Department of Medical and Surgical Sciences, University of Bologna, Bologna, Emilia-Romagna, Italy.
First Department of Internal Medicine, San Matteo Hospital Foundation, University of Pavia, Pavia, Lombardia, Italy.
Gut. 2020 Nov;69(11):1966-1974. doi: 10.1136/gutjnl-2019-319281. Epub 2020 Feb 14.
Non-coeliac gluten sensitivity (NCGS) is characterised by intestinal and extraintestinal symptoms related to the ingestion of gluten-containing foods, in the absence of coeliac disease (CD) and wheat allergy. No biomarkers are available to diagnose NCGS and the gold standard double-blind placebo-controlled gluten challenge is clinically impractical. The aim of our work was to investigate the role of serum zonulin as a diagnostic biomarker of NCGS and to develop a diagnostic algorithm.
In a multicentre study, we enrolled 86 patients with either self-reported or double-blind confirmed NCGS, 59 patients with diarrhoea-predominant IBS (IBS-D), 15 patients with CD and 25 asymptomatic controls (AC). Zonulin serum levels were assessed and the associated diagnostic power calculated. Clinical and symptomatic data were recorded. The effect of diet on zonulin levels was evaluated in a subgroup of patients with NCGS.
Compared with ACs, the NCGS, irrespective of modality of diagnosis, and patients with CD had significantly increased levels of zonulin, as did both NCGS and patients with CD compared with participants with IBS-D. Self-reported NCGS showed increased zonulin levels compared with double-blind confirmed and not-confirmed NCGS. Six-month wheat avoidance significantly reduced zonulin levels only in HLA-DQ2/8-positive participants with NCGS. The diagnostic accuracy of zonulin levels in distinguishing NCGS from IBS-D was 81%. After exclusion of CD, a diagnostic algorithm combining zonulin levels, symptoms and gender improved the accuracy to 89%.
Zonulin can be considered a diagnostic biomarker in NCGS and combined with demographic and clinical data differentiates NCGS from IBS-D with high accuracy. Wheat withdrawal was associated with a reduction in zonulin levels only in NCGS carrying HLA genotype.
非麸质敏感性肠病(NCGS)的特征是在没有乳糜泻(CD)和小麦过敏的情况下,摄入含麸质的食物后出现肠道和肠道外症状。目前尚无用于诊断 NCGS 的生物标志物,而临床不切实际的金标准双盲安慰剂对照麸质挑战。我们的工作旨在研究血清亲环蛋白作为 NCGS 诊断生物标志物的作用,并开发一种诊断算法。
在一项多中心研究中,我们招募了 86 名自我报告或双盲确认的 NCGS 患者、59 名腹泻为主的肠易激综合征(IBS-D)患者、15 名 CD 患者和 25 名无症状对照(AC)。评估了血清亲环蛋白水平,并计算了相关诊断能力。记录了临床和症状数据。在一组 NCGS 患者中评估了饮食对亲环蛋白水平的影响。
与 AC 相比,NCGS (无论诊断方式如何)和 CD 患者的亲环蛋白水平显著升高,NCGS 和 CD 患者与 IBS-D 患者相比也是如此。与双盲确认和未确认的 NCGS 相比,自我报告的 NCGS 显示亲环蛋白水平升高。仅在 HLA-DQ2/8 阳性的 NCGS 参与者中,六个月的小麦回避显著降低了亲环蛋白水平。亲环蛋白水平区分 NCGS 与 IBS-D 的诊断准确性为 81%。排除 CD 后,结合亲环蛋白水平、症状和性别构建的诊断算法可将准确性提高到 89%。
亲环蛋白可视为 NCGS 的诊断生物标志物,与人口统计学和临床数据相结合,可准确地区分 NCGS 与 IBS-D。只有携带 HLA 基因型的 NCGS 患者在停止食用小麦后亲环蛋白水平降低。