Lange Nicholas, Travers Brittany G, Bigler Erin D, Prigge Molly B D, Froehlich Alyson L, Nielsen Jared A, Cariello Annahir N, Zielinski Brandon A, Anderson Jeffrey S, Fletcher P Thomas, Alexander Andrew A, Lainhart Janet E
Department of Psychiatry, Harvard School of Medicine, Boston, Massachusetts; Neurostatistics Laboratory, McLean Hospital, Belmont, Massachusetts.
Autism Res. 2015 Feb;8(1):82-93. doi: 10.1002/aur.1427. Epub 2014 Nov 7.
Since the impairments associated with autism spectrum disorder (ASD) tend to persist or worsen from childhood into adulthood, it is of critical importance to examine how the brain develops over this growth epoch. We report initial findings on whole and regional longitudinal brain development in 100 male participants with ASD (226 high-quality magnetic resonance imaging [MRI] scans; mean inter-scan interval 2.7 years) compared to 56 typically developing controls (TDCs) (117 high-quality scans; mean inter-scan interval 2.6 years) from childhood into adulthood, for a total of 156 participants scanned over an 8-year period. This initial analysis includes between one and three high-quality scans per participant that have been processed and segmented to date, with 21% having one scan, 27% with two scans, and 52% with three scans in the ASD sample; corresponding percentages for the TDC sample are 30%, 30%, and 40%. The proportion of participants with multiple scans (79% of ASDs and 68% of TDCs) was high in comparison to that of large longitudinal neuroimaging studies of typical development. We provide volumetric growth curves for the entire brain, total gray matter (GM), frontal GM, temporal GM, parietal GM, occipital GM, total cortical white matter (WM), corpus callosum, caudate, thalamus, total cerebellum, and total ventricles. Mean volume of cortical WM was reduced significantly. Mean ventricular volume was increased in the ASD sample relative to the TDCs across the broad age range studied. Decreases in regional mean volumes in the ASD sample most often were due to decreases during late adolescence and adulthood. The growth curve of whole brain volume over time showed increased volumes in young children with autism, and subsequently decreased during adolescence to meet the TDC curve between 10 and 15 years of age. The volume of many structures continued to decline atypically into adulthood in the ASD sample. The data suggest that ASD is a dynamic disorder with complex changes in whole and regional brain volumes that change over time from childhood into adulthood.
由于与自闭症谱系障碍(ASD)相关的损伤往往会从儿童期持续到成年期或在成年期恶化,因此研究大脑在这一成长阶段如何发育至关重要。我们报告了100名患有ASD的男性参与者(226次高质量磁共振成像[MRI]扫描;平均扫描间隔2.7年)与56名发育正常的对照者(TDCs)(117次高质量扫描;平均扫描间隔2.6年)从儿童期到成年期的全脑和区域纵向大脑发育的初步研究结果,在8年期间共对156名参与者进行了扫描。这项初步分析包括每位参与者已处理和分割的一至三次高质量扫描,在ASD样本中,21%的人有一次扫描,27%的人有两次扫描,52%的人有三次扫描;TDC样本的相应百分比分别为30%、30%和40%。与典型发育的大型纵向神经影像学研究相比,进行多次扫描的参与者比例(ASD患者中的79%和TDC患者中的68%)较高。我们提供了全脑、总灰质(GM)、额叶GM、颞叶GM、顶叶GM、枕叶GM、总皮质白质(WM)、胼胝体、尾状核、丘脑、全小脑和全心室的体积生长曲线。皮质WM的平均体积显著减少。在整个研究的广泛年龄范围内,ASD样本中的平均心室体积相对于TDCs增加。ASD样本中区域平均体积的减少最常见于青春期后期和成年期。随着时间的推移,全脑体积的生长曲线显示自闭症幼儿的体积增加,随后在青春期减少,在10至15岁之间达到TDC曲线。在ASD样本中,许多结构的体积在成年期继续出现非典型下降。数据表明,ASD是一种动态疾病,全脑和区域脑体积会发生复杂变化,从儿童期到成年期会随时间而改变。