# Bibliometric analysis of research hotspots and emerging trends in mitophagy and atherosclerosis (2004–2024)

**Authors:** Shuchen Ding, He Zhang, Luxia Song, Xinyi Wang, Lifang Song, Wende Tian, Xuanye Chen, Hao Xu

PMC · DOI: 10.3389/fmed.2025.1621079 · Frontiers in Medicine · 2025-07-25

## TL;DR

This paper analyzes research trends in mitophagy and atherosclerosis from 2004 to 2024, identifying key contributors, hotspots, and future directions.

## Contribution

A comprehensive bibliometric analysis of mitophagy and atherosclerosis research, revealing emerging trends and intellectual landscapes.

## Key findings

- Annual publications on mitophagy and atherosclerosis show an overall increasing trend.
- Key research hotspots include NF κB, NLRP3 inflammasome, and mitochondrial DNA.
- Leading contributors are from the United States and China, with Orekhov AN being a prominent researcher.

## Abstract

Mitophagy is closely involved in the onset, progression and pathological mechanisms of atherosclerosis. This study set out to provide a comprehensive overview and identify emerging research trends in the field.

A systematic literature retrieval was conducted across the Web of Science Core Collection (WoSCC) for publications spanning 2004 to 2024. Bibliometric analyses and knowledge mapping were performed utilizing CiteSpace, VOSviewer, R-Bibliometrix, Scimago Graphica and Excel to evaluate the intellectual landscape of the field.

The analysis reveals a fluctuating but overall increasing trend in annual publications. The United States and China are the primary contributors to the body of research, with leading institutions predominantly located in China, the United States, and Russia. Notably, the works of Orekhov AN stand out in terms of both quantity and quality. The most cited studies is Forrester SJ’s 2018 publication in Circulation Research. Additionally, keyword analysis highlights the prevailing research hotspots, including: (1) key molecules such as NF κB, NLRP3 inflammasome, and mitochondrial DNA; (2) critical pathological processes such as oxidative stress, mitochondrial dysfunction, and mitochondrial dynamics; and (3) and the role of mitophagy within vascular smooth muscle cells, endothelial cells, and macrophages in the pathogenesis of atherosclerosis.

The study of mitophagy in atherosclerosis has garnered increasing attention, with substantial progress made in understanding its molecular and cellular mechanisms. This work highlights the current research hotspots and identifies prospective directions for future exploration. Further investigation into the intricate mechanisms governing mitophagy may uncover novel therapeutic strategies that could mitigate the progression of atherosclerosis.

## Linked entities

- **Diseases:** atherosclerosis (MONDO:0005311)

## Full-text entities

- **Genes:** NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** mitochondrial dysfunction (MESH:D028361), atherosclerosis (MESH:D050197)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12331740/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12331740/full.md

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Source: https://tomesphere.com/paper/PMC12331740