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可视化2000年至2022年间巨噬细胞相关糖尿病研究的时间动态和研究趋势:一项文献计量分析

Visualizing temporal dynamics and research trends of macrophage-related diabetes studies between 2000 and 2022: a bibliometric analysis.

作者信息

Wang Sicheng, Zhang Lili, Jin Zishan, Wang Yayun, Zhang Boxun, Zhao Linhua

机构信息

Institute of Metabolic Diseases, Guang' Anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Graduate School, Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Immunol. 2023 Jul 26;14:1194738. doi: 10.3389/fimmu.2023.1194738. eCollection 2023.

DOI:10.3389/fimmu.2023.1194738
PMID:37564641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10410279/
Abstract

BACKGROUND

Macrophages are considered an essential source of inflammatory cytokines, which play a pivotal role in the development of diabetes and its sequent complications. Therefore, a better understanding of the intersection between the development of diabetes and macrophage is of massive importance.

OBJECTIVES

In this study, we performed an informative bibliometric analysis to enlighten relevant research directions, provide valuable metrics for financing decisions, and help academics to gain a quick understanding of the current macrophage-related diabetes studies knowledge domain.

METHODS

The Web of Science Core Collection database was used for literature retrieval and dataset export. Bibliometrix R-package was performed to conduct raw data screening, calculating, and visualizing.

RESULTS

Between 2000 and 2022, the annual publication and citation trends steadily increased. Wu Yonggui was the scholar with the most published papers in this field. The institute with the highest number of published papers was the University of Michigan. The most robust academic collaboration was observed between China and the United States of America. was the journal that published the most relevant publications. The author's keywords with the highest occurrences were "inflammation", "diabetic nephropathy", and "obesity". In addition, "Macrophage polarization" was the current motor topic with potential research prospects.

CONCLUSIONS

These comprehensive and visualized bibliometric results summarized the significant findings in macrophage-related diabetes studies over the past 20 years. It would enlighten subsequent studies from a macro viewpoint and is also expected to strengthen investment policies in future macrophage-related diabetes studies.

摘要

背景

巨噬细胞被认为是炎症细胞因子的重要来源,在糖尿病及其后续并发症的发展中起关键作用。因此,更好地理解糖尿病发展与巨噬细胞之间的交叉点至关重要。

目的

在本研究中,我们进行了一项信息丰富的文献计量分析,以阐明相关研究方向,为资助决策提供有价值的指标,并帮助学者快速了解当前巨噬细胞相关糖尿病研究的知识领域。

方法

使用科学网核心合集数据库进行文献检索和数据集导出。利用Bibliometrix R包进行原始数据筛选、计算和可视化。

结果

2000年至2022年间,年度发表量和被引趋势稳步上升。吴永贵是该领域发表论文最多的学者。发表论文数量最多的机构是密歇根大学。中美之间的学术合作最为密切。 是发表相关出版物最多的期刊。出现频率最高的作者关键词是“炎症”、“糖尿病肾病”和“肥胖”。此外,“巨噬细胞极化”是当前具有潜在研究前景的热门话题。

结论

这些全面且可视化的文献计量结果总结了过去20年巨噬细胞相关糖尿病研究的重要发现。它将从宏观角度启发后续研究,也有望加强未来巨噬细胞相关糖尿病研究的投资政策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/549e0bc84fcc/fimmu-14-1194738-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/27b6caf43440/fimmu-14-1194738-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/da6ea025964a/fimmu-14-1194738-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/4de01105dd61/fimmu-14-1194738-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/d943d316ec5f/fimmu-14-1194738-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/c75f65934494/fimmu-14-1194738-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/fa8512284400/fimmu-14-1194738-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/2d4702f0da81/fimmu-14-1194738-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/d3568a8667ba/fimmu-14-1194738-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/af9911a0ff87/fimmu-14-1194738-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/fc99a43507d3/fimmu-14-1194738-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/549e0bc84fcc/fimmu-14-1194738-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/27b6caf43440/fimmu-14-1194738-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/da6ea025964a/fimmu-14-1194738-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/4de01105dd61/fimmu-14-1194738-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/d943d316ec5f/fimmu-14-1194738-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/c75f65934494/fimmu-14-1194738-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/fa8512284400/fimmu-14-1194738-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/2d4702f0da81/fimmu-14-1194738-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/d3568a8667ba/fimmu-14-1194738-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/af9911a0ff87/fimmu-14-1194738-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/fc99a43507d3/fimmu-14-1194738-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb2d/10410279/549e0bc84fcc/fimmu-14-1194738-g011.jpg

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