TABLE 2.
Differential diagnosis between ARVC and Brugada syndrome
Clinical characteristics | ARVC | Brugada syndrome |
---|---|---|
Age | 25–35 | 35–40 |
Sex (male/female) | M > F (3:1) | M > F (8:1) |
Distribution | Worldwide (Italy) | Worldwide (southeast Asia) |
Inheritance | AD (AR) | AD |
Chromosomes | 1, 2, 3, 10, 1417 | 3 |
Gene | hRYR2, plakobin, desmoplakin | SCN5A |
Symptoms | Palpitations | Syncope |
Syncope | Cardiac arrest | |
Cardiac arrest | ||
Circumstances | Effort | Rest |
Imaging | Morpho-functional RV (and LV) abnormalities | Normal |
Pathology | Fibrofatty replacement | Normal |
ECG repolarization | Inverted T-waves in right precordial leads | High take-off ST-segment V1–V3 |
ECG depolarization | Epsilon-waves | RBBB/LAD |
QRS prolongation | Late potentials | |
Late potentials | ||
AV conduction | Normal | 50% abnormal PR/HV intervals |
Atrial arrhythmias | Late (secondary) | Early (primary 10–25%) |
ECG changes | Fixed (mostly) | Variable |
Ventricular arrhythmias | Monomorphic VT/VF | Polymorphic VT/VF |
Mechanism of arrhythmias | Scar-related reentry | Phase 2 reentry |
Drug effect Class I | ↓ | ↑ |
Drug effect Class II | ↓ | ↑ |
Drug effect Class III | ↓ | −/↑ |
Drug effect Class IV | −/↓ | – |
Beta-stimulation | ↑ | ↓ |
Natural history | Sudden death | Sudden death |
Heart failure |
Arrows denote changes in ST segment elevation (↑, increased; ↓, decreased; −/, small change, if any).
Modified from (4), with permission.