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Role of Fluid Biomarkers and PET Imaging in Early Diagnosis and its Clinical Implication in the Management of Alzheimer's Disease.
Hameed, Shahul; Fuh, Jong-Ling; Senanarong, Vorapun; Ebenezer, Esther Gunaseli M; Looi, Irene; Dominguez, Jacqueline C; Park, Kyung Won; Karanam, Ananda Krishna; Simon, Oliver.
Affiliation
  • Hameed S; Department of Neurology, National Neuroscience Institute, Singapore General Hospital, Singapore.
  • Fuh JL; Duke NUS Medical School, Singapore.
  • Senanarong V; Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Ebenezer EGM; Faculty of Medicine, National Yang-Ming University School of Medicine, Taipei, Taiwan.
  • Looi I; Division of Neurology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Dominguez JC; Faculty of Medicine, University Kula Lumpur, Royal College of Medicine Perak, Ipoh, Malaysia.
  • Park KW; Clinical Research Centre, Hospital Seberang Jaya, Penang, Malaysia.
  • Karanam AK; Department of Medicine, Hospital Seberang Jaya, Penang, Malaysia.
  • Simon O; Institute for Neurosciences, St. Luke's Medical Center, Metro Manila, Philippines.
J Alzheimers Dis Rep ; 4(1): 21-37, 2020 Feb 12.
Article in En | MEDLINE | ID: mdl-32206755
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-ß 42 (Aß42) and tau are used in the clinical diagnosis of AD; nevertheless, blood biomarkers (Aß42 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 Aß 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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Screening_studies Language: En Journal: J Alzheimers Dis Rep Year: 2020 Document type: Article Affiliation country: Singapore

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Screening_studies Language: En Journal: J Alzheimers Dis Rep Year: 2020 Document type: Article Affiliation country: Singapore