P310 Intestinal ultrasound as a tool to assess treatment response in patients with Inflammatory Bowel Diseases

M Katsaros, A Katsoula, M Kalogirou, P Paschos, P Papagiannakis, T Tsionis, O Giouleme
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Abstract

Background The assessment of treatment response in patients with Inflammatory Bowel Disease (IBD) is often based on clinical indices [Harvey Bradshaw index (HBI), Partial Mayo score (PMS)] and biomarkers [C - reactive protein (CRP)]. Intestinal ultrasound (IUS) has been proposed as a modality capable of objectively evaluating therapeutic response. We investigated the utility of the IUS as a tool to assess treatment response, as well as its association with HBI, PMS and CRP. Methods We included patients with an established diagnosis of IBD who initiated biologic agent (infliximab, adalimumab, ustekinumab, vedolizumab) or tofacitinib. Active disease on IUS was defined as an increase in bowel wall thickness (BWT) >3 mm in the most affected bowel segment, while the presence of a Doppler signal (CDS) in the bowel wall was also assessed. Treatment response on IUS was defined according to the International Bowel Ultrasound Group (IBUS) criteria: reduction in bowel wall thickness (in continuous measurements) >25% or >2.0 mm or >1.0 mm with concomitant reduction in CDS by 1 unit at week 14 ± 2 from the initiation of treatment. Results A total of 19 patients (11 men, 11 with Crohn's disease) underwent IUS at week 0 and week 14 ± 2, while CRP, HBI and PMS were calculated at the same time points. We included bio-naïve as well bio experienced patients (table 1). At week 0, 84.2% of patients exhibited clinical activity (HBI ≥5, PMS ≥2), median CRP was 24.7 mg /L (IQR 18.6-42.8) and median BWT was 7.1mm (IQR 6.5-7.6). At week 14 ± 2, 42.1% of patients remained clinically active, median CRP was 6.8 mg/L (IQR 4.6-20.7) and median BWT was 5.2 mm (IQR 4.6- 6.4). Overall 10/19 patients fulfilled the criteria of treatment response on IUS at week 14 ± 2. Clinical remission was observed in 8/10 patients who demonstrated therapeutic response on IUS and 3/9 patients who did not (p=0.07). Normalization of CRP value (<6mg/L) was observed in 8/10 patients who exhibited treatment response on IUS and in none of the patients who did not (p<0.001). Among the IUS parameters at baseline, a statistically significant difference was found only in the presence of fat wrapping between treatment responders and treatment non-responders (table 2). Finally, median CRP was 4.9 mg/L (IQR 2.6-6.2) in IUS treatment responders and 20.7 mg/L (IQR 10.5-28.5) in IUS treatment non-responders. (p<0.001), with median BWT being 4.7mm (IQR 3.3-5.1) and 6.4mm (IQR 6.1-6.9) respectively (p<0.001). Conclusion IUS represents an objective tool for evaluating treatment response in patients with IBD, which demonstrates a significant correlation with CRP but not with clinical indices of activity.
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P310 肠道超声作为评估炎症性肠病患者治疗反应的工具
背景 炎症性肠病(IBD)患者治疗反应的评估通常基于临床指标[哈维-布拉德肖指数(HBI)、部分梅奥评分(PMS)]和生物标志物[C反应蛋白(CRP)]。肠道超声(IUS)被认为是一种能够客观评估治疗反应的方法。我们研究了 IUS 作为治疗反应评估工具的实用性及其与 HBI、PMS 和 CRP 的关联。方法 我们纳入了已确诊并开始使用生物制剂(英夫利昔单抗、阿达木单抗、乌斯特库单抗、维妥珠单抗)或托法替尼的 IBD 患者。IUS上的活动性疾病定义为受影响最严重的肠段肠壁厚度(BWT)增加>3毫米,同时还要评估肠壁是否出现多普勒信号(CDS)。根据国际肠道超声组织(IBUS)的标准,IUS治疗反应的定义是:自开始治疗起第14±2周时,肠壁厚度(连续测量值)减少>25%或>2.0毫米或>1.0毫米,同时CDS减少1个单位。结果 共有 19 名患者(11 名男性,11 名克罗恩病患者)在第 0 周和第 14±2 周接受了 IUS 治疗,并在同一时间点计算了 CRP、HBI 和 PMS。我们的研究对象既包括生物免疫缺陷患者,也包括生物免疫缺陷经验丰富的患者(表 1)。在第 0 周,84.2% 的患者表现出临床活性(HBI ≥5,PMS ≥2),CRP 中位数为 24.7 毫克/升(IQR 18.6-42.8),BWT 中位数为 7.1 毫米(IQR 6.5-7.6)。在第 14±2 周,42.1% 的患者保持临床活动,CRP 中位数为 6.8 mg/L(IQR 4.6-20.7),BWT 中位数为 5.2 mm(IQR 4.6-6.4)。总体而言,10/19 名患者在第 14 周(±2)时达到了 IUS 治疗反应标准。8/10 名患者在 IUS 治疗反应中出现临床缓解,3/9 名患者未出现临床缓解(P=0.07)。8/10名IUS治疗反应患者的CRP值(<6mg/L)趋于正常,而没有治疗反应的患者的CRP值趋于正常(p<0.001)。在基线 IUS 参数中,治疗应答者和治疗无应答者之间只有脂肪包裹存在统计学差异(表 2)。最后,IUS 治疗应答者的 CRP 中位数为 4.9 毫克/升(IQR 2.6-6.2),IUS 治疗无应答者的 CRP 中位数为 20.7 毫克/升(IQR 10.5-28.5)。(p<0.001),BWT 中位数分别为 4.7 毫米(IQR 3.3-5.1)和 6.4 毫米(IQR 6.1-6.9)(p<0.001)。结论 IUS 是评估 IBD 患者治疗反应的客观工具,它与 CRP 有显著相关性,但与临床活动指数无关。
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