Premium
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
Author(s) -
Moore A Russell,
Harris R. Adam,
Jeffries Christina,
Ashton Laura,
Avery Paul R.
Publication year - 2021
Publication title -
veterinary clinical pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 51
eISSN - 1939-165X
pISSN - 0275-6382
DOI - 10.1111/vcp.12993
Subject(s) - paraproteins , immunofixation , capillary electrophoresis , immunoglobulin light chain , multiple myeloma , serum protein electrophoresis , antibody , monoclonal , agarose gel electrophoresis , microbiology and biotechnology , lymphoma , medicine , chemistry , immunology , biology , monoclonal antibody , biochemistry , gene
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.