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Brain Aging Among Racially and Ethnically Diverse Middle-Aged and Older Adults.不同种族和民族的中老年人的大脑衰老。
JAMA Neurol. 2023 Jan 1;80(1):73-81. doi: 10.1001/jamaneurol.2022.3919.
2
Increasing participant diversity in AD research: Plans for digital screening, blood testing, and a community-engaged approach in the Alzheimer's Disease Neuroimaging Initiative 4.增加 AD 研究中的参与者多样性:在阿尔茨海默病神经影像学倡议 4 中进行数字筛查、血液检测和社区参与方法的计划。
Alzheimers Dement. 2023 Jan;19(1):307-317. doi: 10.1002/alz.12797. Epub 2022 Oct 9.
3
An examination of the relationship among plasma brain derived neurotropic factor, peripheral vascular function, and body composition with cognition in midlife African Americans/Black individuals.对中年非裔美国人/黑人血浆脑源性神经营养因子、外周血管功能、身体成分与认知之间关系的研究。
Front Aging Neurosci. 2022 Aug 25;14:980561. doi: 10.3389/fnagi.2022.980561. eCollection 2022.
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Neurovascular Dysfunction in Diverse Communities With Health Disparities-Contributions to Dementia and Alzheimer's Disease.存在健康差异的不同社区中的神经血管功能障碍——对痴呆症和阿尔茨海默病的影响
Front Neurosci. 2022 Jun 29;16:915405. doi: 10.3389/fnins.2022.915405. eCollection 2022.
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Addressing racial and phenotypic bias in human neuroscience methods.解决人类神经科学方法中的种族和表型偏见。
Nat Neurosci. 2022 Apr;25(4):410-414. doi: 10.1038/s41593-022-01046-0. Epub 2022 Apr 5.
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Racial differences in longitudinal Alzheimer's disease biomarkers among cognitively normal adults.认知正常成年人纵向阿尔茨海默病生物标志物的种族差异。
Alzheimers Dement. 2022 Dec;18(12):2570-2581. doi: 10.1002/alz.12608. Epub 2022 Feb 25.
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Associations of deformation-based brain morphometry with cognitive level and decline within older Blacks without dementia.基于形变的脑形态计量学与无痴呆的老年黑人认知水平和下降的关联。
Neurobiol Aging. 2022 Mar;111:35-43. doi: 10.1016/j.neurobiolaging.2021.11.003. Epub 2021 Nov 20.
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Alzheimer disease in African American individuals: increased incidence or not enough data?非裔美国人的阿尔茨海默病:发病率增加还是数据不足?
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The Relationship of ε4, Race, and Sex on the Age of Onset and Risk of Dementia.ε4、种族和性别与痴呆症发病年龄及风险的关系
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黑人和/或非裔美国人阿尔茨海默病神经影像学倡议(ADNI)参与者的阿尔茨海默病生物标志物。

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

机构信息

Department of Anatomy and Neurobiology, Boston University Chobanian and Avedisian School of Medicine, Boston, MA, USA.

Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA; Boston University Alzheimer's Disease Research Center, Boston, MA, USA.

出版信息

Neurobiol Aging. 2023 Nov;131:144-152. doi: 10.1016/j.neurobiolaging.2023.07.021. Epub 2023 Jul 20.

DOI:10.1016/j.neurobiolaging.2023.07.021
PMID:37639768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10528881/
Abstract

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 biomarker 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) ε4, cerebrospinal fluid (CSF) Aβ, 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 Aβ, 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.

摘要

尽管其他种族群体的痴呆症发病率更高,但大多数痴呆症研究都是在非西班牙裔白人群体中进行的。为了更好地了解非西班牙裔白人群体中阿尔茨海默病(AD)的生物标志物表现,本研究仅在阿尔茨海默病神经影像学倡议(ADNI)中检查了 85 名黑人和/或非裔美国参与者的 AD 生物标志物异常。参与者根据 ADNI 被分为 3 个临床组:认知正常、轻度认知障碍或痴呆。检查的数据包括人口统计学、载脂蛋白 E(APOE)ε4、脑脊液(CSF)Aβ、CSF 总 tau(t-tau)、CSF 磷酸化 tau(p-tau)、3T 磁共振成像(MRI)以及认知和功能测量。方差和协方差分析显示,在 7 个选定的 MRI 区域中有 5 个区域的皮质厚度较低,海马体积较小,白质高信号体积较大,认知和功能测量值较低,CSF Aβ 测量值较低,CSF t-tau 和 p-tau 测量值较高。我们的研究结果证实了该样本中临床组之间存在更大的 AD 生物标志物异常。