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Fetal and maternal autonomic interaction in pre-eclampsia

This study investigates the role of RSA in regulating fetal circulatory system in healthy pregnancies and pre-eclampsia. Maternal and fetal HRV and umbilical venous blood flow velocity were studied in 106 patients between 32-38 weeks of gestation.

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Fetal and maternal autonomic interaction in pre-eclampsia

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  1. Fetal and maternal autonomic interaction in pre-eclampsia Igor Lakhno Kharkiv VN Karazin National university, Department of obstetrics and gynecology, Kharkiv, Ukraine 2016

  2. The process of trophoblastic invasion Fetal and maternal territorial distinction

  3. The morphological transformation in the placental vascular bed

  4. Incomplete "independence" or under the influence of maternal vasoconstrictors

  5. The absence of the emphasis on vagal-mediated reactions contributes to sympathetic overactivity, hypovolemia and vasoconstriction.

  6. RSA-associated hemodynamic fluctuations could penetrate through placental barrier?

  7. The aim of the investigation was to determine the role of RSA in the regulation of  fetal circulatory system  in the case of healthy pregnancy and in PE.  Materials and methods. Maternal and fetal HRV were studied and umbilical venous blood flow velocity spectral analysis was performed in 106 patients at 32-38 weeks of gestation. 30 of them had a healthy pregnancy and were included in Group I. In Group II, 44 pregnant women with mild-moderate PE were observed.  32 patients with severe PE were monitored in Group III. Maternal and fetal RR-interval time series were obtained in a non-invasive manner from maternal abdominal ECG recordings. HRV was measured in the time and frequency domains in the maternal sitting position. The root mean square of successive heartbeat interval differences (RMSSD) was considered as a RSA-related parameter.

  8. The inclusion criteria: diagnosed PE based on the blood pressure higher than 140/90 mm Hg in two separate occasions 6 hours apart, a positive proteinuria test in two mild-stream urine samples collected 4 hours apart. The exclusion criteria: multiple pregnancy, eclampsia, pre-existing medical disorders like diabetes mellitus, metabolic syndrome, cardiac diseases, renal disease, thyrotoxycosis and chronic hypertension. If blood pressure was 140 to 159 mmHg systolic and 90 to 109 mmHg diastolic the patient was included in mild-moderate PE Group. Severe PE was diagnosed in case of blood pressure was higher 160 mmHg systolic and 110 mmHg diastolic or (and) thrombocytopenia, serum creatinine more than 1.1 mg/L, elevated blood concentration of liver transaminases to twice normal concentration, pulmonary oedema, cerebral or visual disturbances. The patients who had no gestational complications and medical disorders including chronic infections and tobacco smoking were enrolled in the control Group. The choice of antihypertensive agent was made according to the type of central maternal hemodynamics (CMH) determined by bio-impedance cardiography. It was estimated the values of cardiac index (CI) and total peripheral vascular resistance (TPVR). The hyperkinetic type of CMH was associated with high CI and low TPVR. The pre-eclamptic women with eukinetic type of CMH had high or normal CI and increased TPVR. And the pre-eclamptic patients with low CI and high TPVR had the hypokinetic type of CMH. The pregnant women with hyperkinetic type of CMH took carvedilol 6.25-12.5 mg 2 times daily, in case of the eukinetic type – methyldopa 250-500 mg 4 times a day and in cases of the hypokinetic one – methyldopa 500 mg 4 times daily combined with nifedipine 20 mg 2 times daily.

  9. The fetal and maternal HRV parameters were obtained with the fetal noninvasive computer electrocardiographic system “Cardiolab Baby Card” (“KhAI-Medica”, Ukraine). The recording lasted for 10 minutes in the normal maternal sitting position. The values of total power (TP) and its spectral compounds, i.e. the very low frequency (VLF), the low frequency (LF), the high frequency (HF) and LF/HF ratio or sympatho-vagal balance, were determined. The temporal characteristics of the fetal HRV: the standard deviation of normal to normal intervals (SDNN), the root mean square of successive heartbeat interval differences (RMSSD), the proportion of the number of pairs of NNs differing by more than 50 ms divided by the total number of NNs (pNN50), the amplitude of mode (the most frequent value of NN interval or the highest column in the histogramm) – the number of NN intervals included in the pocket corresponding to the mode measured in percentages (%) (AMo) and the stress index – SI = AMo(%) / (2×Mo×Var); Var = NNmax – NNmin; (SI) were calculated.

  10. Doppler ultrasonography was performed with the ultrasound system “Voluson 730” (GE Healthcare, USA). The Doppler spectrogram of the venous umbilical blood flow was subjected to further processing. The curves of maximum blood flow velocity were isolated and their spectral components were determined. The spectra were calculated with a sampling step of Δ t=0.01 seconds for the sample of 256 points. The resulting spectrum was obtained by averaging over all the samples of this contingent.

