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Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years

OBJECTIVE: Pheochromocytoma is a rare catecholamine-producing neuroendocrine tumour originating from the chromaffin cells of the adrenal medulla or extra-adrenal paraganglia. However, there are few bibliometric studies on Pheochromocytoma. Therefore, this study was employed to summarize the global t...

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Autores principales: Huang, Bi-ling, Liu, Qi, Teng, Yuan-yuan, Peng, Shu-qin, Liu, Ze, Li, Ming-liu, Liang, Jie-yu, Zhang, Yi, Wang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482340/
https://www.ncbi.nlm.nih.gov/pubmed/37680890
http://dx.doi.org/10.3389/fendo.2023.1167796
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author Huang, Bi-ling
Liu, Qi
Teng, Yuan-yuan
Peng, Shu-qin
Liu, Ze
Li, Ming-liu
Liang, Jie-yu
Zhang, Yi
Wang, Min
author_facet Huang, Bi-ling
Liu, Qi
Teng, Yuan-yuan
Peng, Shu-qin
Liu, Ze
Li, Ming-liu
Liang, Jie-yu
Zhang, Yi
Wang, Min
author_sort Huang, Bi-ling
collection PubMed
description OBJECTIVE: Pheochromocytoma is a rare catecholamine-producing neuroendocrine tumour originating from the chromaffin cells of the adrenal medulla or extra-adrenal paraganglia. However, there are few bibliometric studies on Pheochromocytoma. Therefore, this study was employed to summarize the global trends and current status in pheochromocytoma by bibliometric analysis. MATERIALS AND METHODS: The Web of Science (WOS) core collection database was searched for publications relating to pheochromocytoma from 2001 to 2021. Bibliometric analysis was used to examine the data, and Microsoft Excel was utilized to create bar graphs. In addition, VOSviewer was used to carry out co-authorship analysis, co-citation analysis and co-occurrence analysis. CiteSpace was used to analyze the keywords citation bursts. RESULTS: A total of 8,653 publications published in 1,806 journals by 38,590 authors in 6,117 organizations from 100 countries/regions were included in our study. Among them, USA was the leading countries in terms of total publications and sum of time cited, whereas Eunice Kennedy Shriver Natl Inst Child Hlth & Hum was the leading institutions. The main publications for pheochromocytoma-related articles were Journal of clinical endocrinology &metabolism. Pacak karel and Eisenhofer Graeme were the main contributing authors. The studies on pheochromocytoma could be grouped into five clusters: Treatment, Mechanism, Etiology, Radiology and Hormones study. Moreover, the radiology study, etiology study and some specific keywords such germlines mutation, mesenchymal stem-cells, autophagy, neuroinflammation, neurotoxicity, and hemodynamic instability, may become the hot spots of future. CONCLUSION: Although the number of articles on pheochromocytoma has fluctuated slightly over the past 20 years, there has been an overall upward trend. In general, precision medicine research on pheochromocytoma, especially metastatic pheochromocytoma, in terms of diagnosis, treatment, and etiology will be a hot research topic in the future. This study helps to understand the research perspectives, hot spots and trends of pheochromocytoma and provide new insight and a basis for future pheochromocytoma research quickly.
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spelling pubmed-104823402023-09-07 Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years Huang, Bi-ling Liu, Qi Teng, Yuan-yuan Peng, Shu-qin Liu, Ze Li, Ming-liu Liang, Jie-yu Zhang, Yi Wang, Min Front Endocrinol (Lausanne) Endocrinology OBJECTIVE: Pheochromocytoma is a rare catecholamine-producing neuroendocrine tumour originating from the chromaffin cells of the adrenal medulla or extra-adrenal paraganglia. However, there are few bibliometric studies on Pheochromocytoma. Therefore, this study was employed to summarize the global trends and current status in pheochromocytoma by bibliometric analysis. MATERIALS AND METHODS: The Web of Science (WOS) core collection database was searched for publications relating to pheochromocytoma from 2001 to 2021. Bibliometric analysis was used to examine the data, and Microsoft Excel was utilized to create bar graphs. In addition, VOSviewer was used to carry out co-authorship analysis, co-citation analysis and co-occurrence analysis. CiteSpace was used to analyze the keywords citation bursts. RESULTS: A total of 8,653 publications published in 1,806 journals by 38,590 authors in 6,117 organizations from 100 countries/regions were included in our study. Among them, USA was the leading countries in terms of total publications and sum of time cited, whereas Eunice Kennedy Shriver Natl Inst Child Hlth & Hum was the leading institutions. The main publications for pheochromocytoma-related articles were Journal of clinical endocrinology &metabolism. Pacak karel and Eisenhofer Graeme were the main contributing authors. The studies on pheochromocytoma could be grouped into five clusters: Treatment, Mechanism, Etiology, Radiology and Hormones study. Moreover, the radiology study, etiology study and some specific keywords such germlines mutation, mesenchymal stem-cells, autophagy, neuroinflammation, neurotoxicity, and hemodynamic instability, may become the hot spots of future. CONCLUSION: Although the number of articles on pheochromocytoma has fluctuated slightly over the past 20 years, there has been an overall upward trend. In general, precision medicine research on pheochromocytoma, especially metastatic pheochromocytoma, in terms of diagnosis, treatment, and etiology will be a hot research topic in the future. This study helps to understand the research perspectives, hot spots and trends of pheochromocytoma and provide new insight and a basis for future pheochromocytoma research quickly. Frontiers Media S.A. 2023-08-23 /pmc/articles/PMC10482340/ /pubmed/37680890 http://dx.doi.org/10.3389/fendo.2023.1167796 Text en Copyright © 2023 Huang, Liu, Teng, Peng, Liu, Li, Liang, Zhang and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Huang, Bi-ling
Liu, Qi
Teng, Yuan-yuan
Peng, Shu-qin
Liu, Ze
Li, Ming-liu
Liang, Jie-yu
Zhang, Yi
Wang, Min
Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years
title Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years
title_full Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years
title_fullStr Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years
title_full_unstemmed Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years
title_short Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years
title_sort global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482340/
https://www.ncbi.nlm.nih.gov/pubmed/37680890
http://dx.doi.org/10.3389/fendo.2023.1167796
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