Table 1

Participant demographics

CovariateALS cases
(n=125)
Controls
(n=71)
P value
Age at plasma collection (years)*63.0 (53.0–69.0)61.0 (53.0–65.0)0.362
Sex0.972
 Female51 (40.8)28 (39.4)
 Male74 (59.2)43 (60.6)
BMI at study entry (kg/m2)†25.6 (22.8–29.6)26.6 (23.9–30.3)0.116
Smoking0.569
 Non-smoker68 (54.4)33 (46.5)
 Former smoker43 (34.4)26 (36.6)
 Current smoker13 (10.4)10 (14.1)
 Missing1 (0.8)2 (2.8)
Family history of ALS
 No111 (88.8)
 Yes10 (8.0)
 Missing4 (3.2)
Age at diagnosis (years)62.2 (52.7–68.7)
El Escorial criteria
 Suspected3 (2.4)
 Possible19 (15.2)
 Probable, LS37 (29.6)
 Probable42 (33.6)
 Definite23 (18.4)
 Missing1 (0.8)
Onset segment
 Bulbar38 (30.4)
 Cervical38 (30.4)
 Lumbar49 (39.2)
Time between diagnosis and blood draw (years)*0.57 (0.36–0.75)
Time between symptom onset and diagnosis (years)1.01 (0.68–1.51)
PEG tube present (%)6 (4.8)
  • Table of descriptive statistics for the overall participant study population. Continuous variables represented as the median (25th–75th percentile) and for categorical variables as n (%). P values correspond to Wilcoxon rank-sum tests for continuous variables and χ2 tests for categorical variables. C9orf72 status and ALS family history do not have p values because counts were too small for hypothesis testing.

  • *Median, 25th percentile and 75th percentile are computed using 123 cases and 69 controls (2 cases and 2 controls are missing).

  • †Median, 25th percentile and 75th percentile are computed using 117 cases and 61 controls (8 cases and 10 controls are missing).

  • ALS, amyotrophic lateral sclerosis; BMI, body mass index; GED, Graduate Equivalency Diploma; HS, high school; LS, lab supported; m, metres; NA, not available; PEG, percutaneous endoscopic gastrostomy.