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. 2020 Dec 3;11:579094. doi: 10.3389/fneur.2020.579094

Table 1.

Clinical information of patients with ALS and HCs.

ALS HCs
n = 30 n = 20
Male, n (%) 21 (70.0) 5 (25.0)
Age* 59.0 (52.5–64.0) 26.0 (24.0–45.8)
Disease duration (months)* 17.8 (12.4–29.1) NA
Diagnostic delay (months)* (n = 25) 8.0 (4.9–12.0) NA
Site of onset NA
  Spinal onset, n (%) 22 (73.3)
  Bulbar onset, n (%) 8 (26.7)
ALSFRS-r* (n = 26) 33.0 (29.3–42.0) NA
DPR* (n = 26) 0.49 (0.25–0.83) NA
FVC* (n = 18) 74.1 (70.0–79.0) NA
Clinical stage, n (%) NA
  Stage 2 10 (33.3)
  Stage 3 11 (36.7)
  Stage 4 9 (30)
Riluzole, n (%) 20 (66.7) NA

ALS, amyotrophic lateral sclerosis; ALSFRS-r, amyotrophic lateral sclerosis functional rating scale revised; DPR, Disease progression rate; FVC, forced vital capacity; HCs, Healthy controls; NA, not available; NFL, Neurofilament light chain.

*

Data are presented as median (interquartile range).