TY - JOUR
T1 - Standard ECG for differential diagnosis between Anderson-Fabry disease and hypertrophic cardiomyopathy
AU - Vitale, Giovanni
AU - Ditaranto, Raffaello
AU - Graziani, Francesca
AU - Tanini, Ilaria
AU - Camporeale, Antonia
AU - Lillo, Rosa
AU - Rubino, Marta
AU - Panaioli, Elena
AU - Di Nicola, Federico
AU - Ferrara, Valentina
AU - Zanoni, Rossana
AU - Caponetti, Angelo Giuseppe
AU - Pasquale, Ferdinando
AU - Graziosi, Maddalena
AU - Berardini, Alessandra
AU - Ziacchi, Matteo
AU - Biffi, Mauro
AU - Santostefano, Marisa
AU - Liguori, Rocco
AU - Taglieri, Nevio
AU - Nardi, Elena
AU - Linhart, Ales
AU - Olivotto, Iacopo
AU - Rapezzi, Claudio
AU - Biagini, Elena
PY - 2022
Y1 - 2022
N2 - Objectives To evaluate the role of the ECG in the differential diagnosis between Anderson-Fabry disease (AFD) and hypertrophic cardiomyopathy (HCM). Methods In this multicentre retrospective study, 111 AFD patients with left ventricular hypertrophy were compared with 111 patients with HCM, matched for sex, age and maximal wall thickness by propensity score. Independent ECG predictors of AFD were identified by multivariate analysis, and a multiparametric ECG score-based algorithm for differential diagnosis was developed. Results Short PR interval, prolonged QRS duration, right bundle branch block (RBBB), R in augmented vector left (aVL) >= 1.1 mV and inferior ST depression independently predicted AFD diagnosis. A point-by-point ECG score was then derived with the following diagnostic performances: c-statistic 0.80 (95% CI 0.74 to 0.86) for discrimination, the Hosmel-Lemeshow chi(2) 6.14 (p=0.189) for calibration, sensitivity 69%, specificity 84%, positive predictive value 82% and negative predictive value 72%. After bootstrap resampling, the mean optimism was 0.025, and the internal validated c-statistic for the score was 0.78. Conclusions Standard ECG can help to differentiate AFD from HCM while investigating unexplained left ventricular hypertrophy. Short PR interval, prolonged QRS duration, RBBB, R in aVL >= 1.1 mV and inferior ST depression independently predicted AFD. Their systematic evaluation and the integration in a multiparametric ECG score can support AFD diagnosis.
AB - Objectives To evaluate the role of the ECG in the differential diagnosis between Anderson-Fabry disease (AFD) and hypertrophic cardiomyopathy (HCM). Methods In this multicentre retrospective study, 111 AFD patients with left ventricular hypertrophy were compared with 111 patients with HCM, matched for sex, age and maximal wall thickness by propensity score. Independent ECG predictors of AFD were identified by multivariate analysis, and a multiparametric ECG score-based algorithm for differential diagnosis was developed. Results Short PR interval, prolonged QRS duration, right bundle branch block (RBBB), R in augmented vector left (aVL) >= 1.1 mV and inferior ST depression independently predicted AFD diagnosis. A point-by-point ECG score was then derived with the following diagnostic performances: c-statistic 0.80 (95% CI 0.74 to 0.86) for discrimination, the Hosmel-Lemeshow chi(2) 6.14 (p=0.189) for calibration, sensitivity 69%, specificity 84%, positive predictive value 82% and negative predictive value 72%. After bootstrap resampling, the mean optimism was 0.025, and the internal validated c-statistic for the score was 0.78. Conclusions Standard ECG can help to differentiate AFD from HCM while investigating unexplained left ventricular hypertrophy. Short PR interval, prolonged QRS duration, RBBB, R in aVL >= 1.1 mV and inferior ST depression independently predicted AFD. Their systematic evaluation and the integration in a multiparametric ECG score can support AFD diagnosis.
KW - Bundle-Branch Block
KW - Cardiomyopathy, Hypertrophic
KW - Diagnosis, Differential
KW - Electrocardiography
KW - Fabry Disease
KW - Humans
KW - Hypertrophy, Left Ventricular
KW - Retrospective Studies
KW - cardiomyopathy
KW - electrocardiography
KW - genetic diseases
KW - hypertrophic
KW - inborn
KW - metabolic diseases
KW - Bundle-Branch Block
KW - Cardiomyopathy, Hypertrophic
KW - Diagnosis, Differential
KW - Electrocardiography
KW - Fabry Disease
KW - Humans
KW - Hypertrophy, Left Ventricular
KW - Retrospective Studies
KW - cardiomyopathy
KW - electrocardiography
KW - genetic diseases
KW - hypertrophic
KW - inborn
KW - metabolic diseases
UR - http://hdl.handle.net/10807/214624
U2 - 10.1136/heartjnl-2020-318271
DO - 10.1136/heartjnl-2020-318271
M3 - Article
SN - 1468-201X
VL - 108
SP - 54
EP - 60
JO - Heart
JF - Heart
ER -