Neuroimaging Biomarkers Predict Brain Structural Connectivity Change in a Mouse Model of Vascular Cognitive Impairment

Philipp Boehm-Sturm, Martina Füchtemeier, Marco Foddis, Susanne Mueller, Rebecca C. Trueman, Marietta Zille, Jan Leo Rinnenthal, Theodore Kypraios, Laurence Shaw, Ulrich Dirnagl, Tracy D. Farr*

*Corresponding author for this work

Abstract

Background and Purpose - Chronic hypoperfusion in the mouse brain has been suggested to mimic aspects of vascular cognitive impairment, such as white matter damage. Although this model has attracted attention, our group has struggled to generate a reliable cognitive and pathological phenotype. This study aimed to identify neuroimaging biomarkers of brain pathology in aged, more severely hypoperfused mice. Methods - We used magnetic resonance imaging to characterize brain degeneration in mice hypoperfused by refining the surgical procedure to use the smallest reported diameter microcoils (160 μm). Results - Acute cerebral blood flow decreases were observed in the hypoperfused group that recovered over 1 month and coincided with arterial remodeling. Increasing hypoperfusion resulted in a reduction in spatial learning abilities in the water maze that has not been previously reported. We were unable to observe severe white matter damage with histology, but a novel approach to analyze diffusion tensor imaging data, graph theory, revealed substantial reorganization of the hypoperfused brain network. A logistic regression model from the data revealed that 3 network parameters were particularly efficient at predicting group membership (global and local efficiency and degrees), and clustering coefficient was correlated with performance in the water maze. Conclusions - Overall, these findings suggest that, despite the autoregulatory abilities of the mouse brain to compensate for a sudden decrease in blood flow, there is evidence of change in the brain networks that can be used as neuroimaging biomarkers to predict outcome.

Original languageEnglish
JournalStroke
Volume48
Issue number2
Pages (from-to)468-475
Number of pages8
ISSN0039-2499
DOIs
Publication statusPublished - 01.02.2017

Funding

Sources of Funding This work was supported by the German Research Foundation (DFG; Exc 257, NeuroCURE Cluster of Excellence), the Federal Ministry of Education and Research (BMBF; 01EO0801, Center for Stroke Research Berlin), the Herman and Lilly Schilling Foundation, and the European Commission (01EW1201, ERA-NET NEURON).

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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