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评价未经察觉的乳糜泻患者尿液中单一的麦胶致敏肽含量以监测无麸质饮食依从性。

Evaluation of a Single Determination of Gluten Immunogenic Peptides in Urine from Unaware Celiac Patients to Monitor Gluten-Free Diet Adherence.

机构信息

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy; Center for Prevention and Diagnosis of Celiac Disease; Gastroenterology and Endoscopy Unit.

Department of Pathophysiology and Transplantation, Università degli Studi di Milano, 20122 Milan, Italy.

出版信息

Nutrients. 2023 Mar 2;15(5):1259. doi: 10.3390/nu15051259.

Abstract

INTRODUCTION AND AIM

Usually, adherence to the gluten-free diet (GFD) in celiac patients is indirectly assessed through serological analysis, questionnaires, or invasive methods such as intestinal biopsy. The detection of gluten immunogenic peptides in urine (urinary gluten immunogenic peptides-uGIP) is a novel technique that directly evaluates the ingestion of gluten. The aim of this study was to evaluate the clinical efficacy of uGIP in the follow-up of celiac disease (CD).

METHODS

From April 2019 to February 2020, CD patients reporting complete adherence to the GFD were prospectively enrolled but were unaware of the reason for the tests. Urinary GIP, the celiac dietary adherence test (CDAT), symptomatic visual analog scales (VAS), and tissue transglutaminase antibodies (tTGA) titres were evaluated. Duodenal histology and capsule endoscopy (CE) were performed when indicated.

RESULTS

A total of 280 patients were enrolled. Thirty-two (11.4%) had a positive uGIP test (uGIP+). uGIP+ patients did not show significant differences in demographic parameters, CDAT, or VAS scores. The tTGA+ titre was not related to the positivity of uGIP (14.4% vs. 10.9% in patients with tTGA+ and tTGA-). Regarding histology, 66.7% of the GIP+ patients had atrophy compared to 32.7% of the GIP patients (-value 0.01). However, the presence of atrophy did not correlate with tTGA. Mucosal atrophy was detected in 29 (47.5%) out of 61 patients by CE. With this method, no noticeable dependence on uGIP results (24 GIP- vs. 5 GIP+) was observed.

CONCLUSIONS

The single uGIP test was positive in 11% of CD cases referring a correct GFD adherence. Furthermore, uGIP results significantly correlated with the duodenal biopsy, formerly considered the gold standard for assessing CD activity.

摘要

简介和目的

通常,在乳糜泻患者中,对无麸质饮食(GFD)的依从性是通过血清学分析、问卷或肠道活检等侵入性方法间接评估的。尿中谷蛋白免疫原性肽(尿中谷蛋白免疫原性肽-uGIP)的检测是一种直接评估摄入麸质的新技术。本研究旨在评估 uGIP 在乳糜泻(CD)随访中的临床疗效。

方法

从 2019 年 4 月至 2020 年 2 月,前瞻性招募报告完全遵循 GFD 的 CD 患者,但他们并不知道测试的原因。评估尿 GIP、乳糜泻饮食依从性测试(CDAT)、症状视觉模拟量表(VAS)和组织转谷氨酰胺酶抗体(tTGA)滴度。在需要时进行十二指肠组织学和胶囊内镜(CE)检查。

结果

共纳入 280 例患者。32 例(11.4%)uGIP 检测阳性(uGIP+)。uGIP+患者在人口统计学参数、CDAT 或 VAS 评分方面无显著差异。tTGA+滴度与 uGIP 的阳性无关(tTGA+和 tTGA-患者分别为 14.4%和 10.9%)。关于组织学,66.7%的 GIP+患者有萎缩,而 GIP 患者为 32.7%(-值 0.01)。然而,萎缩的存在与 tTGA 无关。CE 检测到 61 例患者中有 29 例(47.5%)黏膜萎缩。用这种方法,没有明显依赖于 uGIP 结果(24 例 GIP-vs.5 例 GIP+)。

结论

在报告正确 GFD 依从性的 CD 病例中,单次 uGIP 检测呈阳性的比例为 11%。此外,uGIP 结果与十二指肠活检显著相关,而十二指肠活检以前被认为是评估 CD 活动的金标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9222/10004805/0b1e22a502f4/nutrients-15-01259-g001.jpg

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