Comprehensive Bibliometric Analysis of Stem Cell Research in Alzheimer's Disease from 2004 to 2022.

IF 2.2 4区 医学 Q3 CLINICAL NEUROLOGY Dementia and Geriatric Cognitive Disorders Pub Date : 2023-01-01 DOI:10.1159/000528886
Rui Wang, Yi Zhu, Lan-Fang Qin, Zhi-Guo Xu, Xi-Ren Gao, Chong-Bin Liu, Guo-Tong Xu, Yi-Zhu Chen
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引用次数: 7

Abstract

Introduction: Stem cell-based regenerative medicine has provided an excellent opportunity to investigate therapeutic strategies and innovative treatments for Alzheimer's disease (AD). However, there is an absence of visual overviews to assess the published literature systematically.

Methods: In this review, the bibliometric approach was used to estimate the searched data on stem cell research in AD from 2004 to 2022, and we also utilized CiteSpace and VOSviewer software to evaluate the contributions and co-occurrence relationships of different countries/regions, institutes, journals, and authors as well as to discover research hot spots and encouraging future trends in this field.

Results: From 2004 to 2022, a total of 3,428 publications were retrieved. The number of publications and citations on stem cell research in AD has increased dramatically in the last nearly 20 years, especially since 2016. North America and Asia were the top 2 highest output regions. The leading country in terms of publications and access to collaborative networks was the USA. Centrality analysis revealed that the UCL (0.05) was at the core of the network. The Journal of Alzheimer's Disease (n = 102, 2.98%) was the most productive academic journal. The analyses of keyword burst detection indicated that exosomes, risk factors, and drug delivery only had burst recently. Citations and co-citation achievements clarified that cluster #0 induced pluripotent stem cells, #2 mesenchymal stem cells, #3 microglia, and #6 adult hippocampal neurogenesis persisted to recent time.

Conclusion: This bibliometric analysis provides a comprehensive guide for clinicians and scholars working in this field. These analysis and results hope to provide useful information and references for future understanding of the challenges behind translating underlying stem cell biology into novel clinical therapeutic potential in AD.

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2004 - 2022年阿尔茨海默病干细胞研究的综合文献计量学分析。
基于干细胞的再生医学为研究阿尔茨海默病(AD)的治疗策略和创新治疗提供了极好的机会。然而,缺乏可视化的概述来系统地评估已发表的文献。方法:采用文献计量学方法对2004 - 2022年AD期刊中干细胞研究的检索数据进行估算,并利用CiteSpace和VOSviewer软件对不同国家/地区、机构、期刊和作者的贡献和共现关系进行评价,发现该领域的研究热点,展望未来发展趋势。结果:2004 - 2022年共检索文献3428篇。近20年来,特别是2016年以来,关于AD干细胞研究的出版物和引用数量急剧增加。北美和亚洲是产量最高的两个地区。在出版物和获取合作网络方面领先的国家是美国。中心性分析显示,UCL(0.05)是网络的核心。《阿尔茨海默病杂志》(n = 102, 2.98%)是生产力最高的学术期刊。关键词爆发检测分析表明外泌体、危险因素和药物传递最近才爆发。引用和共引用的成果表明,第0组诱导的多能干细胞、第2组诱导的间充质干细胞、第3组诱导的小胶质细胞和第6组诱导的成体海马神经发生一直持续到最近。结论:本文的文献计量分析为临床医生和从事该领域工作的学者提供了全面的指导。这些分析和结果希望为今后理解将潜在干细胞生物学转化为阿尔茨海默病新的临床治疗潜力背后的挑战提供有用的信息和参考。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
46
审稿时长
2 months
期刊介绍: As a unique forum devoted exclusively to the study of cognitive dysfunction, ''Dementia and Geriatric Cognitive Disorders'' concentrates on Alzheimer’s and Parkinson’s disease, Huntington’s chorea and other neurodegenerative diseases. The journal draws from diverse related research disciplines such as psychogeriatrics, neuropsychology, clinical neurology, morphology, physiology, genetic molecular biology, pathology, biochemistry, immunology, pharmacology and pharmaceutics. Strong emphasis is placed on the publication of research findings from animal studies which are complemented by clinical and therapeutic experience to give an overall appreciation of the field.
期刊最新文献
Toolkit to Examine Lifelike Language (TELL) v.2.0: Optimizing speech biomarkers of neurodegeneration. Current Advances in Computerised Cognitive Assessment for Mild Cognitive Impairment and Dementia in Older Adults: A systematic Review. Risperidone for the Treatment of Dementia-Related Psychosis: A Systematic Review and Meta-Analysis. Differential Item Functioning and Clinical Utility of the Subjective Memory Complaints Questionnaire in a Multi-Ethnic Cohort. Efficacy of acetylcholinesterase inhibitors in the logopenic variant of primary progressive aphasia.
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