Age-related estimates of aggregate g-ratio of white matter structures assessed using quantitative magnetic resonance neuroimaging

The g-ratio, defined as the inner-to-outer diameter of a myelinated axon, is associated with the speed of nerve impulse conduction, and represents an index of axonal myelination and integrity. It has been shown to be a sensitive and specific biomarker of neurodevelopment and neurodegeneration. Howev...

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Main Authors: Bergeron, C.M (Author), Bouhrara, M. (Author), Ferrucci, L. (Author), Khattar, N. (Author), Kim, R.W (Author), Melvin, D. (Author), Qian, W. (Author), Resnick, S.M (Author), Spencer, R.G (Author), Zukley, L.M (Author)
Format: Article
Language:English
Published: John Wiley and Sons Inc 2021
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age
Online Access:View Fulltext in Publisher
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Summary:The g-ratio, defined as the inner-to-outer diameter of a myelinated axon, is associated with the speed of nerve impulse conduction, and represents an index of axonal myelination and integrity. It has been shown to be a sensitive and specific biomarker of neurodevelopment and neurodegeneration. However, there have been very few magnetic resonance imaging studies of the g-ratio in the context of normative aging; characterizing regional and time-dependent cerebral changes in g-ratio in cognitively normal subjects will be a crucial step in differentiating normal from abnormal microstructural alterations. In the current study, we investigated age-related differences in aggregate g-ratio, that is, g-ratio averaged over all fibers within regions of interest, in several white matter regions in a cohort of 52 cognitively unimpaired participants ranging in age from 21 to 84 years. We found a quadratic, U-shaped, relationship between aggregate g-ratio and age in most cerebral regions investigated, suggesting myelin maturation until middle age followed by a decrease at older ages. As expected, we observed that these age-related differences vary across different brain regions, with the frontal lobes and parietal lobes exhibiting slightly earlier ages of minimum aggregate g-ratio as compared to more posterior structures such as the occipital lobes and temporal lobes; this agrees with the retrogenesis paradigm. Our results provide evidence for a nonlinear association between age and aggregate g-ratio in a sample of adults from a highly controlled population. Finally, sex differences in aggregate g-ratio were observed in several cerebral regions, with women exhibiting overall lower values as compared to men; this likely reflects the greater myelin content in women's brain, in agreement with recent investigations. © 2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
ISBN:10659471 (ISSN)
DOI:10.1002/hbm.25372