Synergistic Effects of Ischemia and β-Amyloid Burden on Cognitive Decline in Patients With Subcortical Vascular Mild Cognitive Impairment

被引:99
作者
Lee, Mi Ji [1 ]
Seo, Sang Won [1 ]
Na, Duk L. [1 ]
Kim, Changsoo [2 ]
Park, Jae Hyun [1 ]
Kim, Geon Ha [3 ]
Kim, Chi Hun [1 ]
Noh, Young [4 ]
Cho, Hanna [1 ,5 ]
Kim, Hee Jin [1 ]
Yoon, Cindy W. [6 ]
Ye, Byoung Seok [1 ]
Chin, Juhee [1 ]
Jeon, Seun [7 ]
Lee, Jong-Min [7 ]
Choe, Yearn Seong [8 ]
Lee, Kyung-Han [8 ]
Kim, Jae Seung [9 ]
Kim, Sung Tae [10 ]
Lee, Jae-Hong [11 ]
Ewers, Michael [12 ]
Werring, David J. [13 ]
Weiner, MichaelW. [14 ,15 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Neurol, Seoul 135710, South Korea
[2] Yonsei Univ, Coll Med, Dept Prevent Med, Seoul, South Korea
[3] Ewha Womans Univ, Sch Med, Mokdong Hosp, Dept Neurol, Seoul, South Korea
[4] Gachon Univ, Gil Med Ctr, Dept Neurol, Inchon, South Korea
[5] Yonsei Univ, Coll Med, Gangnam Severance Hosp, Dept Neurol, Seoul, South Korea
[6] Inha Univ, Sch Med, Dept Neurol, Inchon, South Korea
[7] Hanyang Univ, Dept Biomed Engn, Seoul 133791, South Korea
[8] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Nucl Med, Seoul 135710, South Korea
[9] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul, South Korea
[10] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Radiol, Seoul 135710, South Korea
[11] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul, South Korea
[12] Univ Munich, Inst Stroke & Dementia Res, Munich, Germany
[13] UCL, Inst Neurol, Dept Brain Repair & Rehabil, London, England
[14] Univ Calif San Francisco, Dept Radiol, San Francisco, CA USA
[15] Dept Vet Affairs Med Ctr, Ctr Imaging Neurodegenerat Dis, San Francisco, CA USA
基金
新加坡国家研究基金会;
关键词
WHITE-MATTER HYPERINTENSITIES; ALZHEIMERS-DISEASE; DEMENTIA; DEPOSITION; MEMORY; BRAIN; ATHEROSCLEROSIS; MICROBLEEDS; VERSION; RISK;
D O I
10.1001/jamapsychiatry.2013.4506
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
IMPORTANCE Cerebrovascular disease (CVD) and Alzheimer disease are significant causes of cognitive impairment in the elderly. However, few studies have evaluated the relationship between CVD and beta-amyloid burden in living humans or their synergistic effects on cognition. Thus, there is a need for better understanding of mild cognitive impairment (MCI) before clinical deterioration begins. OBJECTIVE To determine the synergistic effects of beta-amyloid burden and CVD on cognition in patients with subcortical vascular MCI (svMCI). DESIGN, SETTING, AND PARTICIPANTS A cross-sectional study was conducted using a hospital-based sample at a tertiary referral center. We prospectively recruited 95 patients with svMCI; 67 of these individuals participated in the study. Forty-five patients with amnestic MCI (aMCI) were group matched with those with svMCI by the Clinical Dementia Rating Scale Sum of Boxes. MAIN OUTCOMES AND MEASURES We measured beta-amyloid burden using positron emission tomography with carbon 11-labeled Pittsburgh Compound B (PiB). Cerebrovascular disease was quantified as white matter hyperintensity volume detected by magnetic resonance imaging fluid-attenuated inversion recovery. Detailed neuropsychological tests were performed to determine the level of patients' cognitive impairment. RESULTS On evaluation, 22 of the svMCI group (33%) and 28 of the aMCI group (62%) were found to be PiB positive. The mean PiB retention ratio was lower in patients with svMCI than in those with aMCI. In svMCI, the PiB retention ratio was associated with cognitive impairments in multiple domains, including language, visuospatial, memory, and frontal executive functions, but was associated only with memory dysfunction in aMCI. A significant interaction between PiB retention ratio and white matter hyperintensity volume was found to affect visuospatial function in patients with svMCI. CONCLUSIONS AND RELEVANCE Most patients with svMCI do not exhibit substantial amyloid burden, and CVD does not increase beta-amyloid burden as measured by amyloid imaging. However, in patients with svMCI, amyloid burden and white matter hyperintensity act synergistically to impair visuospatial function. Therefore, our findings highlight the need for accurate biomarkers, including neuroimaging tools, for early diagnosis and the need to relate these biomarkers to cognitive measurements for effective use in the clinical setting.
引用
收藏
页码:412 / 422
页数:11
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