Longitudinal cortical thinning and cognitive decline in patients with early- versus late-stage subcortical vascular mild cognitive impairment

被引:12
作者
Lee, J. [1 ,2 ,3 ]
Seo, S. W. [2 ,3 ,4 ,5 ]
Yang, J. -J. [6 ]
Jang, Y. K. [2 ,3 ]
Lee, J. S. [7 ]
Kim, Y. J. [2 ,3 ,8 ]
Chin, J. [2 ,3 ]
Lee, J. M. [6 ]
Kim, S. T. [9 ]
Lee, K. -H. [10 ]
Lee, J. H. [11 ]
Kim, J. S. [12 ]
Kim, S. [13 ]
Yoo, H. [13 ]
Lee, A. Y. [1 ]
Na, D. L. [2 ,3 ,4 ]
Kim, H. J. [2 ,3 ]
机构
[1] Chungnam Natl Univ Hosp, Dept Neurol, Daejeon, South Korea
[2] Sungkyunkwan Univ, Dept Neurol, Samsung Med Ctr, Sch Med, 80 Ilwon Ro, Seoul 06351, South Korea
[3] Samsung Med Ctr, Neurosci Ctr, Seoul, South Korea
[4] Sungkyunkwan Univ, Dept Hlth Sci & Technol, Seoul, South Korea
[5] Sungkyunkwan Univ, Clin Res Design & Evaluat, SAIHST, Seoul, South Korea
[6] Hanyang Univ, Dept Biomed Engn, Seoul, South Korea
[7] Kyung Hee Univ, Grad Sch, Dept Med, Seoul, South Korea
[8] Hallym Univ, Chuncheon Sacred Heart Hosp, Dept Neurol, Coll Med, Chunchon, Gangwon Do, South Korea
[9] Sungkyunkwan Univ, Sch Med, Dept Radiol, Samsung Med Ctr, Seoul, South Korea
[10] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Nucl Med, Seoul, South Korea
[11] Univ Ulsan, Dept Neurol, Asan Med Ctr, Coll Med, Seoul, South Korea
[12] Univ Ulsan, Dept Nucl Med, Asan Med Ctr, Coll Med, Seoul, South Korea
[13] Samsung Biomed Res Inst, Biostat Team, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
cognition; cortical thickness; early stage; late stage; subcortical vascular mild cognitive impairment; SMALL VESSEL DISEASE; ALZHEIMERS-DISEASE; DEMENTIA; THICKNESS; NEURODEGENERATION; BIOMARKERS; PIPELINE;
D O I
10.1111/ene.13500
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purposeBiomarker changes in cognitively impaired patients with small vessel disease are largely unknown. The rate of amyloid/lacune progression, cortical thinning and cognitive decline were evaluated in subcortical vascular mild cognitive impairment (svMCI) patients. MethodsSeventy-two svMCI patients were divided into early stage (ES-svMCI, n = 39) and late stage (LS-svMCI, n = 33) according to their Clinical Dementia Rating Sum of Boxes score. Patients were annually followed up with neuropsychological tests and brain magnetic resonance imaging for 3 years, and underwent a second [C-11] Pittsburgh compound B (PiB) positron emission tomography scan within a mean interval of 32.4 months. ResultsThere was no difference in the rate of increase in PiB uptake or lacune number between the ES-svMCI and LS-svMCI. However, LS-svMCI showed more rapid cortical thinning and cognitive decline than did the ES-svMCI. ConclusionsWe suggest that, whilst the rate of change in pathological burden did not differ between ES-svMCI and LS-svMCI, cortical thinning and cognitive decline progressed more rapidly in the LS-svMCI.
引用
收藏
页码:326 / 333
页数:8
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