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1995年至2023年脊髓性肌萎缩症的研究趋势:一项文献计量分析。

Research trends on spinal muscular atrophy from 1995 to 2023: A bibliometric analysis.

作者信息

Yu Hao, Wei Cuijie, Sun Dan, Zhang Li, Xia Yanyan, Zhu Wenhua

机构信息

Department of Medical Genetics and Center for Rare Diseases, Second Affiliated Hospital, Zhejiang University School of Medicine and Zhejiang Key Laboratory of Rare Diseases for Precision Medicine and Clinical Translation, Hangzhou, China.

Department of Pediatrics, Peking University First Hospital, Beijing, China.

出版信息

Medicine (Baltimore). 2025 Mar 28;104(13):e41801. doi: 10.1097/MD.0000000000041801.

Abstract

BACKGROUND

Spinal muscular atrophy (SMA) is a neuromuscular disease characterized by progressive muscle weakness due to motor neuron degeneration. The discovery of the survival motor neuron 1 (SMN1) gene in 1995 revolutionized SMA research, leading to significant therapeutic advancements. This bibliometric analysis aimed to explore global trends in SMA research and therapy, with a particular focus on China.

METHODS

A comprehensive database search identified 4506 relevant publications (3812 articles, 694 reviews) published between 1995 and 2023. Bibliometric tools were used to analyze publication trends, collaborations, and research topics.

RESULTS

SMA research has experienced substantial growth, with the United States leading in publications followed by the United Kingdom and Germany. China has shown increasing engagement in this field. Key research areas include genetic and molecular mechanisms, survival motor neuron gene therapy, antisense oligonucleotides, and muscle strength-promoting factors. Chinese researchers have contributed significantly to these areas, with a higher reporting frequency of SMA-related topics compared to other countries.

CONCLUSION

This bibliometric analysis provides a comprehensive overview of global SMA research, highlighting significant advancements, and identifying future directions. The findings offer valuable insights for researchers, clinicians, and policymakers in China to ensure alignment with global medical advancements and improve the lives of individuals affected by SMA.

摘要

背景

脊髓性肌萎缩症(SMA)是一种神经肌肉疾病,其特征是由于运动神经元变性导致进行性肌肉无力。1995年生存运动神经元1(SMN1)基因的发现彻底改变了SMA的研究,带来了重大的治疗进展。这项文献计量分析旨在探索SMA研究和治疗的全球趋势,特别关注中国。

方法

通过全面的数据库检索,确定了1995年至2023年期间发表的4506篇相关出版物(3812篇文章,694篇综述)。使用文献计量工具分析出版趋势、合作情况和研究主题。

结果

SMA研究取得了显著增长,美国在出版物数量上领先,其次是英国和德国。中国在该领域的参与度不断提高。关键研究领域包括遗传和分子机制、生存运动神经元基因治疗、反义寡核苷酸和促进肌肉力量的因素。中国研究人员在这些领域做出了重大贡献,与其他国家相比,SMA相关主题的报告频率更高。

结论

这项文献计量分析全面概述了全球SMA研究,突出了重大进展,并确定了未来方向。研究结果为中国的研究人员、临床医生和政策制定者提供了宝贵的见解,以确保与全球医学进展保持一致,并改善受SMA影响的个体的生活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11957644/54f58c088309/medi-104-e41801-g001.jpg

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