Department of Gastroenterology and Hepatology, AG&M Research Institute, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.
Department of Gastroenterology and Hepatology, MUMC+, Maastricht University, 6229 HX Maastricht, The Netherlands.
Sensors (Basel). 2022 Mar 17;22(6):2316. doi: 10.3390/s22062316.
The early prediction of changes in disease state allows timely treatment of patients with inflammatory bowel disease (IBD) to be performed, which improves disease outcome. The aim of this pilot study is to explore the potential of fecal volatile organic compound (VOC) profiles to predict disease course. In this prospective cohort, IBD patients were asked to collect two fecal samples and fill in a questionnaire at set intervals. Biochemically, active disease was defined by FCP ≥ 250 mg/g and remission was defined by FCP < 100 mg/g. Clinically, active disease was defined by a Harvey Bradshaw Index (HBI) ≥ 5 for Crohn’s disease or by a Simple Clinical Colitis Activity Index (SCCAI) ≥ 3 for ulcerative colitis. Clinical remission was defined by an HBI < 4 or SCCAI ≤ 2. Fecal VOC profiles were measured using gas chromatography-ion mobility spectrometry (GC-IMS). The fecal samples collected first were included for VOC analysis to predict disease state at the following collection. A total of 182 subsequently collected samples met the disease-state criteria. The fecal VOC profiles of samples displaying low FCP levels at the first measurements differed between patients preceding exacerbation versus those who remained in remission (AUC 0.75; p < 0.01). Samples with FCP levels at the first time point displayed different VOC profiles in patients preceding remission compared with those whose disease remained active (AUC 0.86; p < 0.01). Based on disease activity scores, there were no significant differences in any of the comparisons. Alterations in fecal VOC profiles preceding changes in FCP levels may be useful to detect disease-course alterations at an early stage. This could lead to earlier treatment, decreased numbers of complications, surgery and hospital admission.
疾病状态的早期预测可使炎症性肠病(IBD)患者得到及时治疗,改善疾病结局。本研究旨在探索粪便挥发性有机化合物(VOC)谱预测疾病进程的潜力。在这项前瞻性队列研究中,要求 IBD 患者定期采集两份粪便样本并填写问卷。生化方面,通过粪便钙卫蛋白(FCP)≥250mg/g 定义为活动期疾病,FCP<100mg/g 定义为缓解期。临床方面,采用 Harvey Bradshaw 指数(HBI)≥5 定义为克罗恩病活动期,或采用简单临床结肠炎活动指数(SCCAI)≥3 定义为溃疡性结肠炎活动期;HBI<4 或 SCCAI≤2 定义为临床缓解期。采用气相色谱-离子迁移谱(GC-IMS)检测粪便 VOC 谱。将首次采集的粪便样本用于 VOC 分析,以预测下一次采集时的疾病状态。共纳入 182 份随后采集的符合疾病状态标准的样本。首次测量时 FCP 水平较低的粪便样本中,即将发生恶化的患者与持续缓解的患者的粪便 VOC 谱存在差异(AUC 0.75;p<0.01)。首次检测 FCP 水平时处于缓解期的患者的粪便样本与疾病持续活动的患者的粪便 VOC 谱存在差异(AUC 0.86;p<0.01)。根据疾病活动评分,这些比较中没有任何一项具有统计学差异。在 FCP 水平变化之前,粪便 VOC 谱的改变可能有助于早期发现疾病进程的改变。这可能导致更早的治疗,减少并发症、手术和住院的次数。