This thesis investigates the neuroimaging and neuropsychological characteristics of
Posterior Cortical Atrophy (PCA) which is most often caused by Alzheimer’s disease
(AD) pathology. Posterior cortical atrophy describes a predominantly posterior pattern of
atrophy and cognitive deficits. PCA has been poorly characterized and is likely to have
been under-recognized. Using magnetic resonance imaging (MRI), patterns of cortical
thickness were assessed in patients with pathologically-confirmed AD and different
clinical presentations during life (including amnestic, visual and behavioural
phenotypes). In addition to atrophy in the medial temporal lobe, tissue loss in posterior
regions is indicative of AD pathology. Since medial temporal lobe atrophy is not specific
to AD, posterior atrophy may aid distinction between AD and other dementias. Using
easily-applied visual rating scales for medial temporal and posterior atrophy in patients
with pathologically-confirmed AD and frontotemporal lobar degeneration (FTLD), it was
shown that posterior atrophy ratings improve classification accuracy of AD from FTLD
and controls.
Cross-sectional and longitudinal image analysis techniques were used to characterize
atrophy patterns in PCA compared with controls and typical amnestic AD. Whilst the
cross-sectional analysis revealed differential patterns of tissue loss in these two groups,
with PCA showing greatest atrophy in posterior parietal regions, and typical AD
predominantly in medial temporal lobe regions, longitudinal results showed that at five
years disease duration, both PCA and typical AD had global grey matter loss and
cortical thinning compared with controls.
The nature of visual deficits in PCA was assessed by administering detailed
neuropsychological tests. The behavioural data showed that visual deficits were not
uniformly affected in PCA, with considerable heterogeneity of visual impairments shown.
Cortical thickness measures were used to assess atrophy patterns in PCA patients with
predominant space versus object perception impairments, revealing overlap in cortical
thinning patterns between these two PCA subgroups.
In summary this thesis investigates the common and differential atrophy patterns of
atypical AD presentations as well as the degree of heterogeneity of deficits which exist
within the PCA presentation