# Intra-voxel angular dispersion of fibers in corpus callosum decreases with healthy aging

## TL;DR

This study shows that the angular dispersion of axonal fibers in the corpus callosum decreases with healthy aging, suggesting a loss of axons with varied orientations.

## Contribution

The study introduces a novel method using fiber orientation density functions to quantify age-related changes in axonal fiber dispersion in the corpus callosum.

## Key findings

- Angular dispersion of axonal fibers in the corpus callosum decreases significantly with age.
- The decrease in dispersion is consistent across the splenium, body, and genu of the corpus callosum.
- The height of the mean fODF peaks increases with age, indicating a loss of axons with non-peak orientations.

## Abstract

The goal of this study was to investigate how the angular dispersion of axonal fibers changes during the course of healthy aging. The angular dispersion was derived from the fiber orientation density function (fODF), which was estimated in vivo with a diffusion MRI technique called fiber ball imaging. Intra-voxel angular dispersion of axonal fibers within the corpus callosum at the midline up to the anterior tip of the frontal horn of the lateral ventricles was quantified for a cohort of 63 healthy older adults (ages 45 to 85 years). The splenium, body, and genu of the corpus callosum were examined separately, and fODFs within each of these regions were averaged across voxels to obtain three mean fODFs for each study participant. For all three regions, we found that the angular dispersion, as quantified by the full width of the mean fODF at half its maximum, decreases significantly with age. However, these decreases were not significantly different across the regions. In addition, the heights of the mean fODF peaks increase with age. This reduction in angular dispersion and increase in height imply axons with orientations deviating further from the fODF peak are more likely to be lost in the course of healthy aging. We propose that this is related to the known preferential loss of thinner myelinated axons with increasing age.