Shin Young Seon, Christensen Danielle, Wang Jingying, Shirley Desirae J, Orlando Ann-Marie, Romero Regilda A, Wilkes Bradley J, Vaillancourt David E, Coombes Stephen, Wang Zheng
Res Sq. 2024 Aug 16:rs.3.rs-4907999. doi: 10.21203/rs.3.rs-4907999/v1.
Autism spectrum disorder (ASD) has long been recognized as a lifelong condition, but brain aging studies in autistic adults aged >30 years are limited. Free water, a novel brain imaging marker derived from diffusion MRI (dMRI), has shown promise in differentiating typical and pathological aging and monitoring brain degeneration. We aimed to examine free water and free water corrected dMRI measures to assess white and gray matter microstructure and their associations with age in autistic adults. Forty-three autistic adults ages 30-73 years and 43 age, sex, and IQ matched neurotypical controls participated in this cross-sectional study. We quantified fractional anisotropy (FA), free water, and free water-corrected FA (fwcFA) across 32 transcallosal white matter tracts and 94 gray matter areas in autistic adults and neurotypical controls. Follow-up analyses assessed age effect on dMRI metrics of the whole brain for both groups and the relationship between dMRI metrics and clinical measures of ASD in regions that significantly differentiated autistic adults from controls. We found globally elevated free water in 24 transcallosal tracts in autistic adults. We identified negligible differences in dMRI metrics in gray matter between the two groups. Age-associated FA reductions and free water increases were featured in neurotypical controls; however, this brain aging profile was largely absent in autistic adults. Additionally, greater autism quotient (AQ) total raw score was associated with increased free water in the inferior frontal gyrus pars orbitalis and lateral orbital gyrus in autistic adults. All autistic adults were cognitively capable individuals, minimizing the generalizability of the research findings across the spectrum. This study also involved a cross-sectional design, which limited inferences about the longitudinal microstructural changes of white and gray matter in ASD. We identified differential microstructural configurations between white and gray matter in autistic adults and that autistic individuals present more heterogeneous brain aging profiles compared to controls. Our clinical correlation analysis offered new evidence that elevated free water in some localized white matter tracts may critically contribute to autistic traits in ASD. Our findings underscored the importance of quantifying free water in dMRI studies of ASD.
自闭症谱系障碍(ASD)长期以来一直被认为是一种终身疾病,但针对30岁以上自闭症成年人的大脑衰老研究有限。自由水是一种源自扩散磁共振成像(dMRI)的新型脑成像标志物,在区分典型衰老和病理性衰老以及监测脑退化方面显示出前景。我们旨在研究自由水和自由水校正后的dMRI测量值,以评估自闭症成年人的白质和灰质微观结构及其与年龄的关系。43名年龄在30至73岁之间的自闭症成年人以及43名年龄、性别和智商相匹配的神经典型对照者参与了这项横断面研究。我们对自闭症成年人和神经典型对照者的32条胼胝体白质束和94个灰质区域的分数各向异性(FA)、自由水和自由水校正后的FA(fwcFA)进行了量化。后续分析评估了年龄对两组全脑dMRI指标的影响,以及在显著区分自闭症成年人与对照者的区域中dMRI指标与ASD临床指标之间的关系。我们发现自闭症成年人的24条胼胝体束中的自由水总体升高。我们发现两组之间灰质的dMRI指标差异可忽略不计。神经典型对照者的特征是与年龄相关的FA降低和自由水增加;然而,自闭症成年人在很大程度上没有这种大脑衰老特征。此外,在自闭症成年人中,更高的自闭症商数(AQ)总分与眶额下回眶部和外侧眶回的自由水增加有关。所有自闭症成年人都是有认知能力的个体,这限制了研究结果在整个谱系中的普遍性。这项研究还采用了横断面设计,限制了对ASD中白质和灰质纵向微观结构变化的推断。我们确定了自闭症成年人白质和灰质之间不同的微观结构构型,并且与对照者相比,自闭症个体呈现出更具异质性的大脑衰老特征。我们的临床相关性分析提供了新的证据,表明某些局部白质束中自由水升高可能对ASD中的自闭症特征有重要影响。我们的研究结果强调了在ASD的dMRI研究中量化自由水的重要性。