Inclusion of African American/Black adults in a pilot brain proteomics study of Alzheimer's disease

被引:16
作者
Stepler, Kaitlyn E. [1 ]
Mahoney, Emily R. [2 ,3 ]
Kofler, Julia [4 ]
Hohman, Timothy J. [2 ,3 ,5 ,6 ]
Lopez, Oscar L. [7 ,8 ]
Robinson, Rena A. S. [1 ,2 ,5 ,6 ,9 ]
机构
[1] Vanderbilt Univ, Dept Chem, 5423 Stevenson Ctr, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Med Ctr, Vanderbilt Memory & Alzheimers Ctr, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Med Ctr, Vanderbilt Genet Inst, Nashville, TN 37232 USA
[4] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15213 USA
[5] Vanderbilt Univ, Med Ctr, Dept Neurol, Nashville, TN 37232 USA
[6] Vanderbilt Univ, Med Ctr, Vanderbilt Brain Inst, Nashville, TN 37232 USA
[7] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15213 USA
[8] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA 15213 USA
[9] Vanderbilt Univ, Vanderbilt Inst Chem Biol, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; Proteomics; Disparities; Brain; African American; Black; Hippocampus; Inferior parietal lobule; Globus pallidus; Proteins; INFERIOR PARIETAL LOBULE; RISK-FACTORS; LIPID-METABOLISM; DIFFERENTIAL EXPRESSION; RACIAL DISPARITIES; APOLIPOPROTEIN-E; WHITE DECEDENTS; CSF BIOMARKERS; TEMPORAL-LOBE; AMYLOID-BETA;
D O I
10.1016/j.nbd.2020.105129
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) disproportionately affects certain racial and ethnic subgroups, such as African American/Black and Hispanic adults. Genetic, comorbid, and socioeconomic risk factors contribute to this disparity; however, the molecular contributions have been largely unexplored. Herein, we conducted a pilot proteomics study of postmortem brains from African American/Black and non-Hispanic White adults neuropathologically diagnosed with AD compared to closely-matched cognitively normal individuals. Examination of hippocampus, inferior parietal lobule, and globus pallidus regions using quantitative proteomics resulted in 568 differentially-expressed proteins in AD. These proteins were consistent with the literature and included glial fibrillary acidic protein, peroxiredoxin-1, and annexin A5. In addition, 351 novel proteins in AD were identified, which could partially be due to cohort diversity. From linear regression analyses, we identified 185 proteins with significant race x diagnosis interactions across various brain regions. These differences generally were reflective of differential expression of proteins in AD that occurred in only a single racial/ethnic group. Overall, this pilot study suggests that disease understanding can be furthered by including diversity in racial/ethnic groups; however, this must be done on a larger scale.
引用
收藏
页数:12
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