Microstructure of Human Corpus Callosum across the Lifespan: Regional Variations in Axon Caliber, Density, and Myelin Content

Author:

Lynn Jonathan D12,Anand Chaitali12,Arshad Muzamil1,Homayouni Roya23,Rosenberg David R1,Ofen Noa234ORCID,Raz Naftali235,Stanley Jeffrey A1ORCID

Affiliation:

1. Department of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit MI 48201, USA

2. Institute of Gerontology, Wayne State University, Detroit MI 48202, USA

3. Department of Psychology, Wayne State University, Detroit MI 48201, USA

4. Lifespan Cognitive Neuroscience, Merrill Palmer Skillman Institute, Wayne State University, Detroit MI 14195, USA

5. Center for Lifespan Psychology, Max Planck Institute for Human Development, Berlin 14195, Germany

Abstract

Abstract The myeloarchitecture of the corpus callosum (CC) is characterized as a mosaic of distinct differences in fiber density of small- and large-diameter axons along the anterior–posterior axis; however, regional and age differences across the lifespan are not fully understood. Using multiecho T2 magnetic resonance imaging combined with multi-T2 fitting, the myelin water fraction (MWF) and geometric-mean of the intra-/extracellular water T2 (geomT2IEW) in 395 individuals (7–85 years; 41% males) were examined. The approach was validated where regional patterns along the CC closely resembled the histology; MWF matched mean axon diameter and geomT2IEW mirrored the density of large-caliber axons. Across the lifespan, MWF exhibited a quadratic association with age in all 10 CC regions with evidence of a positive linear MWF-age relationship among younger participants and minimal age differences in the remainder of the lifespan. Regarding geomT2IEW, a significant linear age × region interaction reflected positive linear age dependence mostly prominent in the regions with the highest density of small-caliber fibers—genu and splenium. In all, these two indicators characterize distinct attributes that are consistent with histology, which is a first. In addition, these results conform to rapid developmental progression of CC myelination leveling in middle age as well as age-related degradation of axon sheaths in older adults.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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