You are viewing the site in preview mode

Skip to main content

Table 4 Logistic regression results for the associations of TDP-43 positivity with the clinical, demographic and biological characteristics of patients with MND

From: TDP-43 seeding activity in the olfactory mucosa of patients with amyotrophic lateral sclerosis

Clinical parameter

Group

TDP-43_SAA result

Univariate OR (95% CI, p value)

Negative

Positive

Sex

Female

18 (64.3%)

10 (35.7%)

ref

Male

30 (51.7%)

28 (48.3%)

1.680 (0.672–4.367, p = 0.2737)

Age, years

Mean (SD)

61.0 (10.3)

63.1 (9.8)

1.021 (0.979–1.068, p = 0.3357)

BMI, kg/m2

Mean (SD)

23.9 (3.4)

24.8 (3.9)

1.077 (0.952–1.228, p = 0.2470)

Genotype

Genetic

12 (57.1%)

9 (42.9%)

ref

Sporadic

36 (55.4%)

29 (44.6%)

1.074 (0.399–2.965, p = 0.8878)

Clinical phenotype*

sALS

29 (60.4%)

19 (39.6%)

ref

bALS

14 (58.3%)

10 (41.7%)

1.090 (0.396–2.950, p = 0.8651)

PLS

4 (36.4%)

7 (63.6%)

2.671 (0.708–11.391, p = 0.1562)

FOSMN

1 (50.0%)

1 (50.0%)

1.526 (0.058–40.182, p = 0.7698)

Cognitive phenotype

Normal

25 (55.6%)

20 (44.4%)

ref

Impaired

17 (56.7%)

13 (43.3%)

0.956 (0.373–2.427, p = 0.9243)

ECAS, ALS-specific

Mean (SD)

68.8 (11.8)

69.3 (13.6)

1.003 (0.965–1.044, p = 0.8703)

ECAS, non-ALS specific

Mean (SD)

26.0 (4.5)

25.4 (4.3)

0.970 (0.867–1.082, p = 0.5826)

ECAS, total

Mean (SD)

94.7 (14.5)

94.6 (16.1)

1.000 (0.968–1.033, p = 0.9822)

Disease duration, months

Mean (SD)

29.9 (29.1)

35.2 (32.5)

1.006 (0.991–1.021, p = 0.4326)

King’s clinical staging

1

7 (53.8%)

6 (46.2%)

ref

2

20 (69.0%)

9 (31.0%)

0.525 (0.134–2.046, p = 0.3476)

3

12 (60.0%)

8 (40.0%)

0.778 (0.186–3.239, p = 0.7269)

4a

2 (66.7%)

1 (33.3%)

0.583 (0.024–7.681, p = 0.6887)

4b

2 (33.3%)

4 (66.7%)

2.333 (0.328–21.558, p = 0.4104)

ΔFS

Mean (SD)

0.6 (0.7)

0.6 (0.6)

1.031 (0.458–2.215, p = 0.9358)

Rate of progression

Slow

26 (61.9%)

16 (38.1%)

ref

Intermediate

9 (60.0%)

6 (40.0%)

1.083 (0.312–3.595, p = 0.8965)

Fast

7 (53.8%)

6 (46.2%)

1.393 (0.386–4.941, p = 0.6050)

Riluzole treatment

Absent

32 (54.2%)

27 (45.8%)

ref

Present

16 (59.3%)

11 (40.7%)

0.815 (0.318–2.039, p = 0.6636)

TDP-43 Simoa, pg/ml

Mean (SD)

3 958.2 (2 472.2)

3 565.8 (2 098.5)

1.000 (1.000–1.000, p = 0.5360)

NfL Lumipulse

Mean (SD)

79.9 (66.8)

87.0 (72.8)

1.002 (0.993–1.010, p = 0.7067)

  1. *Regardless of the genotype. The data reported in the “TDP-43 result” columns are the number of patients and, in parenthesis, percentages, unless otherwise specified. Abbreviations: ref = reference level; SD = standard deviation; OR = odds ratio; CI = confidence interval; BMI = body mass index; sALS = spinal-onset amyotrophic lateral sclerosis; bALS = bulbar-onset amyotrophic lateral sclerosis; PLS = primary lateral sclerosis; FOSMN = facial onset sensory and motor neuronopathy; ECAS = Edinburgh Cognitive and Behavioral ALS Screen; ΔFS = disease progression rate