Lenhardt A, Plebani A, Marchetti F, Gerarduzzi T, Not T, Meini A, Villanacci V, Martelossi S, Ventura A
Department of Paediatrics, IRCCS Burlo Garofolo, University of Trieste, Via dell'Istria 65/1, 34100 Trieste, Italy.
Dig Liver Dis. 2004 Nov;36(11):730-4. doi: 10.1016/j.dld.2004.06.017.
Selective IgA deficiency is associated with coeliac disease, and studies have shown an increased prevalence of coeliac disease in these patients ranging from 0.71 to 30.7%, depending on the test used for screening.
To determine the sensitivity of IgG anti-gliadin-antibodies and of IgG human-tissue-transglutaminase for diagnosing coeliac disease and assessing its prevalence in subjects with IgA deficiency.
We tested serum samples from 126 IgA-deficient children (66 female, median age: 10.8 years).
All samples were analysed to measure IgG anti-gliadin-antibodies and IgG anti-human-tissue-transglutaminase. Patients testing positive to either test underwent intestinal biopsy. Subjects testing positive for IgG anti-human-tissue-transglutaminase underwent genetic testing for the human leucocyte antigen heterodimer.
Twenty-seven of 126 subjects tested positive for IgG anti-gliadin-antibodies (five of whom tested positive also for IgG anti-human-tissue-transglutaminase) and 18 (including the aforementioned five) for IgG anti-human-tissue-transglutaminase. Intestinal biopsy was performed in 37 of the 40 patients who tested positive (three subjects refused). Eleven had positive intestinal biopsies all of whom tested positive for IgG anti-human-tissue-transglutaminase, but only five of these tested positive also for IgG anti-gliadin-antibodies. All 22 patients testing positive for anti-gliadin-antibody alone had normal intestinal mucosa. All the patients who tested positive for IgG anti-human-tissue-transglutaminase and underwent genetic screening (15/18) had the coeliac-related human leucocyte antigen. Overall, coeliac disease was diagnosed in 11 of the 126 subjects with IgA deficiency (8.7%).
The prevalence of coeliac disease in subjects with total IgA deficiency was 8.7%. Assay of IgG anti-human-tissue-transglutaminase can be recommended for screening coeliac disease in IgA-deficient subjects.
选择性IgA缺乏与乳糜泻相关,研究表明这些患者中乳糜泻的患病率有所增加,根据用于筛查的检测方法不同,患病率在0.71%至30.7%之间。
确定IgG抗麦醇溶蛋白抗体和IgG抗人组织转谷氨酰胺酶对诊断乳糜泻以及评估IgA缺乏患者中乳糜泻患病率的敏感性。
我们检测了126名IgA缺乏儿童(66名女性,中位年龄:10.8岁)的血清样本。
对所有样本进行分析以检测IgG抗麦醇溶蛋白抗体和IgG抗人组织转谷氨酰胺酶。任何一项检测呈阳性的患者均接受肠道活检。IgG抗人组织转谷氨酰胺酶检测呈阳性的受试者接受人类白细胞抗原异二聚体的基因检测。
126名受试者中有27名IgG抗麦醇溶蛋白抗体检测呈阳性(其中5名IgG抗人组织转谷氨酰胺酶检测也呈阳性),18名(包括上述5名)IgG抗人组织转谷氨酰胺酶检测呈阳性。40名检测呈阳性的患者中有37名接受了肠道活检(3名受试者拒绝)。11名患者肠道活检呈阳性,所有这些患者IgG抗人组织转谷氨酰胺酶检测均呈阳性,但其中只有5名IgG抗麦醇溶蛋白抗体检测也呈阳性。仅IgG抗麦醇溶蛋白抗体检测呈阳性的所有22名患者肠道黏膜均正常。所有IgG抗人组织转谷氨酰胺酶检测呈阳性并接受基因筛查的患者(15/18)均具有与乳糜泻相关的人类白细胞抗原。总体而言,126名IgA缺乏受试者中有11名被诊断为乳糜泻(8.7%)。
总IgA缺乏患者中乳糜泻的患病率为8.7%。推荐检测IgG抗人组织转谷氨酰胺酶以筛查IgA缺乏受试者中的乳糜泻。