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The clinical and phenotypical assessment of seronegative villous atrophy; a prospective UK centre experience evaluating 200 adult cases over a 15-year period (2000-2015).

机译:血清阴性绒毛萎缩的临床和表型评估;英国中心在15年期间(2000-2015)评估200例成人病例的经验。

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摘要

BACKGROUND: Seronegative villous atrophy (SNVA) is commonly attributed to coeliac disease (CD). However, there are other causes of SNVA. More recently angiotensin-2-receptor-blockers (A2RBs) have been reported as an association but data on SNVA have been limited to centres evaluating complex case referrals and not SNVA in general. OBJECTIVES: To provide clinical outcomes and associations in a large prospective study overseeing all newcomers with SNVA. DESIGN: Over a 15-year period (2000-2015) we evaluated 200 adult patients with SNVA at a UK centre. A diagnosis of either seronegative CD (SNCD) or seronegative non-CD (SN-non-CD) was reached. Baseline comparisons were made between the groups, with 343 seropositive CD subjects serving as controls. RESULTS: Of the 200 SNVA cases, SNCD represented 31% (n=62) and SN-non-CD 69% (n=138). The human leucocyte antigen (HLA)-DQ2 and/or DQ8 genotype was present in 61%, with a 51% positive predictive value for SNCD. The breakdown of identifiable causes in the SN-non-CD group comprised infections (27%, n=54), inflammatory/immune-mediated disorders (17.5%, n=35) and drugs (6.5%, n=13; two cases related to A2RBs). However, no cause was found in 18% (n=36) and of these 72% (n=26/36) spontaneously normalised duodenal histology while consuming a gluten-enriched diet. Following multivariable logistic regression analysis an independent factor associated with SN-non-CD was non-white ethnicity (OR 10.8, 95% CI 2.2 to 52.8); in fact, 66% of non-whites had GI infections. On immunohistochemistry all groups stained positive for CD8-T-cytotoxic intraepithelial lymphocytes. However, additional CD4-T helper intraepithelial lymphocytes were occasionally seen in SN-non-CD mimicking the changes associated with refractory CD. CONCLUSIONS: Most patients with SNVA do not have CD, in particular those who are not white. Furthermore, a subgroup with no obvious aetiology will show spontaneous histological resolution while consuming gluten. These findings suggest caution in empirically prescribing a gluten-free diet without investigation.
机译:背景:阴性的绒毛萎缩症(SNVA)通常归因于乳糜泻(CD)。但是,还有其他原因导致SNVA。最近,有报道称血管紧张素-2-受体阻滞剂(A2RB)是一种关联,但有关SNVA的数据仅限于评估复杂病例转诊的中心,而不是SNVA。目的:在一项大型前瞻性研究中提供临床结果和相关性,以监督所有SNVA的新来者。设计:在15年期间(2000年至2015年),我们在英国中心评估了200名SNVA成人患者。诊断为血清阴性CD(SNCD)或血清阴性非CD(SN-non-CD)。在各组之间进行基线比较,以343名血清阳性CD受试者作为对照。结果:在200例SNVA病例中,SNCD占31%(n = 62),SN-non-CD 69%(n = 138)。人类白细胞抗原(HLA)-DQ2和/或DQ8基因型的存在率为61%,SNCD的阳性预测值为51%。 SN非CD组中可识别原因的细分包括感染(27%,n = 54),炎症/免疫介导的疾病(17.5%,n = 35)和药物(6.5%,n = 13); 2例与A2RB相关)。然而,在食用富含麸质的饮食的同时,自发归一化的十二指肠组织学中的18%(n = 36)和这72%(n = 26/36)中没有发现原因。经过多变量logistic回归分析,与SN-非CD相关的一个独立因素是非白人种族(OR 10.8,95%CI 2.2至52.8)。实际上,有66%的非白人患有胃肠道感染。在免疫组织化学上,所有组均对CD8-T-细胞毒性上皮内淋巴细胞染色阳性。但是,在SN-非CD中偶尔也可以看到其他CD4-T辅助上皮内淋巴细胞,这与难治性CD相关。结论:大多数SNVA患者没有CD,特别是非白人患者。此外,没有明显病因的亚组在食用面筋时会表现出自发的组织学分辨率。这些发现表明,在未经调查的情况下凭经验开无麸质饮食应谨慎行事。

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