Application of an amyloid and tau classification system in subcortical vascular cognitive impairment patients

被引:19
作者
Jang, Hyemin [1 ,2 ]
Kim, Hee Jin [1 ,2 ]
Park, Seongbeom [1 ,2 ]
Park, Yu Hyun [1 ,2 ]
Choe, Yeongsim [1 ,2 ]
Cho, Hanna [2 ,4 ]
Lyoo, Chul Hyoung [4 ]
Yoon, Uicheul [5 ]
Lee, Jin San [6 ]
Kim, Yeshin [7 ]
Kim, Seung Joo [1 ,2 ]
Kim, Jun Pyo [1 ,2 ]
Jung, Young Hee [1 ,2 ]
Ryu, Young Hoon [8 ]
Choi, Jae Yong [9 ]
Moon, Seung Hwan [10 ]
Seong, Joon-Kyung [11 ]
DeCarli, Charles [12 ,13 ]
Weiner, Michael W. [3 ]
Lockhart, Samuel N. [14 ]
Cho, Soo Hyun [15 ]
Na, Duk L. [1 ,2 ,16 ,17 ]
Seo, Sang Won [1 ,2 ,17 ,18 ,19 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Neurol, 50 Ilwon Dong, Seoul 135710, South Korea
[2] Samsung Med Ctr, Neurosci Ctr, Seoul, South Korea
[3] Univ Calif San Francisco, Ctr Imaging Neurodegenerat Dis, San Francisco, CA 94143 USA
[4] Yonsei Univ, Gangnam Severance Hosp, Dept Neurol, Coll Med, Seoul, South Korea
[5] Catholic Univ Daegu, Coll Hlth & Med Sci, Dept Biomed Engn, Gyongsan, South Korea
[6] Kyung Hee Univ Hosp, Dept Neurol, Seoul, South Korea
[7] Kangwon Natl Univ, Coll Med, Kangwon Natl Univ Hosp, Dept Neurol, Chunchon, South Korea
[8] Yonsei Univ, Coll Med, Gangnam Severance Hosp, Dept Nucl Med, Seoul, South Korea
[9] Korea Inst Radiol & Med Sci, Div RI Convergence Res, Seoul, South Korea
[10] Sungkyunkwan Univ, Dept Nucl Med, Samsung Med Ctr, Sch Med, Seoul, South Korea
[11] Korea Univ, Sch Biomed Engn, Seoul, South Korea
[12] Univ Calif Davis, Dept Neurol, Davis, CA 95616 USA
[13] Univ Calif Davis, Ctr Neurosci, Davis, CA 95616 USA
[14] Wake Forest Sch Med, Dept Internal Med, Winston Salem, NC USA
[15] Chonnam Natl Univ Hosp, Dept Neurol, Gwangju, South Korea
[16] Sungkyunkwan Univ, SAIHST, Dept Hlth Sci & Technol, Seoul, South Korea
[17] Samsung Med Ctr, Samsung Alzheimer Res Ctr, Seoul, South Korea
[18] Sungkyunkwan Univ, SAIHST, Dept Clin Res Design & Evaluat, Seoul, South Korea
[19] Samsung Med Ctr, Ctr Clin Epidemiol, Seoul, South Korea
关键词
Amyloid-beta; Tau; Classification; Subcortical vascular cognitive impairment; Longitudinal changes; ALZHEIMERS ASSOCIATION WORKGROUPS; SMALL VESSEL DISEASE; NATIONAL INSTITUTE; DIAGNOSTIC GUIDELINES; CEREBROVASCULAR-DISEASE; CEREBRAL MICROBLEEDS; BRAIN ATROPHY; BETA; DEMENTIA; RECOMMENDATIONS;
D O I
10.1007/s00259-019-04498-y
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objective To apply an AT (A beta/tau) classification system to subcortical vascular cognitive impairment (SVCI) patients following recently developed biomarker-based criteria of Alzheimer's disease (AD), and to investigate its clinical significance. Methods We recruited 60 SVCI patients who underwent the neuropsychological tests, brain MRI, and F-18-florbetaben and F-18-AV1451 PET at baseline. As a control group, we further recruited 27 patients with AD cognitive impairment (ADCI; eight A beta PET-positive AD dementia and 19 amnestic mild cognitive impairment). ADCI and SVCI patients were classified as having normal or abnormal A beta (A-/A+) and tau (T-/T+) based on PET results. Across the three SVCI groups (A-, A+T-, and A+T+SVCI), we compared longitudinal changes in cognition, hippocampal volume (HV), and cortical thickness using linear mixed models. Results Among SVCI patients, 33 (55%), 20 (33.3%), and seven (11.7%) patients were A-, A+T-, and A+T+, respectively. The frequency of T+ was lower in A+SVCI (7/27, 25.9%) than in A+ADCI (14/20, 70.0%, p = 0.003) which suggested that cerebral small vessel disease affected cognitive impairments independently of A+. A+T-SVCI had steeper cognitive decline than A-SVCI. A+T+SVCI also showed steeper cognitive decline than A+T-SVCI. Also, A+T-SVCI had steeper decrease in HV than A-SVCI, while cortical thinning did not differ between the two groups. A+T+SVCI had greater global cortical thinning compared with A+T-SVCI, while declines in HV did not differ between the two groups. Conclusion This study showed that the AT system successfully characterized SVCI patients, suggesting that the AT system may be usefully applied in a research framework for clinically diagnosed SVCI.
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收藏
页码:292 / 303
页数:12
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