Horton Maxwell, Olshan Katherine L, Gleeson Elizabeth, Regis Stephanie, Morson Taylor, Hintze Zackary J, Leonard Maureen M, Silvester Jocelyn A
From the Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.
Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
JPGN Rep. 2023 Jun 9;4(3):e323. doi: 10.1097/PG9.0000000000000323. eCollection 2023 Aug.
This study examines the prevalence of detectable gluten immunogenic peptides (GIPs) as a proxy for gluten exposure in children with celiac disease on a gluten-free diet in the United States, as estimated by gluten breakdown products excreted in urine and stool.
Urine and stool samples were collected in 3 settings (home, gastroenterology clinic, and endoscopy) for pediatric participants (ages 6-21 years old) across 2 medical centers. Commercial ELISA assays were used to quantify the GIPs in each sample.
GIPs were detected in 4 out of 44 (9.1%) of stool samples and 6 out of 125 (4.8%) of urine samples provided by 84 children. These samples were collected across all settings, and most participants (70%) were asymptomatic at the time of sample collection. For the urine samples collected at the time of endoscopy, all subjects found to have persistent enteropathy had no detectable GIPs (0/12).
GIPs provide an additional method for screening for gluten exposures in individuals with celiac disease on a gluten-free diet, and may be used across multiple settings. We found a low detection rate of GIPs in children. Our finding of undetectable GIPs in individuals with persistent enteropathy may be expected of a single determination under close observation or represent a lack of gluten exposure within the detection window. More research is needed to understand the dynamics of gluten absorption and excretion in the US pediatric population.
本研究通过检测尿和粪便中排出的麸质分解产物,来估算美国接受无麸质饮食的乳糜泻患儿中可检测到的麸质免疫原性肽(GIP)的流行情况,以此作为麸质暴露的指标。
在两个医疗中心,针对6至21岁的儿科参与者,在3种环境(家中、胃肠病诊所和内镜检查时)收集尿样和粪便样本。使用商业酶联免疫吸附测定法(ELISA)对每个样本中的GIP进行定量。
84名儿童提供的44份粪便样本中有4份(9.1%)检测到GIP,125份尿样中有6份(4.8%)检测到GIP。这些样本来自所有环境,大多数参与者(70%)在样本采集时无症状。在内镜检查时采集的尿样中,所有被发现患有持续性肠病的受试者均未检测到GIP(0/12)。
GIP为筛查接受无麸质饮食的乳糜泻患者的麸质暴露提供了一种额外的方法,并且可在多种环境中使用。我们发现儿童中GIP的检测率较低。在持续性肠病患者中未检测到GIP这一发现,可能是在密切观察下单次测定的预期结果,或者代表在检测窗口内缺乏麸质暴露。需要更多研究来了解美国儿科人群中麸质吸收和排泄的动态情况。