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Association of blocking acetylcholine receptor antibodies with clinical subtypes and disease severity in myasthenia gravis. | LitMetric

Association of blocking acetylcholine receptor antibodies with clinical subtypes and disease severity in myasthenia gravis.

Clin Chim Acta

Department of Neurology, Huashan Hospital, Fudan University and Institute of Neurology, Fudan University, National Center for Neurological Disorders, Shanghai, China. Electronic address:

Published: September 2025


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Article Abstract

Background And Aim: The identification of serum antibodies, particularly acetylcholine receptor antibodies (AChR-ab), is essential for diagnosing myasthenia gravis (MG). However, the clinical significance of blocking AChR-abs (bAChR-ab) and their correlation with disease severity remain underexplored. This study aims to evaluate the distribution of bAChR-ab across MG subtypes and their correlation with clinical severity.

Methods: 148 MG patients were recruited from Huashan Hospital, Fudan University. The positive ratio of nAChR-ab and bAChR-ab was evaluated, and the correlations of bAChR-ab inhibition rate were analyzed in relation to clinical severity.

Results: Of total148 patients diagnosed with MG, 76 (51.35%) classified as ocular myasthenia gravis (OMG) and 72 (48.65%) as generalized myasthenia gravis (GMG). Thymic abnormalities were more common in GMG, with 19.44% of GMG patients having thymoma compared to 9.21% of OMG patients, though the difference was not statistically significant. 43.24% of patients tested positive for bAChR-ab, with a significantly higher positivity rate observed in GMG (58.33%) compared to patients with OMG. Elevated bAChR-ab inhibition rate significantly correlated with disease severity, while nAChR-ab did not demonstrate any correlation with either the MGC score or the ADL score in either groups.

Conclusion: bAChR-ab was exclusively detected and showed a strong association with severe clinical manifestations, including myasthenic crises. These findings highlight bAChR-ab as a potential biomarker for monitoring MG severity. The role of bAchR-ab in seronegative MG will be further verified. Larger, multi-center studies warrant to validate these results and refine diagnostic and therapeutic strategies for MG management.

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Source
http://dx.doi.org/10.1016/j.cca.2025.120449DOI Listing

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