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. 2015 Sep 14;10(9):e0137921. doi: 10.1371/journal.pone.0137921

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.