Parkinson's disease;
White matter hyperintensities;
Grey matter atrophy;
Deformation based morphometry;
Scoring by Nonlocal Image Patch Estimator;
BRAIN ATROPHY;
RATING-SCALE;
HYPERINTENSITIES;
IMPAIRMENT;
DEMENTIA;
DECLINE;
HOMOCYSTEINE;
LESIONS;
VOLUME;
GAIT;
D O I:
10.1016/j.nicl.2020.102353
中图分类号:
R445 [影像诊断学];
学科分类号:
100207 ;
摘要:
Introduction: Previous studies have found associations between grey matter atrophy and white matter hyperintensities (WMH) of vascular origin with cognitive and motor deficits in Parkinson's disease (PD). Here we investigate these relationships in a sample of PD patients and age-matched healthy controls. Methods: Data included 50 PD patients and 45 age-matched controls with T1-weighted and FLAIR scans at baseline, 18-months, and 36-months follow-up. Deformation-based morphometry was used to measure grey matter atrophy. SNIPE (Scoring by Nonlocal Image Patch Estimator) was used to measure Alzheimer's diseaselike textural patterns in the hippocampi. WMHs were segmented using T1-weighted and FLAIR images. The relationship between MRI features and clinical scores was assessed using mixed-effects models. The motor subscore of the Unified Parkinson's Disease Rating Scale (UPDRSIII), number of steps in a walking trial, and Dementia Rating Scale (DRS) were used respectively as measures of motor function, gait, and cognition. Results: Substantia nigra atrophy was significantly associated with motor deficits, with a greater impact in PDs (p < 0.05). Hippocampal SNIPE scores were associated with cognitve decline in both PD and controls (p < 0.01). WMH burden was significantly associated with cognitive decline and increased motor deficits in the PD group, and gait deficits in both PD and controls (p < 0.03). Conclusion: While substantia nigra atrophy and WMH burden were significantly associated with additional motor deficits, WMH burden and hippocampal atrophy were associated with cognitive deficits in PD patients. These results suggest an additive contribution of both grey and white matter damage to the motor and cognitive deficits in PD.
机构:
Kanto Cent Hosp, Dept Neurol, Tokyo, Japan
Juntendo Univ, Dept Radiol, Tokyo, JapanTokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, Japan
Hattori, Takaaki
Orimo, Satoshi
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机构:
Kanto Cent Hosp, Dept Neurol, Tokyo, JapanTokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, Japan
Orimo, Satoshi
Aoki, Shigeki
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机构:
Juntendo Univ, Dept Radiol, Tokyo, JapanTokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, Japan
Aoki, Shigeki
Ito, Kenji
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机构:
Juntendo Univ, Dept Radiol, Tokyo, Japan
Univ Tokyo, Grad Sch Med, Dept Radiol, Tokyo, JapanTokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, Japan
Ito, Kenji
Abe, Osamu
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机构:
Nihon Univ, Sch Med, Dept Radiol, Tokyo, JapanTokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, Japan
Abe, Osamu
Amano, Atsushi
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机构:
Kanto Cent Hosp, Dept Radiol, Tokyo, JapanTokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, Japan
Amano, Atsushi
Sato, Ryo
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机构:
Juntendo Univ, Dept Radiol, Tokyo, Japan
Tokyo Metropolitan Univ, Grad Sch Human Hlth Sci, Dept Radiol Sci, Tokyo 158, JapanTokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, Japan
Sato, Ryo
Sakai, Kasumi
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Kanto Cent Hosp, Dept Radiol, Tokyo, JapanTokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, Japan
Sakai, Kasumi
Mizusawa, Hidehiro
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机构:
Tokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, JapanTokyo Med & Dent Univ, Grad Sch, Dept Neurol & Neurol Sci, Bunkyo Ku, Tokyo 1138519, Japan