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潜在乳糜泻患者真的是潜在的吗?代谢组学的答案。

Are patients with potential celiac disease really potential? The answer of metabonomics.

机构信息

Magnetic Resonance Center (CERM), University of Florence, Sesto Fiorentino, Italy.

出版信息

J Proteome Res. 2011 Feb 4;10(2):714-21. doi: 10.1021/pr100896s. Epub 2010 Dec 13.

Abstract

Celiac disease (CD) is an autoimmune disorder caused by a permanent sensitivity to gluten in genetically susceptible individuals. Accurate diagnosis of CD at an early stage and its treatment with a gluten-free diet (GFD) are important for optimum treatment and prognosis. Recently, by employing a noninvasive metabonomic approach, we have shown that CD has a well-defined metabonomic signature. Here we address potential CD patients, defined as subjects who do not have, and have never had, a jejunal biopsy consistent with clear CD, and yet have immunological abnormalities similar to those found in celiac patients. Sixty-one overt CD patients at diagnosis, 29 patients with potential CD, and 51 control subjects were examined by (1)H NMR of their serum and urine: out of 29 potential CD patients, 24 were classified as CD and 5 as control subjects. Potential CD largely shares the metabonomic signature of overt CD. Most metabolites found to be significantly different between control and CD subjects were also altered in potential CD. Our results demonstrate that metabolic alterations may precede the development of small intestinal villous atrophy and provide a further rationale for early institution of GFD in patients with potential CD, as recently suggested by prospective clinical studies.

摘要

乳糜泻(CD)是一种由遗传易感个体对麸质产生永久性敏感性引起的自身免疫性疾病。早期准确诊断 CD 并采用无麸质饮食(GFD)治疗对获得最佳疗效和预后非常重要。最近,我们采用非侵入性代谢组学方法表明,CD 具有明确的代谢组学特征。在这里,我们研究了疑似 CD 患者,这些患者没有且从未有过空肠活检明确的 CD,但具有与乳糜泻患者相似的免疫异常。对 61 名初诊 CD 患者、29 名疑似 CD 患者和 51 名对照进行了血清和尿液 (1)H NMR 检测:在 29 名疑似 CD 患者中,24 名被归类为 CD,5 名被归类为对照。疑似 CD 与显性 CD 具有相似的代谢组学特征。在对照组和 CD 组之间发现存在显著差异的大多数代谢物在疑似 CD 患者中也发生了改变。我们的结果表明,代谢改变可能先于小肠绒毛萎缩的发生,并为最近前瞻性临床研究提出的疑似 CD 患者早期采用 GFD 提供了进一步的理论依据。

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