Study on Changes in Single-Fiber Electromyography and Serum Anti-Acetylcholine Receptor Antibody Levels in Myasthenia Gravis Patients

Tạ Hải Ninh Dương1, , Đình Sơn Nhữ1, Văn Quỳnh Trịnh1, Văn Đàn Nguyễn1, Trung Đức Lê1, Minh Anh Trần1, Thị Tuyến Mầu2, Đăng Tôn Nguyễn3, Thị Yến Đỗ4
1 Học viện Quân y
2 Bệnh viện Ung Bướu Hà Nội
3 Viện Nghiên cứu Hệ Gen
4 Bệnh viện 198 - Bộ Công an

Main Article Content

Abstract

Objective: To evaluate certain characteristics of single-fiber electromyography (SFEMG) testing and the serum concentration of anti-acetylcholine receptor (AchR) antibodies in patients with myasthenia gravis (MG). Methods: A descriptive, cross-sectional study was conducted on 116 patients with myasthenia gravis from January 2023 to December 2024. Patient data were collected using a standardized medical record form. Patients were classified clinically based on the Osserman classification and underwent testing for anti-AchR antibodies and single-fiber electromyography (SFEMG). Results: The female-to-male ratio was 1.9:1. Ptosis was observed in 70.68% of cases. Anti-AchR antibodies were positive in 83.33% of patients. SFEMG was positive in 93.33% of group I MG and 97.67% of group II MG patients. The positivity rate of anti-AchR antibodies in MG grade I patients was 58.3% before treatment, 50% during treatment, and 33.33% after stopping treatment. The concentration of anti-AchR antibodies was correlated with clinical severity based on the Osserman classification (group I: mean concentration = 5.47 nmol/l, lower than group IIa: mean = 7.57 nmol/l; lower than group IIb: mean = 8.72 nmol/l; p<0.05). The SFEMG positivity rate remained unchanged before, during, and after treatment. Conclusion: The concentration of anti-AchR antibodies is positively correlated with the clinical severity of MG as classified by Osserman (p<0.05). SFEMG sensitivity was not affected by treatment, unlike anti-AchR antibody testing (p<0.05). SFEMG demonstrated higher sensitivity compared to anti-AchR antibody testing and was significant for diagnosing ocular myasthenia gravis when compared with anti-AchR antibody testing (p<0.05).

Article Details

References

1. Stålberg E, et al. Single fiber Electromyography, 3rd edition. Edshagen Publishing House, Fiskebackskil. 2010.
2. Ferrero B, Aimo G, Pagni R, et al. Modified and improved anti-acetylcholin receptor (AchR) antibody assay: Comparison of analytical and clinical performance with conventional anti-AChR antibody assay. Clin Chem. 1997; 43.
3. Hiroyuki Murai1, Kimiaki Utsugisawa2. The Japanese clinical guidelines 2022 for myasthenia gravis and Lambert-Eaton myasthenic syndrome. 2022.
4. Guan YZ, Cui LY, Liu MS, et al. Single-fiber electro-myography in the extensor digitorum communis for the predictive prognosis of ocular myasthenia gravis: A retrospective study of 102 cases. Chinese Medical Journal. 2015; 128:2783-2786.
5. Bệnh viện Quân y 103. Quy trình kĩ thuật chuyên ngành thần kinh. 2021; 32:73.
6. Long YL, Najjar RP, Teo KY, et al. A reappraisal of diagnostic tests for myasthenia gravis in a large Asian cohort. Journal of the Neurological Sciences. 2017; 376:153-158.
7. Dumitru D, Amato AA. Neuromuscular junction. Electrodiagnotic medicine, 2nd edition, Handley& Belfus. 2002; 1127-1212.