From: Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy
 | Overall | MYBPC3 | MYH7 | p value |
---|---|---|---|---|
Age (years) | 51.1 ± 14.2 | 49.8 ± 14.3 | 55.1 ± 13.3 | 0.211 |
Females, n (%) | 15 (23.8%) | 10 (20.8%) | 5 (33.3%) | 0.321 |
BMI (kg/m2) | 26.4 ± 4.4 | 26.1 ± 4.6 | 27.8 ± 3.1 | 0.260 |
Fatigue, n (%) | 9 (14.3%) | 7 (14.6%) | 2 (13.3%) | 0.881 |
Dyspnea, n (%) | 25 (39.7%) | 21 (43.7%) | 4 (26.7%) | 0.238 |
Chest pain, n (%) | 6 (9.5%) | 4 (8.3%) | 2 (13.3%) | 0.565 |
Palpitations, n (%) | 13 (20.6%) | 8 (16.7%) | 5 (33.3%) | 0.177 |
Syncope, n (%) | 10 (15.9%) | 9 (18.7%) | 1 (6.6%) | 0.264 |
Family history of HCM, n (%) | 23 (36.5%) | 22 (45.8%) | 1 (6.6%) | 0.014* |
Comorbidities | ||||
 Diabetes mellitus, n (%) | 3 (4.8%) | 3 (6.2%) | – | – |
 Chronic obstructive pulmonary disease, n (%) | 2 (3.2%) | 2 (4.2%) | – | – |
 Thyroid dysfunction, n (%) | 8 (12.7%) | 7 (14.6%) | 1 (6.7%) | 0.422 |
 Anemia, n (%) | 1 (1.6%) | 1 (2.1%) | – | – |
Laboratory analyses | ||||
 Glucose (mmol/l) | 5.6 ± 1.2 | 5.8 ± 1.3 | 5.0 ± 0.6 | 0.071 |
 Creatinine (µmol/l) | 84.4 ± 17.7 | 85.5 ± 18.3 | 81.3 ± 16.4 | 0.487 |
 Blood urea nitrogen (mmol/l) | 9.0 ± 12.7 | 10.2 ± 15.6 | 6.9 ± 3.9 | 0.472 |
 ALT (U/l) | 30.1 ± 15.7 | 31.8 ± 17.0 | 25.0 ± 10.4 | 0.268 |
 Total protein (g/l) | 69.1 ± 8.4 | 69.3 ± 7.2 | 68.6 ± 11.1 | 0.853 |
 Albumin (g/l) | 44.0 ± 6.8 | 44.1 ± 6.4 | 43.9 ± 8.0 | 0.948 |
 Sodium (mmol/l) | 140.3 ± 2.1 | 140.4 ± 2.1 | 140.2 ± 2.3 | 0.868 |
 Potassium (mmol/l) | 4.5 ± 0.4 | 4.5 ± 0.3 | 4.6 ± 0.5 | 0.531 |
 Calcium (mmol/l) | 2.3 ± 0.1 | 2.3 ± 0.1 | 2.3 ± 0.2 | 0.689 |
 NT-proBNP (ng/l) | 1328.3 ± 1420.2 | 1304.5 ± 1457.5 | 1757.2 ± 1335.2 | 0.766 |