Correspondence of large-scale functional brain network decline across aging mice and humans

Human aging is marked by progressive reorganization of large-scale functional brain networks; these brain network changes have been linked to cognitive decline and disease vulnerability. Conversely, while mice have served as powerful models for understanding the molecular and cellular changes that occur over the lifespan, an absence of precise characterization of age-related changes in large-scale functional brain network organization has limited cross-species translational insights. Here, using densely sampled resting-state functional MRI data acquired cross-sectionally and longitudinally in awake mice over a broad range of adulthood (n = 82; 3 to 20 mo), we describe organizational features and age-related alterations of the mouse's functional connectome. Mouse resting-state functional connectivity recapitulates known functional circuits, demonstrating the organizational validity of these signals. Graph theoretic analysis applied to functional connectivity reveals that mice exhibit modular architectures of functional brain network organization and that increasing age is associated with decreasing system segregation, indicative of network dedifferentiation analogous to observations in humans. Notably, mouse resting-state brain networks are more segregated than those of humans [determined using data from the Human Connectome Project and its developmental- and aging-counterparts (n = 1,179; 18 to 90 y)], attributable to mice exhibiting a diminished contribution of long-range functional relationships that integrate distributed systems. Mice also exhibit slower rates of age-related decline in brain network organization relative to humans, highlighting important species differences in functional brain network organization and trajectories of brain network aging. These findings establish a model of large-scale functional brain network aging in mice and provide a translational bridge across species and spatial scales of analysis.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-03-27
DOI
https://doi.org/10.1073/pnas.2527522123
Primary Topic
Functional Brain Connectivity Studies
Type
article
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article

Correspondence of large-scale functional brain network decline across aging mice and humans

Jad Asleh, Irit Dolgopyat, Gagan S. Wig, Eyal Bergmann et al.
Proceedings of the National Academy of Sciences
Functional Brain Connectivity Studies
article

Correspondence of large-scale functional brain network decline across aging mice and humans

Jad Asleh, Irit Dolgopyat, Gagan S. Wig, Eyal Bergmann, Alexandra Kavushansky, Micaela Y. Chan, Jennifer D. Whitesell, Itamar Kahn, Ziwei Zhang, Liang Han, Ezra Winter-Nelson, Gabriella Vill
article en

Abstract

Human aging is marked by progressive reorganization of large-scale functional brain networks; these brain network changes have been linked to cognitive decline and disease vulnerability. Conversely, while mice have served as powerful models for understanding the molecular and cellular changes that occur over the lifespan, an absence of precise characterization of age-related changes in large-scale functional brain network organization has limited cross-species translational insights. Here, using densely sampled resting-state functional MRI data acquired cross-sectionally and longitudinally in awake mice over a broad range of adulthood (n = 82; 3 to 20 mo), we describe organizational features and age-related alterations of the mouse's functional connectome. Mouse resting-state functional connectivity recapitulates known functional circuits, demonstrating the organizational validity of these signals. Graph theoretic analysis applied to functional connectivity reveals that mice exhibit modular architectures of functional brain network organization and that increasing age is associated with decreasing system segregation, indicative of network dedifferentiation analogous to observations in humans. Notably, mouse resting-state brain networks are more segregated than those of humans [determined using data from the Human Connectome Project and its developmental- and aging-counterparts (n = 1,179; 18 to 90 y)], attributable to mice exhibiting a diminished contribution of long-range functional relationships that integrate distributed systems. Mice also exhibit slower rates of age-related decline in brain network organization relative to humans, highlighting important species differences in functional brain network organization and trajectories of brain network aging. These findings establish a model of large-scale functional brain network aging in mice and provide a translational bridge across species and spatial scales of analysis.

Proceedings of the National Academy of SciencesVol. 123(13)
Allen Institute for Brain Science (US), The University of Texas at Dallas (US), Rappaport Family Institute for Research in the Medical Sciences (IL), Allen Institute (US), The University of Texas Southwestern Medical Center (US)
Openalex Percentile: Top 9%
Functional Brain Connectivity Studies
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