Skip to main content
. 2024 Dec 3;32(1):e16463. doi: 10.1111/ene.16463

TABLE 1.

Description of demographic and clinical characteristics of the study patients (N=220).

Demographic and clinical characteristics Value
Demographics
Sex female, n (%) 120 (54.5)
Median age at first MG symptom, years (P25–P75) 60.5 (44.3–73.0)
Median age at first visit, years (P25–P75) 70.0 (56–83)
Clinical characteristics
Time from first symptom to diagnosis, months (SD) 8.8 (21.3)
Time from baseline visit to diagnosis, days a (SD) 48 (132.0)
Autoimmunity, n (%) b
Anti‐AChR 186 (84.5)
Anti‐MuSK 13 (5.9)
Seronegative 22 (10.0)
Baseline MGFA clinical classification, n (%)
I 77 (35.0)
IIA 48 (21.8)
IIB 58 (26.4)
IIIA 7 (3.2)
IIIB 17 (7.7)
IVA 1 (0.5)
IVB 9 (4.1)
V 3 (1.4)
MGFA class at maximal worsening during the study follow‐up, n (%)
IIA 48 (21.8)
IIB 49 (22.3)
IIIA 34 (15.5)
IIIB 47 (21.4)
IVA 5 (2.3)
IVB 24 (10.9)
V 13 (5.9)
Drug refractory status during study follow‐up, n (%) 22 (10.0)
Death during study period n, (%) 27 (12.3)

Abbreviations: AChR, acetylcholine receptor; MG, myasthenia gravis; MGFA, Myasthenia Gravis Foundation of America; MuSK, muscle‐specific kinase; P, percentile; SD standard deviation.

a

Among the 133 (60.5%) patients who were diagnosed after their first visit.

b

One patient was anti‐AChR‐positive and anti‐MuSK‐positive.