Gait subgroups among older adults with chronic pain differ in cerebellum and basal ganglia gray matter volumes.

BACKGROUND

Current literature regarding morphological gray matter atrophy in chronic pain is mixed, inhibiting our ability to understand neurological mechanisms of chronic pain. The inconsistent findings may be due to the presence of subgroups within the older adult chronic pain population that differ in gait performance, as gait and gray matter have been previously associated. These gait subgroups, however, have been inadequately characterized in prior work and have not been compared across gray matter measures. Therefore, the purpose of this study was to identify and characterize gait subgroups within the older adult chronic pain population, and to evaluate differences in gray matter measures between subgroups.

METHODS

The present study was a secondary analysis of the Neuromodulatory Examination of Pain and Mobility Across the Lifespan (NEPAL) study. A subset of older participants (n = 40) completed assessments to evaluate psychological status, cognitive abilities, pain characteristics, and spatiotemporal gait performance using an instrumented gait mat. Gray matter measures were obtained from a T1-weighted anatomical scan using Freesurfer's recon-all function.

RESULTS

After data reduction, a hierarchical cluster analysis identified three gait clusters: A Normal Gait cluster (n = 12), a Shuffle Gait cluster (n = 15), and an Unsteady Gait cluster (n = 13). Clusters differed in gait velocity, stride length, step width, double support percentages, and stride length variability. The Shuffle Gait cluster exhibited reduced gray matter volumes in the cerebellum, caudate, putamen, and pallidum, as well as a worse pain severity when compared to the Normal Gait cluster (p < 0.05). The Shuffle Gait cluster also had less gray matter in the cerebellum and caudate when compared to the Unsteady Gait cluster (p < 0.05).

CONCLUSIONS

Our results confirm the existence of gait subgroups among the older adult chronic pain population and gray matter differences observed between groups support the need for the consideration of subgroups within this population for future pain, mobility, and aging studies.