https://doi.org/10.4081/monaldi.2024.3004
A bibliometric analysis of cystic fibrosis transmembrane conductance regulators
Submitted: March 27, 2024
Accepted: June 3, 2024
Published: July 24, 2024
Accepted: June 3, 2024
Abstract Views: 395
PDF_EARLY VIEW: 101
SUPPLEMENTARY MATERIAL: 16
SUPPLEMENTARY MATERIAL: 16
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
Cystic fibrosis (CF), a multisystem disease primarily affecting the lungs, arises due to pathogenic mutations in the CF transmembrane conductance regulator (CFTR) gene. This study embarked on a bibliometric analysis to survey the use of CFTR modulators in CF treatment. Utilizing the Scopus database, a comprehensive search was executed, incorporating terms related to CF and CFTR modulators. Various document types up to July 19, 2023, were included, with citation counts forming the basis of our analyses. Trends, contributor countries, leading institutions, top authors, journals, keywords, and annual citation trends were evaluated. Our search retrieved 2317 records, predominantly articles. The United States dominated in both publications and citations, followed by the United Kingdom. The University of Alabama, Birmingham, and Vertex Pharmaceuticals, Boston, were among the top institutions. Rowe S.M. was identified as a top-cited author. The Journal of Cystic Fibrosis emerged as the leading journal in terms of publication volume, while the New England Journal of Medicine had the highest citation count. The most-cited article addressed a CFTR potentiator's efficacy in patients with the G551D mutation. The keyword "Cystic fibrosis" appeared most frequently. This bibliometric analysis underscores the significant research focus on CF, especially concerning CFTR modulators. The results highlight the pivotal role of certain countries, institutions, authors, and journals in the progression of CF research, offering insights into current trends and future research directions.
Rowe SM, Miller S, Sorscher EJ. Cystic fibrosis. N Engl J Med 2005;352:1992-2001.
DOI: https://doi.org/10.1056/NEJMra043184
Ratjen F, Döring G. Cystic fibrosis. Lancet 2003;361:681-9.
DOI: https://doi.org/10.1016/S0140-6736(03)12567-6
Hamosh A, FitzSimmons SC, Macek MJ, et al. Comparison of the clinical manifestations of cystic fibrosis in black and white patients. J Pediatr 1998;132:255-9.
DOI: https://doi.org/10.1016/S0022-3476(98)70441-X
O’Sullivan BP, Freedman SD. Cystic fibrosis. Lancet 2009;373:1891-904.
DOI: https://doi.org/10.1016/S0140-6736(09)60327-5
Stewart C, Pepper MS. Cystic fibrosis on the African continent. Genet Med 2016;18:653-62.
DOI: https://doi.org/10.1038/gim.2015.157
Yamashiro Y, Shimizu T, Oguchi S, et al. The estimated incidence of cystic fibrosis in Japan. J Pediatr Gastroenterol Nutr 1997;24:544-7.
DOI: https://doi.org/10.1002/j.1536-4801.1997.tb00648.x
Guo X, Liu K, Liu Y, et al. Clinical and genetic characteristics of cystic fibrosis in CHINESE patients: a systemic review of reported cases. Orphanet J Rare Dis 2018;13:224.
DOI: https://doi.org/10.1186/s13023-018-0968-2
Guo J, Garratt A, Hill A. Worldwide rates of diagnosis and effective treatment for cystic fibrosis. J Cyst Fibros 2022;21:456-62.
DOI: https://doi.org/10.1016/j.jcf.2022.01.009
Yankaskas JR, Marshall BC, Sufian B, et al. Cystic fibrosis adult care: consensus conference report. Chest 2004;125:1S-39S.
DOI: https://doi.org/10.1378/chest.125.1_suppl.1S
Stern RC. The diagnosis of cystic fibrosis. N Engl J Med 1997;336:487-91.
DOI: https://doi.org/10.1056/NEJM199702133360707
Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. J Pediatr 1998;132:589-95.
DOI: https://doi.org/10.1016/S0022-3476(98)70344-0
Middleton PG, Taylor-Cousar JL. Development of elexacaftor - tezacaftor - ivacaftor: highly effective CFTR modulation for the majority of people with Cystic Fibrosis. Expert Rev Respir Med 2021;15:723-35.
DOI: https://doi.org/10.1080/17476348.2021.1855980
Skilton M, Krishan A, Patel S, et al. Potentiators (specific therapies for class III and IV mutations) for cystic fibrosis. Cochrane Database Syst Rev 2019;1:CD009841.
DOI: https://doi.org/10.1002/14651858.CD009841.pub3
Ramsey BW, Davies J, McElvaney NG, et al. A CFTR potentiator in patients with cystic fibrosis and the G551D mutation. N Engl J Med 2011;365:1663-72.
DOI: https://doi.org/10.1056/NEJMoa1105185
De Boeck K. Cystic fibrosis in the year 2020: a disease with a new face. Acta Paediatr 2020;109:893-9.
DOI: https://doi.org/10.1111/apa.15155
Reis FJC, Damaceno N. Cystic fibrosis. J Pediatr (Rio J) 1998;74:S76-94. [Article in Portuguese].
DOI: https://doi.org/10.2223/JPED.489
Klimova B, Kuca K, Novotny M, Maresova P. Cystic fibrosis revisited - a review study. Med Chem 2017;13:102-9.
DOI: https://doi.org/10.2174/1573406412666160608113235
Leso V, Romano R, Santocono C, et al. The impact of cystic fibrosis on the working life of patients: a systematic review. J Cyst Fibros 2022;21:361-9.
