Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring (Jan 2017)

Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin

  • Eva Carro,
  • Fernando Bartolomé,
  • Félix Bermejo‐Pareja,
  • Alberto Villarejo‐Galende,
  • José Antonio Molina,
  • Pablo Ortiz,
  • Miguel Calero,
  • Alberto Rabano,
  • José Luis Cantero,
  • Gorka Orive

DOI
https://doi.org/10.1016/j.dadm.2017.04.002
Journal volume & issue
Vol. 8, no. 1
pp. 131 – 138

Abstract

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Abstract Introduction The Alzheimer's disease (AD) process is likely initiated many years before clinical onset. Biomarkers of preclinical disease are critical for the development of disease‐modifying or even preventative therapies. Current biomarkers for early disease, including cerebrospinal fluid tau and amyloid β (Aβ) levels, structural and functional magnetic resonance imaging, and the use of brain amyloid imaging, are limited because they are very invasive or expensive. Noninvasive biomarkers may be a more accessible alternative, but none can currently detect preclinical AD with the required sensitivity and specificity. Methods Here, we show a novel, straight‐forward, and noninvasive approach for assessment of early stages of cognitive decline. Salivary samples from cases of amnestic mild cognitive impairment (aMCI) and AD, and neurology controls were analyzed. Results We have discovered and validated a new single saliva biomarker, lactoferrin, which in our cross‐sectional investigation perfectly discriminates clinically diagnosed aMCI and AD patients from a cognitively healthy control group. The accuracy for AD diagnosis shown by salivary lactoferrin was greater than that obtained from core cerebrospinal fluid (CSF) biomarkers, including total tau and CSF Aβ42. Furthermore, salivary lactoferrin can be used for population screening and for identifying those underdiagnosed subjects with very early stages of mild cognitive impairment and AD. Conclusion This biomarker may offer new insights in the early diagnostics for AD.

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