Interleukin-6 promoter polymorphism: risk and pathology of Alzheimer's disease

Y Zhang, A Hayes, Antonia Pritchard, U Thaker, Mohammad Haque, Judith Harris, J-C Lambert, Corinne Lendon

    Research output: Contribution to journalArticle

    34 Citations (Scopus)

    Abstract

    Inflammatory and immune responses are involved in the pathogenesis of Alzheimer's disease (AD). Interleukin-6 (IL-6), an inflammatory cytokine, is thought to play a role in neurodegeneration of the central nervous system and has been associated with increased amyloid precursor protein expression in vitro and greater cognitive decline. Previously a C-174G polymorphism in the promoter of IL-6, which influences expression in vitro, has been found associated in some studies but not all. We investigated this polymorphism in a large independent UK sample of AD cases (n = 356) and controls (n 434) but found no association. We extended the study to genotype/phenotype correlations but found no correlation with age of onset (n = 338), brain amyloid load (n = 126) or Tau load (n = 101), brain microglial cell load (n = 65) or brain reactive astrocytes (n = 127). Our data do not support a pathogenic role in AD for the C-174G polymorphism in isolation.
    Original languageEnglish
    Pages (from-to)99-102
    Number of pages4
    JournalNeuroscience Letters
    Volume362
    Issue number2
    DOIs
    Publication statusPublished - 1 Jan 2004

    Keywords

    • promoter
    • polymorphism
    • microglial cell load
    • amyloid load
    • Alzheimer's disease
    • interleukin-6
    • brain
    • reactive astrocytes

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