人工智能为罕见疾病赋能:过去二十年的文献计量学视角

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Peiling Ou, Ru Wen, Linfeng Shi, Jian Wang, Chen Liu
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引用次数: 0

摘要

对人工智能(AI)在罕见病(RDs)中的应用进行全面的文献计量分析,重点是分析出版物产出、按国家确定主要贡献者、评估国际合作的程度、跟踪研究热点的出现以及通过关键词突变检测趋势。在这项文献计量学研究中,我们从 "科学网"(WoS)上确定并检索了 2003 年至 2023 年期间有关人工智能在研发中的应用的出版物。我们进行了全球研究格局分析,并利用 CiteSpace 对这一领域进行了关键词聚类和突发性检测。本研究共收录了 1501 篇出版物。人工智能在研发领域的应用发展经历了三个阶段:起步期(2003-2010 年)、稳定发展期(2011-2018 年)和加速增长期(2019-2023 年),反映了该领域在研究期间日益增长的重要性和影响力。这些研究来自 85 个国家,其中美国的贡献最大。"突变"、"诊断 "和 "管理 "是出现频率最高的三个关键词。关键词聚类分析发现,基因鉴定、有效管理和个性化治疗是人工智能应用于 RD 的三个主要研究领域。此外,关键词突发检测表明,人们对 "生物标记"、"预测模型 "和 "数据挖掘 "等领域的兴趣日益浓厚,凸显了这些领域塑造未来研究方向的潜力。二十多年来,人工智能在区域发展中的应用研究取得了令人瞩目的进展,发展成果喜人。推进国际跨界合作至关重要。人工智能的应用将在RDs管理的各个领域发挥更加关键的作用,包括快速诊断、个性化治疗、药物开发、数据整合与共享以及持续监测与护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Artificial intelligence empowering rare diseases: a bibliometric perspective over the last two decades
To conduct a comprehensive bibliometric analysis of the application of artificial intelligence (AI) in Rare diseases (RDs), with a focus on analyzing publication output, identifying leading contributors by country, assessing the extent of international collaboration, tracking the emergence of research hotspots, and detecting trends through keyword bursts. In this bibliometric study, we identified and retrieved publications on AI applications in RDs spanning 2003 to 2023 from the Web of Science (WoS). We conducted a global research landscape analysis and utilized CiteSpace to perform keyword clustering and burst detection in this field. A total of 1501 publications were included in this study. The evolution of AI applications in RDs progressed through three stages: the start-up period (2003–2010), the steady development period (2011–2018), and the accelerated growth period (2019–2023), reflecting this field’s increasing importance and impact at the time of the study. These studies originated from 85 countries, with the United States as the leading contributor. “Mutation”, “Diagnosis”, and “Management” were the top three keywords with high frequency. Keyword clustering analysis identified gene identification, effective management, and personalized treatment as three primary research areas of AI applications in RDs. Furthermore, the keyword burst detection indicated a growing interest in the areas of “biomarker”, “predictive model”, and “data mining”, highlighting their potential to shape future research directions. Over two decades, research on the AI applications in RDs has made remarkable progress and shown promising results in the development. Advancing international transboundary cooperation is essential moving forward. Utilizing AI will play a more crucial role across the spectrum of RDs management, encompassing rapid diagnosis, personalized treatment, drug development, data integration and sharing, and continuous monitoring and care.
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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