de Gamarra-Oca L Fernández, Nosko D, Kvanta H, Broström L, Strindberg M, Svoboda J, Canto Moreira N, Ojeda N, Zubiaurre-Elorza L, Örtqvist M, Padilla N, Ådén U
Department of Psychology, Faculty of Health Sciences, University of Deusto, Bilbao, Bizkaia, Spain.
Department of Paediatrics, Örebro University Hospital, Örebro, Sweden.
Brain Struct Funct. 2024 Dec 24;230(1):18. doi: 10.1007/s00429-024-02874-5.
To describe the cortical brain development and full-IQ performance in middle school age children after extremely preterm (EPT) birth considering discrete white matter abnormalities (WMA). In addition, to assess possible early motor predictors of cortical brain development and full-IQ in children born EPT with and without discrete WMA diagnosed at 10 years.
T1-weighted MRI images from fifty-one children born before 27 weeks' gestation and 40 full-term born controls (M=10.09 years; SD=0.77) were scored for discrete WMA and analyzed with Freesurfer (v7.2.0). The assessments included motor assessments (i.e., fine- and gross motor function) of Bayley Scales of Infant and Toddler Development - Third Edition (BSID-III) at a mean age of 2½ years. Full-IQ was also assessed with Wechsler Intelligence Scale for Children - Fifth Edition (WISC-V) at 12 years.
No differences were displayed in motor function or full-IQ score between children born EPT with and without discrete WMA at 10 years. Moreover, no global differences were found in cortex volume. However, bilateral mean cortical thicknesses (CTh) were exhibited to be thicker in children born EPT with discrete WMA. Children born EPT with discrete WMA exhibited regional increases mainly in the frontal and temporal lobes apart from left caudal anterior cingulate gyrus (mean difference = -0.11 (-0.22, -0.01), p = 0.026). Full-IQ was predicted by impairments in fine motor skills in children born EPT with discrete WMA, explaining 42.9% of the variance.
Bilateral mean and regional CTh were found to be greater in children born EPT with discrete WMA at 10 years compared to those without. Fine motor function at 2½ years was a strong predictor of full-IQ dependent in children with discrete WMA.
考虑离散性白质异常(WMA),描述极早产儿(EPT)出生后中学年龄段儿童的大脑皮质发育和全智商表现。此外,评估10岁时诊断为有或无离散性WMA的EPT出生儿童大脑皮质发育和全智商的可能早期运动预测因素。
对51名妊娠27周前出生的儿童和40名足月出生的对照儿童(平均年龄=10.09岁;标准差=0.77)的T1加权MRI图像进行离散性WMA评分,并使用Freesurfer(v7.2.0)进行分析。评估包括在平均年龄2.5岁时对贝利婴幼儿发展量表第三版(BSID-III)进行运动评估(即精细和粗大运动功能)。12岁时还使用韦氏儿童智力量表第五版(WISC-V)评估全智商。
10岁时,有或无离散性WMA的EPT出生儿童在运动功能或全智商得分上没有差异。此外,在皮质体积上未发现总体差异。然而,有离散性WMA的EPT出生儿童的双侧平均皮质厚度(CTh)显示更厚。有离散性WMA的EPT出生儿童除左尾侧前扣带回外,主要在额叶和颞叶出现区域增厚(平均差异=-0.11(-0.22,-0.01),p=0.026)。有离散性WMA的EPT出生儿童的全智商由精细运动技能受损预测,解释了42.9%的方差。
与无离散性WMA的儿童相比,10岁时患有离散性WMA的EPT出生儿童的双侧平均和区域CTh更大。2.5岁时的精细运动功能是有离散性WMA儿童全智商的一个强有力的预测因素。