A bibliometric and visualization analysis of global trends and frontiers on macrophages in abdominal aortic aneurysms

Liang Zhang1, Dongyu Li2, Shiyang Bao2

  • 1Department of Breast Surgery, Hubei Provincial Clinical Research Center for Breast Cancer, Wuhan Clinical Research Center for Breast Cancer, Hubei Cancer Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

Medicine
|October 29, 2024
PubMed
Abstract

Insights

This bibliometric analysis reveals a growing research landscape on macrophages in abdominal aortic aneurysms (AAA). The United States and China lead, with future directions focusing on animal models and clinical translation.

Area of Science:

  • Immunology
  • Cardiovascular Research
  • Bibliometrics

Background:

  • Macrophages are critical regulators of inflammatory and innate immune responses.
  • Aberrant macrophage expression is linked to abdominal aortic aneurysm (AAA) development.
  • A comprehensive bibliometric analysis of this research area is currently lacking.

Purpose of the Study:

  • To conduct a bibliometric analysis of research on macrophages in abdominal aortic aneurysms (AAA).
  • To map the knowledge landscape and identify research hotspots in this field.

Main Methods:

  • Retrieved 918 publications from the Web of Science Core Collection (2000-2022).
  • Analyzed literature data using CiteSpace and VOSviewer software.

Main Results:

  • Annual publication output shows an increasing trend.
  • China and the United States are the leading contributors, accounting for over 64% of publications.
  • The United States leads in publications, institutions, and researchers; Harvard University is the most productive institution; Arteriosclerosis, Thrombosis, and Vascular Biology published the most articles; Daugherty Alan is the most prolific and cited author.

Conclusions:

  • This study provides valuable insights into the research status and trends of macrophages in AAA.
  • Identified future research directions include animal models, inflammatory microenvironments, immune mechanisms, clinical translation, and molecular imaging.