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抗组织转谷氨酰胺酶抗体在大量乳糜泻儿童开始无麸质饮食后的正常化 - 真实世界的经验。

Antitissue transglutaminase antibodies' normalization after starting a gluten-free diet in a large population of celiac children-a real-life experience.

机构信息

Pediatric Gastroenterology Unit, Department of Pediatrics, Maggiore Hospital, Largo B. Nigrisoli 2, Bologna 40132, Italy.

Specialty School of Pediatrics-Alma Mater Studiorum, Università di Bologna, Italy.

出版信息

Dig Liver Dis. 2022 Mar;54(3):336-342. doi: 10.1016/j.dld.2021.06.026. Epub 2021 Jul 14.

Abstract

INTRODUCTION

Few data are available regarding the trend of IgA anti-transglutaminase antibodies (TGA-IgA) in children with celiac disease (CD) on a gluten-free diet (GFD). Our aim is to examine the normalization time of CD serology in a large pediatric population, and its predictors.

MATERIAL AND METHODS

We retrospectively evaluated the normalization time of TGA-IgA and its predictive factors (age, sex, ethnicity, symptoms, associated diabetes/thyroiditis, Marsh stage, TGA-IgA and endomysial antibody levels at diagnosis, diet adherence), in 1024 children diagnosed from 2000 to 2019 in three pediatric Italian centers, on a GFD.

RESULTS

TGA-IgA remission was reached in 67,3%, 80,7%, 89,8% and 94,9% after 12, 18, 24 and 36 months from starting a GFD, respectively (median time = 9 months). TGA-IgA >10´upper limit of normal at diagnosis (HR = 0.56), age 7-12 years old (HR = 0.83), poor compliance to diet (HR = 0.69), female sex (HR = 0.82), non-Caucasian ethnicity (HR = 0.75), and comorbidities (HR = 0.72) were independent factors significantly associated with longer time to normalization.

CONCLUSIONS

Our population is the largest in the literature, with the majority of patients normalizing CD serology within 24 months from starting a GFD. We suggest a special attention to patients with comorbidities, language barriers or age 7-12 years for a proper management and follow-up.

摘要

简介

在接受无麸质饮食(GFD)治疗的乳糜泻(CD)患儿中,关于 IgA 抗转谷氨酰胺酶抗体(TGA-IgA)趋势的数据很少。我们的目的是在大型儿科人群中检查 CD 血清学的正常化时间及其预测因素。

材料和方法

我们回顾性评估了意大利三个儿科中心的 1024 名儿童在诊断后 000 年至 2019 年期间开始接受 GFD 治疗时 TGA-IgA 的正常化时间及其预测因素(年龄、性别、种族、症状、相关糖尿病/甲状腺炎、Marsh 分期、TGA-IgA 和肠内膜抗体水平)。

结果

分别在开始 GFD 后 12、18、24 和 36 个月时,TGA-IgA 缓解率达到 67.3%、80.7%、89.8%和 94.9%(中位数时间为 9 个月)。TGA-IgA 在诊断时>10´正常值上限(HR=0.56)、年龄 7-12 岁(HR=0.83)、饮食依从性差(HR=0.69)、女性(HR=0.82)、非白种人(HR=0.75)和合并症(HR=0.72)是与正常化时间延长相关的独立因素。

结论

我们的人群是文献中最大的人群,大多数患者在开始 GFD 后 24 个月内 CD 血清学正常化。我们建议对有合并症、语言障碍或 7-12 岁的患者特别注意,以进行适当的管理和随访。

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