Peer-reviewed veterinary case report
How well blood tests find M-proteins in dogs with multiple myeloma
By Moore, A Russell et al.·Published in Veterinary clinical pathology·2021·Department of Microbiology, United States·View original on PubMed →
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Original publication title: Diagnostic performance of routine electrophoresis and immunofixation for the detection of immunoglobulin paraproteins (M-Proteins) in dogs with multiple myeloma and related disorders: Part 1 - Current performance.
- Species:
- dog
Plain-English summary
A group of dogs diagnosed with multiple myeloma and related disorders underwent tests to detect abnormal proteins in their blood. Researchers found that using a combination of two specific tests, immunofixation with either agarose gel electrophoresis or capillary zone electrophoresis, was more effective at identifying these proteins than using either test alone. The combined tests had a sensitivity of about 83%, meaning they correctly identified most cases of the disease. While immunofixation alone could also detect these proteins, it had some technical challenges. Overall, using both tests together improved diagnosis, but there is still potential for better methods in the future.
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Abstract
BACKGROUND: Routine electrophoresis [agarose gel electrophoresis (AGE) and capillary zone electrophoresis (CZE)] and species-specific immunofixation (IF) can be used alone or in combination to detect immunoglobulin paraprotein (M-protein) and diagnose secretory myeloma-related disorders (sMRD). OBJECTIVE: We aimed to evaluate the performance of AGE, CZE, CZE plus IF (CZE-IF), and AGE plus IF (AGE-IF) for detecting canine serum M-proteins. METHODS: One hundred canine cases that had AGE, CZE, and routine IF performed on serum, and where B-cell lineage neoplasia (such as B-cell lymphoma and plasma cell tumors) had been diagnosed or excluded, were evaluated. Routine IF protocols targeted IgG-FC, IgA, and IgM heavy chains and light chains. IgG4 IF and free light chain IF were also performed. B-cell lineage neoplasms with an M-protein detected, using any available method, were classified as sMRD. Datasets from AGE, CZE, IF, CZE-IF, and AGE-IF (electrophoretograms, gel images, and fraction concentrations) were composed and reviewed. The sensitivity, specificity, and Youden's index for M-protein detection were determined for each dataset. RESULTS: The combination of AGE-IF or CZE-IF was more sensitive (82.9%) than CZE alone (72.0%) or AGE alone (64.6%) and more specific (66.1%, 48.3%, 51.7%, respectively). Immunofixation could be used alone to detect M-proteins (sensitivity 82.9%, specificity 61.9%), but there were technical challenges that complicated the performance and evaluation of the test. Myeloma with free light chains only was found in 5/41 cases of sMRD. CONCLUSIONS: Adding routine IF to routine electrophoresis increases the ability to accurately identify M-proteins; however, there is still room for further diagnostic performance improvements.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/33847384/