Bibliometric and Visualization Analysis of DprE1 Inhibitors to Combat Tuberculosis

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Abstract

Background: Tuberculosis (TB) poses a serious threat to public health, particularly owing to the increase in multidrug-resistant tuberculosis (MDR-TB) and extremely drug-resistant tuberculosis (XDR-TB); thus, there is an imperative need for novel treatments to tackle this issue. Decaprenylphosphoryl-β-D-ribose 2′-epimerase (DprE1) is essential for mycobacterial cell wall integrity and viability. As no relevant bibliometric study has been reported, we performed bibliometric and visual analyses to depict the knowledge framework of research related to the involvement of DprE1 in TB. Methods: Relevant studies were sourced from the Web of Science Core Collection database. VOSviewer, CiteSpace, and bibliometrics (http://bibliometric.com/) were used to construct networks based on an analysis of journals, countries, funding, institutions, authors, references, and keywords. Results: A total of 184 publications were retrieved; the total citations were 3405 times and the mean citation was 17.28 per article. The annual number of publications on DprE1 in TB has shown a significantly increasing trend. The European Journal of Medicinal Chemistry is the most published journal, with 19 articles. Lu Yu and Bin Wang contributed the most prolific authors with 18 articles. Stratified by the number of publications, India was the most prolific country that cooperated closely with the USA, UK, Japan, and United Arab Emirates. Burstness analysis of references and keywords showed that the developing research trends in this field mainly woven around “Mtb”, “DprE1” and “inhibitors” during the past years. Conclusion: A systematic bibliometric study indicates that DprE1 remains a focal point in the anti-TB domain. These results can serve as a data-driven reference for future research and offer precise insights into the development of anti-TB agents associated with DprE1. To the best of our knowledge, this study is the first to comprehensively investigate DprE1 in TB by means of bibliometric analysis. Guizhou Province High-level Innovative Talent Training Program [2020] for J. F, GCC[2022]014 for H. F and GCC [2023]037 for J. X., National Engineering Technology Research Center for Miao Medicine Improved Ability (QKHZYD [2023]006), Engineering Research Center of New Dosage Form and New Preparation of Traditional Chinese Medicine (Miao Medicine) in Higher Education Institutions of Guizhou Province (QJJ[2022]022).

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Wang, Q., Fu, H., Zhang, Y., Zhang, M., Xu, J., & Fu, J. (2025). Bibliometric and Visualization Analysis of DprE1 Inhibitors to Combat Tuberculosis. Drug Design, Development and Therapy, 19, 2577–2596. https://doi.org/10.2147/DDDT.S515049

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