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Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study

DC Field Value Language
dc.contributor.authorPark, Hayne C-
dc.contributor.authorRyu, Hyunjin-
dc.contributor.authorKim, Yong-Chul-
dc.contributor.authorAhn, Curie-
dc.contributor.authorLee, Kyu-Beck-
dc.contributor.authorKim, Yeong Hoon-
dc.contributor.authorKim, Yunmi-
dc.contributor.authorHan, Seungyeup-
dc.contributor.authorKim, Yaerim-
dc.contributor.authorBae, Eun hui-
dc.contributor.authorMa, Seong Kwon-
dc.contributor.authorKang, Hee Gyung-
dc.contributor.authorAhn, Yo Han-
dc.contributor.authorPark, Eujin-
dc.contributor.authorJeong, Kyungjo-
dc.contributor.authorLee, Jaewon-
dc.contributor.authorChoi, Jungmin-
dc.contributor.authorOh, Kook-Hwan-
dc.contributor.authorOh, Yun Kyu-
dc.date.accessioned2021-02-23T07:47:15Z-
dc.date.available2021-02-23T16:48:06Z-
dc.date.issued2021-01-06-
dc.identifier.citationBMC Nephrology. 2021 Jan 06;22(1):2ko_KR
dc.identifier.issn1471-2369-
dc.identifier.urihttps://hdl.handle.net/10371/173380-
dc.description.abstractBackground
Inherited cystic kidney disease is a spectrum of disorders in which clusters of renal cysts develop as the result of genetic mutation. The exact methods and pipelines for defining genetic mutations of inherited cystic kidney disease are not clear at this point. This 3-year, prospective, multicenter, cohort study was designed to set up a cohort of Korean patients with inherited cystic kidney disease, establish a customized genetic analysis pipeline for each disease subtype, and identify modifying genes associated with the severity of the disease phenotype.

Methods/design
From May 2020 to May 2022, we aim to recruit 800 patients and their family members to identify pathogenic mutations. Patients with more than 3 renal cysts in both kidneys are eligible to be enrolled. Cases of simple renal cysts and acquired cystic kidney disease that involve cyst formation as the result of renal failure will be excluded from this study. Demographic, laboratory, and imaging data as well as family pedigree will be collected at baseline. Renal function and changes in total kidney volume will be monitored during the follow-up period. Genetic identification of each case of inherited cystic kidney disease will be performed using a targeted gene panel of cystogenesis-related genes, whole exome sequencing (WES) and/or family segregation studies. Genotype-phenotype correlation analysis will be performed to elucidate the genetic effect on the severity of the disease phenotype.

Discussion
This is the first nationwide cohort study on patients with inherited cystic kidney disease in Korea. We will build a multicenter cohort to describe the clinical characteristics of Korean patients with inherited cystic kidney disease, elucidate the genotype of each disease, and demonstrate the genetic effects on the severity of the disease phenotype.

Trial registration
This cohort study was retrospectively registered at the Clinical Research Information Service (
KCT0005580) operated by the Korean Center for Disease Control and Prevention on November 5th, 2020.
ko_KR
dc.description.sponsorshipThis work has been supported by the Research Program funded by the Korea Centers for Disease Control and Prevention (2019-ER-7304-00, 2019-ER7304-01). The funding body has no role in the design of the study, collection, analysis, interpretation of data, or writing of the manuscript.ko_KR
dc.language.isoenko_KR
dc.publisherBMCko_KR
dc.subjectCohort study-
dc.subjectCystic kidney disease-
dc.subjectHigh-throughput nucleotide sequencing-
dc.subjectGenotype-
dc.subjectPhenotype-
dc.subjectGenetic association studies-
dc.subjectGlomerular filtration rate-
dc.titleGenetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort studyko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor류현진-
dc.contributor.AlternativeAuthor김용철-
dc.contributor.AlternativeAuthor이규백-
dc.contributor.AlternativeAuthor김영훈-
dc.contributor.AlternativeAuthor김윤미-
dc.contributor.AlternativeAuthor한승엽-
dc.contributor.AlternativeAuthor김예림-
dc.contributor.AlternativeAuthor배은희-
dc.contributor.AlternativeAuthor마성권-
dc.contributor.AlternativeAuthor강희경-
dc.contributor.AlternativeAuthor안요한-
dc.contributor.AlternativeAuthor박유진-
dc.contributor.AlternativeAuthor정경조-
dc.contributor.AlternativeAuthor이재원-
dc.contributor.AlternativeAuthor오국환-
dc.contributor.AlternativeAuthor오윤규-
dc.identifier.doi10.1186/s12882-020-02207-8-
dc.citation.journaltitleBMC Nephrologyko_KR
dc.language.rfc3066en-
dc.rights.holderThe Author(s)-
dc.date.updated2021-01-27T09:56:53Z-
dc.citation.number1ko_KR
dc.citation.startpage2ko_KR
dc.citation.volume22ko_KR
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