Jul 2026· American Journal of Primatology· Vol 88· 0 citations· 72 references
Medicine
TL;DR
It is found that variation in primate social systems and/or reproductive aging may influence sex and species differences in brain aging, and within the baboons but not the chimpanzees, significant sex differences were found in age‐related differences in cortical folding.
Abstract
In light of the evidence that nonhuman primates naturally develop Alzheimer's disease neuropathologies, there is a renewed interest in research on the comparative biology of aging, including neurological changes across the age groups in species with diverse lifespans. In this paper, we examined age‐related differences in two measures of cortical folding, mean depth and fold opening, in a sample of chimpanzees (Pan troglodytes) and olive baboons (Papio anubis). We found significant species differences in the slope and pattern of age‐related changes in cortical folding. As predicted, chimpanzees showed negative linear associations between age and mean depth and positive linear associations between age and fold opening, as we see in humans. However, contrary to our hypotheses, baboons showed positive quadratic associations between age and mean depth and negative quadratic associations between age and fold opening. Additionally, within the baboons but not the chimpanzees, significant sex differences were found in age‐related differences in cortical folding. Here, male baboons showed significant linear associations between age, sulci depth, and fold opening, much like male and female chimpanzees. However, for female baboons, slopes of age‐related differences in fold opening were flat or showed slight quadratic associations. It is possible that variation in primate social systems and/or reproductive aging may influence sex and species differences in brain aging. Longitudinal studies on primate brain aging, as well as comparative research with additional taxa, could shed light on the causes and implications of these differences.
This work systematically evaluates current knowledge regarding homologies in the insula among model species and humans to propose research directions aimed at strengthening translational insula research and enhancing the understanding of cross-species similarities and differences.
Joey A. Charbonneau, Sarah B. Carp, Jeffrey L. Bennett et al.· Nature Neuroscience· 0 citations
Using high-resolution qMRI, motor cortex subdivisions controlling the leg, hand, and face in humans and chimpanzees are compared and consistently higher myelin and iron content in the hand-knob in both species are found, suggesting an evolutionarily conserved role.
M. Chauvel, E. Kirilina, I. Lipp et al.· bioRxiv· 0 citations
Healthy aging causes heterogeneous limbic structural changes, which are essential for sustaining immediate and delayed memory, and this advances understanding of the neural mechanisms underlying normal cognitive aging.
This resource is made available to provide a normalization target for baboon data across the lifespan, including intermediate timepoints, and facilitate neuroimaging research in baboons, comparative research with humans and nonhuman primate species for which developmental templates are available.
Katherine L. Bryant, Arnaud Le Troter, D. Meunier et al.· Imaging neuroscience· 0 citations
Sex differences in BAG across the AD continuum were largely explained by APOE {epsilon}4-related acceleration rather than by an independent effect of sex alone, which suggests that females may be more vulnerable to APOE {epsilon}4-associated structural brain aging over time.
R. Rajabli, M. Soltaninejad, S. Villeneuve et al.· medRxiv· 0 citations
Progressive, age-dependent remodeling of motor cortex somatotopic remodeling is demonstrated in 5XFAD mice, characterized by early expansion of specific simple movement cortical sites followed by deterioration of both complex and simple motor cortical maps as disease advances.
SE Moss, Cassandra C. Wolsh, Rmii Brown et al.· bioRxiv· 0 citations