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Quantitative age-dependent differences in human brainstem myelination assessed using high-resolution magnetic resonance mapping
Neuroimage. 2020 Feb 1;206:116307. doi: 10.1016/j.neuroimage.2019.116307.
Mustapha Bouhrara 1, Luis E Cortina 2, Abinand C Rejimon 2, Nikkita Khattar 2, Christopher Bergeron 2, Janet Bergeron 2, Denise Melvin 3, Linda Zukley 3, Richard G Spencer 2
Abstract:
Previous in-vivo magnetic resonance imaging (MRI)-based studies of age-related differences in the human brainstem have focused on volumetric morphometry. These investigations have provided pivotal insights into regional brainstem atrophy but have not addressed microstructural age differences. However, growing evidence indicates the sensitivity of quantitative MRI to microstructural tissue changes in the brain. These studies have largely focused on the cerebrum, with very few MR investigations addressing age-dependent differences in the brainstem, in spite of its central role in the regulation of vital functions. Several studies indicate early brainstem alterations in a myriad of neurodegenerative diseases and dementias. The paucity of MR-focused investigations is likely due in part to the challenges imposed by the small structural scale of the brainstem itself as well as of substructures within, requiring accurate high spatial resolution imaging studies. In this work, we applied our recently developed approach to high-resolution myelin water fraction (MWF) mapping, a proxy for myelin content, to investigate myelin differences with normal aging within the brainstem. In this cross-sectional investigation, we studied a large cohort (n = 125) of cognitively unimpaired participants spanning a wide age range (21-94 years) and found a decrease in myelination with age in most brainstem regions studied, with several regions exhibiting a quadratic association between myelin and age. We believe that this study is the first investigation of MWF differences with normative aging in the adult brainstem. Further, our results provide reference MWF values.
PMID: 31669302
Free Full-Text: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981041/