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A bibliometric analysis of complement in IgA nephropathy from 1991 to 2022.

作者信息

Guo Yun, Zhang Haiqiang, Yu Xueqing

机构信息

The First Clinical Medical College, Guangdong Medical University, Zhanjiang, China.

Department of Nephrology, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China.

出版信息

Front Pharmacol. 2023 Jul 27;14:1200193. doi: 10.3389/fphar.2023.1200193. eCollection 2023.


DOI:10.3389/fphar.2023.1200193
PMID:37576817
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10414182/
Abstract

IgA nephropathy is a common glomerular disease on a global scale, which has resulted in significant economic burdens. The complement system plays a vital role in enhancing the efficacy of antibodies and phagocytic cells in eliminating microbes and damaged cells, and promoting inflammation. Complement activation has been found to contribute to the progression of various renal diseases, including IgA nephropathy. In this study, a thorough analysis was conducted on publications related to complement in IgAN from 1991 to 2022, retrieved from the Web of Science Core Collection and Scopus database. The analysis focused on various aspects such as annual publications, country, institution, author, journal, keywords, and co-cited references, utilizing Citespace and Vosviewer. A total of 819 publications were obtained, and while there were slight fluctuations in annual publications, an overall upward trend was observed. China, Japan and the United States were the leading countries in terms of publications, with China having the highest number of publications (201). Collaborative network analysis revealed that England, University of Alabama Birmingham, and Robert J Wyatt were the most influential country, institution, and author, respectively, in this field of research. Furthermore, the analysis of references and keywords indicated that complement activation contributes to IgAN, and immunosuppression in IgAN are a hot topic of research. This study identifies current research hotspots and advanced tendencies in the study of complement in IgAN, providing scholars with crucial directions in this research area.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/f841b89d43eb/fphar-14-1200193-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/58cd36c294aa/fphar-14-1200193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/2e9d0b3c7acd/fphar-14-1200193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/c348eaaaece1/fphar-14-1200193-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/276be6dc7da0/fphar-14-1200193-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/862c0cbbdc66/fphar-14-1200193-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/dfea4d15fa30/fphar-14-1200193-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/ad634d84917c/fphar-14-1200193-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/2aabb675f5e0/fphar-14-1200193-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/f841b89d43eb/fphar-14-1200193-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/58cd36c294aa/fphar-14-1200193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/2e9d0b3c7acd/fphar-14-1200193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/c348eaaaece1/fphar-14-1200193-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/276be6dc7da0/fphar-14-1200193-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/862c0cbbdc66/fphar-14-1200193-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/dfea4d15fa30/fphar-14-1200193-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/ad634d84917c/fphar-14-1200193-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/2aabb675f5e0/fphar-14-1200193-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c93/10414182/f841b89d43eb/fphar-14-1200193-g009.jpg

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A bibliometric analysis of complement in IgA nephropathy from 1991 to 2022.

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本文引用的文献

[1]
Factor H related proteins modulate complement activation on kidney cells.

Kidney Int. 2022-12

[2]
The Role of Complement in Microangiopathic Lesions of IgA Nephropathy.

Kidney Int Rep. 2022-4-4

[3]
C5a receptor inhibitor avacopan in immunoglobulin A nephropathy-an open-label pilot study.

Clin Kidney J. 2022-1-24

[4]
Application of the International IgA Nephropathy Prediction Tool one or two years post-biopsy.

Kidney Int. 2022-7

[5]
The level of urinary C4d is associated with disease progression in IgA nephropathy with glomerular crescentic lesions: a cohort study.

Nephrol Dial Transplant. 2022-10-19

[6]
Glomerular C4d Deposition and Kidney Disease Progression in IgA Nephropathy: A Systematic Review and Meta-analysis.

Kidney Med. 2021-8-6

[7]
Complement activation in IgA nephropathy.

Semin Immunopathol. 2021-10

[8]
IgA vasculitis with nephritis: update of pathogenesis with clinical implications.

Pediatr Nephrol. 2022-4

[9]
C3 inhibition with pegcetacoplan in subjects with paroxysmal nocturnal hemoglobinuria treated with eculizumab.

Am J Hematol. 2020-11

[10]
Relationship between immunoglobulin A1 lectin-binding specificities, mesangial C4d deposits and clinical phenotypes in immunoglobulin A nephropathy.

Nephrol Dial Transplant. 2022-1-25

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