Mattila Juho, Kallio Johanna, Löyttyniemi Eliisa, Nuutila Pirjo, Koffert Jukka
Department of Gastroenterology, Turku University Hospital, P.O. Box 52, Turku, 20521, Finland.
Department of Radiology, Turku University Hospital, Turku, Finland.
Eur J Nucl Med Mol Imaging. 2025 Aug 26. doi: 10.1007/s00259-025-07524-4.
Crohn's disease (CD) is a chronic and relapsing inflammatory disease of the gastrointestinal tract. Diagnostics and follow-up are difficult in small bowel, that can be only partially evaluated by conventional endoscopy. Combined positron emission tomography magnetic resonance enterography (PET-MRE) has shown potential in diagnosing small bowel CD, but its role in monitoring treatment response has not been previously established. This study aimed to evaluate whether PET-MRE can be used to assess the efficacy of medical therapy. We hypothesized that standardized uptake values (SUV) in inflamed small bowel segments would decrease following initiation of standard therapy. A total of 35 volunteer patients with clinically suspected small bowel CD were recruited. All patients underwent ileocolonoscopy and laboratory testing, followed by [F]-FDG PET-MRE. CD diagnosis was confirmed by small bowel capsule endoscopy. Clinicians initiated treatment based on standard diagnostics, blinded to the PET results. Eighteen patients completed follow-up [F]-FDG PET-MRE at three months. Maximum SUV (SUV) was measured in the small intestine and compared with MRE findings. The median SUV decreased significantly from baseline to follow-up (3.2 vs. 2.1, p = 0.0025). The Simplified Magnetic Resonance Index of Activity (sMARIA) was also significantly lower at follow-up (p = 0.001). Representatively, median fecal calprotectin declined (451 µg/g vs. 163 µg/g, p = 0.004). This preliminary prospective study suggests that [F]-FDG PET-MRE may be a useful tool for assessing biochemical response to treatment in newly diagnosed small bowel CD.Trial registration number: NCT06796959 (ClinicalTrials.gov). Retrospectively registered on 21.1.2025. Enrollment of first participant on 1.8.2020.
克罗恩病(CD)是一种胃肠道的慢性复发性炎症性疾病。小肠疾病的诊断和随访较为困难,传统内镜检查只能对其进行部分评估。正电子发射断层扫描磁共振小肠造影(PET-MRE)在诊断小肠克罗恩病方面已显示出潜力,但其在监测治疗反应中的作用此前尚未确立。本研究旨在评估PET-MRE是否可用于评估药物治疗的疗效。我们假设标准治疗开始后,发炎小肠段的标准化摄取值(SUV)会降低。共招募了35例临床疑似小肠克罗恩病的志愿者患者。所有患者均接受了回结肠镜检查和实验室检测,随后进行了[F]-FDG PET-MRE检查。小肠克罗恩病的诊断通过小肠胶囊内镜检查得以证实。临床医生根据标准诊断开始治疗,对PET结果不知情。18例患者在三个月时完成了随访[F]-FDG PET-MRE检查。测量小肠中的最大SUV(SUV)并与MRE结果进行比较。SUV中位数从基线到随访时显著下降(3.2对2.1,p = 0.0025)。随访时简化磁共振活动指数(sMARIA)也显著降低(p = 0.001)。代表性地,粪便钙卫蛋白中位数下降(451µg/g对163µg/g,p = 0.004)。这项初步前瞻性研究表明,[F]-FDG PET-MRE可能是评估新诊断小肠克罗恩病治疗生化反应的有用工具。试验注册号:NCT06796959(ClinicalTrials.gov)。于2025年1月21日进行回顾性注册。2020年8月1日招募第一名参与者。