학술논문
Keratoconus International Consortium (KIC)- advancing keratoconus research
Document Type
Disease/Disorder overview
Author
Sahebjada, Srujana; Chan, Elsie; Sutton, Gerard; Pang, Chi Pui Calvin; Hodge, Christopher; Chong, Elaine W.; Zemani-Fodil, Faouzia; Wiffen, Steve; Snibson, Grant; Morlet, Nigel; Samarawickrama, Chameen; Males, John; Mills, Richard; Beckingsale, Peter; Burdon, Kathryn; Jhanji, Vishal; Krishna, Pravin; Chan, Colin; Tenen, Abi; Roufas, Athena; Huynh, Tess; Vajpayee, Rasik; Gupta, Aanchal; Silva, Marcelo Reyes; Zarei, Mehran; Kumaran, Senthil; Huang, Guofu; Seitz, Berthold; Ren, Shengwei; McGhee, Charles; Barker, Nigel
Source
BMC Ophthalmology. July 27, 2023, Vol. 23 Issue 1
Subject
Language
English
ISSN
1471-2415
Abstract
Author(s): Srujana Sahebjada[sup.1,2], Elsie Chan[sup.1,2,3], Gerard Sutton[sup.4,5], Chi Pui Calvin Pang[sup.6], Christopher Hodge, Elaine W. Chong, Faouzia Zemani-Fodil, Steve Wiffen, Grant Snibson, Nigel Morlet, Chameen Samarawickrama, John Males, Richard Mills, [...]
Clinical relevance The Keratoconus International Consortium (KIC) will allow better understanding of keratoconus. Background Keratoconus is a disorder characterised by corneal elevation and thinning, leading to reduced vision. The current gaps in understanding of this disease will be discussed and the need for a multi-pronged and multi-centre engagement to enhance our understanding of keratoconus will be highlighted. Design KIC has been established to address the gaps in our understanding of keratoconus with the aim of collecting baseline as well as longitudinal data on several fields. Participants Keratoconus and control (no corneal condition) subjects from different sites globally will be recruited in the study. Methods KIC collects data using an online, secure database, which enables standardised data collection at member sites. Data fields collected include medical history, clinical features, quality of life and economic burden questionnaires and possible genetic sample collection from patients of different ethnicities across different geographical locations. Results There are currently 40 Australian and international clinics or hospital departments who have joined the KIC. Baseline data has so far been collected on 1130 keratoconus patients and indicates a median age of 29.70 years with 61% being male. A total of 15.3% report a positive family history of keratoconus and 57.7% self-report a history of frequent eye rubbing. Conclusion The strength of this consortium is its international, collaborative design and use of a common data collection tool. Inclusion and analyses of cross-sectional and longitudinal data will help answer many questions that remain in keratoconus, including factors affecting progression and treatment outcomes. Keywords: Keratoconus, Consortium, Multi-centre project, Keratoconus progression and treatment
Clinical relevance The Keratoconus International Consortium (KIC) will allow better understanding of keratoconus. Background Keratoconus is a disorder characterised by corneal elevation and thinning, leading to reduced vision. The current gaps in understanding of this disease will be discussed and the need for a multi-pronged and multi-centre engagement to enhance our understanding of keratoconus will be highlighted. Design KIC has been established to address the gaps in our understanding of keratoconus with the aim of collecting baseline as well as longitudinal data on several fields. Participants Keratoconus and control (no corneal condition) subjects from different sites globally will be recruited in the study. Methods KIC collects data using an online, secure database, which enables standardised data collection at member sites. Data fields collected include medical history, clinical features, quality of life and economic burden questionnaires and possible genetic sample collection from patients of different ethnicities across different geographical locations. Results There are currently 40 Australian and international clinics or hospital departments who have joined the KIC. Baseline data has so far been collected on 1130 keratoconus patients and indicates a median age of 29.70 years with 61% being male. A total of 15.3% report a positive family history of keratoconus and 57.7% self-report a history of frequent eye rubbing. Conclusion The strength of this consortium is its international, collaborative design and use of a common data collection tool. Inclusion and analyses of cross-sectional and longitudinal data will help answer many questions that remain in keratoconus, including factors affecting progression and treatment outcomes. Keywords: Keratoconus, Consortium, Multi-centre project, Keratoconus progression and treatment