DOI: https://doi.org/10.1016/j.jcf.2021.08.011
Begum M, Lewison G, Wright JSF, et al. European non-communicable respiratory disease research, 2002-13: bibliometric study of outputs and funding. PLoS One 2016;11:e0154197.
DOI: https://doi.org/10.1371/journal.pone.0154197
Zhong H, Zhou Y, Mei SY, et al. Scars of COVID-19: a bibliometric analysis of post-COVID-19 fibrosis. Front Public Health 2022;10:967829.
DOI: https://doi.org/10.3389/fpubh.2022.967829
Bell SC, Mall MA, Gutierrez H, et al. The future of cystic fibrosis care: a global perspective. Lancet Respir Med 2020;8:65-124.
DOI: https://doi.org/10.1016/S2213-2600(19)30337-6
Cutting GR. Cystic fibrosis genetics: from molecular understanding to clinical application. Nat Rev Genet 2015;16:45-56.
DOI: https://doi.org/10.1038/nrg3849
Mogayzel PJ, Naureckas ET, Robinson KA, et al. Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health. Am J Respir Crit Care Med 2013;187:680-9.
DOI: https://doi.org/10.1164/rccm.201207-1160OE
Dodge JA, Lewis PA, Stanton M, Wilsher J. Cystic fibrosis mortality and survival in the UK: 1947-2003. Eur Respir J 2007;29:522-6.
DOI: https://doi.org/10.1183/09031936.00099506
How to Cite
Araiqat, Bashar, Sebawe Syaj, Aseel Al-Khatib, Nour Al-Bzour, Narmine Hussein, Sarah Aqel, and Jamil Ahmad. 2024. “A Bibliometric Analysis of Cystic Fibrosis Transmembrane Conductance Regulators”. Monaldi Archives for Chest Disease, July. https://doi.org/10.4081/monaldi.2024.3004.
Copyright (c) 2024 The Author(s)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
PAGEPress has chosen to apply the Creative Commons Attribution NonCommercial 4.0 International License (CC BY-NC 4.0) to all manuscripts to be published.
Similar Articles
- M. Vitacca, L. Bianchi, A. Bazza, E.M. Clini, Advanced COPD patients under Home Mechanical Ventilation and/or Long Term Oxygen Therapy: Italian Healthcare Costs , Monaldi Archives for Chest Disease: Vol. 75 No. 4 (2011): Pulmonary series
- D. Lykouras, F. Sampsonas, A. Kaparianos, K. Karkoulias, G. Tsoukalas, K. Spiropoulos, Human genes in TB infection: their role in immune response , Monaldi Archives for Chest Disease: Vol. 69 No. 1 (2008): Pulmonary series
- Paolo Piergentili, Roberto Valle, Loredano Milani, Clinical and treatment profiles of patients affected by acute coronary syndromes derived from administrative databases in the ASSL 10 Veneto orientale , Monaldi Archives for Chest Disease: Vol. 76 No. 1 (2011): Cardiac series
- Gianluigi Balestroni, Pantaleo Giannuzzi, Giovanna Omarini, Pierangela Omarini, Analysis of the vital exhaustion construct in a female population during cardiac rehabilitation , Monaldi Archives for Chest Disease: Vol. 76 No. 1 (2011): Cardiac series
- M. Bugiani, S. Bonora, A. Carosso, P. Piccioni, M. Cavallero, A. Mondo, V. Ghisetti, The effect of antituberculosis treatment on interferon-γ release assay results , Monaldi Archives for Chest Disease: Vol. 75 No. 4 (2011): Pulmonary series
- Dimitrios Papadopoulos, Panagiotis Misthos, Maria Chorti, Vlasios Skopas, Alexandra Nakou, Napoleon Karagianidis, Achilleas Lioulias, Vasiliki Filaditaki, Unilateral pulmonary hypoplasia in an adult patient , Monaldi Archives for Chest Disease: Vol. 88 No. 1 (2018)
- Antonello D’Andrea, Giancarlo Scognamiglio, Franco Giordano, Sergio Cuomo, Maria Giovanna Russo, Genny Rinaldi, Raffaele Calabrò, An atypical assessment of Ebstein’s anomaly in an 86-year-old man , Monaldi Archives for Chest Disease: Vol. 76 No. 2 (2011): Cardiac series
- Benedetta Basagni, Luana Pancani, Valerio Brambilla, Paolo Coruzzi, Groups with volunteers cardiac surgery patients: experience in a cardiovascular rehabilitation department , Monaldi Archives for Chest Disease: Vol. 78 No. 1 (2012): Cardiac series
- Elena Costanza dal Piaz, Giovanni Cioffi, Federica Ognibeni, Andrea Dalbeni, Alessandro Giollo, Giovanni Orsolini, Davide Gatti, Luca Idolazzi, Carlo Stefenelli, Maurizio Rossini, Ombretta Viapiana, Incidence and predictors of new onset left ventricular diastolic dysfunction in asymptomatic patients with rheumatoid arthritis without overt cardiac disease , Monaldi Archives for Chest Disease: Vol. 89 No. 3 (2019)
- Donatella Del Sindaco, Giovanni Pulignano, Andrea Di Lenarda, Luigi Tarantini, Giovanni Cioffi, Stefano Tolone, Maria Denitza Tinti, Luca Monzo, Giulia Barbati, Giovanni Minardi, Role of a multidisciplinary program in improving outcomes in cognitively impaired heart failure older patients , Monaldi Archives for Chest Disease: Vol. 78 No. 1 (2012): Cardiac series
<< < 8 9 10 11 12 13 14 15 16 17 > >>
You may also start an advanced similarity search for this article.
