Microstructural alterations in the locus coeruleus‐entorhinal cortex pathway in Alzheimer's disease and frontotemporal dementia

Author:

Quattrini Giulia12ORCID,Pini Lorenzo3,Boscolo Galazzo Ilaria4,Jelescu Ileana O.5,Jovicich Jorge6,Manenti Rosa7,Frisoni Giovanni B.8,Marizzoni Moira19,Pizzini Francesca B.4,Pievani Michela1ORCID

Affiliation:

1. Laboratory of Alzheimer's Neuroimaging and Epidemiology (LANE) IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli Brescia Italy

2. Department of Molecular and Translational Medicine University of Brescia Brescia Italy

3. Padova Neuroscience Center University of Padova Padova Italy

4. Department of Engineering for Innovation Medicine University of Verona Verona Italy

5. Department of Radiology Lausanne University Hospital and University of Lausanne Lausanne Switzerland

6. Center of Mind/Brain Sciences University of Trento Rovereto Italy

7. Neuropsychology Unit IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli Brescia Italy

8. Memory Center and LANVIE ‐ Laboratory of Neuroimaging of Aging University Hospitals and University of Geneva Geneva Switzerland

9. Laboratory of Biological Psychiatry IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli Brescia Italy

Abstract

AbstractINTRODUCTIONWe investigated in vivo the microstructural integrity of the pathway connecting the locus coeruleus to the transentorhinal cortex (LC‐TEC) in patients with Alzheimer's disease (AD) and frontotemporal dementia (FTD).METHODSDiffusion‐weighted MRI scans were collected for 21 AD, 20 behavioral variants of FTD (bvFTD), and 20 controls. Fractional anisotropy (FA), mean, axial, and radial diffusivities (MD, AxD, RD) were computed in the LC‐TEC pathway using a normative atlas. Atrophy was assessed using cortical thickness and correlated with microstructural measures.RESULTSWe found (i) higher RD in AD than controls; (ii) higher MD, RD, and AxD, and lower FA in bvFTD than controls and AD; and (iii) a negative association between LC‐TEC MD, RD, and AxD, and entorhinal cortex (EC) thickness in bvFTD (all p < 0.050).DISCUSSIONLC‐TEC microstructural alterations are more pronounced in bvFTD than AD, possibly reflecting neurodegeneration secondary to EC atrophy.Highlights Microstructural integrity of LC‐TEC pathway is understudied in AD and bvFTD. LC‐TEC microstructural alterations are present in both AD and bvFTD. Greater LC‐TEC microstructural alterations in bvFTD than AD. LC‐TEC microstructural alterations in bvFTD are associated to EC neurodegeneration.

Publisher

Wiley

Subject

Psychiatry and Mental health,Neurology (clinical)

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