De Vis J B, Petersen E T, Alderliesten T, Groenendaal F, de Vries L S, van Bel F, Benders M J N L, Hendrikse J
Department of Radiology, University Medical Centre Utrecht, HP E 01.132, P.O. Box 85500, 3508GA Utrecht, The Netherlands.
Department of Radiology, University Medical Centre Utrecht, HP E 01.132, P.O. Box 85500, 3508GA Utrecht, The Netherlands; Department of Radiotherapy, University Medical Centre Utrecht, HP Q 00.118, P.O. Box 85500, 3508GA Utrecht, The Netherlands.
Neuroimage. 2014 Jul 15;95:185-92. doi: 10.1016/j.neuroimage.2014.03.060. Epub 2014 Mar 29.
Brain oxygen consumption reflects neuronal activity and can therefore be used to investigate brain development or neuronal injury in neonates. In this paper we present the first results of a non-invasive MRI method to evaluate whole brain oxygen consumption in neonates.
For this study 51 neonates were included. The T1 and T2 of blood in the sagittal sinus were fitted using the 'T2 prepared tissue relaxation inversion recovery' pulse sequence (T2-TRIR). From the T1 and the T2 of blood, the venous oxygenation and the oxygen extraction fraction (OEF) were calculated. The cerebral metabolic rate of oxygen (CMRO2) was the resultant of the venous oxygenation and arterial spin labeling whole brain cerebral blood flow (CBF) measurements.
Venous oxygenation was 59±14% (mean±sd), OEF was 40±14%, CBF was 14±5ml/100g/min and CMRO2 was 30±12μmol/100g/min. The OEF in preterms at term-equivalent age was higher than in the preterms and in the infants with hypoxic-ischemic encephalopathy (p<0.01). The OEF, CBF and CMRO2 increased (p<0.01, <0.05 and <0.01, respectively) with postnatal age.
We presented an MRI technique to evaluate whole-brain oxygen consumption in neonates non-invasively. The measured values are in line with reference values found by invasive measurement techniques. Preterms and infants with HIE demonstrated significant lower oxygen extraction fraction than the preterms at term-equivalent age. This could be due to decreased neuronal activity as a reflection of brain development or as a result of tissue damage, increased cerebral blood flow due to immature or impaired autoregulation, or could be caused by differences in postnatal age.
脑氧消耗反映神经元活动,因此可用于研究新生儿脑发育或神经元损伤。在本文中,我们展示了一种用于评估新生儿全脑氧消耗的非侵入性MRI方法的初步结果。
本研究纳入了51例新生儿。使用“T2准备组织弛豫反转恢复”脉冲序列(T2-TRIR)拟合矢状窦中血液的T1和T2。根据血液的T1和T2计算静脉氧合和氧摄取分数(OEF)。脑氧代谢率(CMRO2)是静脉氧合与动脉自旋标记全脑脑血流量(CBF)测量结果的综合值。
静脉氧合为59±14%(平均值±标准差),OEF为40±14%,CBF为14±5ml/100g/min,CMRO2为30±12μmol/100g/min。足月相当年龄早产儿的OEF高于早产儿和患有缺氧缺血性脑病的婴儿(p<0.01)。OEF、CBF和CMRO2随出生后年龄增加(分别为p<0.01、<0.05和<0.01)。
我们展示了一种非侵入性评估新生儿全脑氧消耗的MRI技术。测量值与通过侵入性测量技术获得的参考值一致。早产儿和患有缺氧缺血性脑病的婴儿的氧摄取分数明显低于足月相当年龄的早产儿。这可能是由于作为脑发育反映的神经元活动减少或组织损伤、由于自身调节不成熟或受损导致的脑血流量增加,或者可能是由于出生后年龄差异所致。