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White Matter Diffusion Properties in Chronic Temporomandibular Disorders: An Exploratory Analysis

OBJECTIVE: To determine differences in diffusion metrics in key white matter (WM) tracts between women with chronic temporomandibular disorders (TMDs) and age- and sex-matched healthy controls. DESIGN: Cross sectional study compared diffusion metrics between groups and explored their associations wi...

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Detalles Bibliográficos
Autores principales: Budd, Alexandra S., Huynh, Thi K. T., Seres, Peter, Beaulieu, Christian, Armijo-Olivo, Susan, Cummine, Jacqueline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254396/
https://www.ncbi.nlm.nih.gov/pubmed/35800990
http://dx.doi.org/10.3389/fpain.2022.880831
Descripción
Sumario:OBJECTIVE: To determine differences in diffusion metrics in key white matter (WM) tracts between women with chronic temporomandibular disorders (TMDs) and age- and sex-matched healthy controls. DESIGN: Cross sectional study compared diffusion metrics between groups and explored their associations with clinical variables in subjects with TMDs. METHODS: In a total of 33 subjects with TMDs and 33 healthy controls, we performed tractography to obtain diffusion metrics (fractional anisotropy [FA], mean diffusivity [MD], radial diffusivity [RD], and axial diffusivity [AD]) from the cingulum near the cingulate gyrus (CGC), the cingulum near the hippocampus (CGH), the fornix, the anterior limb of the internal capsule (ALIC), the posterior limb of the internal capsule (PLIC), and the uncinate fasciculus (UF). We compared diffusion metrics across groups and explored the relationships between diffusion metrics and clinical measures (pain chronicity and intensity, central sensitization, somatization, depression, orofacial behavior severity, jaw function limitations, disability, and interference due to pain) in subjects with TMDs. RESULTS: We observed differences in diffusion metrics between groups, primarily in the right side of the brain, with the right CGC having lower FA and the right UF having lower FA and higher MD and RD in subjects with TMDs compared to healthy controls. No clinical measures were consistently associated with diffusion metrics in subjects with TMDs. CONCLUSION: The UF showed potential microstructural damage in subjects with TMDs, but further studies are needed to confirm any associations between diffusion changes and clinical measures.