Neurath M F, Vehling D, Schunk K, Holtmann M, Brockmann H, Helisch A, Orth T, Schreckenberger M, Galle P R, Bartenstein P
Department of Medicine, University of Mainz, Germany.
Am J Gastroenterol. 2002 Aug;97(8):1978-85. doi: 10.1111/j.1572-0241.2002.05836.x.
Detection of disease activity in Crohn's disease (CD) is of crucial importance for diagnosis and management of the disease. Noninvasive methods for monitoring are desirable and comprise hydromagnetic resonance imaging (hydro-MRI) and leukocyte scintigraphy. In addition, a recent case report indicated the potential of 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) to assess CD activity. However, comparative prospective studies are lacking.
Between February, 1999 and August, 2000, 59 patients with CD were enrolled in a prospective study to assess disease activity by FDG-PET, hydro-MRI, and immunoscintigraphy with anti-nonspecific cross-reacting antigen 95 antigranulocyte antibodies. In 28 of these patients, colonoscopy could be performed. Twelve patients with irritable bowel syndrome and 20 tumor patients without gut inflammation served as controls. Results were compared by statistical analysis.
FDG-PET detected 127 pathological findings (average maximum standardized uptake value = 4.4 +/- 1.1) in the terminal/neoterminal ileum (37), small bowel (24), and colon (66) of 54 patients with CD, whereas no pathological findings were seen in five patients with CD, the control patients with irritable bowel syndrome, and the tumor patients without gut inflammation. In contrast, examination with hydro-MRI or granulocyte antibodies detected less pathological findings in CD patients. Forty-five of the detected foci were accessible to endoscopic verification. The correlation of the foci with endoscopic findings showed a high specificity (>89%) of all three methods to detect inflamed areas in the terminal ileum and colon of patients with CD, although analyses by hydro-MRI and granulocyte antibody scan had strikingly lower sensitivities (40.9% and 66.7%) than FDG-PET analysis (85.4%).
FDG-PET appears to be a reliable noninvasive tool for simultaneous detection of inflamed areas in the small and large bowel of patients with CD. FDG-PET can be used to detect disease activity in the terminal ileum and colon of CD patients with high sensitivity and specificity.
检测克罗恩病(CD)的疾病活动度对该病的诊断和管理至关重要。理想的非侵入性监测方法包括磁共振水成像(hydro-MRI)和白细胞闪烁扫描。此外,最近的一份病例报告显示18F-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)评估CD活动度的潜力。然而,缺乏比较性前瞻性研究。
1999年2月至2000年8月期间,59例CD患者被纳入一项前瞻性研究,通过FDG-PET、hydro-MRI和使用抗非特异性交叉反应抗原95抗粒细胞抗体的免疫闪烁扫描来评估疾病活动度。其中28例患者可进行结肠镜检查。12例肠易激综合征患者和20例无肠道炎症的肿瘤患者作为对照。通过统计分析比较结果。
FDG-PET在54例CD患者的回肠末端/新回肠(37处)、小肠(24处)和结肠(66处)检测到127处病理表现(平均最大标准化摄取值=4.4±1.1),而5例CD患者、肠易激综合征对照患者和无肠道炎症的肿瘤患者未发现病理表现。相比之下,hydro-MRI或粒细胞抗体检查在CD患者中检测到的病理表现较少。45个检测到的病灶可通过内镜验证。病灶与内镜检查结果的相关性显示,所有三种方法检测CD患者回肠末端和结肠炎症区域的特异性均较高(>89%),尽管hydro-MRI和粒细胞抗体扫描分析的敏感性(分别为40.9%和66.7%)明显低于FDG-PET分析(85.4%)。
FDG-PET似乎是一种可靠的非侵入性工具,可同时检测CD患者小肠和大肠的炎症区域。FDG-PET可用于高灵敏度和特异性地检测CD患者回肠末端和结肠的疾病活动度。