We exploit time reversibility analysis, checking the invariance of statistical features of a series after time reversal, to detect temporal asymmetries of short-term heart period variability series. Reversibility indexes were extracted from 22 healthy fetuses between 16th to 40th wk of gestation and from 17 healthy humans (aged 21 to 54, median ϭ 28) during graded head-up tilt with table inclination angles randomly selected inside the set {15, 30, 45, 60, 75, 90}. Irreversibility analysis showed that nonlinear dynamics observed in short-term heart period variability are mostly due to asymmetric patterns characterized by bradycardic runs shorter than tachycardic ones. These temporal asymmetries were 1) more likely over short temporal scales than over longer, dominant ones; 2) more frequent during the late period of pregnancy (from 25th to 40th week of gestation); 3) significantly present in healthy humans at rest in supine position; 4) more numerous during 75 and 90°head-up tilt. Results suggest that asymmetric patterns observable in short-term heart period variability might be the result of a fully developed autonomic regulation and that an important shift of the sympathovagal balance toward sympathetic predominance (and vagal withdrawal) can increase their presence. heart rate variability; autonomic nervous system; head-up tilt; fetal maturation; nonlinear dynamics THE VARIABILITY OF HEART PERIOD (usually approximated as the temporal distance between two consecutive R peaks on the ECG, R-R) has been proven to be nonlinear in healthy fetuses between 38th and 40th week of gestation (8) and in healthy humans (1, 4), mostly during experimental conditions periodically forcing cardiovascular regulation (i.e., controlled breathing) (15, 16). However, this finding has not been translated yet into a notion actually helpful in pathophysiology. The main reason is that, until now, the detection of nonlinear dynamics has not been linked to a clear temporal correlate (i.e., a pattern associated with nonlinear dynamics).Time irreversibility analysis checks the invariance of the statistical properties of a time series after time reversal. This analysis might be helpful to translate the involved concept of nonlinear dynamics into a simple, comprehensible notion useful in pathophysiology, since it clearly indicates a time domain scheme responsible for nonlinear dynamics. Indeed, time irreversibility analysis is capable of detecting a specific class of nonlinear dynamics, that is, those characterized by a temporal asymmetry. In other words, when a series is detected as irreversible using simple tests in the two-dimensional phase space (6, 9, 17), it can be stated that the nonlinear behavior is the result of the presence of asymmetric patterns (i.e., waveforms characterized by the upward side shorter or longer than the downward side), thus directly linking the abstract concept of nonlinear dynamics to a clear, easily imaginable, feature (17).The aim of this study is twofold. The first aim is to link the presence of temporal asymme...
We conclude that characteristic spectral bands that increase in spectral density at different rates during the second and third trimester may be identified. They most likely reflect developmental changes and behavioral states during pregnancy.
Pregnant mothers often report a special awareness of and bonding with their unborn child. Little is known about this relationship although it may offer potential for the assessment of the fetal condition. Recently we found evidence of short epochs of fetalmaternal heart rate synchronization under uncontrolled conditions with spontaneous maternal breathing. Here, we examine whether the occurrence of such epochs can be influenced by maternal respiratory arrhythmia induced by paced breathing at several different rates (10, 12, 15, and 20 cycles per minute). To test for such weak and nonstationary synchronizations among the fetal-maternal subsystems, we apply a multivariate synchronization analysis technique and test statistics based on twin surrogates. We find a clear increase in synchronization epochs mostly at high maternal respiratory rates in the original but not in the surrogate data. On the other hand, fewer epochs are found at low respiratory rates both in original and surrogate data. The results suggest that the fetal cardiac system seems to possess the capability to adjust its rate of activation in response to external-i.e., maternal-stimulation. Hence, the pregnant mothers' special awareness to the unborn child may also be reflected by fetal-maternal interaction of cardiac activity. Our approach opens up the chance to examine this interaction between independent but closely linked physiological systems.fetal heart rate ͉ maternal heart rate ͉ respiration ͉ synchronization ͉ surrogate data P renatal development involves increased neural integration as pregnancy progresses. Among other things, this neural integration is indicated by the increasing coincidence of fetal heart rate and fetal motor activity in the second and third trimester (1). Apart from such intrafetal coordination of function, the fetus also interacts with its environment. This interaction can often be documented in the fetal heart rate, which remains one of the primary descriptors of fetal physiological activity accessible to systematic study.The mother is central to the fetal environment. Her condition sets the framework for the state and development of the fetus. So far, however, only anecdotal evidence exists for maternal perception of the condition of the fetus. Physiologically, prenatal interaction between mother and fetus has been postulated and various studies confirm a relationship between maternal and fetal conditions on the basis of fetal heart rate. These studies show changes in fetal heart rate and heart rate variability (HRV) associated with altered maternal arterial oxygen content (2, 3), maternal hypothermia (4) and maternal exercise (5). Furthermore, links between maternal and fetal heart rate have been examined. A positive correlation between these rates has been found over periods of 1 and 24 h (6) and the entrainment of the fetal heart rate rhythm to the maternal diurnal rhythm has been observed (7). However, short-term interaction between fetal and maternal heart rate is elusive.In previous work we have examined a large...
