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阿尔茨海默病中的线粒体自噬:2007年至2022年的文献计量分析

Mitophagy in Alzheimer's Disease: A Bibliometric Analysis from 2007 to 2022.

作者信息

Wang Hongqi, Yan Xiaodong, Zhang Yiming, Wang Peifu, Li Jilai, Zhang Xia

机构信息

Department of Neurology, Peking University Aerospace School of Clinical Medicine, Aerospace Center Hospital, Beijing, China.

Department of Anatomy, Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.

出版信息

J Alzheimers Dis Rep. 2024 Jan 29;8(1):101-128. doi: 10.3233/ADR-230139. eCollection 2024.


DOI:10.3233/ADR-230139
PMID:38312534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10836605/
Abstract

BACKGROUND: The investigation of mitophagy in Alzheimer's disease (AD) remains relatively underexplored in bibliometric analysis. OBJECTIVE: To delve into the progress of mitophagy, offering a comprehensive overview of research trends and frontiers for researchers. METHODS: Basic bibliometric information, targets, and target-drug-clinical trial-disease extracted from publications identified in the Web of Science Core Collection from 2007 to 2022 were assessed using bibliometric software. RESULTS: The study encompassed 5,146 publications, displaying a consistent 16-year upward trajectory. The United States emerged as the foremost contributor in publications, with the ' being the most prolific journal. P. Hemachandra Reddy, George Perry, and Xiongwei Zhu are the top 3 most prolific authors. PINK1 and Parkin exhibited an upward trend in the last 6 years. Keywords (e.g., insulin, aging, epilepsy, tauopathy, and mitochondrial quality control) have recently emerged as focal points of interest within the past 3 years. "Mitochondrial dysfunction" is among the top terms in disease clustering. The top 10 drugs/molecules (e.g., curcumin, insulin, and melatonin) were summarized, accompanied by their clinical trials and related targets. CONCLUSIONS: This study presents a comprehensive overview of the mitophagy research landscape in AD over the past 16 years, underscoring mitophagy as an emerging molecular mechanism and a crucial focal point for potential drug in AD. This study pioneers the inclusion of targets and their correlations with drugs, clinical trials, and diseases in bibliometric analysis, providing valuable insights and inspiration for scholars and readers of JADR interested in understanding the potential mechanisms and clinical trials in AD.

摘要

背景:在文献计量分析中,阿尔茨海默病(AD)中细胞线粒体自噬的研究仍相对未得到充分探索。 目的:深入探究细胞线粒体自噬的进展,为研究人员提供研究趋势和前沿的全面概述。 方法:使用文献计量软件评估从2007年至2022年在科学网核心合集中识别出的出版物中提取的基本文献计量信息、靶点以及靶点-药物-临床试验-疾病。 结果:该研究涵盖5146篇出版物,呈现出持续16年的上升趋势。美国是出版物的首要贡献者,《》是发文量最多的期刊。P. Hemachandra Reddy、George Perry和Xiongwei Zhu是发文量排名前三的作者。PINK1和Parkin在过去6年呈上升趋势。关键词(如胰岛素、衰老、癫痫、tau蛋白病和线粒体质量控制)在过去3年中已成为新的关注焦点。“线粒体功能障碍”是疾病聚类中的高频术语之一。总结了排名前十的药物/分子(如姜黄素、胰岛素和褪黑素)及其临床试验和相关靶点。
结论:本研究全面概述了过去16年AD中细胞线粒体自噬的研究概况,强调细胞线粒体自噬是一种新兴的分子机制,也是AD潜在药物的关键焦点。本研究率先在文献计量分析中纳入靶点及其与药物、临床试验和疾病的相关性,为对AD潜在机制和临床试验感兴趣的《阿尔茨海默病研究与治疗》学者和读者提供了有价值的见解和启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/e5a772cd7c13/adr-8-adr230139-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/6352e8d75daa/adr-8-adr230139-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/c91a5bf49d00/adr-8-adr230139-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/310ae0b481ae/adr-8-adr230139-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/e5a772cd7c13/adr-8-adr230139-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/6352e8d75daa/adr-8-adr230139-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/820ff98ef882/adr-8-adr230139-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/3f2e73e482e3/adr-8-adr230139-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/42ba7724ee4d/adr-8-adr230139-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/644cace12bd4/adr-8-adr230139-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/38c090d703bf/adr-8-adr230139-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/c91a5bf49d00/adr-8-adr230139-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/310ae0b481ae/adr-8-adr230139-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9937/10836605/e5a772cd7c13/adr-8-adr230139-g009.jpg

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本文引用的文献

[1]
Two Phase 3 Trials of Gantenerumab in Early Alzheimer's Disease.

N Engl J Med. 2023-11-16

[2]
Glial-derived mitochondrial signals affect neuronal proteostasis and aging.

Sci Adv. 2023-10-13

[3]
Donanemab in Early Symptomatic Alzheimer Disease: The TRAILBLAZER-ALZ 2 Randomized Clinical Trial.

JAMA. 2023-8-8

[4]
Trial of Solanezumab in Preclinical Alzheimer's Disease.

N Engl J Med. 2023-9-21

[5]
Role of neuroinflammation in neurodegeneration development.

Signal Transduct Target Ther. 2023-7-12

[6]
Research in the genetics of pheochromocytoma and paraganglioma: a bibliometric analysis from 2002 to 2022.

Clin Exp Med. 2023-11

[7]
2023 Alzheimer's disease facts and figures.

Alzheimers Dement. 2023-4

[8]
Autoimmune diseases and gut microbiota: a bibliometric and visual analysis from 2004 to 2022.

Clin Exp Med. 2023-10

[9]
Multi-Targeting Intranasal Nanoformulation as a Therapeutic for Alzheimer's Disease.

Biomolecules. 2023-1-25

[10]
Thirty years of research on negative symptoms of schizophrenia: A scientometric analysis of hotspots, bursts, and research trends.

Neurosci Biobehav Rev. 2023-1

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