Assessment & Research

Quantitative comparison of radial cell columns in children with Down's syndrome and controls.

Buxhoeveden et al. (2002) · Journal of intellectual disability research : JIDR 2002
★ The Verdict

Down syndrome brains show prematurely wide minicolumns, a structural sign of early ageing that links to earlier cognitive plateaus.

✓ Read this if BCBAs designing skill-acquisition programs for school-age or adolescent clients with Down syndrome.
✗ Skip if Clinicians who only serve adults with ID of other etiologies.

01Research in Context

01

What this study did

Wimpory et al. (2002) looked at thin slices of brain tissue from children with Down syndrome and same-age peers. They measured the width of minicolumns, the tiny vertical stacks of neurons that process information. All tissue came from autopsies, so the method is direct but cross-sectional.

02

What they found

Minicolumns in Down syndrome children were already as wide as adult columns, while typical kids still had narrower, child-sized columns. The space between cells, called neuropil, was also wider. The authors call this pattern “precocious cortical ageing,” meaning the brain looks older than the child’s calendar age.

03

How this fits with other research

Takashima et al. (1994) saw the same ageing story earlier. They found fewer dendritic spines in childhood and faster dendrite loss in adulthood, so the widening shown by Wimpory et al. (2002) fits neatly as the structural base.

Amore et al. (2011) extend the finding into real-time brain activity. Young adults with Down syndrome used different brain areas during a word task, suggesting the widened columns change how the brain works, not just how it looks.

Ruser et al. (2007) used the same ruler on gifted scientists and got the opposite picture: ultra-narrow columns. Wide columns in Down syndrome and narrow columns in high IQ minds create a clear anatomical contrast that may guide future teaching strategies.

04

Why it matters

You can’t change brain width, but you can adjust teaching. Expect earlier plateaus in attention and memory because the cortex is “older.” Break lessons into short, concrete steps and review often. Pair visual cues with language tasks, since fMRI shows the brain leans on visual systems. Share the ageing pattern with parents to explain why skills can seem to stall and to plan realistic long-term goals.

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Cut each teaching block to five-minute chunks and add a quick visual preview to offset earlier cortical ageing.

02At a glance

Intervention
not applicable
Design
case study
Population
down syndrome, neurotypical
Finding
not reported

03Original abstract

No one has examined the configuration of the minicolumns in Down's syndrome (DS) brains even though these are a basic functional unit of the cortex. In the present study, the authors used computerized imaging to examine minicolumns in the posterior superior temporal gyrus in both the brains of patients with DS and normal controls. They compared the brains of children aged 4 and 6 years with those of adults for both people with DS and the normal population. Columns in the brains of two DS children aged 4 and 6 years were almost the same size as those of the adults with DS. The neuropil space in the periphery of the columns was also considerably wider. In contrast, minicolumns in aged-matched control children were smaller, both relatively and absolutely, when compared to the mean size of adult columns. The size of the minicolumns in the normal children apparently corresponded to the overall brain size, whereas the large columns in children with DS appeared to be independent of brain size, at least in area Tpt. This seems to reflect a rapid ageing process that is striking when compared to normal controls. Columns in adults with DS were large and less cell dense, while brain volumes were significantly smaller than in controls. This combination suggests reduced neuronal complexity based on a decrease in processing units, which supports previous findings of decreased cell numbers and synaptic diminution in DS brains.

Journal of intellectual disability research : JIDR, 2002 · doi:10.1046/j.1365-2788.2002.00362.x