Lu Shuai, Shen Huaishuang, Li Minjuan, Luo Yiming, Sun Hao, Zhao Xian, Chen Jianming, Bai Ruifeng, Han Pengli, Zha Yejun, Jiang Xieyuan
Department of Orthopedic Trauma, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
Beijing Research Institute of Traumatology and Orthopaedics, Beijing, China.
Front Mol Biosci. 2025 Mar 26;12:1545109. doi: 10.3389/fmolb.2025.1545109. eCollection 2025.
Receptor activator of nuclear factor kappa-B ligand (RANKL) plays a critical role in bone metabolism and the pathogenesis of osteoporotic fractures. This study aims to conduct a bibliometric analysis of global research pertaining to RANKL and osteoporotic fractures to identify key trends, influential studies, and collaborative networks.
A literature search was conducted to identify articles found in the Web of Science Core Collection database regarding RANKL and osteoporotic fractures from 2001 to 2024. A bibliometric analysis was performed using VOSviewer, CiteSpace, and R 4.3.3 for the publication volume, country and institution contributions, journal impact, author influence, and research hotspots.
A total of 214 articles were analyzed. Publication rates have steadily increased, with a peak of 21 papers in 2020. The U.S., China, and South Korea were the top contributing countries, and leading institutions included Harvard University and Dankook University. The , , and were the journals of highest impact. At the level of authors, Heiss-Christian published the highest number and Christiansen-Claus had the strongest citation impact (1,368 citations). Research evolved from basic biological mechanisms (2001-2010) through clinical applications (2011-2017) to recent renewed interest in fundamental RANKL biology (2018-2024). Key research hotspots included postmenopausal osteoporosis, bone mineral density, and osteoclast differentiation, with emerging focus on RANKL's role beyond skeletal metabolism.
This bibliometric analysis provides a comprehensive overview of RANKL research in osteoporotic fractures, highlighting key priorities for future investigation. Future studies should prioritize understanding RANKL's broader physiological roles, developing better predictive markers, and optimizing personalized treatment strategies.
核因子κB受体活化因子配体(RANKL)在骨代谢和骨质疏松性骨折的发病机制中起关键作用。本研究旨在对全球有关RANKL和骨质疏松性骨折的研究进行文献计量分析,以确定关键趋势、有影响力的研究和合作网络。
进行文献检索,以识别2001年至2024年在Web of Science核心合集数据库中找到的有关RANKL和骨质疏松性骨折的文章。使用VOSviewer、CiteSpace和R 4.3.3对发表量、国家和机构贡献、期刊影响力、作者影响力和研究热点进行文献计量分析。
共分析了214篇文章。发表率稳步上升,2020年达到峰值21篇。美国、中国和韩国是贡献最大的国家,主要机构包括哈佛大学和韩国檀国大学。《 》《 》和《 》是影响力最高的期刊。在作者层面,海斯 - 克里斯蒂安发表的文章数量最多,克里斯蒂安森 - 克劳斯的被引影响力最强(1368次引用)。研究从基础生物学机制(2001 - 2010年)发展到临床应用(2011 - 2017年),再到近期对RANKL基础生物学的重新关注(2018 - 2024年)。关键研究热点包括绝经后骨质疏松症、骨密度和破骨细胞分化,新兴关注点是RANKL在骨骼代谢之外的作用。
本文献计量分析全面概述了RANKL在骨质疏松性骨折方面的研究,突出了未来研究的关键重点。未来研究应优先了解RANKL更广泛的生理作用,开发更好的预测标志物,并优化个性化治疗策略。