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用于阿尔茨海默病研究的人类诱导多能干细胞模型:一项文献计量分析

Human induced pluripotent stem cell models for Alzheimer's disease research: a bibliometric analysis.

作者信息

Sun Yuning, Liu Zhilong, Zhang Zongbo, Kang Yufeng, Wang Xinlian, Zhang Yiping, Liu Yan, Zhao Pei

机构信息

School of Pharmacy, Gansu University of Chinese Medicine, Lanzhou, China.

Gansu Provincial People's Hospital, Lanzhou, China.

出版信息

Front Hum Neurosci. 2025 Mar 19;19:1548701. doi: 10.3389/fnhum.2025.1548701. eCollection 2025.

Abstract

INTRODUCTION

Alzheimer's disease (AD), the leading cause of dementia, remains without adequate treatment. Current models do not fully replicate human physiology and pathology. The advent of human induced pluripotent stem cell (hiPSC) technology offers a novel approach to studying AD.

METHODS

Our study conducted a bibliometric analysis to assess the application and development of hiPSC technology in AD research. We retrieved 531 articles on hiPSC models of AD from the Web of Science Core Collection, published between January 2010 and June 2024. CiteSpace and VOSviewer were used to analyze authorship, geographic contributions, journal influence, and citation patterns.

RESULTS

Our findings reveal a steady increase in publications over 14 years, with the United States leading in contributions, followed by China. Li-Huei Tsai from the Massachusetts Institute of Technology is a prominent researcher. emerges as the most influential journal. Research trends have focused on inflammation, astrocytes, microglia, apolipoprotein E (ApoE), and tau.

DISCUSSION

Bibliometric analysis is crucial in identifying research gaps and trends and guiding future studies to address unmet needs in understanding and modeling human physiology and pathology. Leveraging hiPSC models to investigate the molecular mechanisms of familial and sporadic AD is expected to provide a crucial foundation for developing future treatment strategies.

CONCLUSION

In summary, the bibliometric findings from this study provide a comprehensive overview of the current research landscape in hiPSC models for AD. It also highlights emerging trends and research gaps, crucial for guiding future research efforts, particularly in exploring novel therapeutic targets and improving understanding of disease mechanisms.

摘要

引言

阿尔茨海默病(AD)是痴呆症的主要病因,目前仍缺乏有效的治疗方法。现有的模型无法完全复制人类的生理和病理状态。人类诱导多能干细胞(hiPSC)技术的出现为研究AD提供了一种新方法。

方法

我们的研究进行了文献计量分析,以评估hiPSC技术在AD研究中的应用和发展。我们从科学网核心合集检索了2010年1月至2024年6月期间发表的531篇关于AD的hiPSC模型的文章。使用CiteSpace和VOSviewer分析作者身份、地理贡献、期刊影响力和引用模式。

结果

我们的研究结果显示,在14年的时间里,出版物数量稳步增加,美国的贡献最大,其次是中国。麻省理工学院的蔡理慧是一位杰出的研究人员。《》成为最具影响力的期刊。研究趋势集中在炎症、星形胶质细胞、小胶质细胞、载脂蛋白E(ApoE)和tau蛋白上。

讨论

文献计量分析对于识别研究差距和趋势以及指导未来研究以满足在理解和模拟人类生理和病理方面未满足的需求至关重要。利用hiPSC模型研究家族性和散发性AD的分子机制有望为未来治疗策略的开发提供关键基础。

结论

总之,本研究的文献计量结果全面概述了目前AD的hiPSC模型的研究现状。它还突出了新出现的趋势和研究差距,这对于指导未来的研究工作至关重要,特别是在探索新的治疗靶点和增进对疾病机制的理解方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c096/11962003/0bfac2295f16/fnhum-19-1548701-g001.jpg

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