Abstract
The QT variability index (QTVI), which measures the instability of myocardial repolarization, is usually calculated from a single electrocardiogram (ECG) recording and can be easily applied in children. It is well known that frequency analysis of heart rate variability (HRV) can detect autonomic balance, but it is not clear whether QTVI is correlated with autonomic tone. Therefore, we evaluated the association between QTVI and HRV to elucidate whether QTVI is correlated with autonomic nerve activity. Apparently, healthy 320 children aged 0–7 years who visited Fujita Health University Hospital for heart checkup examinations were included. The RR and QT intervals of 60 continuous heart beats were measured, and the QTVI was calculated using the formula of Berger et al. Frequency analysis of HRV, including the QTVI analysis region, was conducted for 2 min and the ratio of low-frequency (LF) components to high-frequency (HF) components (LF/HF) and HF/(LF + HF) ratio was calculated as indicators of autonomic nerve activity. Then, the correlations between QTVI and these parameters were assessed. QTVI showed a significant positive correlation with LF/HF ratio (r = 0.45, p < 0.001) and negative correlation with HF/(LF + HF) ratio (r = −0.429, p < 0.001). These correlations remained after adjustment for sex and age. QTVI, which is calculated from non-invasive ECG and can detect abnormal myocardial repolarization, is significantly correlated with frequency analysis of HRV parameters. QTVI reflects autonomic nerve balance in children.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
Instability of myocardial repolarization detected by the QT interval variability indicates a substrate that can induce lethal arrhythmias [1]. Adult patients with myocardial dysfunction exhibit high QT interval variability following the preceding cardiac cycle, and such increased QT variability may be an ominous sign of cardiac death [2]. On the other hand, heart rate variability (HRV) calculated from the variations in the RR interval reflects autonomic nerve balance. Reduced HRV can predict the poor prognosis in patients with heart diseases [3, 4]. However, there were limited studies assessing the myocardial repolarization in children, and sufficient clinical applications have not been achieved.
The changes in QT interval variability are linked to autonomic and central nervous system [5]. The QT Variability Index (QTVI) is a non-invasive measure to assess repolarization liability that has been applied to a wide variety of subjects with cardiovascular disease [6]. We have used QTVI to evaluate the characteristics of myocardial repolarization in infants. This index changes with age in healthy children from infancy to school age [7, 8]. In healthy 1-month-old infants, the QTVI is negatively correlated with gestational age, which can serve as an index of the maturity of the cardiac autonomic nervous system and myocardial repolarization [9]. In the present study, we examined the correlation between QTVI and the power spectral analysis parameters of HRV, which are commonly used to measure autonomic nerve balance.
Participants and Methods
Apparently healthy 320 children aged 0–7 years who visited Fujita Health University Hospital for heart checkup examinations between April 2012 and November 2015 were included. For children aged younger than 1 year, tricloryl syrup (0.7 mL/kg) was used for sedation to perform such diagnostic procedures. Informed consents were obtained from the children’s parents or guardians.
ECG was performed using a bio-polygraph recorder (MP-150; Biopac Systems Inc., CA, USA) with a sampling rate of 1000 Hz, and signals of the CM5 lead were recorded. All ECG recordings were obtained between 4 PM and 6 PM.
The RR interval was automatically measured using AcqKnowledge version 3.9 (Biopac Systems Inc., CA, USA) on the basis of the ECG recordings with stable baseline. The endpoint of the T wave was identified using the first-order differentiation processing method (Fig. 1). For 60 heart beats, we calculated the instantaneous heart rate, as well as the mean HR (HRm), mean QT interval (QTm), and variance (HRv and QTv). Thereafter, using the formula of Berger et al., we calculated the QTVI [QTVI = log10 (QTv/QTm2)/(HRv/HRm2)], which is an indicator of variability in the QT interval.
