Abstract

.We describe the development of a miniaturized broadband near-infrared spectroscopy system (bNIRS), which measures changes in cerebral tissue oxyhemoglobin () and deoxyhemoglobin ([HHb]) plus tissue metabolism via changes in the oxidation state of cytochrome-c-oxidase ([oxCCO]). The system is based on a small light source and a customized mini-spectrometer. We assessed the instrument in a preclinical study in 27 newborn piglets undergoing transient cerebral hypoxia-ischemia (HI). We aimed to quantify the recovery of the HI insult and estimate the severity of the injury. The recovery in brain oxygenation (), blood volume (), and metabolism () for up to 30 min after the end of HI were quantified in percentages using the recovery fraction (RF) algorithm, which quantifies the recovery of a signal with respect to baseline. The receiver operating characteristic analysis was performed on bNIRS-RF measurements compared to proton () magnetic resonance spectroscopic (MRS)-derived thalamic lactate/N-acetylaspartate (Lac/NAA) measured at 24-h post HI insult; Lac/NAA peak area ratio is an accurate surrogate marker of neurodevelopmental outcome in babies with neonatal HI encephalopathy. The -RF cut-off threshold of 79% within 30 min of HI predicted injury severity based on Lac/NAA with high sensitivity (100%) and specificity (93%). A significant difference in thalamic Lac/NAA was noticed () between the two groups based on this cut-off threshold of 79% -RF. The severe injury group () had smaller recovery in -RF () and no significant difference was observed in -RF between groups. At 48 h post HI, significantly higher -MRS-measured inorganic phosphate/exchangeable phosphate pool (epp) () and reduced phosphocreatine/epp () were observed in the severe injury group indicating persistent cerebral energy depletion. Based on these results, the bNIRS measurement of the oxCCO recovery fraction offers a noninvasive real-time biomarker of brain injury severity within 30 min following HI insult.

Highlights

  • Neonatal hypoxia-ischemia (HI) is primarily caused by systemic hypoxemia and reduced cerebral blood flow to the brain

  • We demonstrated in our recent study by Bainbridge, et al.[10] that 31P-magnetic resonance spectroscopy (MRS) recovery of energetics were correlated with broadband near-infrared spectroscopy system (bNIRS) Δ1⁄2oxCCOŠ recovery within 1 h following HI

  • We have developed and described a miniature bNIRS system based on a miniature white-light source and a customized miniature spectrometer

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Summary

Introduction

Neonatal hypoxia-ischemia (HI) is primarily caused by systemic hypoxemia and reduced cerebral blood flow to the brain. Preclinical studies of perinatal HI, using newborn pigs (similar gross anatomical features of human neonatal brain5) have been used to investigate cerebral energetics and Phosphorous (31P) and proton (1H) magnetic resonance spectroscopy (MRS) are gold standard magnetic resonance (MR) techniques for assessing injury severity, as the decline in cerebral energy measured in this manner correlates strongly with neurodevelopmental outcome.[11,12] Studies have demonstrated that 31P-MRS-measured inorganic phosphate/exchangeable phosphate pool (Pi/epp), phosphocreatine (PCr)/Pi, and total nucleotide triphosphate (NTP)/epp ∼1 to 2 h after HI correlate linearly with the decline in cerebral energetics leading to secondary energy failure.[6,10] 1H-MRS lactate/

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