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A Comprehensive Bibliometric and Visual Analysis of EGR1 in Cardiovascular Disease
Na Dong1,2, Hongmei Yue3,4
1The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.
Insights
Early Growth Response 1 (EGR1) is vital for heart health and disease. This bibliometric analysis maps global research trends and key themes in EGR1 cardiovascular research from 2014-2024.
Area of Science:
- Cardiovascular Research
- Molecular Biology
- Bibliometrics
Background:
- Early Growth Response 1 (EGR1) is a transcription factor regulating critical cellular processes.
- EGR1 is implicated in cardiomyocyte death and cardiovascular diseases, presenting a therapeutic target.
- Understanding the research landscape of EGR1 in cardiovascular disease is essential.
Purpose of the Study:
- To conduct a bibliometric analysis of Early Growth Response 1 (EGR1) research in cardiovascular disease.
- To identify publication trends, leading institutions, authors, and journals.
- To map key research themes and provide a reference for future studies.
Main Methods:
- Bibliometric analysis using Web of Science Core Collection (2014-2024).
- Data retrieval on December 31, 2024.
- Analysis of publication counts, citations, institutions, authors, journals, and keywords.
Main Results:
- 173 publications on EGR1 and cardiovascular disease identified from 2,112 EGR1-related papers.
- Fluctuating research growth observed; China leads in publications and citations.
- Key themes include apoptosis, inflammation, oxidative stress, angiogenesis, and autophagy.
Conclusions:
- The study provides a comprehensive overview of EGR1's role in cardiovascular research.
- Identifies key contributors and emerging research areas.
- Offers a valuable reference for future investigations into EGR1 mechanisms and therapeutic potential in cardiovascular diseases.
Abstract:
Early Growth Response 1 (EGR1) is a crucial transcription factor that regulates diverse cellular processes, including growth, differentiation, proliferation, inflammation, apoptosis, and autophagy. It plays a vital role in maintaining cardiac homeostasis and is deeply implicated in the pathological mechanisms leading to cardiomyocyte death, making it a promising therapeutic target for cardiovascular diseases. To better understand the research landscape of EGR1 in this context, we conducted a bibliometric analysis using data from the Web of Science Core Collection (WoSCC) covering the period from 2014 to 2024, retrieved on 31 December 2024. A total of 2,112 publications related to EGR1 were identified, of which 173 specifically addressed cardiovascular disease and were published across 126 journals. Global research output on this topic has shown fluctuating growth over the past decade, with China contributing the most publications and citations. The Institut national de la santé et de la recherche médicale (Inserm) emerged as the most productive institution. Zhang Y authored the highest number of papers, while Wang J received the most citations. Scientific Reports was the most prolific journal, whereas the Journal of Biological Chemistry was the most influential in terms of citation metrics. Keyword co-occurrence and cluster analysis revealed major research themes such as apoptosis, inflammation, oxidative stress, angiogenesis, and autophagy. These findings provide a comprehensive overview of EGR1-related cardiovascular research and offer a valuable reference for future investigations into its mechanisms and therapeutic potential.
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