Plasma amyloid ß protein is elevated in late-onset Alzheimer disease families

被引:70
作者
Ertekin-Taner, N. [1 ,3 ]
Younkin, L. H. [1 ]
Yager, D. M. [1 ]
Parfitt, F. [2 ]
Baker, M. C. [1 ]
Asthana, S. [4 ]
Hutton, M. L. [1 ]
Younkin, S. G. [1 ]
Graff-Radford, N. R. [2 ]
机构
[1] Mayo Clin, Dept Neurosci, Jacksonville, FL 32224 USA
[2] Mayo Clin, Dept Neurol, Jacksonville, FL 32224 USA
[3] Mayo Clin, Dept Neurol, Rochester, MN USA
[4] Wisconsin Alzheimers Inst & Geriat & Gerontol, Madison, WI USA
关键词
D O I
10.1212/01.wnl.0000278386.00035.21
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Plasma A ss levels are elevated in early-onset Alzheimer disease (AD) caused by autosomal dominant mutations. Our objective was to determine whether similar genetic elevations exist in late-onset AD (LOAD). Methods: We measured plasma A ss in first-degree relatives of patients with LOAD in a cross-sectional series and in extended LOAD families. We screened these subjects for pathogenic mutations in early-onset AD genes and determined their ApoE genotypes. Results: Plasma A ss is significantly elevated in the LOAD first-degree relatives in comparison to unrelated controls and married-in spouses. These elevations are not due to ApoE epsilon 4 or pathogenic coding mutations in the known early-onset AD genes. Conclusions: The findings provide strong evidence for the existence of novel, as yet unknown genetic factors that affect late-onset Alzheimer disease by increasing A ss.
引用
收藏
页码:596 / 606
页数:11
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