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The Alzheimer's Disease Neuroimaging Initiative 2 Biomarker Core: A review of progress and plans

Kang, J. H. (author)
Korecka, M. (author)
Figurski, M. J. (author)
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Toledo, J. B. (author)
Blennow, Kaj, 1958 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Zetterberg, Henrik, 1973 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Waligorska, T. (author)
Brylska, M. (author)
Fields, L. (author)
Shah, N. (author)
Soares, H. (author)
Dean, R. A. (author)
Vanderstichele, H. (author)
Petersen, R. C. (author)
Aisen, P. S. (author)
Saykin, A. J. (author)
Weiner, M. W. (author)
Trojanowski, J. Q. (author)
Shaw, L. M. (author)
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 (creator_code:org_t)
2015-07
2015
English.
In: Alzheimers & Dementia. - : Wiley. - 1552-5260 .- 1552-5279. ; 11:7, s. 772-791
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Introduction: We describe Alzheimer's Disease Neuroimaging Initiative (ADNI) Biomarker Core progress including: the Biobank; cerebrospinal fluid (CSF) amyloid beta (A beta(1-42)), t-tau, and p-tau(181) analytical performance, definition of Alzheimer's disease (AD) profile for plaque, and tangle burden detection and increased risk for progression to AD; AD disease heterogeneity; progress in standardization; and new studies using ADNI biofluids. Methods: Review publications authored or coauthored by ADNI Biomarker core faculty and selected non-ADNI studies to deepen the understanding and interpretation ofCSFA beta(1-42), t-tau, and p-tau(181) data. Results: CSFAD biomarker measurements with the qualified AlzBio3 immunoassay detects neuropathologic AD hallmarks in preclinical and prodromal disease stages, based on CSF studies in nonADNI living subjects followed by the autopsy confirmation of AD. Collaboration across ADNI cores generated the temporal ordering model of AD biomarkers varying across individuals because of genetic/environmental factors that increase/decrease resilience to AD pathologies. Discussion: Further studies will refine this model and enable the use of biomarkers studied in ADNI clinically and in disease-modifying therapeutic trials. (C) 2015 Published by Elsevier Inc. on behalf of the Alzheimer's Association.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Keyword

Alzheimer's disease
Mild cognitive impairment
Cerebrospinal fluid
Plasma
Biomarkers
MILD COGNITIVE IMPAIRMENT
CEREBROSPINAL-FLUID BIOMARKERS
PLASMA
AMYLOID-BETA
APOLIPOPROTEIN-E GENOTYPE
TANDEM MASS-SPECTROMETRY
GENOME-WIDE ASSOCIATION
CSF BIOMARKERS
A-BETA
DIAGNOSTIC GUIDELINES
Clinical Neurology

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