Whole-Brain Diffusion-Tensor Changes in Parkinsonian Patients with Impulse Control Disorders
2
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Background and Purpose The aim of this study was to determine the changes in diffusiontensor images associated with medication-related impulse control disorder (ICD) in Parkinson’sdisease (PD) patients undergoing chronic dopamine-replacement therapy. Methods Nineteen PD patients, comprising 10 with ICD (PD-ICD) and 9 without ICD (PDnonICD), and 18 age-matched healthy controls (HCs) with no cognitive or other psychiatricdisorders 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. Results In 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, rightposterior 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 andPD-nonICD groups in any brain regions. Conclusions The PD-ICD patients appear to have relatively preserved white-matter integrityin the regions involved in reward-related behaviors compared to PD-nonICD patients. Furtherinvestigation is required to determine whether the difference in FA between PD-ICD and PDnonICD patients reflects microstructural differences in the pathological progression of PD or issecondary to ICD.
Abstract
Background and Purpose The aim of this study was to determine the changes in diffusiontensor images associated with medication-related impulse control disorder (ICD) in Parkinson’sdisease (PD) patients undergoing chronic dopamine-replacement therapy. Methods Nineteen PD patients, comprising 10 with ICD (PD-ICD) and 9 without ICD (PDnonICD), and 18 age-matched healthy controls (HCs) with no cognitive or other psychiatricdisorders 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. Results In 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, rightposterior 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 andPD-nonICD groups in any brain regions. Conclusions The PD-ICD patients appear to have relatively preserved white-matter integrityin the regions involved in reward-related behaviors compared to PD-nonICD patients. Furtherinvestigation is required to determine whether the difference in FA between PD-ICD and PDnonICD patients reflects microstructural differences in the pathological progression of PD or issecondary to ICD.
참고문헌 (14)
- Weintraub D, "Impulse control disorders in Parkinson disease: a cross-sectional study of 3090 patients", Arch Neurol, 67, pp.589~595 (2010)
- Lee JY, "Association between the dose of dopaminergic medication and the behavioral disturbances in Parkinson disease", Parkinsonism Relat Disord, 16, pp.202~207 (2010)
- Cilia R, "Functional abnormalities underlying pathological gambling in Parkinson disease", Arch Neurol, 65, pp.1604~1611 (2008)
- fluorodopa uptake in Parkinsonian impulse control disorders, "Mov Disord", 2012, 778~782
- Smith SM, "Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data", Neuroimage, 31, pp.1487~1505 (2006)
- Lawrence AD, "Compulsive use of dopamine replacement therapy in Parkinson’s disease: reward systems gone awry?", Lancet Neurol, 2, pp.595~604 (2003)
- Ouchi Y, "Alterations in binding site density of dopamine transporter in the striatum, orbitofrontal cortex, and amygdala in early Parkinson’s disease: compartment analysis for beta-CFT binding with positron emis-sion tomography", Ann Neurol, 45, pp.601~610 (1999)
- Reuter J, "Pathological gambling is linked to reduced activation of the mesolimbic reward system", Nat Neurosci, 8, pp.147~148 (2005)
- Thiel A, "Activation of basal ganglia loops in idiopathic Parkinson’s disease: a PET study", J Neural Transm, 110, pp.1289~1301 (2003)
- Tzschentke TM, "The medial prefrontal cortex as a part of the brain reward system", Amino Acids, 19, pp.211~219 (2000)
- Moeller FG, "Reduced anterior corpus callosum white matter integrity is related to increased impulsivity and reduced discriminability in cocaine-dependent subjects: diffusion tensor imaging", Neuropsychopharmacology, 30, pp.610~617 (2005)
- Grant JE, "The neurobiology of substance and behavioral addictions", CNS Spectr, 11, pp.924~930 (2006)
- Yoo SY, "White matter abnormalities in drug-naïve patients with obsessive-compulsive disorder: a diffusion tensor study before and after citalopram treatment", Acta Psychiatr Scand, 116, pp.211~219 (2007)
- Li F, "Microstructural brain abnormalities in patients with obsessive-compulsive disorder: diffusion-tensor MR imaging study at 3.0 T", Radiology, 260, pp.216~223 (2011)
