Association of plasma biomarkers of amyloid and neurodegeneration with cerebrovascular disease and Alzheimer's disease

被引:6
|
作者
Graff-Radford, Jonathan [1 ,8 ]
Mielke, Michelle M. [1 ,2 ,7 ]
Hofrenning, Ekaterina I. [2 ]
Kouri, Naomi [3 ]
Lesnick, Timothy G. [2 ]
Moloney, Christina M. [3 ]
Rabinstein, Alejandro [1 ]
Cabrera-Rodriguez, Janisse N. [3 ]
Othberg, Darren M. R. [3 ]
Elski, Scott A. Przyb [2 ]
Petersen, Ronald C. [1 ]
Knopman, David S. [1 ]
Dickson, Dennis W. [3 ]
Jack, Clifford R. [4 ]
Algeciras-Schimnich, Alicia [5 ,6 ]
Nguyen, Aivi T. [5 ,6 ]
Murray, Melissa E. [3 ]
Vemuri, Prashanthi [4 ]
机构
[1] Mayo Clin, Dept Neurol, Rochester, MN USA
[2] Mayo Clin, Dept Quantitat Hlth Sci, Rochester, MN USA
[3] Mayo Clin, Dept Neurosci, Jacksonville, FL USA
[4] Mayo Clin, Dept Radiol, Rochester, MN USA
[5] Dept Pathol, Mayo Clin, Rochester, MN USA
[6] Mayo Clin, Lab Med, Rochester, MN USA
[7] Wake Forest Univ, Sch Med, Div Publ Hlth Sci, Winston Salem, NC USA
[8] Mayo Clin, Coll Med, Dept Neurol, 200 1st St SW, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
Plasma biomarkers; Neurofilament light (NfL); Total tau (T-tau); Cerebrovascular neuropathology; Neurodegenerative biomarkers; Postmortem neuropathology; MILD COGNITIVE IMPAIRMENT; NEUROPATHOLOGIC ASSESSMENT; NEUROFILAMENT LIGHT; NATIONAL INSTITUTE; TAU; GUIDELINES; PATHOLOGY;
D O I
10.1016/j.neurobiolaging.2022.07.006
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The objective of this study was to determine the differential mapping of plasma biomarkers to post-mortem neuropathology measures. We identified 64 participants in a population-based study with anteplasma markers (amyloid-beta [A,beta] x-42, A beta x-40, neurofilament light [NfL], and total tau [T-tau]) who also had neuropathologic assessments of Alzheimer's and cerebrovascular pathology. We conducted weighted linear-regression models to evaluate relationships between plasma measures and neuropathology. Higher plasma NfL and A beta 42/40 ratio were associated with cerebrovascular neuropathologic scales ( p < 0.05) but not with Braak stage, neuritic plaque score, or Thal phase. Plasma A beta 42/40 and NfL explained up to 18% of the variability in cerebrovascular neuropathologic scales. In participants predominantly with modest levels of Alzheimer's pathologic change, biomarkers of amyloid and neurodegeneration were associated with cerebrovascular neuropathology. NfL is a non-specific marker of brain injury, therefore its association with cerebrovascular neuropathology was expected. The association between elevated A beta 42/40 and cerebrovascular disease pathology needs further investigation but could be due to the use of less specific amyloid-beta assays (x-40, x-42).(c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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