Plasma multianalyte profiling in mild cognitive impairment and Alzheimer disease
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Abstract
Objectives: While plasma biomarkers have been proposed to aid in the clinical diagnosis of Alzheimer disease (AD), few biomarkers have been validated in independent patient cohorts. Here we aim to determine plasma biomarkers associated with AD in 2 independent cohorts and validate the findings in the multicenter Alzheimer's Disease Neuroimaging Initiative (ADNI).
Methods: Using a targeted proteomic approach, we measured levels of 190 plasma proteins and peptides in 600 participants from 2 independent centers (University of Pennsylvania, Philadelphia; Washington University, St. Louis, MO), and identified 17 analytes associated with the diagnosis of very mild dementia/mild cognitive impairment (MCI) or AD. Four analytes (apoE, B-type natriuretic peptide, C-reactive protein, pancreatic polypeptide) were also found to be altered in clinical MCI/AD in the ADNI cohort (n = 566). Regression analysis showed CSF Aβ42 levels and t-tau/Aβ42 ratios to correlate with the number of APOE4 alleles and plasma levels of B-type natriuretic peptide and pancreatic polypeptide.
Conclusion: Four plasma analytes were consistently associated with the diagnosis of very mild dementia/MCI/AD in 3 independent clinical cohorts. These plasma biomarkers may predict underlying AD through their association with CSF AD biomarkers, and the association between plasma and CSF amyloid biomarkers needs to be confirmed in a prospective study.
GLOSSARY
- Aβ42=
- βamyloid 1–42;
- AD=
- Alzheimer disease;
- ADNI=
- Alzheimer's Disease Neuroimaging Initiative;
- BNP=
- B-type natriuretic peptide;
- CDR=
- Clinical Dementia Rating;
- CRP=
- C-reactive protein;
- CV=
- coefficient of variation;
- IGF-BP2=
- insulin growth factor binding protein 2;
- IL=
- interleukin;
- IUT=
- Intersection Union Test;
- MCI=
- mild cognitive impairment;
- p-tau181=
- tau phosphorylated at threonine 181;
- Penn=
- University of Pennsylvania;
- RBM=
- Rules-Based Medicine;
- SAM=
- significance analysis of microarrays;
- t-tau=
- total tau;
- TARC=
- Texas Alzheimer's Research Consortium;
- WU=
- Washington University
Footnotes
↵† Deceased.
Coinvestigators are listed on the Neurology® Web site at www.neurology.org.
Additional corresponding authors: holtzman{at}neuro.wustl.edu, Les.Shaw{at}uphs.upenn.edu, trojanow{at}mail.med.upenn.edu, holly.soares{at}bms.com.
Study funding: Funding information is provided at the end of the article.
Editorial, page 846
Supplemental data at www.neurology.org
- Received August 11, 2011.
- Accepted March 8, 2012.
- Copyright © 2012 by AAN Enterprises, Inc.
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Letters: Rapid online correspondence
- Response to Dr. Bennett
- William T Hu, Assistant Professor, Neurology, Emory Universitywthu@emory.edu
- David Holtzman, St. Louis, MO; Leslie Shaw, Philadelphia, PA; John Trojanowski, Philadelphia, PA; Holly Soares, New London, CT
Submitted August 30, 2012 - Proteomics and Alzheimer Disease (AD)
- David A. Bennett, Director and Professor of Neurological Sciences, Rush Alzheimer's Disease Center, Rush University Medical CenterDavid_A_Bennett@rush.edu
- Chicago, IL
Submitted August 28, 2012
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