4.5 Article

Blood Protein Markers of Neocortical Amyloid-beta Burden: A Candidate Study Using SOMAscan Technology

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 46, Issue 4, Pages 947-961

Publisher

IOS PRESS
DOI: 10.3233/JAD-150020

Keywords

Alzheimer's disease; amyloid plaques; blood; positron emission tomography scan; proteomics

Categories

Funding

  1. CogState Ltd.
  2. Hollywood Private Hospital
  3. Sir Charles Gairdner Hospital
  4. CSIRO
  5. Science and Industry Endowment Fund
  6. NHMRC and Dementia Collaborative Research Centres (DCRC)
  7. Alzheimer's Australia (AA)
  8. Alzheimer's Association
  9. McCusker Alzheimer's Research Foundation
  10. Alzheimer's Society
  11. NIHR Biomedical Research Centre for Mental Health and Biomedical Research Unit for Dementia at the South London, Maudsley NHS Foundation Trust
  12. Kings College London
  13. Innovative Medicines Initiative Joint Undertaking [115372]
  14. European Union
  15. MRC [MR/L011859/1]
  16. GE Healthcare
  17. Janssen RD
  18. Alzheimers Research UK [ART-PG2010-4] Funding Source: researchfish
  19. Medical Research Council [MR/L011859/1] Funding Source: researchfish
  20. National Institute for Health Research [NF-SI-0512-10053] Funding Source: researchfish
  21. Alzheimer&quot
  22. s Society [122, 171] Funding Source: researchfish

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Background: Four previously reported studies have tested for association of blood proteins with neocortical amyloid-beta burden (NAB). If shown to be robust, these proteins could have utility as a blood test for enrichment in clinical trials of Alzheimer's disease (AD) therapeutics. Objective: This study aimed to investigate whether previously identified blood proteins also show evidence for association with NAB in serum samples from the Australian Imaging, Biomarker and Lifestyle Flagship Study of Ageing (AIBL). The study considers candidate proteins seen in cohorts other than AIBL and candidates previously discovered in the AIBL cohort. Methods: Our study used the SOMAscan platform for protein quantification in blood serum. Linear and logistic regressions were used to model continuous NAB and dichotomized NAB respectively using single proteins as a predictor. Multiple protein models were built using stepwise regression techniques and support vectors machines. Age and APOE epsilon 4 carriage were used as covariates for all analysis. Results: Of the 41 proteins previously reported, 15 AIBL candidates and 20 non-AIBL candidates were available for testing. Of these candidates, pancreatic polypeptide (PPY) and IgM showed a significant association with NAB. Notably, IgM was found to associate with continuous NAB across cognitively normal control subjects. Conclusions: We have further demonstrated the association of PPY and IgM with NAB, despite technical differences between studies. There are several reasons for a lack of significance for the other candidates including platform differences and the use of serum rather than plasma samples. To investigate the possibility of technical differences causing lack of replication, further studies are required.

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