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. 2020 Sep 14;91(12):1329–1338. doi: 10.1136/jnnp-2020-323611

Table 1.

Participant demographics

Covariate ALS 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
Sex 0.972
 Female 51 (40.8) 28 (39.4)
 Male 74 (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
Smoking 0.569
 Non-smoker 68 (54.4) 33 (46.5)
 Former smoker 43 (34.4) 26 (36.6)
 Current smoker 13 (10.4) 10 (14.1)
 Missing 1 (0.8) 2 (2.8)
Family history of ALS
 No 111 (88.8)
 Yes 10 (8.0)
 Missing 4 (3.2)
Age at diagnosis (years) 62.2 (52.7–68.7)
El Escorial criteria
 Suspected 3 (2.4)
 Possible 19 (15.2)
 Probable, LS 37 (29.6)
 Probable 42 (33.6)
 Definite 23 (18.4)
 Missing 1 (0.8)
Onset segment
 Bulbar 38 (30.4)
 Cervical 38 (30.4)
 Lumbar 49 (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.