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Peripheral transcriptomic biomarkers for early detection of sporadic Alzheimer disease?

Alzheimer disease (AD) is the major epidemic of the 21(st) century, its prevalence rising along with improved human longevity. Early AD diagnosis is key to successful treatment, as currently available therapeutics only allow small benefits for diagnosed AD patients. By contrast, future therapeutics,...

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Detalles Bibliográficos
Autores principales: Hadar, Adva, Gurwitz, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Les Laboratoires Servier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436957/
https://www.ncbi.nlm.nih.gov/pubmed/30936769
Descripción
Sumario:Alzheimer disease (AD) is the major epidemic of the 21(st) century, its prevalence rising along with improved human longevity. Early AD diagnosis is key to successful treatment, as currently available therapeutics only allow small benefits for diagnosed AD patients. By contrast, future therapeutics, including those already in preclinical or clinical trials, are expected to afford neuroprotection prior to widespread brain damage and dementia. Brain imaging technologies are developing as promising tools for early AD diagnostics, yet their high cost limits their utility for screening at-risk populations. Blood or plasma transcriptomics, proteomics, and/or metabolomics may pave the way for cost-effective AD risk screening in middle-aged individuals years ahead of cognitive decline. This notion is exemplified by data mining of blood transcriptomics from a published dataset. Consortia blood sample collection and analysis from large cohorts with mild cognitive impairment followed longitudinally for their cognitive state would allow the development of a reliable and inexpensive early AD screening tool.