TREM2 in Alzheimer's disease: A global bibliometric analysis of research evolution and therapeutic implications

Linjing Cui1, Zhang Yue2, Chen Sun3

  • 1Department of Clinical Laboratory, Changzhou Hospital of Traditional Chinese Medicine, Changzhou, China.

Abstract

Insights

This bibliometric analysis reveals a growing research focus on Triggering Receptor Expressed on Myeloid Cells 2 (TREM2) in Alzheimer's disease (AD). Key areas include neuroinflammation, genetics, and microglia, with emerging trends in protein interactions and cognitive impairment.

Area of Science:

  • Neuroscience
  • Immunology
  • Genetics

Background:

  • Triggering Receptor Expressed on Myeloid Cells 2 (TREM2) is a microglial receptor genetically linked to Alzheimer's disease (AD).
  • TREM2 is recognized as a key regulator of neuroinflammation in the central nervous system.
  • The global research landscape of TREM2 in AD requires comprehensive bibliometric analysis.

Purpose of the Study:

  • To conduct a bibliometric analysis of TREM2 research in Alzheimer's disease.
  • To identify major research themes, development trends, and prospects.
  • To visualize the scientific landscape of TREM2 and AD research.

Main Methods:

  • Bibliometric analysis of 944 publications from 2000-2024 in the Web of Science Core Collection.
  • Utilized tools including GraphPad Prism 9, CiteSpace, VOSviewer, and Metascape.
  • Screened and selected relevant articles focusing on TREM2 and AD.

Main Results:

  • Research on TREM2 and AD shows a consistent upward trend, peaking in 2021-2022.
  • The United States and China are leading in publications, with Washington University as a top institution.
  • Key research areas include molecular biology, genetics, and neuroimmunology, with keywords like microglia, inflammation, and genetic variants.

Conclusions:

  • This study provides a clear overview of TREM2 research in AD using bibliometric analysis.
  • Identified major research themes and emerging topics such as protein interactions and cognitive impairment.
  • Highlights the evolving trends and future prospects in TREM2-related AD research.