TY - JOUR
T1 - Feasibility of EEG Phase‐Amplitude Coupling to Stratify Encephalopathy Severity in Neonatal HIE Using Short Time Window
AU - Wang, Xinlong
AU - Liu, Hanli
AU - Ortigoza, Eric B.
AU - Kota, Srinivas
AU - Liu, Yulun
AU - Zhang, Rong
AU - Chalak, Lina F.
N1 - Funding Information:
This research was funded by NIH, grant number R01NS102617. We thank Pollieanna Sepulveda and Maricel Maxey who helped with data collection and Parkland Hospital support where the study was conducted.
Funding Information:
Funding: This research was funded by NIH, grant number R01NS102617.
Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/7
Y1 - 2022/7
N2 - Goal: It is challenging to clinically discern the severity of neonatal hypoxic ischemic encephalopathy (HIE) within hours after birth in time for therapeutic decision‐making for hypothermia. The goal of this study was to determine the shortest duration of the EEG based PAC index to provide real‐time guidance for clinical decision‐making for neonates with HIE. Methods: Neonates were recruited from a single‐center Level III NICU between 2017 and 2019. A time‐dependent, PAC-frequency‐averaged index, tPACm, was calculated to characterize intrinsic coupling between the amplitudes of 12–30 Hz and the phases of 1–2 Hz oscillation from 6‐h EEG data at electrode P3 during the first day of life, using different sizes of moving windows including 10 s, 20 s, 1 min, 2 min, 5 min, 10 min, 20 min, 30 min, 60 min, and 120 min. Time‐dependent receiver operating characteristic (ROC) curves were generated to examine the performance of the accurate window tPACm as a neurophysiologic biomarker. Results: A total of 33 neonates (mild‐HIE, n = 15 and moderate/severe HIE, n = 18) were enrolled. Mixed effects models demonstrated that tPACm between the two groups was significantly different with window time segments of 3–120 min. By observing the estimates of group differences in tPACm across different window sizes, we found 20 min was the shortest window size to optimally distinguish the two groups (p < 0.001). Time‐varying ROC showed significant average area‐under‐the‐curve of 0.82. Conclusion: We demonstrated the feasibility of using tPACm with a 20min EEG time window to differentiate the severity of HIE and facilitate earlier diagnosis and treatment initiation.
AB - Goal: It is challenging to clinically discern the severity of neonatal hypoxic ischemic encephalopathy (HIE) within hours after birth in time for therapeutic decision‐making for hypothermia. The goal of this study was to determine the shortest duration of the EEG based PAC index to provide real‐time guidance for clinical decision‐making for neonates with HIE. Methods: Neonates were recruited from a single‐center Level III NICU between 2017 and 2019. A time‐dependent, PAC-frequency‐averaged index, tPACm, was calculated to characterize intrinsic coupling between the amplitudes of 12–30 Hz and the phases of 1–2 Hz oscillation from 6‐h EEG data at electrode P3 during the first day of life, using different sizes of moving windows including 10 s, 20 s, 1 min, 2 min, 5 min, 10 min, 20 min, 30 min, 60 min, and 120 min. Time‐dependent receiver operating characteristic (ROC) curves were generated to examine the performance of the accurate window tPACm as a neurophysiologic biomarker. Results: A total of 33 neonates (mild‐HIE, n = 15 and moderate/severe HIE, n = 18) were enrolled. Mixed effects models demonstrated that tPACm between the two groups was significantly different with window time segments of 3–120 min. By observing the estimates of group differences in tPACm across different window sizes, we found 20 min was the shortest window size to optimally distinguish the two groups (p < 0.001). Time‐varying ROC showed significant average area‐under‐the‐curve of 0.82. Conclusion: We demonstrated the feasibility of using tPACm with a 20min EEG time window to differentiate the severity of HIE and facilitate earlier diagnosis and treatment initiation.
KW - EEG
KW - hypoxic ischemia encephalopathy biomarkers
KW - mixed effects models
KW - neonatal hypoxic‐ischemic encephalopathy
KW - time‐dependent phase amplitude coupling
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U2 - 10.3390/brainsci12070854
DO - 10.3390/brainsci12070854
M3 - Article
C2 - 35884659
AN - SCOPUS:85133580638
SN - 2076-3425
VL - 12
JO - Brain Sciences
JF - Brain Sciences
IS - 7
M1 - 854
ER -