Boateng Theresah, Beauchamp Kathryn, Torres Faerl, Ruffaner-Hanson Chaselyn D, Pinner John F L, Vakamudi Kishore, Cerros Cassandra, Hill Dina E, Stephen Julia M
Department of Special Education, The University of New Mexico, Albuquerque, NM, United States.
College of Pharmacy, University of New Mexico Health Sciences Center, Albuquerque, NM, United States.
Front Neurosci. 2023 Aug 9;17:1152038. doi: 10.3389/fnins.2023.1152038. eCollection 2023.
The teratogenic effects of prenatal alcohol exposure (PAE) have been examined in animal models and humans. The current study extends the prior literature by quantifying differences in brain structure for individuals with a fetal alcohol spectrum disorder (FASD) compared to typically developing controls, as well as examining FASD subtypes. We hypothesized the FASD group would reveal smaller brain volume, reduced cortical thickness, and reduced surface area compared to controls, with the partial fetal alcohol syndrome (pFAS)/fetal alcohol syndrome (FAS) subtypes showing the largest effects and the PAE/alcohol-related neurodevelopmental disorder (ARND) subtype revealing intermediate effects.
The sample consisted of 123 children and adolescents recruited from a single site including children with a diagnosis of FASD/PAE (26 males, 29 females) and controls (34 males, 34 females). Structural T1-weighted MRI scans were obtained on a 3T Trio TIM scanner and FreeSurfer v7.2 was used to quantify brain volume, cortical thickness, and surface area. Analyses examined effects by subgroup: pFAS/FAS ( = 32, M = 10.7 years, SE = 0.79), PAE/ARND ( = 23, M = 10.8, SE = 0.94), and controls ( = 68, M = 11.1, SE = 0.54).
Total brain volume in children with an FASD was smaller relative to controls, but subtype analysis revealed only the pFAS/FAS group differed significantly from controls. Regional analyses similarly revealed reduced brain volume in frontal and temporal regions for children with pFAS/FAS, yet children diagnosed with PAE/ARND generally had similar volumes as controls. Notable differences to this pattern occurred in the cerebellum, caudate, and pallidum where children with pFAS/FAS and PAE/ARND revealed lower volume relative to controls. In the subset of participants who had neuropsychological testing, correlations between volume and IQ scores were observed. Goodness-of-Fit analysis by age revealed differences in developmental patterns (linear vs. quadratic) between groups in some cases.
This study confirmed prior results indicating decreased brain volume in children with an FASD and extended the results by demonstrating differential effects by structure for FASD subtypes. It provides further evidence for a complex role of PAE in structural brain development that is likely related to the cognitive and behavioral effects experienced by children with an FASD.
产前酒精暴露(PAE)的致畸作用已在动物模型和人类中进行了研究。本研究通过量化胎儿酒精谱系障碍(FASD)个体与正常发育对照者在脑结构上的差异,并研究FASD亚型,扩展了先前的文献。我们假设,与对照组相比,FASD组的脑容量会更小,皮质厚度会变薄,表面积会减小,其中部分胎儿酒精综合征(pFAS)/胎儿酒精综合征(FAS)亚型的影响最大,而PAE/酒精相关神经发育障碍(ARND)亚型的影响则处于中间水平。
样本包括从单一地点招募的123名儿童和青少年,其中包括诊断为FASD/PAE的儿童(26名男性,29名女性)和对照组(34名男性,34名女性)。在3T Trio TIM扫描仪上进行了结构性T1加权MRI扫描,并使用FreeSurfer v7.2来量化脑容量、皮质厚度和表面积。分析按亚组检查了影响:pFAS/FAS(n = 32,平均年龄 = 10.7岁,标准误 = 0.79)、PAE/ARND(n = 23,平均年龄 = 10.8岁,标准误 = 0.94)和对照组(n = 68,平均年龄 = 11.1岁,标准误 = 0.54)。
FASD儿童的总脑容量相对于对照组较小,但亚型分析显示只有pFAS/FAS组与对照组有显著差异。区域分析同样显示,pFAS/FAS儿童的额叶和颞叶区域脑容量减小,但被诊断为PAE/ARND的儿童的脑容量通常与对照组相似。在小脑、尾状核和苍白球出现了与这种模式明显不同的情况,其中pFAS/FAS和PAE/ARND儿童的这些脑区容量相对于对照组较低。在进行了神经心理测试的参与者子集中,观察到了脑容量与智商分数之间的相关性。按年龄进行的拟合优度分析显示,在某些情况下,各组之间在发育模式(线性与二次)上存在差异。
本研究证实了先前的结果,即FASD儿童的脑容量减小,并通过证明FASD亚型在结构上的差异影响扩展了这些结果。它为PAE在脑结构发育中的复杂作用提供了进一步的证据,这可能与FASD儿童所经历的认知和行为影响有关。