Hippocampus co-atrophy pattern in dementia deviates from covariance patterns across the lifespan

Author:

Plachti Anna12,Kharabian Shahrzad12,Eickhoff Simon B12,Maleki Balajoo Somayeh2,Hoffstaedter Felix2,Varikuti Deepthi P2,Jockwitz Christiane23,Caspers Svenja245,Amunts Katrin246,Genon Sarah27

Affiliation:

1. Institute of Systems Neuroscience, Heinrich Heine University Düsseldorf, Düsseldorf 40225, Germany

2. Institute of Neuroscience and Medicine (INM-1, INM-7), Research Centre Jülich, Jülich, Germany

3. Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, RWTH Aachen University, Aachen, Germany

4. JARA-BRAIN, Jülich-Aachen Research Alliance, Jülich, Germany

5. Institute for Anatomy I, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany

6. C. & O. Vogt Institute for Brain Research, Heinrich Heine University, Düsseldorf, Germany

7. GIGA-CRC In vivo Imaging, University of Liege, Liege, Belgium

Abstract

Abstract The hippocampus is a plastic region and highly susceptible to ageing and dementia. Previous studies explicitly imposed a priori models of hippocampus when investigating ageing and dementia-specific atrophy but led to inconsistent results. Consequently, the basic question of whether macrostructural changes follow a cytoarchitectonic or functional organization across the adult lifespan and in age-related neurodegenerative disease remained open. The aim of this cross-sectional study was to identify the spatial pattern of hippocampus differentiation based on structural covariance with a data-driven approach across structural MRI data of large cohorts (n = 2594). We examined the pattern of structural covariance of hippocampus voxels in young, middle-aged, elderly, mild cognitive impairment and dementia disease samples by applying a clustering algorithm revealing differentiation in structural covariance within the hippocampus. In all the healthy and in the mild cognitive impaired participants, the hippocampus was robustly divided into anterior, lateral and medial subregions reminiscent of cytoarchitectonic division. In contrast, in dementia patients, the pattern of subdivision was closer to known functional differentiation into an anterior, body and tail subregions. These results not only contribute to a better understanding of co-plasticity and co-atrophy in the hippocampus across the lifespan and in dementia, but also provide robust data-driven spatial representations (i.e. maps) for structural studies.

Funder

Alzheimer's Disease Neuroimaging Initiative

ADNI

National Institutes of Health

DOD ADNI

Department of Defense

National Institute on Aging

National Institute of Biomedical Imaging and Bioengineering

Alzheimer’s Association

Alzheimer’s Drug Discovery Foundation

Araclon Biotech

BioClinica, Inc

Biogen

Bristol-Myers Squibb Company

CereSpir, Inc

Cogstate

Eisai Inc

Elan Pharmaceuticals, Inc

Eli Lilly and Company

EuroImmun

F Hoffmann-La Roche Ltd

Genentech, Inc

Fujirebio

GE Healthcare; IXICO Ltd

Janssen Alzheimer Immunotherapy Research and Development, LLC

Johnson and Johnson Pharmaceutical Research and Development LLC

Lumosity

Lundbeck

Merck and Co, Inc

Meso Scale Diagnostics, LLC

NeuroRx Research

Neurotrack Technologies

Novartis Pharmaceuticals Corporation; Pfizer Inc

Piramal Imageng

Servier

Takeda Pharmaceutical Company

Transition Therapeutics.

The Canadian Institutes of Health Research

Northern California Institute for Research and Education

University of Southern California

UK Biotechnology and Biological Sciences Research Council

UK Medical Research Council and University of Cambridge, UK

Deutsche Forschungsgemeinschaft

Helmholtz-Gemeinschaft

Horizon 2020 Framework Programme

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

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