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Bibliometric analysis of treatment modalities in calcific aortic valve stenosis.

作者信息

He Yang, Yang Yue-Jiao, Wang Zhao-Jun, Tang Liang

机构信息

Department of Cardiovascular Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.

出版信息

Front Pharmacol. 2025 Mar 13;16:1431311. doi: 10.3389/fphar.2025.1431311. eCollection 2025.


DOI:10.3389/fphar.2025.1431311
PMID:40183078
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11966050/
Abstract

BACKGROUND: Calcific aortic valve stenosis (CAVS) is a common cardiovascular condition associated with significant adverse events and high mortality rates. Unfortunately, there are currently no effective pharmacological treatments to halt or prevent its progression. Through our analysis of global trends and treatment strategies, we have identified valuable insights and promising therapeutic possibilities. Additionally, by utilizing bibliometric and visualization techniques, we provide a comprehensive overview of the current research landscape in this field. METHOD: According to our design idea, we used the Web of Science database to select publications on aortic stenosis and related treatments. Through our VOSviewer and CiteSpace analysis, a total of 787 articles have been analyzed by September 2024. We also summarize and explore the most prolific authors, the most prolific countries, and the journals and institutions that publish the most articles. RESULTS: A visual analysis of the collected articles reveals that Canada and the United States have the highest publication volumes in this field. Among institutions, Harvard University in the U.S. leads in publication count, followed by Laval University in Canada and the University of California in the U.S. The top three research hotspots are stenosis, calcification, and progression. The journal with the highest number of publications in this area is Frontiers in Cardiovascular Medicine, followed by Catheterization and Cardiovascular Interventions and Arteriosclerosis, Thrombosis and Vascular Biology. Furthermore, research on CAVS treatment spans various directions and focuses, including therapeutic approaches, pathogenesis, and diagnostic methods. CONCLUSION: Research into CAVS treatment has advanced significantly over the years. While interventional and surgical valve replacement remains the mainstay treatments for aortic stenosis, they are insufficient to fully meet the needs of the patient. Emerging priorities now focus on improving diagnostics, exploring innovative therapies, uncovering disease mechanisms, and developing novel drugs. These findings highlight the evolving demands in this field and underscore the need for continued research to address these challenges.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/c74d1d355ef2/fphar-16-1431311-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/f5ce6adaad7f/fphar-16-1431311-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/a4a7d3aee889/fphar-16-1431311-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/d010e3cefcb8/fphar-16-1431311-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/30c025bc74a1/fphar-16-1431311-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/9cd033af882c/fphar-16-1431311-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/8380686396ba/fphar-16-1431311-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/c74d1d355ef2/fphar-16-1431311-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/f5ce6adaad7f/fphar-16-1431311-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/a4a7d3aee889/fphar-16-1431311-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/d010e3cefcb8/fphar-16-1431311-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/30c025bc74a1/fphar-16-1431311-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/9cd033af882c/fphar-16-1431311-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/8380686396ba/fphar-16-1431311-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a01a/11966050/c74d1d355ef2/fphar-16-1431311-g007.jpg

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本文引用的文献

[1]
Role of Lipoprotein (A) in aortic valve stenosis: Novel disease mechanisms and emerging pharmacotherapeutic approaches.

Int J Cardiol Heart Vasc. 2024-10-30

[2]
The Off-Treatment Effects of Olpasiran on Lipoprotein(a) Lowering: OCEAN(a)-DOSE Extension Period Results.

J Am Coll Cardiol. 2024-8-27

[3]
Grading of Aortic Valve Calcification Severity and Risk Stratification in Aortic Stenosis.

J Am Heart Assoc. 2024-8-6

[4]
Enhancing aortic valve drug delivery with PAR2-targeting magnetic nano-cargoes for calcification alleviation.

Nat Commun. 2024-1-16

[5]
Novel Pharmacological Therapies for the Management of Hyperlipoproteinemia(a).

Int J Mol Sci. 2023-9-3

[6]
Impact of low-density lipoprotein cholesterol on progression of aortic valve sclerosis and stenosis.

Front Cardiovasc Med. 2023-7-17

[7]
The Complex Relationship between Hypoxia Signaling, Mitochondrial Dysfunction and Inflammation in Calcific Aortic Valve Disease: Insights from the Molecular Mechanisms to Therapeutic Approaches.

Int J Mol Sci. 2023-7-5

[8]
Multi-modality imaging in aortic stenosis: an EACVI clinical consensus document.

Eur Heart J Cardiovasc Imaging. 2023-10-27

[9]
Activation of Piezo1 promotes osteogenic differentiation of aortic valve interstitial cell through YAP-dependent glutaminolysis.

Sci Adv. 2023-6-2

[10]
Cardiovascular Calcification Heterogeneity in Chronic Kidney Disease.

Circ Res. 2023-4-14

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