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抗GM1神经节苷脂血清学的诊断价值及INCAT-ELISA的验证

Diagnostic value of anti-GM1 ganglioside serology and validation of the INCAT-ELISA.

作者信息

Kuijf Mark L, van Doorn Pieter A, Tio-Gillen Anne P, Geleijns Karin, Ang C Wim, Hooijkaas Herbert, Hop Wim C J, Jacobs Bart C

机构信息

Department of Neurology, Erasmus Medical Center, Dr. Molewaterplein 50, 3015 GE, Rotterdam, The Netherlands.

出版信息

J Neurol Sci. 2005 Dec 15;239(1):37-44. doi: 10.1016/j.jns.2005.07.009. Epub 2005 Sep 8.

Abstract

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.

摘要

炎症性神经病与治疗(INCAT)小组开发了一种标准化酶联免疫吸附测定(ELISA)方法,用于检测血清抗GM1抗体。通过该方法测定的抗GM1抗体的诊断价值尚未在大量患者群体中得到确立。我们评估了其可重复性、变异来源、最佳临界值,并在不同患者组和对照组(N = 1232)中评估了INCAT-ELISA的诊断相关性。IgM的变异系数为11.2%,IgG为3.8%。高IgG滴度仅在吉兰-巴雷综合征(GBS)和其他炎症性多发性神经病中发现。高IgM滴度与GBS和多灶性运动神经病相关。低IgM滴度没有额外的诊断价值。INCAT-ELISA是一种可靠的检测方法,在特定临床情况下具有额外的诊断价值。

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