Polygenic analysis of inflammatory disease variants and effects on microglia in the aging brain.

Mol Neurodegener
Authors
Keywords
Abstract

BACKGROUND: The role of the innate immune system in Alzheimer's disease (AD) and neurodegenerative disease susceptibility has recently been highlighted in genetic studies. However, we do not know whether risk for inflammatory disease predisposes unaffected individuals to late-life cognitive deficits or AD-related neuropathology. We investigated whether genetic risk scores for seven immune diseases and central nervous system traits were related to cognitive decline (n = 1601), classical AD neuropathology (n = 985), or microglial density (n = 184).

METHODS: Longitudinal cognitive decline, postmortem amyloid and tau neuropathology, microglial density, and gene module expression from bulk brain tissue were all measured in participants from two large cohorts (the Rush Religious Orders Study and Memory and Aging Project; ROS/MAP) of elderly subjects (mean age at entry 78 +/- 8.7 years). We analyzed data primarily using robust regression methods. Neuropathologists were blind to clinical data.

RESULTS: The AD genetic risk scores, including and excluding APOE effects, were strongly associated with cognitive decline in all domains (min P = 3.2 × 10). Multiple sclerosis (MS), Parkinson's disease, and schizophrenia risk did not influence cognitive decline in older age, but the rheumatoid arthritis (RA) risk score alone was significantly associated with microglial density after correction (t = - 3.88, P = 1.6 × 10). Post-hoc tests found significant effects of the RA genetic risk score in multiple regions and stages of microglial activation (min P = 1.5 × 10). However, these associations were driven by only one or two variants, rather than cumulative polygenicity. Further, individual MS (P 

CONCLUSIONS: Our results demonstrate that global risk of inflammatory disease does not strongly influence aging-related cognitive decline but that susceptibility variants that influence peripheral immune function also alter microglial density and immune gene expression in the aging brain, opening a new perspective on the control of microglial and immune responses within the central nervous system. Further study on the molecular mechanisms of peripheral immune disease risk influencing glial cell activation will be required to identify key regulators of these pathways.

Year of Publication
2018
Journal
Mol Neurodegener
Volume
13
Issue
1
Pages
38
Date Published
2018 07 24
ISSN
1750-1326
DOI
10.1186/s13024-018-0272-6
PubMed ID
30041668
PubMed Central ID
PMC6057096
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Grant list
RF1 AG015819 / AG / NIA NIH HHS / United States
R01AG30146 / NH / NIH HHS / United States
R01 AG030146 / AG / NIA NIH HHS / United States
R01NS084965 / NH / NIH HHS / United States
R01 AG017917 / AG / NIA NIH HHS / United States
CIHR / Canada
P30 AG010161 / AG / NIA NIH HHS / United States
R01 NS084965 / NS / NINDS NIH HHS / United States
R01AG15819 / NH / NIH HHS / United States
R01AG17917 / NH / NIH HHS / United States
R01 AG015819 / AG / NIA NIH HHS / United States
P30AG10161 / NH / NIH HHS / United States