TY - JOUR
T1 - Resting-state brain networks in neonatal hypoxic-ischemic brain damage
T2 - A functional near-infrared spectroscopy study
AU - Zhang, Shen
AU - Peng, Cheng
AU - Yang, Yang
AU - Wang, Daifa
AU - Hou, Xinlin
AU - Li, Deyu
N1 - Publisher Copyright:
© The Authors. Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
PY - 2021/4/1
Y1 - 2021/4/1
N2 - Significance: There is an emerging need for convenient and continuous bedside monitoring of full-Term newborns with hypoxic-ischemic brain damage (HIBD) to determine whether early intervention is required. Functional near-infrared spectroscopy (fNIRS)-based resting-state brain network analysis, which could provide an effective evaluation method, remains to be extensively studied. Aim: Our study aims to verify the feasibility of fNIRS-based resting-state brain networks for evaluating brain function in infants with HIBD to provide a new and effective means for clinical research in neonatal HIBD. Approach: Thirteen neonates with HIBD were scanned using fNIRS in the resting state. The brain network properties were explored to attempt to extract effective features as recognition indicators. Results: Compared with healthy controls, newborns with HIBD showed decreased brain functional connectivity. Specifically, there were severe losses of long-range functional connectivity of the contralateral parietal-Temporal lobe, contralateral parietal-frontal lobe, and contralateral parietal lobe. The node degree showed a widespread decrease in the left frontal middle gyrus, left superior frontal gyrus dorsal, and right central posterior gyrus. However, newborns with HIBD showed a significantly higher local network efficiency (∗p < 0.05). Subsequently, network indicators based on small-worldness, local efficiency, modularity, and normalized clustering coefficient were extracted for HIBD identification with the accuracy observed as 79.17%. Conclusions: Our findings indicate that fNIRS-based resting-state brain network analysis could support early HIBD diagnosis.
AB - Significance: There is an emerging need for convenient and continuous bedside monitoring of full-Term newborns with hypoxic-ischemic brain damage (HIBD) to determine whether early intervention is required. Functional near-infrared spectroscopy (fNIRS)-based resting-state brain network analysis, which could provide an effective evaluation method, remains to be extensively studied. Aim: Our study aims to verify the feasibility of fNIRS-based resting-state brain networks for evaluating brain function in infants with HIBD to provide a new and effective means for clinical research in neonatal HIBD. Approach: Thirteen neonates with HIBD were scanned using fNIRS in the resting state. The brain network properties were explored to attempt to extract effective features as recognition indicators. Results: Compared with healthy controls, newborns with HIBD showed decreased brain functional connectivity. Specifically, there were severe losses of long-range functional connectivity of the contralateral parietal-Temporal lobe, contralateral parietal-frontal lobe, and contralateral parietal lobe. The node degree showed a widespread decrease in the left frontal middle gyrus, left superior frontal gyrus dorsal, and right central posterior gyrus. However, newborns with HIBD showed a significantly higher local network efficiency (∗p < 0.05). Subsequently, network indicators based on small-worldness, local efficiency, modularity, and normalized clustering coefficient were extracted for HIBD identification with the accuracy observed as 79.17%. Conclusions: Our findings indicate that fNIRS-based resting-state brain network analysis could support early HIBD diagnosis.
KW - brain network
KW - functional near-infrared spectroscopy
KW - hypoxic-ischemic brain damage
KW - infants
KW - resting state
UR - https://www.scopus.com/pages/publications/85117359020
U2 - 10.1117/1.NPh.8.2.025007
DO - 10.1117/1.NPh.8.2.025007
M3 - 文章
AN - SCOPUS:85117359020
SN - 2329-423X
VL - 8
JO - Neurophotonics
JF - Neurophotonics
IS - 2
M1 - 025007
ER -