Meanwhile, to evaluate the autonomic nerve function, we performed power spectrum analysis of HRV during a short period of 2 min including the QTVI analysis region using AcqKnowledge version 3.9. In power spectrum analysis, we measured the frequency density of the low-frequency region (LF: 0.036–0.146 Hz) and the high-frequency region (HF: 0.146–0.390 Hz) according to the method shown in The Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology [10]. Then, LF/HF and HF/(LF + HF) were calculated as indicators of autonomic nerve balance. Then, the correlations between QTVI and these parameters were assessed. The association of time domain HRV and QTVI was also assessed. In this study, standard deviation of NN intervals (SDNN) and root mean square of successive RR interval differences (rMSSD) were used. These values were expressed in original units or as the logarithm from (log10) to obtain normal distribution.
Statistical Analysis
Statistical processing was performed using the JMP version 12.2.0 (SAS Institute Inc., Cary, NC, USA). The Wilcoxon signed rank test was used for Sex-specific comparison. Correlation between QTVI and age was assessed using logarithmic curve regression analysis. Correlations between QTVI and LF/HF or HF/(LF + HF) were assessed using Pearson’s linear regression analysis. Additionally, correlations between QTVI and SDNN or rMSSD were assessed using logarithmic curve regression analysis.
Multiple regression analysis was performed to assess whether QTVI was associated with HRV parameters independent of age and sex. A p value of < 0.05 was accepted as statistically significant.
Results
Participants’ Characteristics, ECG Parameters and HRV Parameters
Table 1 presents the characteristics of the participants. The median age was 3 years. Median QT interval was 318.6 ms with a median heart rate of 103.3 beats per minutes. The corrected QT intervals by Bazett’s and Fridericia’s formulas were 414.8 and 380.0 ms, respectively. None of the children had a corrected QT interval exceeding 440 ms. In the HRV parameters, median LF/HF ratio, reflecting sympathetic nerve activity, was 1.75, whereas median HF/(LF + HF), reflecting vagal nerve activity, was 0.36.
Gender Differences in QTVI and HRV Parameters
There were no gender differences for the QTVI, log10HRVN, and log10QTVN (Table 2).
Relationships Between QTVI and Age, Between LF/HF and Age
Figure 1 presents the relationship between QTVI and age and between LF/HF and age. Both indices decreased rapidly up to 12 months of age and slowly decreased thereafter.
Relationship Between QTVI and LF/HF, Between QTVI and HF/(LF + HF)
Figure 2 presents the relationship between QTVI and LF/HF and between QTVI and HF/(LF + HF). A significant positive correlation was observed between QTVI and LF/HF (r = 0.450, p < 0.001), whereas a significant negative correlation was observed between QTVI and HF/(LF + HF) (r = − 0.429, p < 0.001). A significant correlation between Log10HRVN and LF/HF, HF/(LF + HF) were observed (r = − 0.415, p < 0.001, r = 0.386, p < 0.001, respectively). Similar correlation between log10QTVN and LF/HF, HF/(LF + HF) were observed (r = 0.144, p = 0.010, r = −0.151, p = 0.007, respectively), but the correlations were weak (Fig. 3).
Relationship Between QTVI and SDNN, Between QTVI and rMSSD
A significant correlation between QTVI and log10SDNN and log10rMSSD was observed (r = − 0.784, p < 0.001, r = 0.756, p < 0.001, respectively).
Multivariate Analysis
Table 3 shows multiple regression analysis. QTVI was significantly correlated with LF/HF and HF/(LF + HF) after adjustment for age and sex.
Discussion
The present study demonstrated that the QTVI is correlated with autonomic nerve activity in prepubescent healthy children aged 0–7 years. Namely, QTVI showed a significant positive correlation with LF/HF ratio reflecting sympathetic nerve activity and negative correlation with HF/(LF +HF) ratio, reflecting vagal nerve activity. QTVI showed a significant negative correlation with SDNN reflecting the sympatho-vagal nervous balance and negative correlation with rMSSD, reflecting vagal nerve activity.
