基于CiteSpace的1985年至2024年的英语和中国数据库中罕见疾病的文献统计研究
Mengru Tian1, Shuyi Wang1, Zhihui Meng1
1Key Laboratory for Biotech-Drugs of National Health Commission, Key Laboratory for Rare & Uncommon Diseases of Shandong Province, Biomedical Sciences College & Shandong Medicinal Biotechnology Centre, Shandong First Medical University & Shandong Academy of Medical Sciences, Ji'nan, China.
这项研究使用CiteSpace分析了罕见疾病研究趋势,揭示了全球对孤儿药物和基因疗法的研究增加. 国际合作更加强大,需要更多的高质量研究和在中国的核心作者.
科学领域:
- 医疗信息学 医疗信息学
- 图书统计学 图书统计学
- 罕见疾病研究 罕见疾病研究
背景情况:
- 罕见疾病在全球范围内带来了重大的诊断和治疗挑战.
- 了解研究趋势对于推进罕见疾病诊断和治疗至关重要.
研究的目的:
- 使用CiteSpace,对罕见疾病的文献进行视觉分析.
- 总结目前罕见病领域的研究状况,热点和未来方向.
主要方法:
- 在CNKI和Web of Science (1985-2024) 进行了全面的文献搜索.
- 使用CiteSpace软件对出版物量,作者,机构和关键词进行视觉分析.
- 在选后,包括了2,293篇中文和2,262篇英语文章.
主要成果:
- 关于罕见疾病的研究每年都在增加,主要关注的是孤儿药物,遗传突变和儿科病例.
- 在研究深度和广度方面,中国与外国之间存在重大差距.
- 中国面临着核心作者和高质量文献的短缺,与国际水平相比,研究团队合作率较低.
结论:
- 孤儿药物开发,新型治疗剂和基因疗法是关键的研究方向.
- 强调早期发现,预防和治疗罕见疾病至关重要.
- 基因诊断技术对临床应用和未来研究有着广泛的前景.
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