index (BMI) affects response to IFX during the first year of treatment in patients with CD.
All patients with luminal CD who began IFX between January 2010 and May 2014 were prospectively included. BMI was calculated before IFX treatment was begun, and patients were divided into 3 groups: normal BMI (BMI < 25 kg/m), overweight patients (BMI of 25.0-30 kg/m), and obese patients (BMI > 30.0 kg/m). The primary outcome was to evaluate the rate and delay of IFX optimization during the first year of treatment among normal weight, overweight, and obese patients.
One hundred forty patients were included. Demographic and clinical characteristics at IFX initiation were comparable among the 3 groups. Within 12 months after the initiation of IFX, the rate of IFX optimization was significantly higher in overweight and obese patients than in the normal BMI group: 52%, 56%, and 20%, respectively (P = 0.0002). The median time until optimization of IFX was significantly shorter in overweight and obese patients than in the normal BMI group: 7, 7, and 10 months, respectively (P = 0.03). A BMI >25 kg/m was significantly associated with IFX optimization within 12 months on multivariate analysis.
This is the first study to show that optimization of IFX is more frequent and faster in obese and overweight patients with CD and occurs within 12 months after beginning IFX, suggesting that an induction regimen with higher doses of IFX and a tight control of IFX concentrations may be needed in these patients.
英夫利昔单抗(IFX)在诱导和维持腔型和肛型克罗恩病(CD)患者缓解方面有效。然而,在开始使用 IFX 的 12 个月内,相当一部分患者出现治疗失败。本研究旨在确定 CD 患者在开始 IFX 治疗的第一年中,体重指数(BMI)是否影响 IFX 的反应。
前瞻性纳入 2010 年 1 月至 2014 年 5 月期间开始接受 IFX 治疗的所有腔型 CD 患者。在开始 IFX 治疗前计算 BMI,并将患者分为 3 组:正常 BMI(BMI<25kg/m)、超重患者(BMI 为 25.0-30kg/m)和肥胖患者(BMI>30.0kg/m)。主要结局是评估正常体重、超重和肥胖患者在治疗的第一年中 IFX 优化的速度和延迟。
共纳入 140 例患者。3 组患者在开始 IFX 时的人口统计学和临床特征无差异。在开始 IFX 后 12 个月内,超重和肥胖患者的 IFX 优化率明显高于正常 BMI 组:分别为 52%、56%和 20%(P=0.0002)。超重和肥胖患者 IFX 优化的中位时间明显短于正常 BMI 组:分别为 7、7 和 10 个月(P=0.03)。多变量分析显示,BMI>25kg/m 与 12 个月内 IFX 优化显著相关。
这是第一项表明 CD 肥胖和超重患者 IFX 优化更频繁、更快的研究,且在开始 IFX 后 12 个月内发生,这表明这些患者可能需要更高剂量的 IFX 诱导方案和更严格的 IFX 浓度控制。