McGowan Kelly E, Lyon Martha E, Butzner J Decker
Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.
Clin Chem. 2008 Jul;54(7):1203-9. doi: 10.1373/clinchem.2008.103606. Epub 2008 May 16.
IgA deficiency causes false-negative IgA-based celiac serology results in patients with celiac disease. Using a case-finding strategy, we examined the prevalence of IgA deficiency, physician evaluation, and management of IgA deficiency during serological testing for celiac disease.
We reviewed consecutive IgA-endomysial antibody (EMA) and serum IgA results from the laboratory database over 17 months. We cross-referenced seronegative patients with IgA deficiency (IgA <0.06 g/L) to the pathology database to evaluate intestinal biopsy results. Ordering physicians received a questionnaire regarding the management of seronegative patients with IgA deficiency who had no biopsy record.
Among the 9533 patients tested for IgA-EMA, 4698 (49%) were tested for IgA deficiency. IgA deficiency occurred in 35 of 4698 (0.75%) patients screened for IgA deficiency. Only 19 of 35 (54%) IgA-deficient patients were diagnosed appropriately with either intestinal biopsy (17 patients) or measurement of IgG-tissue transglutaminase (2 patients). Thirteen (76%) of the 17 IgA-deficient patients who underwent upper endoscopy with or without colonoscopy displayed gastrointestinal pathology on biopsies, including 3 (18%) with celiac disease. No further evaluation to exclude celiac disease was performed for the remaining 16 of 35 (46%) IgA-deficient, EMA-negative patients because of inappropriate management (6 patients), administrative error (7 patients), or patient/physician refusal (3 patients).
IgA deficiency occurred in 1:131 patients tested for celiac disease, and celiac disease occurred in 1:6 of those properly evaluated. Inadequate evaluation of IgA deficiency while testing for celiac disease occurred frequently and resulted in the underdiagnosis of both. Changes in testing algorithms and reporting of results were made to improve testing for celiac disease and IgA deficiency.
IgA缺乏症会导致乳糜泻患者基于IgA的乳糜泻血清学检测结果呈假阴性。我们采用病例发现策略,研究了乳糜泻血清学检测期间IgA缺乏症的患病率、医生评估及对IgA缺乏症的处理情况。
我们回顾了实验室数据库中连续17个月的IgA-肌内膜抗体(EMA)和血清IgA检测结果。我们将IgA缺乏(IgA<0.06g/L)的血清学阴性患者与病理数据库进行交叉对照,以评估肠道活检结果。给开单医生发放一份问卷,询问关于无活检记录的IgA缺乏血清学阴性患者的处理情况。
在9533例接受IgA-EMA检测的患者中,4698例(49%)进行了IgA缺乏检测。在4698例接受IgA缺乏筛查的患者中,有35例(0.75%)存在IgA缺乏。35例IgA缺乏患者中,仅19例(54%)通过肠道活检(17例)或IgG-组织转谷氨酰胺酶检测(2例)得到了正确诊断。17例接受上消化道内镜检查(无论是否同时接受结肠镜检查)的IgA缺乏患者中,有13例(76%)活检显示存在胃肠道病变,其中3例(18%)患有乳糜泻。由于处理不当(6例)、行政失误(7例)或患者/医生拒绝(3例),其余16例(46%)IgA缺乏且EMA阴性的患者未进行进一步评估以排除乳糜泻。
在接受乳糜泻检测的患者中,IgA缺乏症的发生率为1:131,在经过正确评估的患者中,乳糜泻的发生率为1:6。在进行乳糜泻检测时,对IgA缺乏症的评估不足经常发生,导致两者均诊断不足。我们对检测算法和结果报告进行了更改,以改进乳糜泻和IgA缺乏症的检测。