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Detection of Alzheimer's disease at mild cognitive impairment and disease progression using autoantibodies as blood-based biomarkers
Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring (2016)
Abstract
Introduction:
There is an urgent need to identify biomarkers that can accurately detect and diagnose Alzheimer's disease (AD). Autoantibodies are abundant and ubiquitous in human sera and have been previously demonstrated as disease-specific biomarkers capable of accurately diagnosing mild-moderate stages of AD and Parkinson's disease.

Methods:
Sera from 236 subjects, including 50 mild cognitive impairment (MCI) subjects with confirmed low CSF Aβ42 levels, were screened with human protein microarrays to identify potential biomarkers for MCI. Autoantibody biomarker performance was evaluated using Random Forest and Receiver Operating Characteristic curves.

Results:
Autoantibody biomarkers can differentiate MCI patients from age-matched and gender-matched controls with an overall accuracy, sensitivity, and specificity of 100.0%. They were also capable of differentiating MCI patients from those with mild-moderate AD and other neurologic and non-neurologic controls with high accuracy.

Discussion:
Autoantibodies can be used as noninvasive and effective blood-based biomarkers for early diagnosis and staging of AD.
Keywords
  • Mild Cognitive Impairment,
  • Alzheimer's disease,
  • Autoantibodies,
  • Biomarkers,
  • Blood biomarkers,
  • Microarray,
  • Autoantibody Biomarker,
  • Antibody,
  • Diagnostics
Publication Date
2016
DOI
10.1016/j.dadm.2016.03.002
Citation Information
"Detection of Alzheimer's disease at mild cognitive impairment and disease progression using autoantibodies as blood-based biomarkers" Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring Vol. 3 (2016) p. 51 - 62 ISSN: 2352-8729
Available at: http://works.bepress.com/umashanger-thayasivam/1/
Creative Commons license
Creative Commons License
This work is licensed under a Creative Commons CC_BY-NC-ND International License.