Plasma Tau Association with Brain Atrophy in Mild Cognitive Impairment and Alzheimer's Disease

被引:63
作者
Deters, Kacie D. [1 ,2 ,3 ]
Shannon, L. Risachera [1 ,2 ]
Kim, Sungeun [1 ,2 ,4 ]
Nhoa, Kwangsik [1 ,2 ]
West, John D. [1 ]
Blennow, Kaj [5 ]
Zetterberge, Henrik [5 ,6 ]
Shaw, Leslie M. [7 ]
Trojanowski, John Q. [7 ]
Weiner, Michael W. [8 ]
Saykin, Andrew J. [1 ,2 ,3 ]
机构
[1] Indiana Univ Sch Med, Ctr Neuroimaging, Dept Radiol & Imaging Sci, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Indiana Alzheimer Dis Ctr, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Paul & Carole Stark Neurosci Res Inst, Program Med Neurosci, Indianapolis, IN 46202 USA
[4] SUNY Coll Oswego, Dept Elect & Comp Engn, Oswego, NY USA
[5] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Molndal, Sweden
[6] UCL, Inst Neurol, Dept Mol Neurosci, London, England
[7] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[8] Univ Calif San Francisco, Dept Radiol Med & Psychiat, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
Alzheimer disease; magnetic resonance imaging; mild cognitive impairment; plasma; tau protein; SURFACE-BASED ANALYSIS;
D O I
10.3233/JAD-161114
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Peripheral (plasma) and central (cerebrospinal fluid, CSF) measures of tau are higher in Alzheimer's disease (AD) relative to prodromal stages and controls. While elevated CSF tau concentrations have been shown to be associated with lower grey matter density (GMD) in AD-specific regions, this correlation has yet to be examined for plasma in a large study. Objective: Determine the neuroanatomical correlates of plasma tau using voxel-based analysis. Methods: Cross-sectional data for 508 ADNI participants were collected for clinical, plasma total-tau (t-tau), CSF amyloid (A beta(42)) and tau, and MRI variables. The relationship between plasma tau and GMD and between CSF t-tau and GMD were assessed on a voxel-by-voxel basis using regression models. Age, sex, APOE epsilon 4 status, diagnosis, and total intracranial volume were used as covariates where appropriate. Participants were defined as amyloid positive (A beta+) if CSF A beta(42) was <192 pg/mL. Results: Plasma tau was negatively correlated with GMD in the medial temporal lobe (MTL), precuneus, thalamus, and striatum. The associations with thalamus and striatum were independent of diagnosis. A negative correlation also existed between plasma tau and GMD in A beta+ participants in the MTL, precuneus, and frontal lobe. When compared to CSF t-tau, plasma tau showed a notably different associated brain atrophy pattern, with only small overlapping regions in the fusiform gyrus. Conclusion: Plasma tau may serve as a non-specific marker for neurodegeneration but is still relevant to AD considering low GMD was associated with plasma tau in A beta+ participants and not A beta-participants.
引用
收藏
页码:1245 / 1254
页数:10
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