The effect of white matter signal abnormalities on default mode network connectivity in mild cognitive impairment

被引:18
|
作者
Wang, Zhuonan [1 ,2 ]
Williams, Victoria J. [3 ]
Stephens, Kimberly A. [1 ]
Kim, Chan-Mi [1 ]
Bai, Lijun [4 ]
Zhang, Ming [2 ]
Salat, David H. [1 ,5 ]
机构
[1] Massachusetts Gen Hosp, Athinoula A Martinos Ctr Biomed Imaging, Dept Radiol, 149 Thirteenth St, Charlestown, MA 02129 USA
[2] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Med Imaging, 277 Yanta West Rd, Xian 710061, Shaanxi, Peoples R China
[3] Massachusetts Gen Hosp, Dept Neurol, Alzheimers Clin & Translat Res Unit, Charlestown, MA 02129 USA
[4] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Dept Biomed Engn, Key Lab Biomed Informat Engn,Minist Educ, Xian, Shaanxi, Peoples R China
[5] VA Boston Healthcare Syst, Neuroimaging Res Vet Ctr, Boston, MA USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
cortical thickness; default mode network; mild cognitive impairment; vascular; white matter signal abnormalities; SURFACE-BASED ANALYSIS; HUMAN CEREBRAL-CORTEX; SMALL VESSEL DISEASE; ALZHEIMERS-DISEASE; FUNCTIONAL CONNECTIVITY; POSTERIOR CINGULATE; LOBE FUNCTION; HYPERINTENSITIES; SEGMENTATION; DEMENTIA;
D O I
10.1002/hbm.24871
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Regions within the default mode network (DMN) are particularly vulnerable to Alzheimer's disease pathology and mechanisms of DMN disruption in mild cognitive impairment (MCI) are still unclear. White matter lesions are presumed to be mechanistically linked to vascular dysfunction whereas cortical atrophy may be related to neurodegeneration. We examined associations between DMN seed-based connectivity, white matter lesion load, and cortical atrophy in MCI and cognitively healthy controls. MCI showed decreased functional connectivity (FC) between the precuneus-seed and bilateral lateral temporal cortex (LTC), medial prefrontal cortex (mPFC), posterior cingulate cortex, and inferior parietal lobe compared to those with controls. When controlling for white matter lesion volume, DMN connectivity differences between groups were diminished within bilateral LTC, although were significantly increased in the mPFC explained by significant regional associations between white matter lesion volume and DMN connectivity only in the MCI group. When controlling for cortical thickness, DMN FC was similarly decreased across both groups. These findings suggest that white matter lesions and cortical atrophy are differentially associated with alterations in FC patterns in MCI. Associations between white matter lesions and DMN connectivity in MCI further support at least a partial but important vascular contribution to age-associated neural and cognitive impairment.
引用
收藏
页码:1237 / 1248
页数:12
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