Back to Search Start Over

The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure

Authors :
Soo Yeon Kim
Seungbok Lee
Hyewon Woo
Jiyeon Han
Young Jun Ko
Youngkyu Shim
Soojin Park
Se Song Jang
Byung Chan Lim
Jung Min Ko
Ki Joong Kim
Anna Cho
Hunmin Kim
Hee Hwang
Ji Eun Choi
Man Jin Kim
Jangsup Moon
Moon-Woo Seong
Sung Sup Park
Sun Ah Choi
Ji Eun Lee
Young Se Kwon
Young Bae Sohn
Jon Soo Kim
Won Seop Kim
Yun Jeong Lee
Soonhak Kwon
Young Ok Kim
Hoon Kook
Yong Gon Cho
Chong Kun Cheon
Ki-Soo Kang
Mi-Ryoung Song
Young-Joon Kim
Hyuk-Jin Cha
Hee-Jung Choi
Yun Kee
Sung-Gyoo Park
Seung Tae Baek
Murim Choi
Dong-Sung Ryu
Jong-Hee Chae
Source :
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-11 (2022)
Publication Year :
2022
Publisher :
BMC, 2022.

Abstract

Abstract Background Phase I of the Korean Undiagnosed Diseases Program (KUDP), performed for 3 years, has been completed. The Phase I program aimed to solve the problem of undiagnosed patients throughout the country and develop infrastructure, including a data management system and functional core laboratory, for long-term translational research. Herein, we share the clinical experiences of the Phase I program and introduce the activities of the functional core laboratory and data management system. Results During the program (2018–2020), 458 patients were enrolled and classified into 3 groups according to the following criteria: (I) those with a specific clinical assessment which can be verified by direct testing (32 patients); (II) those with a disease group with genetic and phenotypic heterogeneity (353 patients); and (III) those with atypical presentations or diseases unknown to date (73 patients). All patients underwent individualized diagnostic processes based on the decision of an expert consortium. Confirmative diagnoses were obtained for 242 patients (52.8%). The diagnostic yield was different for each group: 81.3% for Group I, 53.3% for Group II, and 38.4% for Group III. Diagnoses were made by next-generation sequencing for 204 patients (84.3%) and other genetic testing for 35 patients (14.5%). Three patients (1.2%) were diagnosed with nongenetic disorders. The KUDP functional core laboratory, with a group of experts, organized a streamlined research pipeline covering various resources, including animal models, stem cells, structural modeling and metabolic and biochemical approaches. Regular data review was performed to screen for candidate genes among undiagnosed patients, and six different genes were identified for functional research. We also developed a web-based database system that supports clinical cohort management and provides a matchmaker exchange protocol based on a matchbox, likely to reinforce the nationwide clinical network and further international collaboration. Conclusions The KUDP evaluated the unmet needs of undiagnosed patients and established infrastructure for a data-sharing system and future functional research. The advancement of the KUDP may lead to sustainable bench-to-bedside research in Korea and contribute to ongoing international collaboration.

Details

Language :
English
ISSN :
17501172
Volume :
17
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.31df2b66d24f748e7b60795882af11
Document Type :
article
Full Text :
https://doi.org/10.1186/s13023-022-02520-5