Amyloid β concentrations and stable isotope labeling kinetics of human plasma specific to central nervous system amyloidosis

被引:435
作者
Ovod, Vitaliy [1 ]
Ramsey, Kara N. [1 ]
Mawuenyega, Kwasi G. [1 ]
Bollinger, Jim G. [1 ]
Hicks, Terry [1 ]
Schneider, Theresa [1 ]
Sullivan, Melissa [1 ]
Paumier, Katrina [1 ]
Holtzman, David M. [1 ,2 ,3 ]
Morris, John C. [1 ,3 ]
Benzinger, Tammie [3 ,4 ]
Fagan, Anne M. [1 ,2 ,3 ]
Patterson, Bruce W. [5 ]
Bateman, Randall J. [1 ,2 ,3 ]
机构
[1] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Neurol, Hope Ctr Neurol Disorders, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Neurol, Knight Alzheimers Dis Res Ctr, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Radiol, St Louis, MO USA
[5] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
关键词
Amyloid beta; A beta 42; Turnover; Kinetics; Human; Plasma; CEREBROSPINAL-FLUID TAU; ALZHEIMERS-DISEASE; AGE; BIOMARKERS; DIAGNOSIS; A-BETA-42;
D O I
10.1016/j.jalz.2017.06.2266
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Cerebrospinal fluid analysis and other measurements of amyloidosis, such as amyloid-binding positron emission tomography studies, are limited by cost and availability. There is a need for a more practical amyloid beta (A beta) biomarker for central nervous system amyloid deposition. Methods: We adapted our previously reported stable isotope labeling kinetics protocol to analyze the turnover kinetics and concentrations of A beta 38, A beta 40, and A beta 42 in human plasma. Results: A beta isoforms have a half-life of approximately 3 hours in plasma. A beta 38 demonstrated faster turnover kinetics compared with A beta 40 and A beta 42. Faster fractional turnover of A beta 42 relative to A beta 40 and lower A beta 42 and A beta 42/A beta 40 concentrations in amyloid-positive participants were observed. Discussion: Blood plasma A beta 42 shows similar amyloid-associated alterations as we have previously reported in cerebrospinal fluid, suggesting a blood-brain transportation mechanism of A beta. The stability and sensitivity of plasma A beta measurements suggest this may be a useful screening test for central nervous system amyloidosis. (C) 2017 the Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:841 / 849
页数:9
相关论文
共 17 条
[1]   Human amyloid-β synthesis and clearance rates as measured in cerebrospinal fluid in vivo [J].
Bateman, Randall J. ;
Munsell, Ling Y. ;
Morris, John C. ;
Swarm, Robert ;
Yarasheski, Kevin E. ;
Holtzman, David M. .
NATURE MEDICINE, 2006, 12 (07) :856-861
[2]   Accuracy of the Clinical Diagnosis of Alzheimer Disease at National Institute on Aging Alzheimer Disease Centers, 2005-2010 [J].
Beach, Thomas G. ;
Monsell, Sarah E. ;
Phillips, Leslie E. ;
Kukull, Walter .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2012, 71 (04) :266-273
[3]   Cerebrospinal fluid tau and β-amyloid -: How well do these biomarkers reflect autopsy-confirmed dementia diagnoses? [J].
Clark, CM ;
Xie, S ;
Chittams, J ;
Ewbank, D ;
Peskind, E ;
Galasko, D ;
Morris, JC ;
McKeel, DW ;
Farlow, M ;
Weitlauf, SL ;
Quinn, J ;
Kaye, J ;
Knopman, D ;
Arai, H ;
Doody, RS ;
DeCarli, C ;
Leight, S ;
Lee, VMY ;
Trojanowski, JQ .
ARCHIVES OF NEUROLOGY, 2003, 60 (12) :1696-1702
[4]   Early detection of Alzheimer's disease using PiB and FDG PET [J].
Cohen, Ann D. ;
Klunk, William E. .
NEUROBIOLOGY OF DISEASE, 2014, 72 :117-122
[5]   LRP/amyloid β-peptide interaction mediates differential brain efflux of Aβ isoforms [J].
Deane, R ;
Wu, ZH ;
Sagare, A ;
Davis, J ;
Yan, SD ;
Hamm, K ;
Xu, F ;
Parisi, M ;
LaRue, B ;
Hu, HW ;
Spijkers, P ;
Guo, H ;
Song, XM ;
Lenting, PJ ;
Van Nostrand, WE ;
Zlokovic, BV .
NEURON, 2004, 43 (03) :333-344
[6]   RAGE mediates amyloid-β peptide transport across the blood-brain barrier and accumulation in brain [J].
Deane, R ;
Yan, SD ;
Submamaryan, RK ;
LaRue, B ;
Jovanovic, S ;
Hogg, E ;
Welch, D ;
Manness, L ;
Lin, C ;
Yu, J ;
Zhu, H ;
Ghiso, J ;
Frangione, B ;
Stern, A ;
Schmidt, AM ;
Armstrong, DL ;
Arnold, B ;
Liliensiek, B ;
Nawroth, P ;
Hofman, F ;
Kindy, M ;
Stern, D ;
Zlokovic, B .
NATURE MEDICINE, 2003, 9 (07) :907-913
[7]   Age but not diagnosis is the main predictor of plasma amyloid β-protein levels [J].
Fukumoto, H ;
Tennis, M ;
Locascio, JJ ;
Hyman, BT ;
Growdon, JH ;
Irizarry, MC .
ARCHIVES OF NEUROLOGY, 2003, 60 (07) :958-964
[8]   High cerebrospinal fluid tau and low amyloid β42 levels in the clinical diagnosis of Alzheimer disease and relation to apolipoprotein E genotype [J].
Galasko, D ;
Chang, L ;
Motter, R ;
Clark, CM ;
Kaye, J ;
Knopman, D ;
Thomas, R ;
Kholodenko, D ;
Schenk, D ;
Lieberburg, I ;
Miller, B ;
Green, R ;
Basherad, R ;
Kertiles, L ;
Boss, MA ;
Seubert, P .
ARCHIVES OF NEUROLOGY, 1998, 55 (07) :937-945
[9]   Amyloid-beta isoform metabolism quantitation by stable isotope-labeled kinetics [J].
Mawuenyega, Kwasi G. ;
Kasten, Tom ;
Sigurdson, Wendy ;
Bateman, Randall J. .
ANALYTICAL BIOCHEMISTRY, 2013, 440 (01) :56-62
[10]   Plasma Aβ40 and Aβ42 and Alzheimer's disease -: Relation to age, mortality, and risk [J].
Mayeux, R ;
Honig, LS ;
Tang, MX ;
Manly, J ;
Stern, Y ;
Schupf, N ;
Mehta, PD .
NEUROLOGY, 2003, 61 (09) :1185-1190