Biomarkers of Alzheimer's disease in Black and/or African American Alzheimer's Disease Neuroimaging Initiative (ADNI) participants

被引:2
|
作者
Groechel, Renee C. [1 ]
Tripodis, Yorghos [2 ,3 ]
Alosco, Michael L. [3 ,4 ]
Mez, Jesse [3 ,4 ]
Qiu, Wei Qiao [3 ,5 ]
Goldstein, Lee [3 ,4 ]
Budson, Andrew E. [3 ,4 ]
Kowall, Neil W. [3 ,4 ]
Shaw, Leslie M. [6 ]
Weiner, Michael [7 ]
Jack, Clifford R., Jr. [8 ]
Killiany, R. J.
机构
[1] Boston Univ, Chobanian & Avedisian Sch Med, Dept Anat & Neurobiol, Boston, MA USA
[2] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
[3] Boston Univ, Alzheimers Dis Res Ctr, Boston, MA USA
[4] Boston Univ, Chobanian & Avedisian Sch Med, Dept Neurol, Boston, MA USA
[5] Boston Univ, Chobanian & Avedisian Sch Med, Dept Psychiat, Boston, MA USA
[6] Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA USA
[7] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA USA
[8] Mayo Clin, Dept Radiol, Rochester, MN USA
关键词
Amyloid-beta; Biomarkers; Black or African American; Cerebrospinal fluid; Cognition; Dementia; Magnetic resonance imaging; Mild cognitive impairment; Race; Tau; MILD COGNITIVE IMPAIRMENT; CLINICAL CORE; MRI; SEGMENTATION; PROGRESS; CORTEX; MODEL; APOE4; TOOL;
D O I
10.1016/j.neurobiolaging.2023.07.021
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Majority of dementia research is conducted in non-Hispanic White participants despite a greater prevalence of dementia in other racial groups. To obtain a better understanding of biomarker presentation of Alzheimer's disease (AD) in the non-Hispanic White population, this study exclusively examined AD bio-marker abnormalities in 85 Black and/or African American participants within the Alzheimer's Disease Neuroimaging Initiative (ADNI). Participants were classified by the ADNI into 3 clinical groups: cognitively normal, mild cognitive impairment, or dementia. Data examined included demographics, apolipoprotein E (APOE) & epsilon;4, cerebrospinal fluid (CSF) A & beta;1-42, CSF total tau (t-tau), CSF phosphorylated tau (p-tau), 3T magnetic resonance imaging (MRI), and measures of cognition and function. Analyses of variance and covariance showed lower cortical thickness in 5 of 7 selected MRI regions, lower hippocampal volume, greater volume of white matter hyperintensities, lower measures of cognition and function, lower measures of CSF A & beta;1-42, and greater measures of CSF t-tau and p-tau between clinical groups. Our findings confirmed greater AD biomarker abnormalities between clinical groups in this sample.& COPY; 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:144 / 152
页数:9
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