过去至 2023 年阿尔茨海默病中铁细胞增多症、坏死性细胞增多症和热细胞增多症的全球研究趋势和热点:文献计量学综述》。

IF 2.8 Q2 NEUROSCIENCES Journal of Alzheimer's disease reports Pub Date : 2024-01-29 eCollection Date: 2024-01-01 DOI:10.3233/ADR-230092
Jianishaya Yeerlan, Binhong He, Xianliang Hu, LuShun Zhang
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引用次数: 0

摘要

背景:阿尔茨海默病(AD)是一种遗传复杂的神经退行性疾病。有关 "AD 中的铁蜕变"、"AD 中的热蜕变 "和 "AD 中的坏死 "的研究越来越多,越来越多的证据表明它们与 AD 密切相关。然而,目前尚未对这一主题进行基于文献计量学的深入研究:本研究采用文献计量学方法对 AD 中三种不同类型的细胞死亡领域的文献进行可视化分析,并探讨当前的研究热点和未来的研究方向:我们从Web of Science中收集了相关文章,并使用CiteSpace、VOS viewer和Pajek进行了可视化分析:结果:以 "AD 中的铁突变"、"AD 中的热突变 "和 "AD 中的坏死 "为主题的文章分别为 123 篇、95 篇和 84 篇。根据关键词分析,我们可以发现 "氧化应激 "和 "脂质过氧化"、"细胞死亡 "和 "激活"、"Nlrp3炎性体 "和 "激活 "分别是 "AD中的铁蛋白沉积"、"AD中的热蛋白沉积 "和 "AD中的坏死 "领域最突出的三个词。针对关键词分析中的突围词,我们回顾了 AD 中铁细胞增多症、裂解症和坏死症的机制。通过绘制关键词的时区图,我们推测了 AD 中铁变病、热变病和坏死病的演变趋势:我们的研究结果有助于研究人员掌握 AD 中三种细胞死亡的研究现状,并尽快确定未来研究的新方向。
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Global Research Trends and Hotspots for Ferroptosis, Necroptosis, and Pyroptosis in Alzheimer's Disease from the Past to 2023: A Combined Bibliometric Review.

Background: Alzheimer's disease (AD) is a genetically intricate neurodegenerative disorder. Studies on "Ferroptosis in AD", "Pyroptosis in AD", and "Necroptosis in AD" are becoming more prevalent and there is increasing evidence that they are closely related to AD. However, there has not yet been a thorough bibliometrics-based investigation on this subject.

Objective: This study uses a bibliometric approach to visualize and analyze the literature within the field of three distinct types of cell death in AD and explores the current research hotspots and prospective research directions.

Methods: We collected relevant articles from the Web of Science and used CiteSpace, VOS viewer, and Pajek to perform a visual analysis.

Results: A total of 123, 95, and 84 articles were published in "Ferroptosis in AD", "Pyroptosis in AD", and "Necroptosis in AD", respectively. Based on keywords analysis, we can observe that "oxidative stress" and "lipid peroxidation", "cell death" and "activation", and "Nlrp3 inflammasome" and "activation" were the three most prominent words in the field of "Ferroptosis in AD", "Pyroptosis in AD", and "Necroptosis in AD", respectively. Focusing on the breakout words in the keyword analysis, we reviewed the mechanisms of ferroptosis, pyroptosis, and necroptosis in AD. By mapping the time zones of the keywords, we speculated on the evolutionary trends of ferroptosis, pyrotosis, and necroptosis in AD.

Conclusions: Our findings can help researchers grasp the research status of three types of cell death in AD and determine new directions for future research as soon as possible.

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