From adult data, it is known that numerous factors, such as age, state of the autonomic nervous system, diurnal rhythms or mean R-R interval mRR, influence heart rate variability (HRV). The aim of this study was the examination of the influence of gestational age, mRR, gender and time of day on fetal HRV. The analysis was based on 66 fetal magnetocardiograms (FMCGs) of 22 healthy fetuses between the 16th and 42nd week. FMCGs were recorded for 5 min using a multichannel biomagnetometer. On the basis of the time series of fetal R-R intervals, mRR as well as the standard deviation sdRR, root mean square of successive differences rmssdRR and approximate entropy ApEn were calculated. The influence of gestational age, mRR and gender on sdRR, rmssdRR and ApEn was determined by regression analysis. The relationship between time of day and HRV was evaluated by visual inspection of scatterplots. The logarithmised HRV measures increased significantly with the logarithm of gestational age (regression coefficients: sdRR = 1.28, rmssdRR = 1.12, ApEn = 1.30) and mRR (regression coefficients: sdRR = 0.008, rmssdRR = 0.011, ApEn = 0.012) There was no significant influence of gender. With respect to time of day (between 0800 h and 1800 h), no dependency of the HRV measures was apparent. In summary, when fetal HRV is assessed, it is essential to take gestational age and mRR into account. In contrast, time of day, with respect to daytime, and gender need not be considered. In future studies, the influence of fetal activity state on HRV should be examined.
We investigated several factors which may affect the accuracy of fetal cardiac time intervals (CTI) determined in magnetocardiographic (MCG) recordings: observer differences, the number of available recording sites and the type of sensor used in acquisition. In 253 fetal MCG recordings, acquired using different biomagnetometer devices between the 15th and 42nd weeks of gestation, P-wave, QRS complex and T-wave onsets and ends were identified in signal averaged data sets independently by different observers. Using a defined procedure for setting signal events, interobserver reliability was high. Increasing the number of registration sites led to more accurate identification of the events. The differences in wave morphology between magnetometer and gradiometer configurations led to deviations in timing whereas the differences between low and high temperature devices seemed to be primarily due to noise. Signal-to-noise ratio played an important overall role in the accurate determination of CTI and changes in signal amplitude associated with fetal maturation may largely explain the effects of gestational age on reproducibility. As fetal CTI may be of value in the identification of pathologies such as intrauterine growth retardation or fetal cardiac hypertrophy, their reliable estimation will be enhanced by strategies which take these factors into account.
BackgroundMagnetocardiography enables the precise determination of fetal cardiac time intervals (CTI) as early as the second trimester of pregnancy. It has been shown that fetal CTI change in course of gestation. The aim of this work was to investigate the dependency of fetal CTI on gestational age, gender and postnatal biometric data in a substantial sample of subjects during normal pregnancy.MethodsA total of 230 fetal magnetocardiograms were obtained in 47 healthy fetuses between the 15th and 42nd week of gestation. In each recording, after subtraction of the maternal cardiac artifact and the identification of fetal beats, fetal PQRST courses were signal averaged. On the basis of therein detected wave onsets and ends, the following CTI were determined: P wave, PR interval, PQ interval, QRS complex, ST segment, T wave, QT and QTc interval. Using regression analysis, the dependency of the CTI were examined with respect to gestational age, gender and postnatal biometric data.ResultsAtrioventricular conduction and ventricular depolarization times could be determined dependably whereas the T wave was often difficult to detect. Linear and nonlinear regression analysis established strong dependency on age for the P wave and QRS complex (r2 = 0.67, p < 0.001 and r2 = 0.66, p < 0.001) as well as an identifiable trend for the PR and PQ intervals (r2 = 0.21, p < 0.001 and r2 = 0.13, p < 0.001). Gender differences were found only for the QRS complex from the 31st week onward (p < 0.05). The influence on the P wave or QRS complex of biometric data, collected in a subgroup in whom recordings were available within 1 week of birth, did not display statistical significance.ConclusionWe conclude that 1) from approximately the 18th week to term, fetal CTI which quantify depolarization times can be reliably determined using magnetocardiography, 2) the P wave and QRS complex duration show a high dependency on age which to a large part reflects fetal growth and 3) fetal gender plays a role in QRS complex duration in the third trimester. Fetal development is thus in part reflected in the CTI and may be useful in the identification of intrauterine growth retardation.
Background:The univariate approaches used to analyze heart rate variability have recently been extended by several bivariate approaches with respect to cardiorespiratory coordination. Some approaches are explicitly based on mathematical models which investigate the synchronization between weakly coupled complex systems. Others use an heuristic approach, i.e. characteristic features of both time series, to develop appropriate bivariate methods.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.