Li Juanqin, Wang Yanli, Huang Jing, Gong Daokai
Department of Neurology, Jingzhou Hospital Affiliated to Yangtze University, Jingzhou, China.
Hubei Provincial Clinical Research Center for Parkinson's Disease, Xiangyang, China.
Front Aging Neurosci. 2024 Aug 30;16:1433325. doi: 10.3389/fnagi.2024.1433325. eCollection 2024.
Ferroptosis is a crucial pathogenic mechanism in Parkinson's disease, offering significant potential for pharmacological intervention. Despite its importance, the number of bibliometric analyses examining the relationship between ferroptosis and Parkinson's disease remains limited. This study aims to elucidate the knowledge structure and primary research focuses within this field using various bibliometric tools search.
We conducted a comprehensive literature son ferroptosis in Parkinson's disease using the Web of Science Core Collection database. Bibliometric analyses and visualizations were performed with VOSviewer, examining the geographical and institutional distribution of publications, journal interconnections, and keyword prevalence. Furthermore, CiteSpace was used to visually explore and analyze journal interactions and citation dynamics. The bibliometrix R package facilitated the delineation of collaborative networks across different countries and the construction of visual network representations illustrating relationships among authors, keywords, and journals. Data visualization was further enhanced with Microsoft Office Excel 2021.
Recently, there has been a significant increase in publications on ferroptosis, with China emerging as a leading contributor in this research area. Keyword analysis highlights the critical role of ferroptosis in the pathogenesis of Parkinson's disease, identifying GPX4 as a key enzyme mitigating lipid peroxidation. This study also elucidates the connections and distinctions between ferroptosis and other cell death processes such as apoptosis, autophagy, and pyroptosis. Current research primarily focuses on immunotherapy, prognosis, oxidative stress, lipid peroxidation, and the tumor microenvironment.
This study provides a comprehensive initial analysis of the research landscape, identifying current focal points and potential future directions for ferroptosis research in Parkinson's disease. The findings leverage a variety of bibliometric methodologies to offer valuable insights into this emerging field.
铁死亡是帕金森病的一种关键致病机制,为药物干预提供了巨大潜力。尽管其重要性,但研究铁死亡与帕金森病之间关系的文献计量分析数量仍然有限。本研究旨在使用各种文献计量工具搜索来阐明该领域的知识结构和主要研究重点。
我们使用科学网核心合集数据库对帕金森病中铁死亡的文献进行了全面检索。使用VOSviewer进行文献计量分析和可视化,研究出版物的地理和机构分布、期刊互联情况以及关键词流行度。此外,使用CiteSpace直观地探索和分析期刊互动及引文动态。bibliometrix R包有助于描绘不同国家之间的合作网络,并构建可视化网络表示,展示作者、关键词和期刊之间的关系。使用Microsoft Office Excel 2021进一步增强了数据可视化效果。
最近,关于铁死亡的出版物显著增加,中国已成为该研究领域的主要贡献者。关键词分析突出了铁死亡在帕金森病发病机制中的关键作用,确定谷胱甘肽过氧化物酶4(GPX4)是减轻脂质过氧化的关键酶。本研究还阐明了铁死亡与其他细胞死亡过程(如凋亡、自噬和焦亡)之间的联系与区别。当前研究主要集中在免疫治疗、预后、氧化应激、脂质过氧化和肿瘤微环境方面。
本研究对该研究领域进行了全面的初步分析,确定了帕金森病中铁死亡研究的当前重点和潜在的未来方向。研究结果利用了多种文献计量方法,为这个新兴领域提供了有价值的见解。