The Inflammatory Neuropathy and Treatment (INCAT) group developed a standardized ELISA method for the detection of serum anti-GM1 antibodies. The diagnostic value of anti-GM1 antibodies determined by this method has not yet been established in large groups of patients. We assessed the reproducibility, sources of variation, optimal cut-off values and evaluated the diagnostic relevance of the INCAT-ELISA in various groups of patients and controls (N = 1232). The coefficient of variance was 11.2% for IgM and 3.8% for IgG. High IgG titers were only found in Guillain-Barré syndrome (GBS) and other inflammatory polyneuropathies. High IgM titers were associated with GBS and multifocal motor neuropathy. Low IgM titers had no additional diagnostic value. The INCAT-ELISA is a reliable test with additional diagnostic value in specific clinical situations.

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doi.org/10.1016/j.jns.2005.07.009, hdl.handle.net/1765/73505
Journal of the Neurological Sciences
Department of Immunology

Kuijf, M., van Doorn, P., Tio-Gillen, A., Geleijns, K., Ang, W., Hooijkaas, H., … Jacobs, B. (2005). Diagnostic value of anti-GM1 ganglioside serology and validation of the INCAT-ELISA. Journal of the Neurological Sciences, 239(1), 37–44. doi:10.1016/j.jns.2005.07.009