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前瞻性纵向研究:使用粪便谷蛋白免疫原性肽监测诊断为乳糜泻的儿童在过渡到无麸质饮食期间的情况。

Prospective longitudinal study: use of faecal gluten immunogenic peptides to monitor children diagnosed with coeliac disease during transition to a gluten-free diet.

机构信息

Sevilla, Spain.

Tenerife, Spain.

出版信息

Aliment Pharmacol Ther. 2019 Jun;49(12):1484-1492. doi: 10.1111/apt.15277. Epub 2019 May 10.

Abstract

BACKGROUND

Treatment for coeliac disease is a lifelong strict gluten-free diet. Although guidelines recommend regular follow-up with dietary interviews and coeliac serology, these methods may be inaccurate.

AIM

To evaluate the usefulness of faecal gluten immunogenic peptides to support the diagnosis and to determine the adherence to the gluten-free diet in coeliac children.

METHODS

Multicentre prospective observational study including 64 coeliac children. Faecal gluten peptides, and tissue transglutaminase and deamidated gliadin peptide antibodies were analyzed at diagnosis, and 6, 12 and 24 months thereafter. Gluten consumption was estimated from gluten peptide levels.

RESULTS

Most children (97%) had detectable gluten peptides at diagnosis. On a gluten-free diet, the rate of gluten peptides increased from 13% at 6 months to 25% at 24 months. Mean estimated gluten exposure dropped from 5543 mg/d at diagnosis to 144 mg/d at 6 months, then increased to 606 mg/d by 24 months. In contrast, deamidated gliadin peptide antibodies normalised and only 20% had elevated tissue transglutaminase antibody by 24 months. The elevation of tissue transglutaminase antibody was more prolonged in patients with detectable gluten peptides (P < 0.05). Nevertheless, absolute levels of tissue transglutaminase antibody had low sensitivity to identify patients with detectable gluten peptides (P > 0.1). Dietitian assessment was only moderately correlated with gluten peptide detection (κ = 0.5).

CONCLUSIONS

Faecal gluten peptides testing may guide treatment of coeliac disease prior to diagnosis and during the assessment diet adherence. Further studies could determine if early identification of gluten exposure reduces the need for expensive/invasive investigations for non-responsive coeliac disease. ClinicalTrials.gov Number: NCT02711397.

摘要

背景

治疗乳糜泻需要终生严格遵循无麸质饮食。尽管指南建议定期进行饮食访谈和乳糜泻血清学检查,但这些方法可能并不准确。

目的

评估粪便麸质免疫肽在支持乳糜泻诊断和确定乳糜泻儿童对无麸质饮食的依从性方面的作用。

方法

这项多中心前瞻性观察性研究纳入了 64 名乳糜泻患儿。在诊断时以及此后 6、12 和 24 个月时,分析粪便麸质肽、组织转谷氨酰胺酶和脱酰胺麦胶肽抗体。通过麸质肽水平估计麸质摄入量。

结果

大多数患儿(97%)在诊断时可检测到麸质肽。在无麸质饮食时,麸质肽水平从 6 个月时的 13%增加到 24 个月时的 25%。估计的平均麸质暴露量从诊断时的 5543mg/d 降至 6 个月时的 144mg/d,然后在 24 个月时增加到 606mg/d。相比之下,脱酰胺麦胶肽抗体恢复正常,只有 20%的患儿在 24 个月时出现组织转谷氨酰胺酶抗体升高。在可检测到麸质肽的患者中,组织转谷氨酰胺酶抗体的升高更为持久(P<0.05)。然而,组织转谷氨酰胺酶抗体的绝对水平对识别可检测到麸质肽的患者的敏感性较低(P>0.1)。营养师评估与检测到麸质肽仅有中度相关性(κ=0.5)。

结论

粪便麸质肽检测可在诊断前和评估饮食依从性期间指导乳糜泻的治疗。进一步的研究可以确定早期识别麸质暴露是否可以减少对非应答性乳糜泻进行昂贵/有创检查的需求。临床试验注册编号:NCT02711397。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b55/6767519/8f617b21a9e2/APT-49-1484-g001.jpg

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