Department of Gastroenterology and Hepatology, The Queen Elizabeth Hospital, Woodville South, South Australia, Australia.
Clin Transl Gastroenterol. 2011 Aug 18;2(8):e4. doi: 10.1038/ctg.2011.3.
Traditional celiac disease guidelines recommend follow-up endoscopy and duodenal biopsies at 6-12 months after commencing a gluten-free diet (GFD). However, histology may remain abnormal even 1-2 years later. We evaluated the role of capsule endoscopy in patients with celiac disease after treatment with a GFD.
Twelve adult patients with newly diagnosed celiac disease were prospectively enrolled. All patients had baseline symptom assessment, celiac serology (tissue transglutaminase antibody, tTG), and capsule endoscopy. Twelve months after commencing a GFD, patients underwent repeat symptom assessment, celiac serology, upper gastrointestinal endoscopy, and capsule endoscopy.
At baseline, capsule endoscopy detected endoscopic markers of villous atrophy in the duodenum and extending to a variable distance along the small intestine. On the basis of small bowel transit time, the mean±s.e.m. percentage of small intestine with villous atrophy was 18.2±3.7%. After 12 months on a GFD, repeat capsule endoscopy demonstrated mucosal healing from a distal to proximal direction, and the percentage of small intestine with villous atrophy was significantly reduced to 3.4±1.2% (P=0.0014) and this correlated with improvement in the symptom score (correlation 0.69, P=0.01). There was a significant improvement in symptom score (5.2±1.0 vs. 1.7±0.4, P=0.0012) and reduction in immunoglobulin A-tTG levels (81.5±10.6 vs. 17.5±8.2, P=0.0005). However, 42% of subjects demonstrated persistent villous abnormality as assessed by duodenal histology.
After 12 months on a GFD, patients with celiac disease demonstrate an improvement in symptoms, celiac serology, and the extent of disease as measured by capsule endoscopy. Mucosal healing occurs in a distal to proximal direction. The extent of mucosal healing correlates with improvement in symptoms. Duodenal histology does not reflect the healing that has occurred more distally.
传统的乳糜泻指南建议在开始无麸质饮食(GFD)后 6-12 个月进行内镜检查和十二指肠活检。然而,即使在 1-2 年后,组织学可能仍然异常。我们评估了在接受 GFD 治疗后乳糜泻患者胶囊内镜的作用。
前瞻性纳入 12 例新诊断为乳糜泻的成年患者。所有患者均进行基线症状评估、乳糜泻血清学(组织转谷氨酰胺酶抗体,tTG)和胶囊内镜检查。在开始 GFD 治疗 12 个月后,患者再次进行症状评估、乳糜泻血清学、上消化道内镜和胶囊内镜检查。
在基线时,胶囊内镜检测到十二指肠和沿小肠延伸的绒毛萎缩的内镜标志物。基于小肠通过时间,绒毛萎缩的小肠平均±标准误百分比为 18.2±3.7%。在 GFD 治疗 12 个月后,重复胶囊内镜显示从远端到近端的黏膜愈合,绒毛萎缩的小肠百分比显著降低至 3.4±1.2%(P=0.0014),并且与症状评分的改善相关(相关系数 0.69,P=0.01)。症状评分显著改善(5.2±1.0 与 1.7±0.4,P=0.0012),免疫球蛋白 A-tTG 水平降低(81.5±10.6 与 17.5±8.2,P=0.0005)。然而,42%的患者通过十二指肠组织学评估显示持续的绒毛异常。
在 GFD 治疗 12 个月后,乳糜泻患者的症状、乳糜泻血清学和胶囊内镜测量的疾病程度均有所改善。黏膜愈合从远端到近端发生。黏膜愈合程度与症状改善相关。十二指肠组织学不能反映更远处发生的愈合。