Whole-Brain Diffusion-Tensor Changes in Parkinsonian Patients with Impulse Control Disorders

脉冲控制 磁共振弥散成像 脉冲(物理) 心理学 医学 神经科学 精神科 认知心理学 物理 经典力学 放射科 磁共振成像
作者
Hye Bin Yoo,Jee‐Young Lee,Jae Sung Lee,Hyejin Kang,Yu Kyeong Kim,In Chan Song,Dong Soo Lee,Beom Seok Jeon
出处
期刊:The Journal of Clinical Neurology [Korean Neurological Association]
卷期号:11 (1): 42-42 被引量:35
标识
DOI:10.3988/jcn.2015.11.1.42
摘要

Background and PurposezzThe aim of this study was to determine the changes in diffusiontensor images associated with medication-related impulse control disorder (ICD) in Parkinson's disease (PD) patients undergoing chronic dopamine-replacement therapy.MethodszzNineteen PD patients, comprising 10 with ICD (PD-ICD) and 9 without ICD (PD-nonICD), and 18 age-matched healthy controls (HCs) with no cognitive or other psychiatric disorders were analyzed.All subjects underwent 3-T magnetic resonance diffusion-tensor imaging.For all PD patients, clinical data on PD duration, antiparkinsonian medication dosages, Unified Parkinson's Disease Rating Scale and Mini-Mental State Examination were collected.Whole-brain voxel-based measures of fractional anisotropy (FA) and mean diffusivity (MD) were analyzed.ResultszzIn comparison with HCs, the PD-nonICD subjects had low FA at the bilateral orbitofrontal areas.While the PD-ICD subjects exhibited no such difference, their FA was significantly elevated at the anterior corpus callosum.Analysis of FA between the two PD groups revealed that FA in the anterior corpus callosum, right internal capsule posterior limbs, right posterior cingulum, and right thalamic radiations were significantly higher (corrected p<0.05) in the PD-ICD than in the PD-nonICD patients.MD did not differ between the PD-ICD and PD-nonICD groups in any brain regions.ConclusionszzThe PD-ICD patients appear to have relatively preserved white-matter integrity in the regions involved in reward-related behaviors compared to PD-nonICD patients.Further investigation is required to determine whether the difference in FA between PD-ICD and PD-nonICD patients reflects microstructural differences in the pathological progression of PD or is secondary to ICD.
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