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麸质敏感性肠病的确诊。体外器官培养模型的应用。

Definitive diagnosis of gluten-sensitive enteropathy. Use of an in vitro organ culture model.

作者信息

Katz A J, Falchuk Z M

出版信息

Gastroenterology. 1978 Oct;75(4):695-700.

PMID:710838
Abstract

The flat mucosal lesion of the small intestine is not pathognomonic of gluten-sensitive enteropathy (GSE). Frequently, the definitive diagnosis of this condition can only be established after three intestinal biopsies are performed: an initial one to show a flat mucosal lesion, one after a gluten-free diet to show morphological recovery, and one after a gluten challenge to show morphological deterioration. We used an organ culture model of GSE to determine the usefulness of this technique in establishing a diagnosis of GSE on the basis of the initial biopsy. Seventy-five patients with diarrhea, and/or malabsorption were evaluated prospectively; 40 had a flat mucosal lesion of variable degree; of these 26 were ultimately determined to have gluten-sensitive enteropathy by the above criteria. A rise in alkaline phosphatase activity of intestinal tissue from 22 of these 26 patients was inhibited when the tissue was cultured in gluten-containing medium as compared to enzyme activities of cultures in a gluten-free medium (108 +/- 69 versus 206 +/- 96, mean +/- SD, P less than 0.001). Mean enzyme values in the similarly cultured intestinal tissue from 13 of 14 patients ultimately shown not to have GSE were not affected by gluten (224 +/- 94 versus 201 +/- 109, P greater than 0.4). Examination of the data by stepwise discriminant analysis provided a function which correctly classified 35 of the 40 patients (88%). The false-positive and false-negative rate for establishing the diagnosis of GSE was 7% (1 of 14) and 15% (4 of 26), respectively. All patients with normal biopsies were classified correctly. The model can be used to establish prospectively the definitive diagnosis of GSE, obviate the need for additional diagnostic biopsies, and allow for the prompt pursuit of alternative diagnoses when gluten sensitivity is not shown.

摘要

小肠扁平黏膜病变并非麸质敏感性肠病(GSE)所特有。通常,只有在进行三次肠道活检后才能确诊该病:首次活检显示扁平黏膜病变,无麸质饮食后活检显示形态恢复,麸质激发试验后活检显示形态恶化。我们使用GSE器官培养模型来确定该技术在基于首次活检确诊GSE方面的实用性。对75例腹泻和/或吸收不良患者进行了前瞻性评估;40例有不同程度的扁平黏膜病变;其中26例最终根据上述标准被确定为患有麸质敏感性肠病。与无麸质培养基中培养的组织相比,这26例患者中有22例的肠道组织碱性磷酸酶活性在含麸质培养基中培养时受到抑制(108±69对206±96,平均值±标准差,P<0.001)。最终显示未患GSE的14例患者中,有13例在类似培养的肠道组织中的平均酶值不受麸质影响(224±94对201±109,P>0.4)。通过逐步判别分析对数据进行检查,得出一个函数,该函数正确分类了40例患者中的35例(88%)。确诊GSE的假阳性率和假阴性率分别为7%(14例中的1例)和15%(26例中的4例)。所有活检正常的患者分类均正确。该模型可用于前瞻性地确诊GSE,无需进行额外的诊断性活检,并在未显示麸质敏感性时允许迅速寻求其他诊断。

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J Clin Invest. 1980 Aug;66(2):227-33. doi: 10.1172/JCI109848.
6
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