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
- Maryam Hassan, Akbar Shoukat Ali, Ali Bin Sarwar Zubairi, Zahra Ali Padhani, Salman Kirmani, Huzaifa Ahmad, Zafar Fatmi, Jai K Das, Gene polymorphisms and risk of idiopathic pulmonary fibrosis: a systematic review and meta-analysis , Monaldi Archives for Chest Disease: Early Access
- Laura Miranda, Sarwat Gilani, Liying Han, Oleg Epelbaum, Three's company: A woman with rash, uterine mass and cystic lungs , Monaldi Archives for Chest Disease: Vol. 90 No. 1 (2020)
- Nikhilesh Ladha, Pankaj Bhardwaj, Nishant Kumar Chauhan, Kikkeri Hanumantha Setty Naveen, Vijaya Lakshmi Nag, Dandabathula Giribabu, Determinants, risk factors and spatial analysis of multi-drug resistant pulmonary tuberculosis in Jodhpur, India , Monaldi Archives for Chest Disease: Vol. 92 No. 4 (2022)
- Ivan Comelli, Alessandra Bologna, Andrea Ticinesi, Andrea Magnacavallo, Denis Comelli, Tiziana Meschi, Gianfranco Cervellin, Incidence of primary spontaneous pneumothorax is not associated with microclimatic variations. Results of a seven-year survey in a temperate climate area , Monaldi Archives for Chest Disease: Vol. 87 No. 1 (2017)
- Filippo M. Sarullo, Luigi Americo, Salvatore Accardo, Sergio Cicero, Rossella Schicchi, Maria Schirò, Antonio Castello, Tako-tsubo cardiomyopathy observed in a patient with sepsis and transient hyperthyroidism , Monaldi Archives for Chest Disease: Vol. 72 No. 1 (2009): Cardiac series
- Astha Guliani, Abhishek Tandon, Amartya Chakroborty, Prem Parkash Gupta, Predictors of post COVID complications in patients admitted with moderate to severe COVID symptoms: A single center, prospective, observational study , Monaldi Archives for Chest Disease: Vol. 93 No. 2 (2023)
- Shayan Shahid, Kausar Jabeen, Nousheen Iqbal, Joveria Farooqi, Muhammad Irfan, Respiratory pathogens in patients with acute exacerbation of non-cystic fibrosis bronchiectasis from a developing country , Monaldi Archives for Chest Disease: Vol. 91 No. 2 (2021)
- Cuneyt Tetikkurt, Buket Caliskaner Ozturk, Nejdiye Gungordu, Diagnosis of pleuroparenchymal fibroelastosis: A review , Monaldi Archives for Chest Disease: Vol. 93 No. 3 (2023)
- Veronica Rossi, Martina Santambrogio, Cesare Del Monaco, Mariangela Retucci, Serena Tammaro, Clara Ceruti, Laura Saderi, Stefano Aliberti, Emilia Privitera, Giacomo Grasselli, Giovanni Sotgiu, Francesco Blasi, Safety and feasibility of physiotherapy in ICU-admitted severe COVID-19 patients: an observational study , Monaldi Archives for Chest Disease: Vol. 92 No. 4 (2022)
- K. Ahmad Dar, M. Shahid, A. Mubeen, R. Bhargava, Z. Ahmad, I. Ahmad, N. Islam, The role of noninvasive methods in assessing airway inflammation and structural changes in asthma and COPD , Monaldi Archives for Chest Disease: Vol. 77 No. 1 (2012): Pulmonary series
<< < 1 2 3 4 5 6 7 8 9 10 > >>
You may also start an advanced similarity search for this article.
