Abstract
The bibliometric analysis uses the citation count of an article to measure its impact in the scientific community, but no study has been undertaken to determine the most influential papers in the field of primary biliary cholangitis (PBC). This study aimed to investigate the global research interest regarding PBC in dentistry using a bibliometric approach. We searched the Web of Science Core Collection database to find the top 100 most cited (T100) articles focusing on PBC. The information about each article including citations, authors, journals, countries, institutions, and keywords was recorded for bibliometric analysis. The T100 articles related to PBC were published from 1983 to 2019 and were originated from 26 countries. A total of 805 different authors were from 342 different institutions, and articles written by them were published in 35 journals. The five most frequently occurring keywords were “biochemical response,” “ursodeoxycholic acid,” “primary biliary cirrhosis,” “antimitochondrial antibody,” and “autoimmunity.” The T100 articles were classified into different research focuses: pathogenesis (41%), treatment (20%), prognosis (12%), epidemiology (9%), diagnosis (8%), and others (10%). These 100 articles included 32 observational studies, 29 basic research articles, 15 reviews, eight meta-analyses, 12 clinical trials, and four clinical guidelines. The 100 top-cited articles are marked with the leading countries, institutions, journals, hotspots, and development trends in the PBC field that could provide the foundation for further investigations.
Similar content being viewed by others
References
Tsuneyama K, Baba H, Morimoto Y, Tsunematsu T, Ogawa H. Primary biliary cholangitis: its pathological characteristics and immunopathological mechanisms. J Med Investig. 2017;64(12):7–13. https://doi.org/10.2152/jmi.64.7.
Beuers U, Gershwin ME, Gish RG, et al. Changing nomenclature for PBC: from “cirrhosis” to “cholangitis.” Gastroenterology. 2015;149(6):1627–9. https://doi.org/10.1053/j.gastro.2015.08.031.
Carey EJ, Ali AH, Lindor KD. Primary biliary cirrhosis. Lancet. 2015;386(10003):1565–75. https://doi.org/10.1016/s0140-6736(15)00154-3.
Hirschfield GM, Dyson JK, Alexander GJM, et al. The British Society of Gastroenterology/UK-PBC primary biliary cholangitis treatment and management guidelines. Gut. 2018;67(9):1568–94. https://doi.org/10.1136/gutjnl-2017-315259.
Pandit S, Samant H (2021) Primary biliary cholangitis. In StatPearls. Copyright© 2021, StatPearls Publishing LLC
Carbone M, Nardi A, Flack S, et al. Pretreatment prediction of response to ursodeoxycholic acid in primary biliary cholangitis: development and validation of the UDCA response score. Lancet Gastroenterol Hepatol. 2018;3(9):626–34. https://doi.org/10.1016/s2468-1253(18)30163-8.
Jin B, Wu X, Xu G, et al. Evolutions of the management of colorectal cancer liver metastasis: a bibliometric analysis. J Cancer. 2021;12(12):3660–70. https://doi.org/10.7150/jca.52842.
Powell AG, Hughes DL, Wheat JR, Lewis WG. The 100 most influential manuscripts in gastric cancer: a bibliometric analysis. Int J Surg. 2016;28:83–90. https://doi.org/10.1016/j.ijsu.2016.02.028.
Murray MR, Wang T, Schroeder GD, Hsu WK. The 100 most cited spine articles. Eur Spine J. 2012;21(10):2059–69. https://doi.org/10.1007/s00586-012-2303-2.
Qin B, Liang Y, Yang Z, Zhong R. Scientific publications on primary biliary cirrhosis from 2000 through 2010: an 11-year survey of the literature. PLoS ONE. 2012;7(4):e35366. https://doi.org/10.1371/journal.pone.0035366.
Yu Y, Li Y, Zhang Z, et al. A bibliometric analysis using VOSviewer of publications on COVID-19. Ann Transl Med. 2020;8(13):816. https://doi.org/10.21037/atm-20-4235.
van Eck NJ, Waltman L. Software survey: VOSviewer, a computer program for bibliometric mapping. Scientometrics. 2010;84(2):523–38. https://doi.org/10.1007/s11192-009-0146-3.
