TY - JOUR
T1 - Characterization of the fetal diaphragmatic magnetomyogram and the effect of breathing movements on cardiac metrics of rate and variability
AU - Gustafson, Kathleen M.
AU - Allen, John J.B.
AU - Yeh, Hung wen
AU - May, Linda E.
N1 - Funding Information:
The authors acknowledge the contributions of JoAnn Liermann, RNC, PhD and Lori Blanck, R. EEG/EP T. for their assistance with ultrasonography, data acquisition and processing and recognize E. Anda Popescu, PhD, for her intellectual contribution and helpful discussions. This study was supported in part by pilot funding from the Hoglund Brain Imaging Center , made possible by a generous gift from Forrest and Sally Hoglund; and an intramural grant from the Kansas City University of Medicine and Biosciences (May). K. M. Gustafson is supported in part by NICHD R21 HD059019.
PY - 2011/7
Y1 - 2011/7
N2 - Breathing movements are one of the earliest fetal motor behaviors to emerge and are a hallmark of fetal well-being. Fetal respiratory sinus arrhythmia (RSA) has been documented but efforts to quantify the influence of breathing on heart rate (HR) and heart rate variability (HRV) are difficult due to the episodic nature of fetal breathing activity. We used a dedicated fetal biomagnetometer to acquire the magnetocardiogram (MCG) between 36 and 38. weeks gestational age (GA). We identified and characterized a waveform observed in the raw data and independent component decomposition that we attribute to fetal diaphragmatic movements during breathing episodes. RSA and increased high frequency power in a time-frequency analysis of the IBI time-series was observed during fetal breathing periods. Using the diaphragmatic magnetomyogram (dMMG) as a marker, we compared time and frequency domain metrics of heart rate and heart rate variability between breathing and non-breathing epochs. Fetal breathing activity resulted in significantly lower HR, increased high frequency power, greater sympathovagal balance, increased short-term HRV and greater parasympathetic input relative to non-breathing episodes confirming the specificity of fetal breathing movements on parasympathetic cardiac influence. No significant differences between breathing and non-breathing epochs were found in two metrics reflecting total HRV or very low, low and intermediate frequency bands. Using the fetal dMMG as a marker, biomagnetometry can help to elucidate the electrophysiologic mechanisms associated with diaphragmatic motor function and may be used to study the longitudinal development of human fetal cardiac autonomic control and breathing activity.
AB - Breathing movements are one of the earliest fetal motor behaviors to emerge and are a hallmark of fetal well-being. Fetal respiratory sinus arrhythmia (RSA) has been documented but efforts to quantify the influence of breathing on heart rate (HR) and heart rate variability (HRV) are difficult due to the episodic nature of fetal breathing activity. We used a dedicated fetal biomagnetometer to acquire the magnetocardiogram (MCG) between 36 and 38. weeks gestational age (GA). We identified and characterized a waveform observed in the raw data and independent component decomposition that we attribute to fetal diaphragmatic movements during breathing episodes. RSA and increased high frequency power in a time-frequency analysis of the IBI time-series was observed during fetal breathing periods. Using the diaphragmatic magnetomyogram (dMMG) as a marker, we compared time and frequency domain metrics of heart rate and heart rate variability between breathing and non-breathing epochs. Fetal breathing activity resulted in significantly lower HR, increased high frequency power, greater sympathovagal balance, increased short-term HRV and greater parasympathetic input relative to non-breathing episodes confirming the specificity of fetal breathing movements on parasympathetic cardiac influence. No significant differences between breathing and non-breathing epochs were found in two metrics reflecting total HRV or very low, low and intermediate frequency bands. Using the fetal dMMG as a marker, biomagnetometry can help to elucidate the electrophysiologic mechanisms associated with diaphragmatic motor function and may be used to study the longitudinal development of human fetal cardiac autonomic control and breathing activity.
KW - Autonomic nervous system
KW - Diaphragm activation
KW - Fetal biomagnetometry
KW - Magnetocardiogram
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U2 - 10.1016/j.earlhumdev.2011.03.012
DO - 10.1016/j.earlhumdev.2011.03.012
M3 - Article
C2 - 21497027
AN - SCOPUS:79958254499
SN - 0378-3782
VL - 87
SP - 467
EP - 475
JO - Early Human Development
JF - Early Human Development
IS - 7
ER -