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Table 1 Participant clinical information and demographics

From: Impairment of brain short association fibers across clinical stages in amyotrophic lateral sclerosis: a new biomarker mirroring disease progression

 

HC

Stage 1

Stage 2

Stage 3

Stage 4

p value

Age (years)

54.4 ± 7.0

55.9 ± 10.0

54.2 ± 10.7

56.1 ± 9.1

56.2 ± 12.3

0.902 a

Sex (male/female)

22/15

10/5

24/12

12/13

6/5

0.632 b

Education (years)

7.5 ± 3.2

7.1 ± 4.8

7.3 ± 3.8

6.4 ± 4.0

6.8 ± 4.8

0.702 c

Site of onset (spinal/bulbar)

-

13/2

31/5

22/3

9/2

 

Diagnosis (possible/probable laboratory-supported/probable/definite)

-

7/3/2/3

7/2/21/6

3/1/12/9

3/0/5/3

 

ASLFRS-R score

-

43.9 ± 2.1

41.4 ± 2.6

35.0 ± 6.8 *, #

33.0 ± 6.0 *, #

 < 0.001 c

Disease duration (months)

-

14.7 ± 12.0

12.5 ± 7.8

14.4 ± 9.2

19.5 ± 15.1

0.562 c

Disease progression rate

-

0.5 ± 0.4

0.8 ± 0.5

1.2 ± 0.8 *

1.5 ± 1.8

0.001 c

  1. The numbers are the means ± standard deviations. a, b, and c were determined by one-way analysis of variance, the chi-square test, and the Kruskal‒Wallis test, respectively. The superscript symbols * and # indicate significant differences (Bonferroni-corrected for multiple comparisons) compared with the ALS Stage 1 group and Stage 2 group, respectively. ALSFRS-R, revised amyotrophic lateral sclerosis functional rating scale; HC, healthy control