Comino Isabel, Fernández-Bañares Fernando, Esteve María, Ortigosa Luís, Castillejo Gemma, Fambuena Blanca, Ribes-Koninckx Carmen, Sierra Carlos, Rodríguez-Herrera Alfonso, Salazar José Carlos, Caunedo Ángel, Marugán-Miguelsanz J M, Garrote José Antonio, Vivas Santiago, Lo Iacono Oreste, Nuñez Alejandro, Vaquero Luis, Vegas Ana María, Crespo Laura, Fernández-Salazar Luis, Arranz Eduardo, Jiménez-García Victoria Alejandra, Antonio Montes-Cano Marco, Espín Beatriz, Galera Ana, Valverde Justo, Girón Francisco José, Bolonio Miguel, Millán Antonio, Cerezo Francesc Martínez, Guajardo César, Alberto José Ramón, Rosinach Mercé, Segura Verónica, León Francisco, Marinich Jorge, Muñoz-Suano Alba, Romero-Gómez Manuel, Cebolla Ángel, Sousa Carolina
Department of Microbiology and Parasitology, Faculty of Pharmacy, University of Seville, Seville, Spain.
Department of Gastroenterology, Hospital Universitari Mutua Terrassa, and CIBERehd, Terrassa, Barcelona, Spain.
Am J Gastroenterol. 2016 Oct;111(10):1456-1465. doi: 10.1038/ajg.2016.439. Epub 2016 Sep 20.
Treatment for celiac disease (CD) is a lifelong strict gluten-free diet (GFD). Patients should be followed-up with dietary interviews and serology as CD markers to ensure adherence to the diet. However, none of these methods offer an accurate measure of dietary compliance. Our aim was to evaluate the measurement of gluten immunogenic peptides (GIP) in stools as a marker of GFD adherence in CD patients and compare it with traditional methods of GFD monitoring.
We performed a prospective, nonrandomized, multicenter study including 188 CD patients on GFD and 84 healthy controls. Subjects were given a dietary questionnaire and fecal GIP quantified by enzyme-linked immunosorbent assay (ELISA). Serological anti-tissue transglutaminase (anti-tTG) IgA and anti-deamidated gliadin peptide (anti-DGP) IgA antibodies were measured simultaneously.
Of the 188 celiac patients, 56 (29.8%) had detectable GIP levels in stools. There was significant association between age and GIP in stools that revealed increasing dietary transgressions with advancing age (39.2% in subjects ≥13 years old) and with gender in certain age groups (60% in men ≥13 years old). No association was found between fecal GIP and dietary questionnaire or anti-tTG antibodies. However, association was detected between GIP and anti-DGP antibodies, although 46 of the 53 GIP stool-positive patients were negative for anti-DGP.
Detection of gluten peptides in stools reveals limitations of traditional methods for monitoring GFD in celiac patients. The GIP ELISA enables direct and quantitative assessment of gluten exposure early after ingestion and could aid in the diagnosis and clinical management of nonresponsive CD and refractory CD. Trial registration number NCT02711397.
乳糜泻(CD)的治疗是终身严格的无麸质饮食(GFD)。应通过饮食访谈和血清学检查作为CD标志物对患者进行随访,以确保其坚持饮食。然而,这些方法均无法准确衡量饮食依从性。我们的目的是评估粪便中麸质免疫原性肽(GIP)的检测作为CD患者GFD依从性的标志物,并将其与传统的GFD监测方法进行比较。
我们进行了一项前瞻性、非随机、多中心研究,纳入了188名接受GFD治疗的CD患者和84名健康对照。受试者接受饮食问卷调查,并通过酶联免疫吸附测定(ELISA)对粪便GIP进行定量。同时检测血清抗组织转谷氨酰胺酶(抗tTG)IgA和抗脱酰胺麦醇溶蛋白肽(抗DGP)IgA抗体。
在188名乳糜泻患者中,56名(29.8%)粪便中可检测到GIP水平。粪便中年龄与GIP之间存在显著关联,表明随着年龄增长饮食违规情况增加(≥13岁受试者中为39.2%),并且在特定年龄组中与性别有关(≥13岁男性中为60%)。未发现粪便GIP与饮食问卷或抗tTG抗体之间存在关联。然而,检测到GIP与抗DGP抗体之间存在关联,尽管53名粪便GIP阳性患者中有46名抗DGP为阴性。
粪便中麸质肽的检测揭示了乳糜泻患者监测GFD传统方法的局限性。GIP ELISA能够在摄入后早期直接定量评估麸质暴露情况,并有助于诊断和临床管理无反应性CD和难治性CD。试验注册号NCT02711397。