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Fluid Biomarkers and APOE Status of Early Onset Alzheimer's Disease Variants: A Systematic Review and Meta-Analysis.
Kaur, Gurjeet; Poljak, Anne; Braidy, Nady; Crawford, John D; Lo, Jessica; Sachdev, Perminder S.
Afiliação
  • Kaur G; Centre for Healthy Brain Ageing, School of Psychiatry, University of New South Wales, Sydney, NSW, Australia.
  • Poljak A; Centre for Healthy Brain Ageing, School of Psychiatry, University of New South Wales, Sydney, NSW, Australia.
  • Braidy N; Mark Wainwright Analytical Centre, Bioanalytical Mass Spectrometry Facility, University of New South Wales, Sydney, NSW, Australia.
  • Crawford JD; School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.
  • Lo J; Centre for Healthy Brain Ageing, School of Psychiatry, University of New South Wales, Sydney, NSW, Australia.
  • Sachdev PS; Centre for Healthy Brain Ageing, School of Psychiatry, University of New South Wales, Sydney, NSW, Australia.
J Alzheimers Dis ; 75(3): 827-843, 2020.
Article em En | MEDLINE | ID: mdl-32333592
ABSTRACT

BACKGROUND:

Numerous studies have reported on cerebrospinal fluid (CSF) and blood biomarkers of Alzheimer's disease (AD); however, to date, none has compared biomarker patterns across the early-onset subtypes, i.e., early onset sporadic AD (EOsAD) and autosomal dominant AD (ADAD), qualitatively and quantitatively.

OBJECTIVE:

To compare the fluid biomarker patterns in early-onset subtypes of AD; EOsAD and ADAD.

METHODS:

Six scientific databases were searched for peer-reviewed research publications. The total number of individuals used in all the meta-analysis were 2,427, comprised of 1,337 patients and 1,090 controls.

RESULTS:

In the subset of EOsAD cases without APP, PSEN1/PSEN2 mutations, CSF Aß42 and tau levels were higher when compared to the EOsAD group as a whole. Prevalence of the APOEɛ4 allele was more elevated in EOsAD relative to controls, and not significantly elevated in ADAD cases.

CONCLUSION:

Established CSF biomarkers confirmed quantitative differences between variants of EOAD. EOsAD is enriched with APOEɛ4, but the level is not higher than generally reported in late-onset AD. The results prompt further exploration of the etiopathogenesis of EOsAD, which accounts for ∼4-10% of all AD cases, but the reasons for the early onset remain poorly understood.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Doença de Alzheimer Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Doença de Alzheimer Idioma: En Ano de publicação: 2020 Tipo de documento: Article