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. Author manuscript; available in PMC: 2017 May 31.
Published in final edited form as: Neurotoxicology. 2016 Apr 13;54:119–126. doi: 10.1016/j.neuro.2016.03.022

Table 1.

Characteristics of study participants.

Controls (n=229)
N (%)
ALS Cases (n=163)
N (%)
MND Cases (n=193)
N (%)
Age (years), mean ± (SD) 63.4 (9.9) 62.9 (10.8) 63.5 (10.8)

Quartiles*, N (%)

 34–57 65 (28) 41 (25) 48 (25)
 58–64 58 (25) 48 (29) 55 (28)
 65–71 50 (22) 30 (18) 32 (17)
 72–84 56 (24) 44 (27) 58 (30)

Gender, N (%)

 Male 216 (94) 160 (98) 190 (98)
 Female 13 (6) 3 (2) 3 (2)

Race and Ethnicity, N (%)

 Non-Hispanic White 201 (88) 152 (93) 179 (93)
 Other 28 (12) 11 (7) 14 (7)

Cigarette Smoking, N (%)

 Ever 154 (67) 104 (65) 122 (65)
 Never 75 (33) 56 (35) 67 (35)
 Missing 0 3 4

Diagnosis, N (%)

 Clinically definite ALS - 31 (19) 31 (16)
 Clinically probable ALS - 108 (66) 108 (56)
 Clinically possible ALS - 24 (15) 24 (12)
 Progressive muscular atrophy - - 30 (16)

Site of Onset, N (%)

 Spinal - 127 (78) 156 (81)
 Bulbar - 36 (22) 37 (19)

Diagnostic Delay (years), N (%)

 ≤ 1 - 88 (54) 100 (52)
 > 1 - 75 (46) 93 (48)

Collection Delay (months), N (%)

 ≤ 13 - 76 (47) 91 (47)
 > 13 - 87 (53) 102 (53)

ALS Functional Rating Scale-Revised Score, N (%)

 ≤ 29 - 82 (51) 92 (49)
 > 29 - 78 (49) 97 (51)
 Missing - 3 4

Abbreviations: SD, standard deviation.

*

Categorized at quartiles among the controls.

Dichotomized at the median among ALS cases.