Department of Epidemiology, Center for Aging and Population Health, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Alzheimer Dis Assoc Disord. 2013 Jul-Sep;27(3):244-9. doi: 10.1097/WAD.0b013e318260a8cb.
Plasma amyloid β-42 (Aβ42) and Aβ42/Aβ40 are increasingly recognized as biomarkers for dementia, with low levels indicating increased risk. Little is known about the demographic and medical correlates of plasma Aβ40 or Aβ42. In 997 community-dwelling, nondemented older adults from the Health, Aging, and Body Composition Study, we determined the cross-sectional association between a wide range of demographic and medical variables with Aβ40 and Aβ42. In multivariate stepwise linear regression models, Aβ40 was significantly associated with race (β=-14.70, F=22.01, P<0.0001), age (β=1.34, F=6.39, P=0.01), creatinine (β=52.91, F=151.77, P<0.0001), and the serum brain-derived neurotrophic factor (β=-0.0004, F=7.34, P=0.007); Aβ42 was significantly associated with race (β=-3.72, F=30.83, P<0.0001), sex (β=1.39, F=4.32, P=0.04), education (β=1.50, F=4.78, P=0.03), apolipoprotein E e4 genotype (β=-2.82, F=16.57, P<0.0001), and creatinine (β=9.32, F=120.09, P<0.0001). These correlates should be considered as potential confounders in future studies investigating plasma Aβ as a biomarker of dementia. Understanding fully how these correlates mediate or modify the association between plasma Aβ and dementia will be a fundamental step in determining the biological pathways through which plasma Aβ40 and Aβ42 are associated with dementia, and in determining their full potential as biomarkers.
血浆淀粉样蛋白β-42(Aβ42)和 Aβ42/Aβ40 越来越被认为是痴呆的生物标志物,其水平较低表明风险增加。关于血浆 Aβ40 或 Aβ42 的人口统计学和医学相关性知之甚少。在健康、衰老和身体成分研究中,我们对来自 997 名居住在社区、没有痴呆的老年人进行了横断面研究,以确定广泛的人口统计学和医学变量与 Aβ40 和 Aβ42 之间的关联。在多元逐步线性回归模型中,Aβ40 与种族(β=-14.70,F=22.01,P<0.0001)、年龄(β=1.34,F=6.39,P=0.01)、肌酐(β=52.91,F=151.77,P<0.0001)和血清脑源性神经营养因子(β=-0.0004,F=7.34,P=0.007)显著相关;Aβ42 与种族(β=-3.72,F=30.83,P<0.0001)、性别(β=1.39,F=4.32,P=0.04)、教育程度(β=1.50,F=4.78,P=0.03)、载脂蛋白 E e4 基因型(β=-2.82,F=16.57,P<0.0001)和肌酐(β=9.32,F=120.09,P<0.0001)显著相关。在未来研究中,这些相关性应被视为研究血浆 Aβ作为痴呆生物标志物的潜在混杂因素。充分了解这些相关性如何介导或改变血浆 Aβ 与痴呆之间的关联,将是确定与痴呆相关的血浆 Aβ40 和 Aβ42 生物途径及其作为生物标志物的全部潜力的重要步骤。