White matter microstructures in Parkinson's disease with and without impulse control behaviors

Ann Clin Transl Neurol. 2022 Mar;9(3):253-263. doi: 10.1002/acn3.51504. Epub 2022 Feb 9.

Abstract

Background: Impulse control behaviors (ICBs) in Parkinson's disease (PD) are thought to be caused by an overdose of dopaminergic therapy in the relatively spared ventral striatum, or by hypersensitivity of this region to dopamine. Alterations in brain networks are now also thought to contribute to the development of ICBs.

Objective: To comprehensively assess white matter microstructures in PD patients with ICBs using advanced diffusion MRI and magnetization transfer saturation (MT-sat) imaging.

Methods: This study included 19 PD patients with ICBs (PD-ICBs), 18 PD patients without ICBs (PD-nICBs), and 20 healthy controls (HCs). Indices of diffusion tensor imaging (DTI), diffusion kurtosis imaging, neurite orientation dispersion and density imaging, and MT-sat imaging were evaluated using tract-based spatial statistics (TBSS), regions of interest (ROIs), and tract-specific analysis (TSA).

Results: Compared with HCs, PD-nICBs had significant alterations in many major white matter tracts in most parameters. In contrast, PD-ICBs had only partial changes in several parameters. Compared with PD-ICBs, TBSS, ROI, and TSA analyses revealed that PD-nICBs had lower axial kurtosis, myelin volume fraction, and orientation dispersion index in the uncinate fasciculus and external capsule, as well as in the retrolenticular part of the internal capsule. These are components of the reward system and the visual and emotional perception areas, respectively.

Interpretation: Myelin and axonal changes in fibers related to the reward system and visual emotional recognition might be more prominent in PD-nICBs than in PD-ICBs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain / diagnostic imaging
  • Diffusion Magnetic Resonance Imaging
  • Diffusion Tensor Imaging / methods
  • Humans
  • Parkinson Disease* / diagnostic imaging
  • Parkinson Disease* / psychology
  • White Matter* / diagnostic imaging

Grants and funding

This work was funded by Grants‐in‐Aid for Scientific Research grant 24390224; Japan Agency for Medical Research and Development grants 21ak0101112, 19dm0107156, 21dk0207055, and 21wm0425015; Japan Society for the Promotion of Science grants JP21H04820, 21K07424, 21K20698, and JP19K17244; Ministry of Health, Labour and Welfare, Japan ; the Setsuro Fujii Memorial Osaka Foundation for Promotion of Fundamental Medical Research.