Serum IgG anti-GD1a antibody and mEGOS predict outcome in Guillain-Barré syndrome

Author:

Yamagishi Yuko,Kuwahara Motoi,Suzuki Hidekazu,Sonoo MasahiroORCID,Kuwabara SatoshiORCID,Yokota Takanori,Nomura Kyoichi,Chiba Atsuro,Kaji Ryuji,Kanda Takashi,Kaida Ken-ichi,Mutoh TatsuroORCID,Yamasaki RyoORCID,Takashima Hiroshi,Matsui Makoto,Nishiyama Kazutoshi,Sobue GenORCID,Kusunoki SusumuORCID

Abstract

ObjectiveApproximately 15%–20% of patients with Guillain-Barré syndrome (GBS) are unable to walk independently at 6 months from the onset of neurological symptom. The modified Erasmus GBS outcome score (mEGOS) has been reported as a prognostic tool.Herein we investigated the association between a poor outcome, inability to walk independently at 6 months and presence of antiganglioside antibodies.MethodsThe clinical and serological data of 177 patients with GBS were retrospectively collected in Japan to assess the associations between a poor outcome and serum IgG antibodies against each ganglioside (GM1, GD1a, GalNAc-GD1a, GQ1b and GT1a). In addition, we investigated whether the combination of mEGOS and serum IgG antibodies against gangliosides is useful in predicting a poor outcome.ResultsThe patients with IgG anti-GD1a antibodies more frequently showed poor outcomes than those without these antibodies (9 (36%) of 25 vs 8 (6%) of 127 patients, p<0.001). Particularly, 80% showed a poor outcome when they had both serum IgG anti-GD1a antibody and a high mEGOS of ≥10 on day 7 of admission.ConclusionsThe combination of serum IgG anti-GD1a antibodies and a high mEGOS could help in making a more accurate prognosis of patients than mEGOS alone, especially for predicting poor outcomes.

Funder

Japan Agency for Medical Research and Development

The Ministry of Health, Labour and Welfare of Japan

Japan Society for the Promotion of Science

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

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