Author:
LENEMAN MICHAL,BUCHANAN LORI,ROVET JOANNE
Abstract
Visuospatial processing is accomplished in distinct neuroanatomic
pathways. One such pathway, known as the where
pathway, involves a dorsal route through magnocellular
thalamic cells to occipital and parietal cortices and conveys
location and motion information. A second pathway, known
as the what pathway, involves a ventral route
through parvocellular thalamic cells to occipital and temporal
cortices and conveys color and form information. The where
pathway is thought to be responsible for processing spatial
relationships while the what pathway is responsible
for object identification. Children with early-treated
congenital hypothyroidism (CH) who exhibit selective visuospatial
deficits may provide a good model to study the differential
development of these pathways. Because children with CH
lacked thyroid hormone at a time when needed by developing
brain regions such as the parietal cortex, these children
may be affected to a greater degree on tasks tapping where
but not what pathway processing. We tested this
hypothesis via retrospective analysis of their performance
on 6 spatial tasks. Compared were 49 adolescents with CH
and 49 matched control participants. On the basis of confirmatory
factor analysis, tasks were assigned to either where
or what pathway groupings. A repeated measures
ANOVA showed the CH group was impaired relative to a normal
comparison group only on where pathway tasks.
Regression analyses indicated that severity of early hypothyroidism
was the strongest predictor of where pathway processing
but had no effect on what pathway tasks. It is
concluded that thyroid hormone is required during late
gestation and early life for the normal development of
the where aspects of visuospatial processing.
(JINS, 2001, 7, 556–562.)
Publisher
Cambridge University Press (CUP)
Subject
Psychiatry and Mental health,Clinical Neurology,Clinical Psychology,General Neuroscience
Cited by
26 articles.
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