Abstract

ObjectivesTo investigate the global cortical and regional quantitative features of cortical neural architecture in the brains of patients with posterior cortical atrophy (PCA) and typical Alzheimer’s disease (tAD) compared with elderly healthy controls (HC).MethodsA novel diffusion MRI method, that has been shown to correlate with minicolumnar organization changes in the cerebral cortex, was used as a surrogate of neuropathological changes in dementia. A cohort of 15 PCA patients, 23 tAD and 22 healthy elderly controls (HC) were enrolled to investigate the changes in cortical diffusivity among groups. For each subject, 3 T MRI T1-weighted images and diffusion tensor imaging (DTI) scans were analysed to extract novel cortical DTI derived measures (AngleR, PerpPD and ParlPD). Receiver operating characteristics (ROC) curve analysis and the area under the curve (AUC) were used to assess the group discrimination capability of the method.ResultsThe results showed that the global cortical DTI derived measures were able to detect differences, in both PCA and tAD patients compared to healthy controls. The AngleR was the best measure to discriminate HC from tAD (AUC = 0.922), while PerpPD was the best measure to discriminate HC from PCA (AUC = 0.961). Finally, the best global measure to differentiate the two patient groups was ParlPD (AUC = 0.771). The comparison between PCA and tAD patients revealed a different pattern of damage within the AD spectrum and the regional comparisons identified significant differences in key regions including parietal and temporal lobe cortical areas. The best AUCs were shown by PerpPD right lingual cortex (AUC = 0.856), PerpPD right superior parietal cortex (AUC = 0.842) and ParlPD right lateral occipital cortex (AUC = 0.826).ConclusionsDiagnostic group differences were found, suggesting that the new cortical DTI analysis method may be useful to investigate cortical changes in dementia, providing better characterization of neurodegeneration, and potentially aiding differential diagnosis and prognostic accuracy.

Highlights

  • Posterior cortical atrophy (PCA) is typically an early onset neurodegenerative condition, characterised by progressive visuospatial and visuo-perceptual deficits, but relatively preserved memory [1,2,3,4,5].For most patients, the underlying aetiology is Alzheimer’s disease (AD) [5, 6] so PCA is considered a rare variant, different from typical AD [7,8,9]

  • The present study aimed to investigate cortical features in PCA, typical AD (tAD) and elderly healthy controls (HC), using diffusion tensor imaging (DTI) as a surrogate measure for cortical micro-anatomical alterations that are well known in neurodegenerative pathologies

  • Twenty-three tAD patients were recruited from the Oxford Project to Investigate Memory and Aging (OPTIMA) [28] and the Memory and Amnesia Project, University of Oxford, UK

Read more

Summary

Introduction

The underlying aetiology is Alzheimer’s disease (AD) [5, 6] so PCA is considered a rare variant, different from typical AD (tAD) [7,8,9]. Other neurodegenerative processes sometimes underlie PCA [4,5,6] so PCA could be a distinct nosological entity [10, 11], frequently misclassified. Neuroimaging studies have shown different patterns of grey matter (GM) damage for PCA patients compared to controls or tAD, where the main differences involved occipito-temporal and parietal regions [11,12,13,14,15,16,17]. There is still poor knowledge about the microstructural alterations underlying these patterns of GM damage

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call