Key result
Novel multiscale entropy analysis successfully differentiates symptomatic from asymptomatic LQT1 mutation carriers.
Why the study?
Does refined multiscale self-entropy and conditional entropy analysis of Holter ECGs distinguish between symptomatic and asymptomatic LQT1 mutation carriers?
Cross-Sectional (n=47)
Yes
Does refined multiscale self-entropy and conditional entropy analysis of Holter ECGs distinguish between symptomatic and asymptomatic LQT1 mutation carriers?
Answers are grounded in this paper and cite their sources.
Joint evaluation of RMSCE and RMSsE over heart period and QT variabilities can help typify autonomic function and clarify differences between asymptomatic and symptomatic LQT1 patients.
The study proposes the contemporaneous assessment of conditional entropy (CE) and self-entropy (sE), being the two terms of the Shannon entropy (ShE) decomposition, as a function of the time scale via refined multiscale CE (RMSCE) and sE (RMSsE) with the aim at gaining insight into cardiac control in long QT syndrome type 1 (LQT1) patients featuring the KCNQ1-A341V mutation. CE was estimated via the corrected CE (CCE) and sE as the difference between the ShE and CCE. RMSCE and RMSsE were computed over the beat-to-beat series of heart period (HP) and QT interval derived from 24-hour Holter electrocardiographic recordings during daytime (DAY) and nighttime (NIGHT). LQT1 patients were subdivided into asymptomatic and symptomatic mutation carriers (AMCs and SMCs) according to the severity of symptoms and contrasted with non-mutation carriers (NMCs). We found that RMSCE and RMSsE carry non-redundant information, separate experimental conditions (i.e., DAY and NIGHT) within a given group and distinguish groups (i.e., NMC, AMC and SMC) assigned the experimental condition. Findings stress the importance of the joint evaluation of RMSCE and RMSsE over HP and QT variabilities to typify the state of the autonomic function and contribute to clarify differences between AMCs and SMCs.
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Bari et al. (2015) conducted a cross-sectional in Long QT syndrome type 1 (LQT1) (n=47). KCNQ1-A341V mutation and symptomatic status vs. Non-mutation carriers (NMCs) was evaluated on Refined multiscale conditional entropy (RMSCE) and refined multiscale self-entropy (RMSsE) evaluated over heart period and QT interval (p=<0.05). The joint evaluation of refined multiscale conditional entropy and self-entropy provided non-redundant information that successfully differentiated asymptomatic from symptomatic LQT1 mutation carriers and distinguished day-night autonomic variations.
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