Lindor KD, Gershwin ME, Poupon R, Kaplan M, Bergasa NV, Heathcote EJ. Primary biliary cirrhosis. Hepatology. 2009;50(1):291–308. https://doi.org/10.1002/hep.22906.
Moritoki Y, Zhang W, Tsuneyama K, et al. B cells suppress the inflammatory response in a mouse model of primary biliary cirrhosis. Gastroenterology. 2009;136(3):1037–47. https://doi.org/10.1053/j.gastro.2008.11.035.
Hamlyn AN, Macklon AF, James O. Primary biliary cirrhosis: geographical clustering and symptomatic onset seasonality. Gut. 1983;24(10):940–5. https://doi.org/10.1136/gut.24.10.940.
Hwang JW, Kim H, Lee DJ. The 100 most influential manuscripts on hepatocellular carcinoma: a bibliometric analysis. J Int Med Res. 2019;47(4):1467–82. https://doi.org/10.1177/0300060519835974.
Nevens F, Andreone P, Mazzella G, et al. A placebo-controlled trial of obeticholic acid in primary biliary cholangitis. N Engl J Med. 2016;375(7):631–43. https://doi.org/10.1056/NEJMoa1509840.
Corpechot C, Chazouillères O, Rousseau A, et al. A placebo-controlled trial of bezafibrate in primary biliary cholangitis. N Engl J Med. 2018;378(23):2171–81. https://doi.org/10.1056/NEJMoa1714519.
Shuaib W, Acevedo JN, Khan MS, Santiago LJ, Gaeta TJ. The top 100 cited articles published in emergency medicine journals. Am J Emerg Med. 2015;33(8):1066–71. https://doi.org/10.1016/j.ajem.2015.04.047.
Tian J, Li M, Lian F, Tong X. The hundred most-cited publications in microbiota of diabetes research: a bibliometric analysis. Medicine (Baltimore). 2017;96(37):e7338. https://doi.org/10.1097/md.0000000000007338.
Lleo A, Wang GQ, Gershwin ME, Hirschfield GM. Primary biliary cholangitis. Lancet. 2020;396(10266):1915–26. https://doi.org/10.1016/s0140-6736(20)31607-x.
Shimoda S, van de Water J, Ansari A, et al. Identification and precursor frequency analysis of a common T cell epitope motif in mitochondrial autoantigens in primary biliary cirrhosis. J Clin Investig. 1998;102:1831–40. https://doi.org/10.1172/jci4213.
Li Y, Tang R, Ma X. Epigenetics of primary biliary cholangitis. Adv Exp Med Biol. 2020;1253:259–83. https://doi.org/10.1007/978-981-15-3449-2_10.
Juran BD, Hirschfield GM, Invernizzi P, et al. Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. Hum Mol Genet. 2012;21(23):5209–21. https://doi.org/10.1093/hmg/dds359.
Lan RY, Salunga TL, Tsuneyama K, et al. Hepatic IL-17 responses in human and murine primary biliary cirrhosis. J Autoimmun. 2009;32(1):43–51. https://doi.org/10.1016/j.jaut.2008.11.001.
Yang CY, Ma X, Tsuneyama K, et al. IL-12/Th1 and IL-23/Th17 biliary microenvironment in primary biliary cirrhosis: implications for therapy. Hepatology. 2014;59(5):1944–53. https://doi.org/10.1002/hep.26979.
Qiu F, Tang R, Zuo X, et al. A genome-wide association study identifies six novel risk loci for primary biliary cholangitis. Nat Commun. 2017;8:14828. https://doi.org/10.1038/ncomms14828.
Hirschfield GM, Liu X, Han Y, et al. Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis. Nat Genet. 2015;42(8):655–7. https://doi.org/10.1038/ng.631.