Berger et al. [2] proposed that temporal variations in the QT interval—instability in myocardial repolarization—could serve as an electrophysiological indicator. QT interval is affected by the heart rate; larger HRV could induce larger QT interval variability, whereas smaller HRV could induce smaller QT interval variability. Either overestimation or underestimation of QT variability might occur without considering the degree of HRV. Therefore, the authors proposed the formula: QTVI = log10 (QTv/QTm2)/(HRv/HRm2)] taking into account the effects of HRV. In fact, this formula has been evaluated in clinical studies and proved to be useful in distinguishing patients with high risk for sudden cardiac death in hypertrophic cardiomyopathy and patients with a history of ventricular fibrillation [11]. Although all studies did not always present data of the numerator (QTVN: QT variance/QTmean2) and denominator (HRVN: HR variance/HRmean2), increased QTVN rather than decreased HRVN might usually be the cause of QTVI to increase. Dobson suggested that evaluating both QTVN and HRVN is important in assessing the pathophysiology of QTVI. [6] As previously shown, HRVN changes with age; however, QTVN was not affected by age and remained stable without sex-related differences in children [7]. Thus, increase in QTVI might not necessarily indicate increase in QTVN, but could be due to decrease in HRVN. Actually, our analysis revealed a significant relationship between LF/HF and HF/(LF + HF) with log10HRVN; however, only weak relationship was observed with log10QTVN. Therefore, it might be possible that increased sympathetic nerve activity reduces RR interval variability but has no marked effect on the QT interval variability. Schmidt M and colleagues showed that QTV was increased in rapid eye movement sleep, reflective of high sympathetic drive and predicts death from cardiovascular disease [12]. However, HRV was not assessed in the paper. Likewise, augmented vagal nerve activity increases RR interval variability and could decrease QTVI, but its effect on QTVN is not clear. Further studies are required to evaluate the relationship between autonomic nerve balance and QTVN.
Potential Clinical Implication
Sudden Infant Death Syndrome (SIDS) is one of the leading causes of death in infants. Although the exact mechanisms contributing SIDS have not been fully elucidated until now, it is estimated that dysfunction of the autonomic nervous system regulation either respiratory or cardiovascular systems might play a part. The advantage of this study is that QTVI, which reflects myocardial repolarization variability, calculated from short-term ECG recording, can be used to assess the degree of autonomic tone. Thus, QTVI could be potentially used for predicting lethal arrhythmias, including SIDS. This should be explored in the future studies.
Limitations
This study has some limitations. First, this was a single-center study with a limited number of patients.
Second, we collected only one data in each subject. Thus, reproducibility of the parameters could not be assessed. Third, it may be true that sedatives affect the autonomic nervous activity and should be avoided to assess the autonomic balance, but in fact, it was impossible to ask the infant to rest on supine position for more than 2 min. However, the amount of tricloryl syrup (0.7 mg/kg) used in this study is small so that we think effects of this medication on autonomic nervous activity is limited. Finally, we included only healthy infants, therefore it is unclear whether our results could be applied to infants with heart disease including hereditary channelopathies.
Conclusion
QTVI, which is calculated from non-invasive ECG and can detect abnormal myocardial repolarization instability, is significantly correlated with power spectral HRV parameters. QTVI reflects autonomic nerve balance in children.
