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Bibliometric analysis of the inflammation in diabetic cardiomyopathy
BACKGROUND: Maladaptive inflammation is implicated in the development of diabetic cardiomyopathy (DCM). This study aimed to visually analyze the global scientific output over the past two decades regarding research on inflammation associated with DCM. METHODS: All relevant articles and reviews were...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792483/ https://www.ncbi.nlm.nih.gov/pubmed/36582738 http://dx.doi.org/10.3389/fcvm.2022.1006213 |
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author | Zhu, Ning Huang, Bingwu Zhu, Liuyan |
author_facet | Zhu, Ning Huang, Bingwu Zhu, Liuyan |
author_sort | Zhu, Ning |
collection | PubMed |
description | BACKGROUND: Maladaptive inflammation is implicated in the development of diabetic cardiomyopathy (DCM). This study aimed to visually analyze the global scientific output over the past two decades regarding research on inflammation associated with DCM. METHODS: All relevant articles and reviews were retrieved in the Web of Science (WOS) Core Collection (limited to SCIE) using “inflammation” and “diabetic cardiomyopathy” as search terms. Articles and reviews published from 1 January 2001 to 28 February 2021 were collected. Visualization analysis and statistical analysis were conducted by Microsoft 365 Excel and VOSviewer 1.6.18. RESULTS: A total of 578 documents were finally selected for further analysis. The publications regarding inflammation and DCM increased gradually over approximately 20 years. The most prolific country was China, with 296 documents and the most citations (9,366). The most influential author groups were Lu Cai and Yihui Tan who were from the United States. The bibliometric analysis of co-occurrence keywords showed that inflammation in DCM is composed of numerous molecules (NF-κB, NLRP3 inflammasome, Nrf-2, TNF-α, protein kinase C, PPARα, TLR4, p38 mitogen-activated protein kinase, TGF-β, Sirt1, and AKT), a variety of cardiac cell types (stem cell, fibroblast, and cardiomyocyte), physiological processes (apoptosis, oxidative stress, autophagy, endoplasmic reticulum stress, hypertrophy, mitochondrion dysfunction, and proliferation), and drugs (sulforaphane, metformin, empagliflozin, and rosuvastatin). CONCLUSION: Our bibliometric analysis presents the characteristics and trends of inflammation in DCM and shows that research on inflammation in DCM will continue to be a hotspot. |
format | Online Article Text |
id | pubmed-9792483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97924832022-12-28 Bibliometric analysis of the inflammation in diabetic cardiomyopathy Zhu, Ning Huang, Bingwu Zhu, Liuyan Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Maladaptive inflammation is implicated in the development of diabetic cardiomyopathy (DCM). This study aimed to visually analyze the global scientific output over the past two decades regarding research on inflammation associated with DCM. METHODS: All relevant articles and reviews were retrieved in the Web of Science (WOS) Core Collection (limited to SCIE) using “inflammation” and “diabetic cardiomyopathy” as search terms. Articles and reviews published from 1 January 2001 to 28 February 2021 were collected. Visualization analysis and statistical analysis were conducted by Microsoft 365 Excel and VOSviewer 1.6.18. RESULTS: A total of 578 documents were finally selected for further analysis. The publications regarding inflammation and DCM increased gradually over approximately 20 years. The most prolific country was China, with 296 documents and the most citations (9,366). The most influential author groups were Lu Cai and Yihui Tan who were from the United States. The bibliometric analysis of co-occurrence keywords showed that inflammation in DCM is composed of numerous molecules (NF-κB, NLRP3 inflammasome, Nrf-2, TNF-α, protein kinase C, PPARα, TLR4, p38 mitogen-activated protein kinase, TGF-β, Sirt1, and AKT), a variety of cardiac cell types (stem cell, fibroblast, and cardiomyocyte), physiological processes (apoptosis, oxidative stress, autophagy, endoplasmic reticulum stress, hypertrophy, mitochondrion dysfunction, and proliferation), and drugs (sulforaphane, metformin, empagliflozin, and rosuvastatin). CONCLUSION: Our bibliometric analysis presents the characteristics and trends of inflammation in DCM and shows that research on inflammation in DCM will continue to be a hotspot. Frontiers Media S.A. 2022-12-13 /pmc/articles/PMC9792483/ /pubmed/36582738 http://dx.doi.org/10.3389/fcvm.2022.1006213 Text en Copyright © 2022 Zhu, Huang and Zhu. 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 | Cardiovascular Medicine Zhu, Ning Huang, Bingwu Zhu, Liuyan Bibliometric analysis of the inflammation in diabetic cardiomyopathy |
title | Bibliometric analysis of the inflammation in diabetic cardiomyopathy |
title_full | Bibliometric analysis of the inflammation in diabetic cardiomyopathy |
title_fullStr | Bibliometric analysis of the inflammation in diabetic cardiomyopathy |
title_full_unstemmed | Bibliometric analysis of the inflammation in diabetic cardiomyopathy |
title_short | Bibliometric analysis of the inflammation in diabetic cardiomyopathy |
title_sort | bibliometric analysis of the inflammation in diabetic cardiomyopathy |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9792483/ https://www.ncbi.nlm.nih.gov/pubmed/36582738 http://dx.doi.org/10.3389/fcvm.2022.1006213 |
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