Selmi C, Meda F, Kasangian A, et al. Experimental evidence on the immunopathogenesis of primary biliary cirrhosis. Cell Mol Immunol. 2010;7(1):1–10. https://doi.org/10.1038/cmi.2009.104.
Prince MI, Ducker SJ, James OF. Case-control studies of risk factors for primary biliary cirrhosis in two United Kingdom populations. Gut. 2010;59(4):508–12. https://doi.org/10.1136/gut.2009.184218.
Boonstra K, Beuers U, Ponsioen CY. Epidemiology of primary sclerosing cholangitis and primary biliary cirrhosis: a systematic review. J Hepatol. 2012;56(5):1181–8. https://doi.org/10.1016/j.jhep.2011.10.025.
Mason AL, Zhang G. Linking human beta retrovirus infection with primary biliary cirrhosis. Gastroenterol Clin Biol. 2010;34(6–7):359–66. https://doi.org/10.1016/j.gcb.2010.04.014.
Gershwin ME, Selmi C, Worman HJ, et al. Risk factors and comorbidities in primary biliary cirrhosis: a controlled interview-based study of 1032 patients. Hepatology. 2005;42(5):1194–202. https://doi.org/10.1002/hep.20907.
Walker JG, Doniach D, Roitt IM, Sherlock S. Serological tests in diagnosis of primary biliary cirrhosis. Lancet. 1965;1(7390):827–31. https://doi.org/10.1016/s0140-6736(65)91372-3.
Li CP, Hwang SJ, Chan CY, et al. Clinical evaluation of primary biliary cirrhosis in Chinese patients without serum anti-mitochondrial antibody. Zhonghua Yi Xue Za Zhi (Taipei). 1997;59(6):334–40.
Invernizzi P, Crosignani A, Battezzati PM, et al. Comparison of the clinical features and clinical course of antimitochondrial antibody-positive and -negative primary biliary cirrhosis. Hepatology. 1997;25(5):1090–5. https://doi.org/10.1002/hep.510250507.
Witt-Sullivan H, Heathcote J, Cauch K, et al. The demography of primary biliary cirrhosis in Ontario, Canada. Hepatology. 1990;12(1):98–105. https://doi.org/10.1002/hep.1840120116.
Zhang Q, Liu Z, Wu S, et al. Meta-analysis of antinuclear antibodies in the diagnosis of antimitochondrial antibody-negative primary biliary cholangitis. Gastroenterol Res Pract. 2019. https://doi.org/10.1155/2019/8959103.
Bogdanos DP, Baum H, Butler P, et al. Association between the primary biliary cirrhosis specific anti-sp100 antibodies and recurrent urinary tract infection. Dig Liver Dis. 2003;35(11):801–5. https://doi.org/10.1016/s1590-8658(03)00466-3.
Hu CJ, Zhang FC, Li YZ, Zhang X. Primary biliary cirrhosis: what do autoantibodies tell us? World J Gastroenterol. 2010;16(29):3616–29. https://doi.org/10.3748/wjg.v16.i29.3616.
Laschtowitz A, de Veer RC, Van der Meer AJ, Schramm C. Diagnosis and treatment of primary biliary cholangitis. United Eur Gastroenterol J. 2020;8(6):667–74. https://doi.org/10.1177/2050640620919585.
Huang YQ. Recent advances in the diagnosis and treatment of primary biliary cholangitis. World J Hepatol. 2016;8(33):1419–41. https://doi.org/10.4254/wjh.v8.i33.1419.
Quarneti C, Muratori P, Lalanne C, et al. Fatigue and pruritus at onset identify a more aggressive subset of primary biliary cirrhosis. Liver Int. 2015;35(2):636–41. https://doi.org/10.1111/liv.12560.
Hegade VS, Mells GF, Lammert C, Juran B, Jones DE. P1152: a comparative study of pruritus in PBC cohorts from UK, USA and Italy. J Hepatol. 2015;62(2):S785–S785.
