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Comparative neuropathology in aging primates

A perspective

Bibliographic Data

ID19388698
AuthorsCarmen Freire‐Cobo (0000-0003-4596-0227, Nash Family Department of Neuroscience and Friedman Brain Institute Icahn School of Medicine at Mount Sinai New York New York USA), Melissa K Edler (0000-0002-9084-9539, School of Biomedical Sciences Kent State University Kent Ohio USA), Merina Varghese (0000-0001-7162-9883, Nash Family Department of Neuroscience and Friedman Brain Institute Icahn School of Medicine at Mount Sinai New York New York USA), Emily Munger (School of Biomedical Sciences Kent State University Kent Ohio USA), Emily L Munger (0000-0001-7437-2032, Kent State University), Jessie Laffey (0000-0002-7473-5558, Nash Family Department of Neuroscience and Friedman Brain Institute Icahn School of Medicine at Mount Sinai New York New York USA), Sophia Raia (0000-0003-3859-8442, Nash Family Department of Neuroscience and Friedman Brain Institute Icahn School of Medicine at Mount Sinai New York New York USA), Selena S In (Nash Family Department of Neuroscience and Friedman Brain Institute Icahn School of Medicine at Mount Sinai New York New York USA), Bridget Wicinski (0000-0002-2972-7081, Nash Family Department of Neuroscience and Friedman Brain Institute Icahn School of Medicine at Mount Sinai New York New York USA), Maria Medalla (0000-0003-4890-2532, Department of Anatomy and Neurobiology, Center for Systems Neuroscience Boston University School of Medicine Boston Massachusetts USA), Sylvia E Perez (0009-0009-1412-5721, Department of Neurobiology Barrow Neurological Institute Phoenix Arizona USA), Elliott J Mufson (0000-0003-4438-7334, Department of Neurobiology Barrow Neurological Institute Phoenix Arizona USA), Joseph M Erwin (Department of Anthropology, Center for the Advanced Study of Human Paleobiology The George Washington University Washington District of Columbia USA), Joseph Erwin (George Washington University), Elaine E Guevara (0000-0003-1480-474X, Department of Anthropology, Center for the Advanced Study of Human Paleobiology The George Washington University Washington District of Columbia USA), Chet C Sherwood (0000-0001-6711-449X, Department of Anthropology, Center for the Advanced Study of Human Paleobiology The George Washington University Washington District of Columbia USA), Jennifer I Luebke (0000-0003-1399-6073, Department of Anatomy and Neurobiology, Center for Systems Neuroscience Boston University School of Medicine Boston Massachusetts USA), Agnès Lacreuse (0000-0003-2890-9649, Psychological and Brain Sciences University of Massachusetts Amherst Massachusetts USA), Mary Ann Raghanti (0000-0002-6842-1907, Kent State University), Patrick R Hof (0000-0002-3208-1154, Nash Family Department of Neuroscience and Friedman Brain Institute Icahn School of Medicine at Mount Sinai New York New York USA, corresponding author)
Year2021
Volume83
Issue11
Pagese23299-e23299
Publication date2021-11-01
Open AccessYes
TypeARTICLE
VenueAmerican Journal of Primatology (JOURNAL)
Journal identifiersISSN: 0275-2565 • E-ISSN: 1098-2345
PublisherWiley (PUBLISHER • GB)
DOI10.1002/ajp.23299
PMID34255875
OpenAlexW3180738139
LanguageEN
Citations received3
References cited253

While humans exhibit a significant degree of neuropathological changes associated with deficits in cognitive and memory functions during aging, non‐human primates (NHP) present with more variable expressions of pathological alterations among individuals and species. As such, NHP with long life expectancy in captivity offer an opportunity to study brain senescence in the absence of the typical cellular pathology caused by age‐related neurodegenerative illnesses commonly seen in humans. Age‐related changes at neuronal population, single cell, and synaptic levels have been well documented in macaques and marmosets, while age‐related and Alzheimer's disease‐like neuropathology has been characterized in additional species including lemurs as well as great apes. We present a comparative overview of existing neuropathologic observations across the primate order, including classic age‐related changes such as cell loss, amyloid deposition, amyloid angiopathy, and tau accumulation. We also review existing cellular and ultrastructural data on neuronal changes, such as dendritic attrition and spine alterations, synaptic loss and pathology, and axonal and myelin pathology, and discuss their repercussions on cellular and systems function and cognition

Biology · Cerebral amyloid angiopathy · Cognitive decline · Dementia · Dendritic spine · Disease · Neuropathology · Pathological · Pathology · Primate · Senescence · Alzheimer's disease research and treatments · Medicine · Neurogenesis and neuroplasticity mechanisms · Neuroinflammation and Neurodegeneration Mechanisms · Neuroscience · Psychology

  • Differential amyloid-beta sensitivity across human and nonhuman primate neurons

    Open Access•Isabel August, Sheila Steiner et al.•Journal of Human Evolution•2026

  • Nonhuman primates at the intersection of aging biology, chronic disease, and health

    Open Access•Carol A Shively, Agnès Lacreuse et al.•American Journal of Primatology•2021

  • Potential trade‐off between olfactory and visual discrimination learning in common marmosets ( Callithrix jacchus )

    Open Access•Elena M Golub, Bryce Conner et al.•American Journal of Primatology•2022

  • Age‐related changes in myelin of axons of the corpus callosum and cognitive decline in common marmosets

    Open Access•Kimberley A Phillips, Chase M Watson et al.•American Journal of Primatology•2019

  • Loss of ferritin‐positive microglia relates to increased iron, RNA oxidation, and dystrophic microglia in the brains of aged male marmosets

    Open Access•Juan de Dios Rodríguez‐Callejas, Juan D Rodríguez-Callejas et al.•American Journal of Primatology•2019

Citations per year0.6
Citation span2021 - 2026 (6)
Highly citedNo

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