sTREM2 and GFAP Mediated the Association of IGF-1 Signaling Biomarkers with Alzheimer's Disease Pathology

J Alzheimers Dis. 2023;92(3):791-797. doi: 10.3233/JAD-220725.

Abstract

Defects in insulin-like growth factor 1 (IGF-1) signaling is a key contributor to Alzheimer's disease (AD). However, the mechanism of how IGF-1 signaling relates to AD remained unclear. Here, we investigated the association of IGF-1 signaling associated biomarkers with AD pathology, sTREM2, and GFAP. Finally, insulin-like growth factor binding protein 2 (IGFBP-2) was associated with AD pathology, and the association was partly medicated by sTREM2 (Aβ42, β= 0.794, p = 0.016; T-tau, β= 0.291, p < 0.001; P-tau181, β= 0.031, p < 0.001) and GFAP (T-tau, β= 0.427, p < 0.001; P-tau181, β= 0.044, p < 0.001). It suggested that sTREM2 and GFAP mediated the relationship between IGF-1 signaling and AD pathology.

Keywords: AD pathology; Alzheimer’s disease; GFAP; IGF-1 signaling; IGFBP-2; sTREM2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease* / pathology
  • Amyloid beta-Peptides
  • Biomarkers
  • Humans
  • Insulin-Like Growth Factor I
  • tau Proteins

Substances

  • Amyloid beta-Peptides
  • Biomarkers
  • Insulin-Like Growth Factor I
  • tau Proteins
  • TREM2 protein, human
  • GFAP protein, human