4.5 Article

Pain differences in neurite orientation dispersion and density imaging measures among community-dwelling older adults

期刊

EXPERIMENTAL GERONTOLOGY
卷 154, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exger.2021.111520

关键词

Brain; White matter; Aging; Pain

资金

  1. National Institutes of Health (NIA) [K01AG048259, R01AG059809, R01AG067757]
  2. University of Florida Clinical Translational Sciences Institute [NCATSUL1TR001427]
  3. Cognitive Aging & Memory Clinical Translational Program, McKnight Brain Foundation
  4. University of Florida Claude D. Pepper Older Americans Independence Center [P30 AG028740]

向作者/读者索取更多资源

NODDI imaging technique revealed lower neurite density and less geometric complexity in older adults with chronic musculoskeletal pain. The lower neurite density was associated with higher pain intensity and anatomical pain sites. Pain-by-sex differences in neurite density and geometric complexity were also observed.
Neurite orientation dispersion and density imaging (NODDI) is a technique providing more detailed information on the microstructural bases of white matter. Given the previously reported white matter contributions to chronic pain, the present study aims to investigate pain-specific differences in NODDI measures across white matter tracts in a sample of community-dwelling older adults with (n = 29) and without (n = 18) chronic musculoskeletal pain. We further aimed to investigate associations between NODDI measures and clinical and experimental pain measures. As part of the Nepal study, a subset of older adults (>60 years old), underwent multiple laboratory sessions providing self-reported and experimental pain measures and a diffusion weighted neuroimaging sequence. Older adults with chronic musculoskeletal pain had a lower neurite density with less geometric complexity across a number of white matter tracts compared to older pain-free controls (corrected p's < 0.05). Lower neurite density was associated with greater self-reported pain intensity and anatomical pain sites, as well as greater experimental pain sensitivity (p's < 0.05). There were also significant pain-by-sex differences in neurite density and geometric complexity across multiple white matter tracts mainly around the hippocampus (corrected p's < 0.05). Finally, there were no pain differences with respect to extra-cellular water diffusion (corrected p's > 0.05). Our study demonstrates less geometric complexity in neurite density and architecture in chronic musculoskeletal pain, partly in a sex-dependent manner. An increased understanding of neurobiological mechanisms such as those measured by NODDI may contribute to the potential targeting of interventions in our older population suffering from chronic pain.

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