Newton JL, Hudson M, Tachtatzis P, et al. Population prevalence and symptom associations of autonomic dysfunction in primary biliary cirrhosis. Hepatology. 2007;45(6):1496–505. https://doi.org/10.1002/hep.21609.
Gu EL, Yao GB. The clinical characteristics of primary biliary cirrhosis in China: a systematic review. Zhonghua Gan Zang Bing Za Zhi. 2009;17(11):861–6.
Al-Harthy N, Kumagi T, Coltescu C, Hirschfield GM. The specificity of fatigue in primary biliary cirrhosis: evaluation of a large clinic practice. Hepatology. 2010;52(2):562–70. https://doi.org/10.1002/hep.23683.
Purohit T, Cappell MS. Primary biliary cirrhosis: pathophysiology, clinical presentation and therapy. World J Hepatol. 2015;7(7):926–41. https://doi.org/10.4254/wjh.v7.i7.926.
Hohenester S, Oude-Elferink RP, Beuers U. Primary biliary cirrhosis. Semin Immunopathol. 2009;31(3):283–307. https://doi.org/10.1007/s00281-009-0164-5.
Corpechot C, Abenavoli L, Rabahi N, et al. Biochemical response to ursodeoxycholic acid and long-term prognosis in primary biliary cirrhosis. Hepatology. 2008;48(3):871–7. https://doi.org/10.1002/hep.22428.
Myers RP, Swain MG, Lee SS, Shaheen AA, Burak KW. B-cell depletion with rituximab in patients with primary biliary cirrhosis refractory to ursodeoxycholic acid. Am J Gastroenterol. 2013;108(6):933–41. https://doi.org/10.1038/ajg.2013.51.
Moritoki Y, Lian ZX, Lindor K, et al. B-cell depletion with anti-CD20 ameliorates autoimmune cholangitis but exacerbates colitis in transforming growth factor-beta receptor II dominant negative mice. Hepatology. 2009;50(6):1893–903. https://doi.org/10.1002/hep.23238.
Lammers WJ, Hirschfield GM, Corpechot C, et al. Development and validation of a scoring system to predict outcomes of patients with primary biliary cirrhosis receiving ursodeoxycholic acid therapy. Gastroenterology. 2015;149(7):1804-1812.e4. https://doi.org/10.1053/j.gastro.2015.07.061.
Carbone M, Sharp SJ, Flack S, et al. The UK-PBC risk scores: Derivation and validation of a scoring system for long-term prediction of end-stage liver disease in primary biliary cholangitis. Hepatology (Baltimore, MD). 2016;63(3):930–50. https://doi.org/10.1002/hep.28017.
Kuiper EMM, Hansen BE, de Vries RA, et al. Improved prognosis of patients with primary biliary cirrhosis that have a biochemical response to ursodeoxycholic acid. Gastroenterology. 2009;136(4):1281–7. https://doi.org/10.1053/j.gastro.2009.01.003.
Corpechot C, Chazouillères O, Poupon R. Early primary biliary cirrhosis: biochemical response to treatment and prediction of long-term outcome. J Hepatol. 2011;55(6):1361–7. https://doi.org/10.1016/j.jhep.2011.02.031.
Funding
This work was supported by the "Natural Science Foundation of Fujian Province, China" (No. 2020J01120297) to Hongbin Chen which provided funds for our research.
Author information
Authors and Affiliations
Contributions
HC, YZ, and ZY designed the study. YZ and ZY conducted the literature search and analyzed the data. YZ drafted the manuscript. HD and KH drew the pictures. ZY and FZ prepared the tables. HC and YZ reviewed and revised the manuscript. All authors contributed to the article and approved the submitted version.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Zhao, Y., Yin, Z., Du, H. et al. The latest research trends in primary biliary cholangitis: a bibliometric analysis. Clin Exp Med 23, 347–355 (2023). https://doi.org/10.1007/s10238-022-00825-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10238-022-00825-0