Frontiers in Aging Neuroscience (Jun 2023)

Serial deep gray nuclear DTI changes in Parkinson’s disease over twelve years

  • Yao-Chia Shih,
  • Yao-Chia Shih,
  • Yao-Chia Shih,
  • Leon Qi Rong Ooi,
  • Hui-Hua Li,
  • Hui-Hua Li,
  • John Carson Allen,
  • Septian Hartono,
  • Septian Hartono,
  • Thomas Welton,
  • Thomas Welton,
  • Eng-King Tan,
  • Eng-King Tan,
  • Ling Ling Chan,
  • Ling Ling Chan

DOI
https://doi.org/10.3389/fnagi.2023.1169254
Journal volume & issue
Vol. 15

Abstract

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BackgroundDeep gray nuclear pathology relates to motor deterioration in idiopathic Parkinson’s disease (PD). Inconsistent deep nuclear diffusion tensor imaging (DTI) findings in cross-sectional or short-term longitudinal studies have been reported. Long-term studies in PD are clinically challenging; decade-long deep nuclear DTI data are nonexistent. We investigated serial DTI changes and clinical utility in a case-control PD cohort of 149 subjects (72 patients/77 controls) over 12 years.MethodsParticipating subjects underwent brain MRI at 1.5T; DTI metrics from segmented masks of caudate, putamen, globus pallidus and thalamus were extracted from three timepoints with 6-year gaps. Patients underwent clinical assessment, including Unified Parkinson Disease Rating Scale Part 3 (UPDRS-III) and Hoehn and Yahr (H&Y) staging. A multivariate linear mixed-effects regression model with adjustments for age and gender was used to assess between-group differences in DTI metrics at each timepoint. Partial Pearson correlation analysis was used to correlate clinical motor scores with DTI metrics over time.ResultsMD progressively increased over time and was higher in the putamen (p < 0.001) and globus pallidus (p = 0.002). FA increased (p < 0.05) in the thalamus at year six, and decreased in the putamen and globus pallidus at year 12. Putaminal (p = 0.0210), pallidal (p = 0.0066) and caudate MD (p < 0.0001) correlated with disease duration. Caudate MD (p < 0.05) also correlated with UPDRS-III and H&Y scores.ConclusionPallido-putaminal MD showed differential neurodegeneration in PD over 12 years on longitudinal DTI; putaminal and thalamic FA changes were complex. Caudate MD could serve as a surrogate marker to track late PD progression.

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