Table 1.
ALS patients (N = 35) | Controls (N = 34) | |
---|---|---|
Age (y), mean ± SD | 69.54 ± 10.64 | 68.06 ± 9.59 |
Females, n (%) | 18 (51.4) | 18 (52.9) |
Arterial hypertension, n (%) | 16 (45.7) | 11 (32.4) |
Diabetes, n (%) | 7 (20) | 1 (3) |
Body mass index mean ± SD (kg/m2) | 25.0 ± 5.3 | 25.8 ± 4.2 |
ALS functional rating scale, points | 32.4 ± 8.5 | – |
Forced vital capacity, % | 66.11 ± 25.30 | – |
Spinal/bulbar, n | 23/12 | – |
Creatine kinase (norm <171), U/l | 244 ± 266 | – |
Myocardial creatine kinase (norm <25), U/l | 24 ± 14 | – |
Troponin T (norm <14), ng/l | 0 ± 0 | – |
N-terminal pro brain natriuretic peptide (norm 0–125), pg/ml | 149 ± 206 | – |
Angiotensin converting enzyme inhibitor and angiotensin 1 receptor blockers, n | 10/35 | – |
Beta-blocker, n | 8/35 | – |
Other antihypertensive medication, n | 4/35 | – |
AVB grade II, n | 0 | – |
Atrial fibrillation, n | 0 | – |
Supraventricular tachycardia, n | 0 | – |
NSVT, n | 0 | – |
VCP/h (0–100), n | 20/26 | – |
NSVT, non-sustained ventricular tachycardia; AVB, atrioventricular block; VPC/h, ventricular premature contractions/hour.