Table 5.
Predictive value of novel or alternative biomarkers in hereditary cardiomyopathies.
Genetic | Biomarker | Underlying Condition | Pacemaker/ICD | Arrhythmias | Outcome | Number of Patients | Study Design | FU-Duration | Specific Endpoint | Effect on SCD |
---|---|---|---|---|---|---|---|---|---|---|
Oz et al., 2017 [92] | Galectin-3 | ARVD | ICD | VF, VT | Correlation with Galectin-3 | 29 vs. 24 controls | Retrospective, multicenter | - | nsVT/sVT | SCD not directly investigated |
Daidoji et al., 2016 [93] | H-FABP | Brugada syndrome | ICD | Appropriate ICD shock, VF | Correlation with VA | 31 | Prospective, single-center | 5 years | appropriate ICD shock | Independent predictor of SCD * |
Zachariah et al., 2012 [94] | MMP3 | HCM | ICD | VT/VF | MMP3 predicts VA | 45 | Retrospective, single Center | 6 months | CA, sVT/VF with ICD shock | SCD not directly investigated |
Emet et al., 2018 [95] | Galectin-3 | HCM | ICD | SCD | Predictive 5 year risk of SCD | 52 | Cross-sectional data | - | Correlation between the estimated 5-year risk of SCD | SCD not directly investigated |
ARVD, arrhythmogenic right ventricular dysplasia; CA, cardiac arrest; HCM, hypertrophic cardiomyopathy; H-FABP, Heart-type fatty acid binding protein; ICD, implantable cardiac defibrillator; MMP-9, matrix metallo-proteinase; nsVT, non-sustained ventricular tachycardia; SCD, sudden cardiac death; VA, ventricular arrhythmias; VF, ventricular fibrillation; VT ventricular tachycardia. * If patient had ICD, appropriate ICD therapy was defined as sudden cardiac death.