B-122 Discrepant transglutaminase IgA results between Bioplex 2200 and Phadia 250 assays

IF 6.3 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Katherine Turner, Karie McDonald
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引用次数: 0

Abstract

Background Transglutaminase (tTg) IgA plus total IgA is the recommended screening test for patients over two years old for Celiac Disease. Other tests, such as Endomysial IgA (EMA), may be useful in diagnosing patients when the tTg IgA is equivocal due to the higher specificity of EMA compared to tTg IgA. For patients with Celiac Disease, tTg IgA is a useful marker to monitor disease activity when subscribing to a gluten-free diet. To consolidate antibody testing to a single vendor, tTg IgA was moved from a Phadia 250 assay (EliA Celikey IgA) to a Bioplex 2200 assay (Celiac IgA). Methods To verify the accuracy of tTg IgA on the Bioplex 2200 assay, 65 residual patient sera samples were analyzed on both the Phadia 250 and Bioplex 2200 assay. Results 90.7% were qualitatively concordant between instruments (table 1). Conclusion In our laboratory we offer a Celiac Cascade consisting of tTg IgA plus total IgA. In the cascade when tTg IgA is equivocal it is reflexed to EMA. With the implementation of the Bioplex 2200 assay there is no longer an equivocal range. In our accuracy study we identified a small cohort of patients that tested equivocal on the Phadia 250 assay (7-10 U/mL) and as low positives on the Bioplex 2200 assay (reference range <15 U/mL). The five samples that were equivocal on the Phadia 250 assay resulted in a median (min, max) Bioplex 2200 result of 34.4 U/mL (29.6-73.3). As a result, we modified our cascade so any weakly positive tTg IgA (15-30 U/mL) will reflex to EMA. Post go-live there have been three clinical reports of Celiac Disease patients adhering to a gluten-free diet who tested either as high negative or equivocal on the Phadia 250 assay before the assay transition and are now weakly positive (<30 U/mL) on the Bioplex 2200 assay with a negative EMA. In conclusion, it is recommended that if the tTg IgA is a low positive (15-30 U/mL) by the Bioplex 2200 assay, reflex to EMA. If the EMA is negative, it can be concluded that the patient does not have active disease and is most likely compliant with a gluten-free diet.
B-122转谷氨酰胺酶IgA在Bioplex 2200和Phadia 250检测中的差异
背景:转谷氨酰胺酶(tTg) IgA加总IgA是推荐用于2岁以上乳糜泻患者的筛查试验。由于EMA比tTg IgA特异性更高,其他测试,如肌内膜IgA (EMA)可能对tTg IgA模棱两可的患者诊断有用。对于乳糜泻患者,tTg IgA是监测疾病活动的有用标记,当他们订阅无麸质饮食时。为了将抗体检测整合到单一供应商,tTg IgA从Phadia 250检测(EliA Celikey IgA)转移到Bioplex 2200检测(乳糜泻IgA)。方法为验证Bioplex 2200法检测tTg IgA的准确性,采用Phadia 250法和Bioplex 2200法分析65例患者剩余血清样本。结果90.7%仪器间定性一致(表1)。结论我们提供了由tTg IgA加总IgA组成的乳糜泻级联反应。在级联中,当tTg IgA模棱两可时,它会反射到EMA。随着Bioplex 2200测定法的实施,不再有一个模棱两可的范围。在我们的准确性研究中,我们确定了一小群患者,他们在Phadia 250检测(7-10 U/mL)中检测结果模棱两可,在Bioplex 2200检测(参考范围15 U/mL)中检测结果低阳性。Phadia 250检测结果不确定的5个样品中位(最小、最大)Bioplex 2200结果为34.4 U/mL(29.6-73.3)。因此,我们修改了我们的级联,使任何弱阳性的tTg IgA (15-30 U/mL)都会反射到EMA。在此之后,已有3例乳糜泻患者坚持无麸质饮食的临床报告,他们在检测转换前的Phadia 250检测结果为高阴性或模棱两可,而现在在Bioplex 2200检测结果为弱阳性(30 U/mL), EMA为阴性。总之,如果tTg IgA通过Bioplex 2200检测呈低阳性(15-30 U/mL),建议对EMA进行反射。如果EMA为阴性,则可以得出结论,患者没有活动性疾病,并且很可能符合无麸质饮食。
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来源期刊
Clinical chemistry
Clinical chemistry 医学-医学实验技术
CiteScore
11.30
自引率
4.30%
发文量
212
审稿时长
1.7 months
期刊介绍: Clinical Chemistry is a peer-reviewed scientific journal that is the premier publication for the science and practice of clinical laboratory medicine. It was established in 1955 and is associated with the Association for Diagnostics & Laboratory Medicine (ADLM). The journal focuses on laboratory diagnosis and management of patients, and has expanded to include other clinical laboratory disciplines such as genomics, hematology, microbiology, and toxicology. It also publishes articles relevant to clinical specialties including cardiology, endocrinology, gastroenterology, genetics, immunology, infectious diseases, maternal-fetal medicine, neurology, nutrition, oncology, and pediatrics. In addition to original research, editorials, and reviews, Clinical Chemistry features recurring sections such as clinical case studies, perspectives, podcasts, and Q&A articles. It has the highest impact factor among journals of clinical chemistry, laboratory medicine, pathology, analytical chemistry, transfusion medicine, and clinical microbiology. The journal is indexed in databases such as MEDLINE and Web of Science.
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