학술논문

Dissociations in Cortical Morphometry in Youth with Down Syndrome: Evidence for Reduced Surface Area but Increased Thickness
Document Type
article
Source
Cerebral Cortex. 26(7)
Subject
Cognitive and Computational Psychology
Psychology
Brain Disorders
Aging
Intellectual and Developmental Disabilities (IDD)
Neurodegenerative
Pediatric
Down Syndrome
Alzheimer's Disease
Biomedical Imaging
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Dementia
Mental Health
Acquired Cognitive Impairment
Neurosciences
Clinical Research
Aetiology
2.1 Biological and endogenous factors
Adolescent
Alzheimer Disease
Analysis of Variance
Cerebral Cortex
Child
Child
Preschool
Female
Humans
Intelligence
Intelligence Tests
Magnetic Resonance Imaging
Male
Organ Size
Young Adult
Alzheimer's disease
cerebral cortex
intellectual disability
magnetic resonance imaging
Trisomy 21
Cognitive Sciences
Experimental Psychology
Biological psychology
Cognitive and computational psychology
Language
Abstract
Detailed descriptions of cortical anatomy in youth with Down syndrome (DS), the most common genetic cause of intellectual disability (ID), are scant. Thus, the current study examined deviations in cortical thickness (CT) and surface area (SA), at high spatial resolution, in youth with DS, to identify focal differences relative to typically developing (TD) youth. Participants included 31 youth with DS and 45 age- and sex-matched TD controls (mean age ∼16 years; range = 5-24 years). All participants completed T1-weighted ASSET-calibrated magnetization prepared rapid gradient echo scans on a 3-T magnetic resonance imaging scanner. Replicating prior investigations, cortical volume was reduced in DS compared with controls. However, a novel dissociation for SA and CT was found-namely, SA was reduced (predominantly in frontal and temporal regions) while CT was increased (notably in several regions thought to belong to the default mode network; DMN). These findings suggest that reductions in SA rather than CT are driving the cortical volume reductions reported in prior investigations of DS. Moreover, given the link between DMN functionality and Alzheimer's symptomatology in chromosomally typical populations, future DS studies may benefit from focusing on the cortex in DMN regions, as such investigations may provide clues to the precocious onset of Alzheimer's disease in this at-risk group.