Simões Rui V, Cruz-Lemini Mónica, Bargalló Núria, Gratacós Eduard, Sanz-Cortés Magdalena
BCNatal, Barcelona Center for Maternal-Fetal and Neonatal Medicine, Hospital Clínic and Hospital Sant Joan de Deu, Fetal i+D Fetal Medicine Research Center, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Centre for Biomedical Research on Rare Diseases (CIBER-ER), Barcelona, Spain; Fundació Hospital Sant Joan de Déu, Barcelona, Spain.
Department of Obstetrics, Maternal-Fetal Medicine Unit, Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain.
Am J Obstet Gynecol. 2015 Aug;213(2):210.e1-210.e11. doi: 10.1016/j.ajog.2015.04.011. Epub 2015 Apr 16.
We assessed brain metabolite levels by magnetic resonance spectroscopy (MRS) in 1-year-old infants born small at term, as compared with infants born appropriate for gestational age (AGA), and their association with neurodevelopment at 2 years of age.
A total of 40 infants born small (birthweight <10th centile for gestational age) and 30 AGA infants underwent brain MRS at age 1 year on a 3-T scanner. Small-born infants were subclassified as late intrauterine growth restriction or as small for gestational age, based on the presence or absence of prenatal Doppler and birthweight predictors of an adverse perinatal outcome, respectively. Single-voxel proton magnetic resonance spectroscopy ((1)H-MRS) data were acquired from the frontal lobe at short echo time. Neurodevelopment was evaluated at 2 years of age using the Bayley Scales of Infant and Toddler Development, Third Edition, assessing cognitive, language, motor, social-emotional, and adaptive behavior scales.
As compared with AGA controls, infants born small showed significantly higher levels of glutamate and total N-acetylaspartate (NAAt) to creatine (Cr) ratio at age 1 year, and lower Bayley Scales of Infant and Toddler Development, Third Edition scores at 2 years. The subgroup with late intrauterine growth restriction further showed lower estimated glutathione levels at age 1 year. Significant correlations were observed for estimated glutathione levels with adaptive scores, and for myo-inositol with language scores. Significant associations were also noticed for NAA/Cr with cognitive scores, and for glutamate/Cr with motor scores.
Infants born small show brain metabolite differences at 1 year of age, which are correlated with later neurodevelopment. These results support further research on MRS to develop imaging biomarkers of abnormal neurodevelopment.
我们通过磁共振波谱(MRS)评估了足月小样儿1岁时的脑代谢物水平,并与适于胎龄儿(AGA)进行比较,以及这些代谢物水平与2岁时神经发育的关联。
共有40例小样儿(出生体重<胎龄的第10百分位数)和30例AGA婴儿在1岁时接受了3-T扫描仪的脑部MRS检查。根据是否存在产前多普勒检查结果以及出生体重等围产期不良结局预测指标,将小样儿进一步分为晚期宫内生长受限或小于胎龄儿。在短回波时间从额叶获取单体素质子磁共振波谱((1)H-MRS)数据。使用贝利婴幼儿发育量表第三版在2岁时评估神经发育,评估认知、语言、运动、社会情感和适应性行为量表。
与AGA对照组相比,小样儿在1岁时谷氨酸水平和总N-乙酰天门冬氨酸(NAAt)与肌酸(Cr)的比值显著更高,而在2岁时贝利婴幼儿发育量表第三版得分更低。晚期宫内生长受限亚组在1岁时估计的谷胱甘肽水平进一步降低。观察到估计的谷胱甘肽水平与适应性得分之间、肌醇与语言得分之间存在显著相关性。还注意到NAA/Cr与认知得分之间、谷氨酸/Cr与运动得分之间存在显著关联。
小样儿在1岁时显示出脑代谢物差异,这些差异与后期神经发育相关。这些结果支持进一步开展MRS研究以开发异常神经发育的成像生物标志物。