Leonard Maureen M, Weir Dascha C, DeGroote Maya, Mitchell Paul D, Singh Prashant, Silvester Jocelyn A, Leichtner Alan M, Fasano Alessio
*Department of Pediatric Gastroenterology and Nutrition, MassGeneral Hospital for Children†Celiac Research Program, Harvard Medical School‡Division of Gastroenterology and Nutrition§Clinical Research Center, Boston Children's Hospital||Department of Medicine, Massachusetts General Hospital, Boston, MA¶University of Manitoba, Winnipeg, Manitoba, Canada.
J Pediatr Gastroenterol Nutr. 2017 Feb;64(2):286-291. doi: 10.1097/MPG.0000000000001460.
Our objective was to determine the rate of mucosal recovery in pediatric patients with celiac disease on a gluten-free diet. We also sought to determine whether immunoglobulin A tissue transglutaminase (tTG) correlates with mucosal damage at the time of a repeat endoscopy with duodenal biopsy in these patients.
We performed a retrospective chart review of 103 pediatric patients, younger than 21 years, with a diagnosis of celiac disease defined as Marsh 3 histology, and who underwent a repeat endoscopy with duodenal biopsy at least 12 months after initiating a gluten-free diet.
We found that 19% of pediatric patients treated with a gluten-free diet had persistent enteropathy. At the time of the repeat biopsy, tTG was elevated in 43% of cases with persistent enteropathy and 32% of cases in which there was mucosal recovery. Overall the positive predictive value of the autoantibody tTG was 25% and the negative predictive value was 83% in patients on a gluten-free diet for a median of 2.4 years.
Nearly 1 in 5 children with celiac disease in our population had persistent enteropathy despite maintaining a gluten-free diet and immunoglobulin A tTG was not an accurate marker of mucosal recovery. Neither the presence of symptoms nor positive serology were predictive of a patient's histology at the time of repeat biopsy. These findings suggest a revisitation of monitring and management criteria of celiac disease in childhood.
我们的目的是确定采用无麸质饮食的乳糜泻患儿的黏膜恢复率。我们还试图确定免疫球蛋白A组织转谷氨酰胺酶(tTG)与这些患者再次进行十二指肠活检的内镜检查时的黏膜损伤是否相关。
我们对103名年龄小于21岁、诊断为乳糜泻(定义为马什3级组织学)且在开始无麸质饮食至少12个月后接受了再次十二指肠活检的内镜检查的儿科患者进行了回顾性病历审查。
我们发现,采用无麸质饮食治疗的儿科患者中有19%患有持续性肠病。在再次活检时,43%的持续性肠病病例和32%黏膜已恢复的病例中tTG升高。总体而言,在无麸质饮食中位数为2.4年的患者中,自身抗体tTG的阳性预测值为25%,阴性预测值为83%。
在我们的研究人群中,近五分之一的乳糜泻患儿尽管坚持无麸质饮食仍患有持续性肠病,且免疫球蛋白A tTG并非黏膜恢复的准确标志物。症状的存在和血清学阳性均不能预测患者再次活检时的组织学情况。这些发现提示需重新审视儿童乳糜泻的监测和管理标准。