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. 2024 Apr 22;15:1382320. doi: 10.3389/fimmu.2024.1382320

Table 1.

Clinical features of 30 participants.

Healthy control (n=10) AChR-positive MG (n=10) Seronegative MG (n=10)
Age, years 41.3 ± 10.7 45.2 ± 11.3 43.1 ± 9.8
Female sex 10 (100%) 10 (100%) 10 (100%)
Onset age, years 33.9 31.8
Disease duration, years 11.3 11.2
MGFA classification
Mild generalized 8 (80%) 0 (0%)
Moderate generalized 2 (20%) 8 (80%)
Severe generalized 0 2 (20%)
Bulbar symptoms 4 (40%) 10 (100%)
Myasthenic crisis 0 (0%) 0 (0%)
AChR Ab positive 10 (100%) 0 (0%)
Treatment
Thymectomy 4 (40%) 1 (10%)
Prednisolone 0 (0%) 10 (100%)
Calcineurin inhibitors 0 (0%) 10 (100%)
IVIg 0 (0%) 10 (100%)
Plasmapheresis 0 (0%) 4 (40%)
Postinterventional status
Minimal manifestations 5 (50%) 0 (0%)
Improved 4 (40%) 3 (30%)
Unchanged 1 (10%) 7 (70%)
Clinical scales*
MGC 4.2 ± 3.1 21.1 ± 3.8/16.8 ± 2.9
MG-ADL 3.2 ± 2.0 14.0 ± 1.3/10.7 ± 1.3
15-item MG-QOL 5.8 ± 4.6 20.1 ± 5.0/15.4 ± 3.8

*Clinical scales were evaluated pre- and post-intravenous immunoglobulin (IVIg) treatment in seronegative myasthenia gravis (MG) patients (indicated as pre- and post- IVIg).

AChR, acetylcholine receptor; MGC, MG composite scale; MG-ADL, MG-Activities of Daily Living.