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网硬蛋白自身抗体血清学转换可预测胰岛素依赖型糖尿病患者的乳糜泻。

Seroconversion of reticulin autoantibodies predicts coeliac disease in insulin dependent diabetes mellitus.

作者信息

Mäki M, Huupponen T, Holm K, Hällström O

机构信息

Department of Clinical Medicine, University of Tampere, Finland.

出版信息

Gut. 1995 Feb;36(2):239-42. doi: 10.1136/gut.36.2.239.

Abstract

Serum IgA class reticulin autoantibody test was performed prospectively once a year on 238 children and adolescents with insulin dependent diabetes mellitus (IDDM). At the initial testing, within one year after onset of IDDM, five were positive and 233 were negative. During follow up a further 11 of the initially antibody negative children became positive (6.7%). Jejunal biopsy was performed at the appearance of the autoantibodies and silent coeliac disease was shown in nine (3.8%). One of these children showed on initial biopsy after the onset of IDDM to have normal jejunal mucosal architecture deteriorating later to a flat lesion. Jejunal immunohistochemical studies of another of the patients positive for reticulin autoantibodies but normal on routine biopsy showed an increased density of intraepithelially located gamma/delta T cells and aberrant HLA-DR expression in the crypts pointing to ongoing mucosal inflammation and potential coeliac disease. This study shows that in IDDM patients, reticulin autoantibody negative subjects become antibody positive, which may be followed by coeliac disease. Repeated serological screening and rebiopsy should be considered to detect late developing clinically silent coeliac disease among patients with IDDM.

摘要

对238例胰岛素依赖型糖尿病(IDDM)儿童和青少年前瞻性地每年进行一次血清IgA类网硬蛋白自身抗体检测。在初次检测时,即IDDM发病后一年内,5例呈阳性,233例呈阴性。在随访期间,最初抗体阴性的儿童中有另外11例转为阳性(6.7%)。在自身抗体出现时进行空肠活检,9例(3.8%)显示为无症状性乳糜泻。其中1例儿童在IDDM发病后的初次活检显示空肠黏膜结构正常,后来恶化为扁平病变。另1例网硬蛋白自身抗体阳性但常规活检正常的患者的空肠免疫组化研究显示,上皮内γ/δT细胞密度增加,隐窝中HLA-DR表达异常,提示存在持续的黏膜炎症和潜在的乳糜泻。这项研究表明,在IDDM患者中,网硬蛋白自身抗体阴性的受试者会转为抗体阳性,随后可能会发生乳糜泻。应考虑进行重复血清学筛查和再次活检,以在IDDM患者中检测出晚期发生的临床无症状性乳糜泻。

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