Table 1

ALS and control participant demographics

CovariateCases (n=164)Controls (n=105)P value
Age at sample collection (years)65.3 (57.2–72.1)62.4 (55.2–68.5)0.016
Body mass index (kg/m2)*26.3 (23.2–30.1)26.5 (23.4–29.7)0.747
Sex0.001
 Female82 (50.0)74 (70.5)
 Male82 (50.0)31 (29.5)
Military service0.414
 No148 (90.2)93 (88.6)
 Yes14 (8.5)5 (4.8)
 Missing2 (1.2)7 (6.7)
Education<0.001
 High school or less54 (32.9)8 (7.6)
 Some postsecondary58 (35.4)24 (22.9)
 Bachelor’s degree29 (17.7)36 (34.3)
 Graduate degree19 (11.6)30 (28.6)
 Missing4 (2.4)7 (6.7)
RaceNA
 American Indian/Alaska Native1 (0.6)0 (0.0)
 Asian3 (1.8)3 (2.9)
 Black or African American3 (1.8)5 (4.8)
 White157 (95.7)97 (92.4)
ALSFRS-R†36 (31–41)
Time between symptom onset and diagnosis (years)‡1.02 (0.59–1.67)
Time between diagnosis and sample acquisition (years)0.48 (0.26–0.94)
Observed death
 Yes147 (89.6)
 No17 (10.4)
El Escorial criteria
 Possible/suspected28 (17.1)
 Probable, lab supported32 (19.5)
 Probable47 (28.7)
 Definite57 (34.8)
Onset segment
 Bulbar55 (33.5)
 Cervical49 (29.9)
 Lumbar59 (36.0)
 Cannot be determined1 (0.6)
  • Table of descriptive statistics for the study population. For continuous variables, median (25th–75th percentile), and for categorical variables, N (%). P values for continuous and categorical variables correspond to t-tests and χ2 tests, respectively.

  • *Body mass index is observed for 157 cases and 93 controls.

  • †ALSFRS-R is observed for 162 cases.

  • ‡Time between symptom onset and diagnosis is observed for 163 cases.

  • ALS, amyotrophic lateral sclerosis; ALSFRS-R, revised amyotrophic lateral sclerosis functional rating scale.