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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

BACKGROUND: 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,...

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Autores principales: Park, Hayne Cho, Ryu, Hyunjin, Kim, Yong-Chul, Ahn, Curie, Lee, Kyu-Beck, Kim, Yeong Hoon, Kim, Yunmi, Han, Seungyeup, Kim, Yaerim, Bae, Eun hui, Ma, Seong Kwon, Kang, Hee Gyung, Ahn, Yo Han, Park, Eujin, Jeong, Kyungjo, Lee, Jaewon, Choi, Jungmin, Oh, Kook-Hwan, Oh, Yun Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786983/
https://www.ncbi.nlm.nih.gov/pubmed/33407230
http://dx.doi.org/10.1186/s12882-020-02207-8
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author Park, Hayne Cho
Ryu, Hyunjin
Kim, Yong-Chul
Ahn, Curie
Lee, Kyu-Beck
Kim, Yeong Hoon
Kim, Yunmi
Han, Seungyeup
Kim, Yaerim
Bae, Eun hui
Ma, Seong Kwon
Kang, Hee Gyung
Ahn, Yo Han
Park, Eujin
Jeong, Kyungjo
Lee, Jaewon
Choi, Jungmin
Oh, Kook-Hwan
Oh, Yun Kyu
author_facet Park, Hayne Cho
Ryu, Hyunjin
Kim, Yong-Chul
Ahn, Curie
Lee, Kyu-Beck
Kim, Yeong Hoon
Kim, Yunmi
Han, Seungyeup
Kim, Yaerim
Bae, Eun hui
Ma, Seong Kwon
Kang, Hee Gyung
Ahn, Yo Han
Park, Eujin
Jeong, Kyungjo
Lee, Jaewon
Choi, Jungmin
Oh, Kook-Hwan
Oh, Yun Kyu
author_sort Park, Hayne Cho
collection PubMed
description BACKGROUND: 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.
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spelling pubmed-77869832021-01-07 Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study Park, Hayne Cho Ryu, Hyunjin Kim, Yong-Chul Ahn, Curie Lee, Kyu-Beck Kim, Yeong Hoon Kim, Yunmi Han, Seungyeup Kim, Yaerim Bae, Eun hui Ma, Seong Kwon Kang, Hee Gyung Ahn, Yo Han Park, Eujin Jeong, Kyungjo Lee, Jaewon Choi, Jungmin Oh, Kook-Hwan Oh, Yun Kyu BMC Nephrol Study Protocol BACKGROUND: 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. BioMed Central 2021-01-06 /pmc/articles/PMC7786983/ /pubmed/33407230 http://dx.doi.org/10.1186/s12882-020-02207-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Park, Hayne Cho
Ryu, Hyunjin
Kim, Yong-Chul
Ahn, Curie
Lee, Kyu-Beck
Kim, Yeong Hoon
Kim, Yunmi
Han, Seungyeup
Kim, Yaerim
Bae, Eun hui
Ma, Seong Kwon
Kang, Hee Gyung
Ahn, Yo Han
Park, Eujin
Jeong, Kyungjo
Lee, Jaewon
Choi, Jungmin
Oh, Kook-Hwan
Oh, Yun Kyu
Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study
title Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study
title_full Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study
title_fullStr Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study
title_full_unstemmed Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study
title_short Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study
title_sort genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786983/
https://www.ncbi.nlm.nih.gov/pubmed/33407230
http://dx.doi.org/10.1186/s12882-020-02207-8
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