This study assesses the complexity of heart period (HP) and QT variability series through sample entropy (SampEn) in long QT syndrome type 1 individuals. In order to improve signal-to-noise ratio SampEn was evaluated over the original series (SampEn0) and over the residual computed by subtracting the first oscillatory mode identified by empirical mode decomposition (SampEnEMD1R). HP and QT interval were continuously extracted during daytime (2:00-6:00 PM) from 24 hour Holter recordings in 14 non mutation carriers (NMCs) and 34 mutation carriers (MCs) subdivided in 11 asymptomatic (ASYMP) and 23 symptomatic (SYMP). Both NMCs and MCs belonged to the same family line. While SampEn0 did not show differences among the three groups, SampEnEMD1R assessed over the QT series significantly decreased in ASYMP subjects. SampEnEMD1R identified a possible factor (i.e. the lower short scale QT complexity) that might contribute to the different risk profile of the ASYMP group.
Bari, V., Marchi, A., Girardengo, G., George, A., Brink, P., Cerutti, S., et al. (2014). Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 population. In 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBC 2014 (pp. 6671-6674). Institute of Electrical and Electronics Engineers Inc. [10.1109/EMBC.2014.6945158].
Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 population
Crotti, L;
2014
Abstract
This study assesses the complexity of heart period (HP) and QT variability series through sample entropy (SampEn) in long QT syndrome type 1 individuals. In order to improve signal-to-noise ratio SampEn was evaluated over the original series (SampEn0) and over the residual computed by subtracting the first oscillatory mode identified by empirical mode decomposition (SampEnEMD1R). HP and QT interval were continuously extracted during daytime (2:00-6:00 PM) from 24 hour Holter recordings in 14 non mutation carriers (NMCs) and 34 mutation carriers (MCs) subdivided in 11 asymptomatic (ASYMP) and 23 symptomatic (SYMP). Both NMCs and MCs belonged to the same family line. While SampEn0 did not show differences among the three groups, SampEnEMD1R assessed over the QT series significantly decreased in ASYMP subjects. SampEnEMD1R identified a possible factor (i.e. the lower short scale QT complexity) that might contribute to the different risk profile of the ASYMP group.File | Dimensione | Formato | |
---|---|---|---|
Bari 2014 EMBC14_1229_FI FINAL published.pdf
Solo gestori archivio
Dimensione
255.51 kB
Formato
Adobe PDF
|
255.51 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.