Table 2. Demographic and clinical characteristics of captured and non-captured ALS cases.
Captured cases (n = 106) | Non-captured cases(n = 10) | p Value | |
---|---|---|---|
Age at evaluation (years) | 51.3±10.4 | 56.0±11.7 | 0.173 |
Educational level (years) | 10.5±3.7 | 11.1±4.1 | 0.696 |
Gender (male, %) | 63.2 | 50.0 | 0.462 |
Onset type (bulbar, %) | 20.8 | 50.0 | 0.036 |
Disease duration (months) | 14.2±11.6 | 14.9±12.2 | 0.726 |
Swallowing subscale of ALSSS | 9.2±1.2 | 7.4±2.0 | 0.002 |
ALSFRS-R | 40.8±4.6 | 31.4±8.1 | <0.001 |
Progression rate | 0.7±0.6 | 1.5±1.0 | 0.011 |
ALS, amyotrophic lateral sclerosis; ALSFRS-R, revised ALS functional rating scale; ALSSS, ALS severity scale; the disease progression rate was calculated according to the formula of (48-ALSFRS-R score)/disease duration(month).
Data were means±SD.