Côté-Corriveau Gabriel, Simard Marie-Noëlle, Beaulieu Olivia, Chowdhury Rasheda Arman, Gagnon Marie-Michèle, Gagnon Mélanie, Ledjiar Omar, Bernard Catherine, Nuyt Anne Monique, Dehaes Mathieu, Luu Thuy Mai
Research Center, Sainte-Justine University Hospital Center, Montreal, QC, Canada.
Department of Epidemiology, Biostatistics and Occupational Health, Faculty of Medicine, McGill University, Montreal, QC, Canada.
Front Neurosci. 2023 Mar 2;17:1105638. doi: 10.3389/fnins.2023.1105638. eCollection 2023.
Infants born at 29-36 weeks gestational age (GA) are at risk of experiencing neurodevelopmental challenges. We hypothesize that cerebral hemodynamics and oxygen metabolism measured by bedside optical brain monitoring are potential biomarkers of brain development and are associated with neurological examination at term-equivalent age (TEA).
Preterm infants ( = 133) born 29-36 weeks GA and admitted in the neonatal intensive care unit were enrolled in this prospective cohort study. Combined frequency-domain near infrared spectroscopy (FDNIRS) and diffuse correlation spectroscopy (DCS) were used from birth to TEA to measure cerebral hemoglobin oxygen saturation and an index of microvascular cerebral blood flow (CBF ) along with peripheral arterial oxygen saturation (SpO). In combination with hemoglobin concentration in the blood, these parameters were used to derive cerebral oxygen extraction fraction (OEF) and an index of cerebral oxygen metabolism (CMRO ). The Amiel-Tison and Gosselin Neurological Assessment was performed at TEA. Linear regression models were used to assess the associations between changes in FDNIRS-DCS parameters from birth to TEA and GA at birth. Logistic regression models were used to assess the associations between changes in FDNIRS-DCS parameters from birth to TEA and neurological examination at TEA.
Steeper increases in CBF ( < 0.0001) and CMRO ( = 0.0003) were associated with higher GA at birth. Changes in OEF, CBF , and CMRO from birth to TEA were not associated with neurological examination at TEA.
In this population, cerebral FDNIRS-DCS parameters were not associated with neurological examination at TEA. Larger increases in CBF and CMRO from birth to TEA were associated with higher GA. Non-invasive bedside FDNIRS-DCS monitoring provides cerebral hemodynamic and metabolic parameters that may complement neurological examination to assess brain development in preterm infants.
孕29 - 36周出生的婴儿有面临神经发育挑战的风险。我们假设通过床边光学脑监测测量的脑血流动力学和氧代谢是脑发育的潜在生物标志物,并且与足月等效年龄(TEA)时的神经学检查相关。
本前瞻性队列研究纳入了29 - 36周孕龄出生并入住新生儿重症监护病房的133名早产儿。从出生到TEA期间,联合使用频域近红外光谱(FDNIRS)和扩散相关光谱(DCS)测量脑血红蛋白氧饱和度、微血管脑血流量指数(CBF )以及外周动脉血氧饱和度(SpO)。结合血液中的血红蛋白浓度,这些参数用于计算脑氧摄取分数(OEF)和脑氧代谢指数(CMRO )。在TEA时进行阿米尔 - 蒂森和戈斯林神经学评估。使用线性回归模型评估从出生到TEA期间FDNIRS - DCS参数变化与出生时孕龄之间的关联。使用逻辑回归模型评估从出生到TEA期间FDNIRS - DCS参数变化与TEA时神经学检查之间的关联。
出生时较高的孕龄与CBF ( < 0.0001)和CMRO( = 0.0003)更显著的增加相关。从出生到TEA期间OEF、CBF 和CMRO的变化与TEA时的神经学检查无关。
在该人群中,脑FDNIRS - DCS参数与TEA时的神经学检查无关。从出生到TEA期间CBF 和CMRO更大幅度的增加与较高的孕龄相关。非侵入性床边FDNIRS - DCS监测提供的脑血流动力学和代谢参数可能补充神经学检查,以评估早产儿的脑发育情况。