Table 1

Clinical characteristics of the study population

All patients (n=115)Men (n=76)Women (n=39)P value*
Age at diagnosis, years45.8±13.743.2±12.350.8±15.1 0.009
Probands71 (62%)50 (66%)21 (54%)0.230
Family history93 (81%)58 (76%)35 (90%)0.130
Diabetes9 (8%)7 (9%)2 (5%)0.716
Hypertension15 (13%)7 (9%)8 (21%)0.142
NYHA III–IV56 (49%)41 (54%)15 (38%)0.167
LVEF at diagnosis, %28.3±12.727.0±12.130.8±13.60.152
LVEDD at diagnosis, mm/m2 31.7±4.631.2±4.432.5±5.00.197
ACE-inhibitor/ARB94 (82%)63 (83%)31 (79%)0.607
Beta blocker82 (71%)55 (%)27 (69%)0.665
Diuretic60 (52%)42 (55%)18 (46%)0.331
Aldosterone antagonist50 (43%)33 (43%)17 (44%)0.999
ICD22 (19%)17 (22%)5 (13%)0.317
CRT-P2 (2%)0 (0%)2 (5%)0.113
CRT-D9 (8%)7 (9%)2 (5%)0.716
AV-block†29 (29%)17 (27%)12 (32%)0.658
Left bundle branch block‡21 (20%)15 (23%)6 (16%)0.456
  • Bold text indicates a statistically significant difference between the sexes.

  • *P values are based on comparisons between men and women.

  • †On latest available ECG without pace rhythm or AF (n=100).

  • ‡On latest available ECG without pace rhythm (n=104).

  • AF, atrial fibrillation; ARB, angiotensin receptor blocker; CRT-D, cardiac resynchronisation therapy defibrillator; CRT-P, cardiac resynchronisation therapy pacemaker; ICD, implantable cardioverter-defibrillator; LVEDD, left ventricular end diastolic diameter; LVEF, left ventricular ejection fraction; NYHA, New York Heart Association functional class.