{"title":"B-122转谷氨酰胺酶IgA在Bioplex 2200和Phadia 250检测中的差异","authors":"Katherine Turner, Karie McDonald","doi":"10.1093/clinchem/hvaf086.519","DOIUrl":null,"url":null,"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.","PeriodicalId":10690,"journal":{"name":"Clinical chemistry","volume":"28 1","pages":""},"PeriodicalIF":6.3000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"B-122 Discrepant transglutaminase IgA results between Bioplex 2200 and Phadia 250 assays\",\"authors\":\"Katherine Turner, Karie McDonald\",\"doi\":\"10.1093/clinchem/hvaf086.519\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":10690,\"journal\":{\"name\":\"Clinical chemistry\",\"volume\":\"28 1\",\"pages\":\"\"},\"PeriodicalIF\":6.3000,\"publicationDate\":\"2025-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical chemistry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/clinchem/hvaf086.519\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/clinchem/hvaf086.519","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
B-122 Discrepant transglutaminase IgA results between Bioplex 2200 and Phadia 250 assays
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.
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.