A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains

  • Patrick C.G. Haddick
  • , Jessica L. Larson
  • , Nisha Rathore
  • , Tushar R. Bhangale
  • , Qui T. Phung
  • , Karpagam Srinivasan
  • , David V. Hansen
  • , Jennie R. Lill
  • , Margaret A. Pericak-Vance
  • , Jonathan Haines
  • , Lindsay A. Farrer
  • , John S. Kauwe
  • , Gerard D. Schellenberg
  • , Carlos Cruchaga
  • , Alison M. Goate
  • , Timothy W. Behrens
  • , Ryan J. Watts
  • , Robert R. Graham
  • , Joshua S. Kaminker
  • , Marcel Van Der Brug

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

The common p.D358A variant (rs2228145) in IL-6R is associated with risk for multiple diseases and with increased levels of soluble IL-6R in the periphery and central nervous system (CNS). Here, we show that the p.D358A allele leads to increased proteolysis of membrane bound IL-6R and demonstrate that IL-6R peptides with A358 are more susceptible to cleavage by ADAM10 and ADAM17. IL-6 responsive genes were identified in primary astrocytes and microglia and an IL-6 gene signature was increased in the CNS of late onset Alzheimer's disease subjects in an IL6R allele dependent manner. We conducted a screen to identify variants associated with the age of onset of Alzheimer's disease in APOE ϵ4 carriers. Across five datasets, p.D358A had a meta P 3 ×10-4 and an odds ratio 1.3, 95 confidence interval 1.12-1.48. Our study suggests that a common coding region variant of the IL-6 receptor results in neuroinflammatory changes that may influence the age of onset of Alzheimer's disease in APOE ϵ4 carriers.

Original languageEnglish
Pages (from-to)1037-1054
Number of pages18
JournalJournal of Alzheimer's Disease
Volume56
Issue number3
DOIs
StatePublished - 2017

Keywords

  • Alzheimer's disease
  • IL-6
  • astrocytes
  • metalloproteases
  • microglia

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