阿尔茨海默病大脑中Tau蛋白的可视化分析:范围文献综述。

IF 1.9
Dan-Qi Zhang, Xu Yang, Han-Bin Niu, Xu-Chen Sun, Dan-Na Cao, Ang Li, Jin-Huan Yue, Xiao-Ling Li, Qin-Hong Zhang
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引用次数: 0

摘要

本研究分析了阿尔茨海默病(AD)中tau蛋白研究的现状、热点和发展趋势,为今后该领域的研究提供参考。利用CiteSpace软件对Web of Science Core Collection数据库1991 - 2022年AD脑tau蛋白领域相关文章进行科学测量和可视化。方法:共纳入568篇文献,1991 - 2022年,文献数量呈指数增长,平均每年17.8篇。美国是这一领域最多产的国家,占总文献的46.83%。纽约州基础研究所是最具生产力的组织,其次是英国的MRC实验室分子生物学。最有影响力的是伦敦国王学院、加州大学旧金山分校等。伊克巴尔·K是最多产的作家。结果:影响因子最高的期刊为《journal of Biological Chemistry》,影响因子最高的期刊为《Acta neuropath》。累积影响因子最高的期刊是《自然》。研究热点主要集中在tau蛋白配对螺旋细丝的形成和降解机制及异常磷酸化、AD神经原纤维缠结和退行性改变,以及模型研究,主要涉及tau蛋白异常磷酸化、磷酸化位点、去磷酸化、聚集螺旋细丝、神经原纤维缠结小鼠模型。结论:研究前沿趋势主要集中在tau蛋白的病理变化、干预机制的研究以及临床治疗药物的开发与实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visualization Analysis of Tau Protein in the Brain of Alzheimer's Disease: A Scoping Literature Review.

Introduction: This study analyzed the current status, hotspots, and development trends of tau protein research in Alzheimer's disease (AD) and to provide a reference for future research in this field. CiteSpace software was used to scientifically measure and visualize the relevant articles in the field of tau protein in AD brain from the Web of Science Core Collection database from 1991 to 2022.

Methods: A total of 568 articles were included, with an exponential growth in the number of articles published from 1991 to 2022, with an average of 17.8 articles per year. The United States is the most productive country in this field, accounting for 46.83% of the total literature. The New York State Institute for Basic Research is the most productive organization, followed by MRC Laboratory Molecular Biology in the UK. The most influential are Kings College London, University of California, San Francisco, and others. Iqbal K is the most productive author.

Results: The most productive journal is the Journal of Biological Chemistry, and the journal with the highest impact factor is Acta Neuropathologica. The journal with the highest cumulative impact factor is Nature. The research hotspots mainly focus on the formation and degradation mechanisms of tau protein paired helical filaments and abnormal phosphorylation, AD neurofibrillary tangles and degenerative changes, and model research, mainly involving tau protein abnormal phosphorylation, phosphorylation sites, dephosphorylation, aggregate helical filaments, neurofibrillary tangles mouse models.

Conclusion: The research frontier trends mainly focus on the study of pathological changes in tau protein, intervention mechanisms, and the development and practice of clinical therapeutic drugs.

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