Table 2 Demographic, clinical and laboratory data of ALS patients from Halle and Milan (n = 130)

From: Phosphorylated tau 181 and 217 are elevated in serum and muscle of patients with amyotrophic lateral sclerosis

Age (years) at blood collection mean ± SD

63.24 ± 10.50

Female %

41 (31.6)

BMI mean ± SD

24.12 ± 3.73

Site of symptom onset N (%)

 

Bulbar

27 (20.8)

Spinal: upper limbs, trunk, lower limbs

98 (75.4): 49 (37.7), 3 (2.3), 46 (35.4)

Generalised

4 (3.1)

Cognitive

1 (0.7)

Disease duration at blood collection (months) mean ± SD

21.82 ± 20.33

Clinical phenotype N(%)

 

Classic

83 (63.9)

Bulbar

16 (12.3)

UMN-predominant

9 (6.9)

LMN-predominant

22 (16.9)

Diagnosis according to revised El Escorial criteria

Definite

31 (23.8)

Probable

30 (23.1)

Probable laboratory supported

46 (35.4)

Possible

23 (17.7)

King’s staging system

 

1

4 (3.1)

2

65 (50.0)

3

46 (35.4)

4

15 (11.5)

ALSFRS-R score mean ± SD

38.54 ± 8.17

Disease progression rate at blood sampling mean ± SD

0.71 ± 0.62

ECAS total score mean ± SD

100.57 ± 17.58

Blood Creatine Kinase (U/L) Median (IQR) (normal values < 171 U/L)

% of cases with normal values

133.0 (65.9-253.4)

59.3

Blood Troponin T (ng/L) Median (IQR) (normal values < 14 ng/L)

% of cases with normal values

51.0 (16.9-74.3)

19.2

Blood Myoglobin (µg/L) Median (IQR) (normal values 25-72 µg/L)

% of cases with normal values

43.0 (30.6-89.5)

70.6

  1. ALSFRS-R ALS Functional Rating Scale-Revised, BMI body mass index, ECAS Edinburgh Cognitive and Behavioural ALS Screen, IQR interquartile range, LMN lower motor neuron, SD standard deviation, UMN upper motor neuron.