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. 2022 Mar 15;14:827500. doi: 10.3389/fnagi.2022.827500

TABLE 1.

Subjects’ demographic and clinical information.

Healthy controls
(n = 55)
ALS patients
(n = 50)
P-value
Age (years) 52.8 ± 6.9 52.3 ± 9.0 0.99
Gender (females/males) 19/36 19/31 0.71
Education (years) 7.8 ± 3.4 7.3 ± 3.9 0.40
Site of onset (bulbar/cervical/lumbosacral) 8/33/9
Diagnostic category (definite/probable/possible) 11/22/17
ALSFRS-R score 40.7 ± 5.3
Disease duration (months) 17.4 ± 16.1
Disease progression rate 0.64 ± 0.59

ALS, amyotrophic lateral sclerosis; ALSFRS-R, revised ALS Functional Rating Scale. “–”, no data available.