Alzheimer’s disease (AD) has been associated with human brain softening, but the underlying biomechanical mechanism is not fully elucidated. We used magnetic resonance elastography to investigate the effect of amyloid-beta accumulation on hippocampal and whole brain (WB) stiffness in transgenic AD and wild-type (WT) mice at 11 and 14 months of age. The only differences observed between AD and WT mice were that the longitudinal change in the loss modulus between 11 and 14 months for female AD mice was significantly different than that of either the WT or male AD mice.
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