4.6 Article

Cortical Thickness in Dementia with Lewy Bodies and Alzheimer's Disease: A Comparison of Prodromal and Dementia Stages

Journal

PLOS ONE
Volume 10, Issue 6, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0127396

Keywords

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Funding

  1. Appel a Projet Interne (API) of the University Hospital of Strasbourg
  2. Alsace Alzheimer 67
  3. Fondation Universite de Strasbourg and famille Jean Amrhein
  4. Projet Hospitalier de Recherche Clinique (PHRC) [IDRCB 2012-A00992-41]
  5. Newcastle Healthcare Charity [BH0070250]
  6. Academy of Medical Sciences, Wellcome Trust [BH090112]
  7. Wellcome Intermediate Clinical Fellowship [BH083281]
  8. National Institute for Health Research (NIHR) Newcastle Biomedical Research Centre in Ageing and Chronic Disease
  9. Newcastle University
  10. NIHR Dementia Biomedical Research Unit at Cambridge University Hospitals NHS Foundation Trust
  11. University of Cambridge
  12. Biomedical Research Unit in Lewy Body Dementia based at Newcastle upon Tyne Hospitals NHS Foundation Trust
  13. National Institute for Health Research [NF-SI-0611-10048] Funding Source: researchfish

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Objectives To assess and compare cortical thickness (CTh) of patients with prodromal Dementia with Lewy bodies (pro-DLB), prodromal Alzheimer's disease (pro-AD), DLB dementia (DLB-d), AD dementia (AD-d) and normal ageing. Methods Study participants(28 pro-DLB, 27 pro-AD, 31 DLB-d, 54 AD-d and 33 elderly controls) underwent 3Tesla T1 3D MRI and detailed clinical and cognitive assessments. We used Free-Surfer analysis package to measure CTh and investigate patterns of cortical thinning across groups. Results Comparison of CTh between pro-DLB and pro-AD (p<0.05, FDR corrected) showed more right anterior insula thinning in pro-DLB, and more bilateral parietal lobe and left parahippocampal gyri thinning in pro-AD. Comparison of prodromal patients to healthy elderly controls showed the involvement of the same regions. In DLB-d (p<0.05, FDR corrected) cortical thinning was found predominantly in the right temporo-parietal junction, and insula, cingulate, orbitofrontal and lateral occipital cortices. In AD-d(p<0.05, FDR corrected), the most significant areas affected included the entorhinal cortices, parahippocampal gyri and parietal lobes. The comparison of AD-d and DLB-d demonstrated more CTh in AD-d in the left entorhinal cortex (p<0.05, FDR corrected). Conclusion Cortical thickness is a sensitive measure for characterising patterns of grey matter atrophy in early stages of DLB distinct from AD. Right anterior insula involvement may be a key region at the prodromal stage of DLB and needs further investigation.

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