Affiliations 

  • 1 Department of Neurology, National Neuroscience Institute, Singapore General Hospital, Singapore
  • 2 Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan
  • 3 Division of Neurology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand
  • 4 Faculty of Medicine, University Kula Lumpur, Royal College of Medicine Perak, Ipoh, Malaysia
  • 5 Clinical Research Centre, Hospital Seberang Jaya, Penang, Malaysia
  • 6 Institute for Neurosciences, St. Luke's Medical Center, Metro Manila, Philippines
  • 7 Department of Neurology and Cognitive Disorders and Dementia Center, Institute of Convergence Bio-Health, Dong-A University College of Medicine, Busan, Republic of Korea
  • 8 Novartis Healthcare Private Limited, Hyderabad, India
  • 9 Novartis (Singapore) Pte. Ltd., Singapore, Singapore
J Alzheimers Dis Rep, 2020 Feb 12;4(1):21-37.
PMID: 32206755 DOI: 10.3233/ADR-190143

Abstract

Clinical diagnosis of Alzheimer's disease (AD) is based on symptoms; however, the challenge is to diagnose AD at the preclinical stage with the application of biomarkers and initiate early treatment (still not widely available). Currently, cerebrospinal fluid (CSF) amyloid-β 42 (Aβ42) and tau are used in the clinical diagnosis of AD; nevertheless, blood biomarkers (Aβ42 and tau) are less predictive. Amyloid-positron emission tomography (PET) imaging is an advancement in technology that uses approved radioactive diagnostic agents (florbetapir, flutemetamol, or florbetaben) to estimate Aβ neuritic plaque density in adults with cognitive impairment evaluated for AD and other causes of cognitive decline. There is no cure for AD to date-the disease progression cannot be stopped or reversed; approved pharmacological agents (donepezil, galantamine, and rivastigmine; memantine) provide symptomatic treatment. However, the disease-modifying therapies are promising; aducanumab and CAD106 are in phase III trials for the early stages of AD. In conclusion, core CSF biomarkers reflect pathophysiology of AD in the early and late stages; the application of approved radiotracers have potential in amyloid-PET brain imaging to detect early AD.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.