  11. Table. The parameters of bioimpedance cardiography in the study population. * – the differences were statistically significant compared to the control group (p<0,05); † – the differences were statistically significant compared to the group II (p<0,05).

  12. Figure. Maternal frequency domain HRV parameters in the study population.

  13. Table. Maternal HRV parameters in the study population. Notes: * – the differences were statistically significant compared to Group I (p<0.05); †– the differences were statistically significant compared to Group II (p<0.05).

  14. Figure. Fetal frequency domain HRV parameters in the study population.

  15. Table. Fetal HRV parameters in the study population. Notes: * – the differences were statistically significant compared to Group I (p<0.05); † – the differences were statistically significant compared to Group II (p<0.05).

  16. Table. The amplitudes of the spectral peaks of umbilical blood flow velocity in the study population. Notes: * – the differences were statistically significant compared to Group I (p<0.05); † – the differences were statistically significant compared to Group II (p<0.05).

  17. Figure. The spectral characteristics of the umbilical venous blood flow velocity of a patient from healthy pregnancy Group.

  18. Table. Statistically significant (p<0.05) Spearman’s correlations between the maternal sympatho-vagal balance and CI, maternal sympatho-vagal balance and TPVR in the study population.

  19. Table. Statistically significant (p<0.05) Spearman’s correlations between the maternal RMSSD and the amplitude of RSA associated peak, the maternal and fetal RMSSDs in the study population.

  20. PE reduced the role of RSA in maternal hemodynamics

  21. Figure. The values of the sympathetic-vagal balance in the study population.

  22. Optimal utero-placental hemodynamics is one of the main mechanisms of beneficial perinatal outcome. All catastrophical events such as preterm placental abruption could be associated with placental bed pathology. So the function of utero-placental hemodynamics is strongly depended on arterial inflow and venous outflow: Vp = (F a − F v )dt; dV p = (F a − F v ),Vp –the volume of blood in the placental circuit; Fa –arterial inflow;Fv –venous outflow. As hemodynamical oscillations are obviously connected with maternal HRV it is possible to create such mathematical model of the utero-placental circulation: де Vp – the volume of blood in the placental circuit;Fa – arterial inflow;Fv­ – venous outflow;w – natural frequency of the system. However this model does not describe the enropy (losses) in the system associated with an increased vascular resistance in PE. That is why the more realistic model could be formulated as: It is similar to van der Pol equation . Maternal regulatory mechanisms provide utero-placental hemodynamics. And maternal pace-makers are probably could be considered as a natural frequency of the system in the above model.

  23. Vagal repercussions theory

  24. Areactive non-stress test (7 decelations)

  25. Reactive non-stress test (7 accelerations)

  26. Additional evaluation of the morphological parameters of the fetal ECG average complex Lakhno I. Fetal non-invasive electrocardiography contributes to better diagnostics of fetal distress: a cross-sectional study among patients with pre-eclampsia // Ann Acad Med Singapore. – 2015. – Vol. 44, No 11. – P. 519-523.Lakhno I. The use of fetal noninvasive electrocardiographyScientifica (Cairo). 2016;2016:5386595. Doi: 10.1155/2016/5386595.

  27. Findings and prospects of the study 1. The increased maternal autonomic balance supported perfusion of the end organs and coupling with fetal hemodynamics in mild-moderate PE while vagal-mediated reactions were safe. 2. Hypokinetic type of CMH in severe PE was associated with the reduction of RSA. 3. The deteriorated placental perfusion and the decreased motion of the RSA-associated hemodynamic fluctuations were due to hemodynamic failure. 4. the fetal cardiovascular system was absolutely separated from the maternal organism and lost the control in severe PE (confirmed with the considerable reduction of an RSA-associated peak and the pulsatile pattern of umbilical hemodynamics). 5. the loss of fetal and maternal hemodynamic coupling could be considered a presumable pathogenetic mechanism of the fetal distress in PE; this hypothesis, though, requires further investigations. 6. It is possible to speculate that the testing for maternal sympatho-vagal balance, fetal and maternal RMSSD could be used in future as biophysical markers of the severe PE and fetal distress.

  28. CONCLUSION The maternal RSA propagated its influence on the fetal umbilical venous blood flow and the fetal autonomic nervous regulation in healthy pregnancy. The hypokinetic type of CMH in severe PE decreased the RSA-mediated hemodynamic fluctuations. It was associated with umbilical vein pulsatile pattern and fetal deterioration.

  29. HRV is a convenient instrument for the neurodevelopmental investigations

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