现代乳糜泻:诊断时小肠黏膜损伤的严重程度、临床相关性分析和无麸质饮食的改善率

Oliver Cronin, Emma Flanagan, Damian Dowling
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引用次数: 1

摘要

目的:分析新诊断乳糜泻(CD)的现代队列中乳糜泻诊断前血清学、十二指肠组织病理学、原发症状、乳糜泻相关合并症和治疗反应的关系。方法:一项回顾性队列研究,包括1999年至2013年间诊断为乳糜泻的99名参与者。所有患者均记录了以下数据:基线特征、乳糜泻血清学、小肠组织病理学。该队列的一个子集接受了重复的小肠活检。用逻辑回归评估独立关联。结果:诊断时的平均年龄为43岁(四分位数范围为30-53岁),68%的队列为女性。诊断时49例(49%)患者为全绒毛钝化(MS 3c), 12例(12%)患者为次全绒毛钝化(MS 3b), 29例(29%)患者为部分绒毛钝化(MS 3a)。诊断前症状的发生率与绒毛钝化的严重程度无关(P = 0.490)。87例(88%)患者在中位7个月(IQR 6-11个月)后再次进行小肠活检。34例(39%)患者活检结果≥MS 3a,而初始活检时为90例(90%)。该组中有24人(71%)报告坚持无麸质饮食(GFD)。重复活检时持续性MS≥3a与症状(P = 0.358)或乳糜泻血清学持续性阳性(P = 0.485)无关。结论:症状和血清学均不能预测小肠黏膜病变的严重程度。虽然GFD与组织学改善相关,但许多新诊断为乳糜泻的患者尽管限制了数月的麸质,但仍有持续的粘膜损伤。乳糜泻血清学阴性不能排除持续的粘膜损伤。
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Coeliac disease in the modern era: Severity of small bowel mucosal injury at diagnosis with analysis of clinical correlates and rate of improvement on a gluten free diet.

Aim: To analyze the relationships between pre-diagnosis coeliac serology, duodenal histopathology, primary presenting symptoms, coeliac-related comorbidity and response to treatment in a modern cohort with new diagnosis of coeliac disease (CD).

Methods: A retrospective cohort study including 99 participants diagnosed with CD between 1999 and 2013. All patients had the following data recorded: baseline characteristics, coeliac serology, small bowel histopathology. A subset of this cohort underwent a repeat small bowel biopsy. Independent associations were assessed with logistic regression.

Results: The mean age at diagnosis was 43 years (Interquartile range 30-53 years) and 68% of the cohort was female. At diagnosis 49 (49%) patients had total villous blunting (MS 3c), 12 (12%) had subtotal villous blunting (MS 3b), and 29 (29%) had partial villous blunting (MS 3a). The prevalence of symptoms pre diagnosis was not related to the severity of villous blunting (P = 0.490). 87 (88%) of the cohort underwent repeat small bowel biopsy after a median of 7 mo (IQR 6-11 mo). 34 (39%) patients had biopsy results ≥ MS 3a which compared to 90 (90%) at the initial biopsy. 24 (71%) of this group reported adherence to a gluten free diet (GFD). Persistent MS ≥ 3a at repeat biopsy was not associated with symptoms (P = 0.358) or persistent positive coeliac serology (P = 0.485).

Conclusion: Neither symptoms nor serology predict the severity of the small bowel mucosal lesion at CD diagnosis. Whilst a GFD was associated with histological improvement many patients with newly diagnosed CD had persistent mucosal damage despite many months of gluten restriction. Negative CD serology did not exclude ongoing mucosal injury.

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