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Published on: October 28, 2022
Neurophysiologic Profiling of At-Risk Low and Very Low Birth-Weight Infants Using Magnetic Resonance Imaging
1Department of Radiology, Shengjing Hospital of China Medical University, Shenyang, China.
Insights
Low birth-weight newborns show significantly lower cerebral oxygen metabolism. Advanced MRI techniques identified these neonates at higher risk for brain injury, aiding early detection.
Area of Science:
- Neonatal neuroscience
- Medical imaging
- Physiology
Background:
- Low birth-weight (LBW) and very low birth-weight (VLBW) newborns face elevated risks for brain injuries, developmental delays, and future vascular diseases.
- The precise neurobiological factors contributing to these vulnerabilities remain incompletely understood.
Purpose of the Study:
- To investigate the neurobiologic underpinnings of pathophysiologic vulnerabilities in LBW-VLBW neonates.
- To utilize advanced magnetic resonance imaging (MRI) techniques to quantify key cerebral physiological parameters.
Main Methods:
- Employed T2-relaxation-under-spin-tagging (TRUST) and phase-contrast (PC) MRI to measure oxygen extraction fraction (OEF), global cerebral blood flow (CBF), and cerebral metabolic rate of oxygen (CMRO2).
- Studied 50 neonates: 41 LBW-VLBW infants (stratified into those with (LBW-VLBW-a) and without (LBW-VLBW-n) structural MRI abnormalities) and 9 term controls.
Main Results:
- LBW-VLBW neonates exhibited significantly lower CMRO2 compared to term controls (p=0.01).
- Both LBW-VLBW-a and LBW-VLBW-n subgroups showed greater physiological deficits than term controls (p=0.03 and p=0.04, respectively).
- Physiological parameters, particularly OEF, CBF, and CMRO2, demonstrated higher accuracy in distinguishing LBW-VLBW-a neonates compared to brain volume or body weight.
Conclusions:
- Cerebral metabolic rate of oxygen (CMRO2) is significantly reduced in LBW-VLBW neonates, indicating impaired brain energy metabolism.
- Physiological imaging using TRUST and PC MRI can effectively identify LBW-VLBW newborns at high risk for irreversible brain damage.
- Distinct cerebral metabolic and hemodynamic alterations were observed in LBW-VLBW neonates with structural abnormalities, suggesting targeted interventions may be beneficial.
Abstract:
Low birth-weight (LBW) and very low birth-weight (VLBW) newborns have increased risks of brain injuries, growth failure, motor difficulties, developmental coordination disorders or delay, and adult-onset vascular diseases. However, relatively little is known of the neurobiologic underpinnings. To clarify the pathophysiologic vulnerabilities of such neonates, we applied several advanced techniques for assessing brain physiology, namely T2-relaxation-under-spin-tagging (TRUST) magnetic resonance imaging (MRI) and phase-contrast (PC) MRI. This enabled quantification of oxygen extraction fraction (OEF), global cerebral blood flow (CBF), and cerebral metabolic rate of oxygen (CMRO2). A total of 50 neonates (LBW-VLBW, 41; term controls, 9) participated in this study. LBW-VLBW neonates were further stratified as those with (LBW-VLBW-a, 24) and without (LBW-VLBW-n, 17) structural MRI (sMRI) abnormalities. TRUST and PC MRI studies were undertaken to determine OEF, CBF, and CMRO2. Ultimately, CMRO2 proved significantly lower (p = 0.01) in LBW-VLBW (vs term) neonates, both LBW-VLBW-a and LBW-VLBW-n subsets showing significantly greater physiologic deficits than term controls (p = 0.03 and p = 0.04, respectively). CMRO2 and CBF in LBW-VLBW-a and LBW-VLBW-n subsets did not differ significantly (p > 0.05), although OEF showed a tendency to diverge (p = 0.15). However, OEF values in the LBW-VLBW-n subset differed significantly from those of term controls (p = 0.02). Compared with brain volume or body weight, these physiologic parameters yield higher area-under-the-curve (AUC) values for distinguishing neonates of the LBW-VLBW-a subset. The latter displayed distinct cerebral metabolic and hemodynamic, whereas changes were marginal in the LBW-VLBW-n subset (i.e., higher OEF and lower CBF and CMRO2) by comparison. Physiologic imaging may therefore be useful in identifying LBW-VLBW newborns at high risk of irreversible brain damage.
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