References
Atiga WL, Calkins H, Lawrence JH, Tomaselli GF, Smith JM, Berger RD (1998) Beat-to-beat Repolarization lability identifies patients at risk for sudden cardiac death. J Cardiovasc Electrophysiol 9:899–908. https://doi.org/10.1111/j.1540-8167.1998.tb00130.x
Berger RD, Kasper EK, Baughman KL, Marban E, Calkins H, Tomaselli GF (1997) Beat-to-beat QT interval variability: novel evidence for repolarization lability in ischemic and nonischemic dilated cardiomyopathy. Circulation 96:1557–1565. https://doi.org/10.1161/01.CIR.96.5.1557
Massin MM, Maeyns K, Withofs N, Ravet F, Gérard P (2000) Circadian rhythm of heart rate and heart rate variability. Arch Dis Child 83:179–182. https://doi.org/10.1136/adc.83.2.179
Sassi R, Cerutti S, Lombardi F et al (2015) Advances in heart rate variability signal analysis: joint position statement by the e-Cardiology ESC Working Group and the European Heart Rhythm Association co-endorsed by the Asia Pacific Heart Rhythm Society. Europace 17:1341–1353. https://doi.org/10.1093/europace/euv015
Baumert M, Porta A, Vos MA, Malik M, Couderc JP, Laguna P, Piccirillo G, Smith GL, Tereshchenko LG, Volders PG (2016) QT interval variability in body surface ECG: measurement, physiological basis, and clinical value: position statement and consensus guidance endorsed by the European Heart Rhythm Association jointly with the ESC Working Group on Cardiac Cellular Electrophysiology. Europace 18:925–944. https://doi.org/10.1093/europace/euv405
Dobson CP, Kim A, Haigney M (2013) QT variability index. Prog Cardiovasc Dis 56:186–194. https://doi.org/10.1016/j.pcad.2013.07.004
Kusuki H, Kuriki M, Horio K, Hosoi M, Matsuura H, Fujino M, Eryu Y, Miyata M, Yasuda T, Yamazaki T, Nagaoka S, Hata T (2011) Beat-to-beat QT interval variability in children: normal and physiologic data. J Electrocardiol 44:326–329. https://doi.org/10.1016/j.jelectrocard.2010.07.016
Takeuchi Y, Omeki Y, Horio K, Nishio M, Nagata R, Oikawa S, Mizutani Y, Nagatani A, Funamoto Y, Uchida H, Fujino M, Eryu Y, Boda H, Miyata M, Hata T (2017) Relationship between QT and JT peak interval variability in prepubertal children. Ann Noninvasive Electrocardiol 22(4):1–6. https://doi.org/10.1111/anec.12444(Epub 2017 Feb 17)
Kojima A, Hata T, Sadanaga T, Mizutani Y, Uchida H, Kawai Y, Manabe M, Fujino M, Eryu Y, Boda H, Miyata M, Yoshikawa T (2018) Maturation of the QT variability index is impaired in preterm infants. Pediatr Cardiol 39(5):902–905. https://doi.org/10.1007/s00246-018-1839-2(Epub 2018 Mar 12)
Heart rate variability. Standards of measurement, physiological interpretation, and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. (1996) Eur Heart. 17:354–81.
Atiga WL, Fananapazir L, McAreavey D, Calkins H, Berger RD (2000) Temporal repolarization lability in hypertrophic cardiomyopathy caused by beta-myosin heavy-chain gene mutations. Circulation 101:1237–1242. https://doi.org/10.1161/01.CIR.101.11.1237
Schmidt M, Baumert M, Penzel T, Malberg H, Zaunseder S (2019) Nocturnal ventricular repolarization lability predicts cardiovascular mortality in the Sleep Heart Health Study. Am J Physiol Heart Circ Physiol 316:H495–H505. https://doi.org/10.1152/ajpheart.00649.2018
Acknowledgements
We express our gratitude to the Ministry of Health, Labor and Welfare of Japan for their funding to this study.
Funding
This work was supported in part by the Japan Society for the Promotion of Science (KAKENHI) (#26350944).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of Interest
The authors declare that they have no conflict of interest.
Ethical Approval
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Informed Consent
Informed consent was obtained from all individual participants or parents/guardians included in the study.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Kusuki, H., Tsuchiya, Y., Mizutani, Y. et al. QT Variability Index is Correlated with Autonomic Nerve Activity in Healthy Children. Pediatr Cardiol 41, 1432–1437 (2020). https://doi.org/10.1007/s00246-020-02399-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00246-020-02399-8