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. 2014 Nov 25:8:948.
doi: 10.3389/fnhum.2014.00948. eCollection 2014.

Fetal autonomic brain age scores, segmented heart rate variability analysis, and traditional short term variability

Affiliations

Fetal autonomic brain age scores, segmented heart rate variability analysis, and traditional short term variability

Dirk Hoyer et al. Front Hum Neurosci. .

Abstract

Disturbances of fetal autonomic brain development can be evaluated from fetal heart rate patterns (HRP) reflecting the activity of the autonomic nervous system. Although HRP analysis from cardiotocographic (CTG) recordings is established for fetal surveillance, temporal resolution is low. Fetal magnetocardiography (MCG), however, provides stable continuous recordings at a higher temporal resolution combined with a more precise heart rate variability (HRV) analysis. A direct comparison of CTG and MCG based HRV analysis is pending. The aims of the present study are: (i) to compare the fetal maturation age predicting value of the MCG based fetal Autonomic Brain Age Score (fABAS) approach with that of CTG based Dawes-Redman methodology; and (ii) to elaborate fABAS methodology by segmentation according to fetal behavioral states and HRP. We investigated MCG recordings from 418 normal fetuses, aged between 21 and 40 weeks of gestation. In linear regression models we obtained an age predicting value of CTG compatible short term variability (STV) of R (2) = 0.200 (coefficient of determination) in contrast to MCG/fABAS related multivariate models with R (2) = 0.648 in 30 min recordings, R (2) = 0.610 in active sleep segments of 10 min, and R (2) = 0.626 in quiet sleep segments of 10 min. Additionally segmented analysis under particular exclusion of accelerations (AC) and decelerations (DC) in quiet sleep resulted in a novel multivariate model with R (2) = 0.706. According to our results, fMCG based fABAS may provide a promising tool for the estimation of fetal autonomic brain age. Beside other traditional and novel HRV indices as possible indicators of developmental disturbances, the establishment of a fABAS score normogram may represent a specific reference. The present results are intended to contribute to further exploration and validation using independent data sets and multicenter research structures.

Keywords: cardiotocography; fetal autonomic brain age; magnetocardiography; prenatal diagnosis.

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Figures

Figure 1
Figure 1
Tachograms of 30 min recordings of four different fetuses. Upper part: changes between sections of active (marked by red horizontal bar) and quiet sleep related heart rate patterns in a younger (28 WGA) and an older (37 WGA) fetus. Lower part: quiet sleep related heart rate patterns at 22 and 33 WGA. DC and AC (>10 bpm deviation from floating baseline, marked by blue *) are identified in the quiet sleep sections only.
Figure 2
Figure 2
Relative frequency of recordings that meet the Dawes-Redman criteria (1 = 100%) vs. chronological age (in weeks GA) of 30 min recordings. In absolute values, 134 of 167 cases met the criteria in the subset of ≤32 WGA and 130 of 146 in the subset of >32 WGA, respectively.
Figure 3
Figure 3
Fetal autonomic brain age score [AMP, skewness, pNN5, lnVLF/LF, gMSE3] vs. chronological age (in WGA) of 30 min recordings, mean ± standard deviation.
Figure 4
Figure 4
Fetal autonomic brain age score [Skewness, gMSE3, pNN5] for quiet sleep segments ○ and [AMP, Skewness, gMSE3, pNN5, lnVLF/LF] for active sleep segments Δ vs. chronological age (in WGA), mean ± standard deviation, notice that 21–24 WGA and 37–40 WGA, respectively, are merged due to the small number of samples.

References

    1. Barker D. J. (1998). In utero programming of chronic disease. Clin. Sci. (Lond) 95, 115–128. 10.1042/cs19980019 - DOI - PubMed
    1. Barker D. J. (2002). Fetal programming of coronary heart disease. Trends Endocrinol. Metab. 13, 364–368. 10.1016/s1043-2760(02)00689-6 - DOI - PubMed
    1. Barker D. J., Eriksson J. G., Forsén T., Osmond C. (2002). Fetal origins of adult disease: strength of effects and biological basis. Int. J. Epidemiol. 31, 1235–1239. 10.1093/ije/31.6.1235 - DOI - PubMed
    1. David M., Hirsch M., Karin J., Toledo E., Akselrod S. (2007). An estimate of fetal autonomic state by time-frequency analysis of fetal heart rate variability. J. Appl. Physiol. (1985) 102, 1057–1064. 10.1152/japplphysiol.00114.2006 - DOI - PubMed
    1. Hoyer D., Heinicke E., Jaekel S., Tetschke F., Di Pietro Paolo D., Haueisen J., et al. . (2009). Indices of fetal development derived from heart rate patterns. Early Hum. Dev. 85, 379–386. 10.1016/j.earlhumdev.2009.01.002 - DOI - PubMed

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