4.5 Article

Different patterns of gray matter density in early- and middle-late-onset Parkinson's disease: a voxel-based morphometry study

期刊

BRAIN IMAGING AND BEHAVIOR
卷 13, 期 1, 页码 172-179

出版社

SPRINGER
DOI: 10.1007/s11682-017-9745-4

关键词

Parkinson's disease; Middle-late-onset Parkinson's disease; Early-onset Parkinson's disease; Cerebellum; DARTEL-VBM

资金

  1. 12th Five-year Plan for National Science and Technology Supporting Program of China [2012BAI10B04]
  2. National Natural Science Foundation of China [81571654, 81371519, 81301190]

向作者/读者索取更多资源

Early-onset Parkinson's disease (EOPD) has a clinical course and characteristics distinct from middle-late-onset Parkinson's disease (M-LOPD). Although many studies have investigated these differences, the neural mechanisms of these characteristics remain unclear. This study aimed to investigate the morphological differences, and their related clinical significance, between EOPD and M-LOPD patients. We recruited two groups of patients, 28 EOPD patients and 37M-LOPD patients, and two age- and sex-matched control groups (23 controls in each group). The voxel-based morphometry (VBM) technique was used to examine changes in gray matter (GM) density between patients and their corresponding controls. Compared with controls, EOPD patients had lower GM density in the left putamen, inferior frontal gyrus and insula, and higher GM density in the right occipital lobe and bilateral cerebellum posterior lobes. M-LOPD patients had lower GM density in the left cerebellum posterior lobe, occipital lobe and right supplementary motor area (SMA), and higher GM density in the left middle temporal gyrus. Correlation analyses showed that GM density values in the right cerebellum posterior lobe positively correlated with the Unified Parkinson's Disease Rating Scale (UPDRS) motor scores and the Hoehn-Yahr stages in EOPD patients. Our results reveal different patterns of structural changes in EOPD and M-LOPD patients. A probable compensatory effect of the cerebellum was observed and may partly explain the slower decline of motor function in EOPD patients.

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