Serum Soluble Triggering Receptor Expressed on Myeloid Cells 2 as a Biomarker for Incident Dementia: The Hisayama Study

Ann Neurol. 2019 Jan;85(1):47-58. doi: 10.1002/ana.25385. Epub 2018 Dec 28.

Abstract

Objective: To investigate the association between serum soluble triggering receptor expressed on myeloid cells 2 (sTREM2), a soluble type of an innate immune receptor expressed on the microglia, and the risk of dementia.

Methods: A total of 1,349 Japanese community residents aged 60 and older without dementia were followed prospectively for 10 years (2002-2012). Serum sTREM2 levels were quantified by using an enzyme-linked immunosorbent assay and divided into quartiles. Cox proportional hazards model was used to estimate the hazard ratios (HRs) of serum sTREM2 levels on the risk of dementia.

Results: During the follow-up, 300 subjects developed all-cause dementia; 193 had Alzheimer's disease (AD), and 85 had vascular dementia (VaD). The age- and sex-adjusted incidences of all-cause dementia, AD, and VaD elevated significantly with higher serum sTREM2 levels (all p for trend < 0.012). These associations were not altered after adjustment for confounding factors, including high-sensitive C-reactive protein. Subjects with the highest quartile of serum sTREM2 levels had significantly higher multivariable-adjusted risks of developing all-cause dementia, AD, and VaD than those with the lowest quartile (HR = 2.03, 95% confidence interval [CI] = 1.39-2.97, p < 0.001 for all-cause dementia; HR = 1.62, 95% CI = 1.02-2.55, p = 0.04 for AD; HR = 2.85, 95% CI = 1.35-6.02, p = 0.006 for VaD). No significant heterogeneity in the association of serum sTREM2 levels with the development of dementia was observed among the other risk factor subgroups (all p for heterogeneity > 0.11).

Interpretation: The present findings suggest a significant association between increased serum sTREM2 levels and the risk of developing all-cause dementia, AD, and VaD in the general elderly Japanese population. ANN NEUROL 2019;85:47-58.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Biomarkers / blood
  • Dementia / blood*
  • Dementia / diagnosis
  • Dementia / epidemiology*
  • Female
  • Follow-Up Studies
  • Gene Expression
  • Humans
  • Incidence
  • Japan / epidemiology
  • Longitudinal Studies
  • Male
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / blood*
  • Membrane Glycoproteins / genetics
  • Middle Aged
  • Myeloid Cells / metabolism*
  • Prospective Studies
  • Receptors, Immunologic / biosynthesis
  • Receptors, Immunologic / blood*
  • Receptors, Immunologic / genetics
  • Risk Factors

Substances

  • Biomarkers
  • Membrane Glycoproteins
  • Receptors, Immunologic
  • TREM2 protein, human