Research Article
Intra-QT Spectral Coherence as a Possible Noninvasive Marker
of Sustained Ventricular Tachycardia
Gianfranco Piccirillo,
1
Federica Moscucci,
1
Alessandro Persi,
1
Daniele Di Barba,
1
Maria Antonella Pappadà,
1
Pietro Rossi,
2
Raffaele Quaglione,
1
Bich Lien Nguyen,
1
Francesco Barillà,
1
Matteo Casenghi,
3
and Damiano Magrì
3
1
Dipartimento di Scienze Cardiovascolari, Respiratorie, Nefrologiche, Anestesiologiche e Geriatriche, Policlinico Umberto I,
“Sapienza” University of Rome, Viale del Policlinico No. 155, 00185 Roma, Italy
2
Division of Cardiology, S. Giovanni Calibita Fatebenefratelli Hospital, Isola Tiberina, Piazza Ponte dei Quattro Capi,
39 186 Roma, Italy
3
Dipartimento di Medicina Clinica e Molecolare, S. Andrea Hospital, “Sapienza” University of Rome, Via di Grottarossa 1035/1039,
00189 Roma, Italy
Correspondence should be addressed to Gianfranco Piccirillo; gianfranco.piccirillo@uniroma1.it
Received 18 March 2014; Accepted 28 May 2014; Published 15 July 2014
Academic Editor: Jason Ng
Copyright © 2014 Gianfranco Piccirillo et al. his is an open access article distributed under the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly
cited.
Sudden cardiac death is the main cause of mortality in patients afected by chronic heart failure (CHF) and with history of
myocardial infarction. No study yet investigated the intra-QT phase spectral coherence as a possible tool in stratifying the
arrhythmic susceptibility in patients at risk of sudden cardiac death (SCD). We, therefore, assessed possible diference in spectral
coherence between the ECG segment extending from the wave to the T wave peak (QT
) and the one from T wave peak to the
T wave end (T
e
) between patients with and without Holter ECG-documented sustained ventricular tachycardia (VT). None of the
QT variability indexes as well as most of the coherences and RR power spectral variables signiicantly difered between the two
groups except for the QT
-T
e
spectral coherence. he latter was signiicantly lower in patients with sustained VT than in those
without (0.508±0.150 versus 0.607±0.150, < 0.05). Although the responsible mechanism remains conjectural, the QT
-T
e
spectral coherence holds promise as a noninvasive marker predicting malignant ventricular arrhythmias.
1. Introduction
A prospective multicenter study indicates the myocardial
temporal repolarization dispersion, measured with the beat-
to-beat QT variability index (QTVI), as a marker predicting
cardiac death without speciically predicting sudden cardiac
death (SCD) in patients with chronic heart failure (CHF)
[1]. A possible explanation might be that QTVI results in
a better electrocardiographic (ECG) marker for the severity
of CHF than for SCD, being closely inluenced also by
the severity of let ventricular dysfunction and neurohu-
moral activation [2–5]. Nonetheless, the QTVI is custom-
arily calculated together with another marker that assesses
changes in myocardial temporal repolarization, namely, the
spectral coherence between the QT and RR intervals [2–5].
he QT-RR spectral coherence uses a value ranging from 0
to 1 to express whether the two ECG signals yield coherent
oscillations over time, and it reaches maximum when QT
and RR interval oscillations proportionally correspond [2–
5]. Unfortunately, this speciic index is more complex to
calculatethan the simple correlation between the myocardial
action potential duration and the diastolic interval expressed
with ventricular electrical restitution curves. Indeed, QT-RR
interval spectral coherence evaluates temporal patterns in
oscillating signals whereas regression curves or lines measure
QT variations as a function of RR interval variations. In
healthy subjects, QT-RR interval spectral coherence tends to
remain relatively low (less than 0.400) but it logically tends
to decrease further in CHF (less than 0.300) [2–5]. Because
Hindawi Publishing Corporation
BioMed Research International
Volume 2014, Article ID 583035, 9 pages
http://dx.doi.org/10.1155/2014/583035