4.5 Article

Cortical thinning related to periventricular and deep white matter hyperintensities

期刊

NEUROBIOLOGY OF AGING
卷 33, 期 7, 页码 1156-+

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2010.12.003

关键词

White matter hyperintensities; Periventricle white matter hyperintensities; Deep white matter hyperintensities; Cortical thickness; Cognitive impairment; Dementia; Mild cognitive impairment

资金

  1. Ministry for Health, Welfare and family Affairs, Republic of Korea [A050079]
  2. Korean Science and Engineering Foundation (KOSEF) NRL
  3. Korean government (MEST) [R0A-2007-000-20068-0]
  4. Samsung Medical Center [CRL-108011, CRS 110-14-1]

向作者/读者索取更多资源

Previous studies showed that white matter hyperintensities (WMH) are related to cognitive decline in patients with mild cognitive impairment (MCI) or dementia. Moreover, periventricular WMH (periventricular white matter hyperintensities (PWMH)) and deep WMH (deep white matter hyperintensities (DWMH)) may have different effects on cognition. The purpose of this study is to investigate the contributions of PWMH and DWMH to the topography of cortical thinning and to investigate the relationship among WMH, cortical thinning, and cognitive impairments. Participants included 226 patients with Alzheimer's disease or subcortical vascular dementia, and 135 patients with amnestic MCI or subcortical vascular MCI. Cortical thickness was measured using the surface based method. The topography of cortical thinning related to WMH was distributed in the frontal and perisylvian regions, which was similar to that of PWMH. In contrast, there were only small areas of cortical thinning inversely associated with DWMH, which were distributed in medial frontal and lingual gyrus. PWMH, but not DWMH, were associated with the frontal thinning and executive dysfunction; where both PWMH and frontal thinning were independently associated with executive dysfunction. Our results suggest that PWMH are associated with frontal thinning, which is further associated with frontal executive dysfunction. (C) 2012 Elsevier Inc. All rights reserved.

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