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The Gaucher Earlier Diagnosis Consensus point-scoring system for children and young adults: a retrospective and prospective evaluation in Korea

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dc.contributor.author유철주-
dc.contributor.author한승민-
dc.contributor.author오지영-
dc.contributor.author고홍-
dc.contributor.author남정모-
dc.contributor.author김세희-
dc.date.accessioned2025-11-18T03:09:35Z-
dc.date.available2025-11-18T03:09:35Z-
dc.date.issued2025-11-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/209005-
dc.description.abstractPurpose: Gaucher disease (GD) is an autosomal recessive condition caused by insufficient glucocerebrosidase activity. The Gaucher Earlier Diagnosis Consensus (GED-C) initiative created a point-scoring system (PSS) to facilitate the early identification of GD based on significant indicators and covariables. This study aimed to evaluate the applicability and utility of the GED-C PSS in pediatric and young adult patients in Korea. Results: This study included both retrospective analysis and prospective recruitment. Subject recruitment involved 14 sites across 13 hospitals in Korea, where patients of any age meeting GED-C criteria were recruited, and blood samples were collected. Data of 513 subjects were analyzed and two patients were confirmed to have GD during prospective enrollment. The median age of participants was 10 years (range: 1 month to 40 years). Receiver operating characteristic analysis revealed a cutoff point of 6.5 for GED-C PSS (area under the curve of 0.9883) demonstrated high sensitivity (1.0) and specificity (0.97). A histogram indicated that the PSS scores of the two confirmed GD patients were distinct from those of other participants. Conclusions: The study suggests that GED-C PSS shows potential for the early diagnosis of GD, supporting its broader clinical use for both children and adults.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherBioMed Central-
dc.relation.isPartOfORPHANET JOURNAL OF RARE DISEASES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdolescent-
dc.subject.MESHAdult-
dc.subject.MESHChild-
dc.subject.MESHChild, Preschool-
dc.subject.MESHEarly Diagnosis-
dc.subject.MESHFemale-
dc.subject.MESHGaucher Disease* / diagnosis-
dc.subject.MESHHumans-
dc.subject.MESHInfant-
dc.subject.MESHMale-
dc.subject.MESHProspective Studies-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHYoung Adult-
dc.titleThe Gaucher Earlier Diagnosis Consensus point-scoring system for children and young adults: a retrospective and prospective evaluation in Korea-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pediatrics (소아과학교실)-
dc.contributor.googleauthorSeung Min Hahn-
dc.contributor.googleauthorMinseok Kim-
dc.contributor.googleauthorYouna Kim-
dc.contributor.googleauthorJiyoung Oh-
dc.contributor.googleauthorSe Hee Kim-
dc.contributor.googleauthorHong Koh-
dc.contributor.googleauthorSung-Eun Kim-
dc.contributor.googleauthorNack-Gyun Chung-
dc.contributor.googleauthorYe Jee Shim-
dc.contributor.googleauthorHawk Kim-
dc.contributor.googleauthorJae Min Lee-
dc.contributor.googleauthorSung-Soo Yoon-
dc.contributor.googleauthorHo Joon Im-
dc.contributor.googleauthorHyoung Jin Kang-
dc.contributor.googleauthorYoung Rok Do-
dc.contributor.googleauthorChung Mo Nam-
dc.contributor.googleauthorChuhl Joo Lyu-
dc.identifier.doi10.1186/s13023-025-03891-1-
dc.contributor.localIdA02524-
dc.contributor.localIdA04299-
dc.contributor.localIdA02399-
dc.contributor.localIdA00156-
dc.contributor.localIdA01264-
dc.relation.journalcodeJ03433-
dc.identifier.eissn1750-1172-
dc.identifier.pmid41214801-
dc.subject.keywordEarly diagnosis-
dc.subject.keywordGaucher disease-
dc.subject.keywordLysosomal storage disorder-
dc.contributor.alternativeNameLyu, Chuhl Joo-
dc.contributor.affiliatedAuthor유철주-
dc.contributor.affiliatedAuthor한승민-
dc.contributor.affiliatedAuthor오지영-
dc.contributor.affiliatedAuthor고홍-
dc.contributor.affiliatedAuthor남정모-
dc.citation.volume20-
dc.citation.number1-
dc.citation.startPage569-
dc.identifier.bibliographicCitationORPHANET JOURNAL OF RARE DISEASES, Vol.20(1) : 569, 2025-11-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Preventive Medicine (예방의학교실) > 1. Journal Papers

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