4.4 Review

Pathways to Brain Aging and Their Modifiers: Free-Radical-Induced Energetic and Neural Decline in Senescence (FRIENDS) Model - A Mini-Review

Journal

GERONTOLOGY
Volume 64, Issue 1, Pages 49-57

Publisher

KARGER
DOI: 10.1159/000479508

Keywords

Mitochondria; Reactive oxygen species; Magnetic resonance spectroscopy; Magnetic resonance imaging; Longitudinal studies; Brain energy metabolism; White matter; Myelin; Neuropil

Funding

  1. National Institute on Aging [R01AG011230]
  2. Beckman Institute Postdoctoral Fellowship (University of Illinois at Urbana-Champaign)
  3. Arnold and Mabel Beckman Foundation
  4. NATIONAL INSTITUTE ON AGING [R01AG011230, R37AG011230] Funding Source: NIH RePORTER

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In this mini-review, we survey the extant literature on brain aging, with the emphasis on longitudinal studies of neuroanatomy, including regional brain volumes and white matter microstructure. We assess the impact of vascular, metabolic, and inflammatory risk factors on the trajectories of change in regional brain volumes and white matter properties, as well as the relationships between neuroanatomical and physiological changes and their influence on cognitive performance. We examine these findings in the context of current biological theories of aging and propose the means of integrating noninvasive measures - spectroscopic indices of brain energy metabolism and regional iron deposits - as valuable proxies for elucidating the basic neurobiology of human brain aging. In a brief summary of the recent findings pertaining to age-related changes in the brain structure and their impact on cognition, we discuss the role of vascular, metabolic, and inflammatory risk factors in shaping the trajectories of change. Drawing on the extant biological theories of aging and mindful of the brain's role as a disproportionately voracious energy consumer in mammals, we emphasize the importance of the fundamental bioenergetic mechanisms as drivers of age-related changes in brain structure and function. We sketch out a model that builds on the conceptualization of aging as an expression of cumulative cellular damage inflicted by reactive oxygen species and ensuing declines in energy metabolism. We outline the ways and means of adapting this model, Free-Radical-Induced Energetic and Neural Decline in Senescence (FRIENDS), to human aging and testing it within the constraints of non-invasive neuroimaging. (c) 2017 S. Karger AG, Basel

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