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Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol

INTRODUCTION: Recent advances in genomic technology have allowed better delineation of renal conditions, the identification of new kidney disease genes and subsequent targets for therapy. To date, however, the utility of genomic testing in a clinically ascertained, prospectively recruited kidney dis...

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Autores principales: Jayasinghe, Kushani, Stark, Zornitza, Patel, Chirag, Mallawaarachchi, Amali, McCarthy, Hugh, Faull, Randall, Chakera, Aron, Sundaram, Madhivanan, Jose, Matthew, Kerr, Peter, Wu, You, Wardrop, Louise, Goranitis, Ilias, Best, Stephanie, Martyn, Melissa, Quinlan, Catherine, Mallett, Andrew J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687024/
https://www.ncbi.nlm.nih.gov/pubmed/31383705
http://dx.doi.org/10.1136/bmjopen-2019-029541
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author Jayasinghe, Kushani
Stark, Zornitza
Patel, Chirag
Mallawaarachchi, Amali
McCarthy, Hugh
Faull, Randall
Chakera, Aron
Sundaram, Madhivanan
Jose, Matthew
Kerr, Peter
Wu, You
Wardrop, Louise
Goranitis, Ilias
Best, Stephanie
Martyn, Melissa
Quinlan, Catherine
Mallett, Andrew J
author_facet Jayasinghe, Kushani
Stark, Zornitza
Patel, Chirag
Mallawaarachchi, Amali
McCarthy, Hugh
Faull, Randall
Chakera, Aron
Sundaram, Madhivanan
Jose, Matthew
Kerr, Peter
Wu, You
Wardrop, Louise
Goranitis, Ilias
Best, Stephanie
Martyn, Melissa
Quinlan, Catherine
Mallett, Andrew J
author_sort Jayasinghe, Kushani
collection PubMed
description INTRODUCTION: Recent advances in genomic technology have allowed better delineation of renal conditions, the identification of new kidney disease genes and subsequent targets for therapy. To date, however, the utility of genomic testing in a clinically ascertained, prospectively recruited kidney disease cohort remains unknown. The aim of this study is to explore the clinical utility and cost-effectiveness of genomic testing within a national cohort of patients with suspected genetic kidney disease who attend multidisciplinary renal genetics clinics. METHODS AND ANALYSIS: This is a prospective observational cohort study performed at 16 centres throughout Australia. Patients will be included if they are referred to one of the multidisciplinary renal genetics clinics and are deemed likely to have a genetic basis to their kidney disease by the multidisciplinary renal genetics team. The expected cohort consists of 360 adult and paediatric patients recruited by December 2018 with ongoing validation cohort of 140 patients who will be recruited until June 2020. The primary outcome will be the proportion of patients who receive a molecular diagnosis via genomic testing (diagnostic rate) compared with usual care. Secondary outcomes will include change in clinical diagnosis following genomic testing, change in clinical management following genomic testing and the cost-effectiveness of genomic testing compared with usual care. ETHICS AND DISSEMINATION: The project has received ethics approval from the Melbourne Health Human Research Ethics Committee as part of the Australian Genomics Health Alliance protocol: HREC/16/MH/251. All participants will provide written informed consent for data collection and to undergo clinically relevant genetic/genomic testing. The results of this study will be published in peer-reviewed journals and will also be presented at national and international conferences.
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spelling pubmed-66870242019-08-23 Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol Jayasinghe, Kushani Stark, Zornitza Patel, Chirag Mallawaarachchi, Amali McCarthy, Hugh Faull, Randall Chakera, Aron Sundaram, Madhivanan Jose, Matthew Kerr, Peter Wu, You Wardrop, Louise Goranitis, Ilias Best, Stephanie Martyn, Melissa Quinlan, Catherine Mallett, Andrew J BMJ Open Genetics and Genomics INTRODUCTION: Recent advances in genomic technology have allowed better delineation of renal conditions, the identification of new kidney disease genes and subsequent targets for therapy. To date, however, the utility of genomic testing in a clinically ascertained, prospectively recruited kidney disease cohort remains unknown. The aim of this study is to explore the clinical utility and cost-effectiveness of genomic testing within a national cohort of patients with suspected genetic kidney disease who attend multidisciplinary renal genetics clinics. METHODS AND ANALYSIS: This is a prospective observational cohort study performed at 16 centres throughout Australia. Patients will be included if they are referred to one of the multidisciplinary renal genetics clinics and are deemed likely to have a genetic basis to their kidney disease by the multidisciplinary renal genetics team. The expected cohort consists of 360 adult and paediatric patients recruited by December 2018 with ongoing validation cohort of 140 patients who will be recruited until June 2020. The primary outcome will be the proportion of patients who receive a molecular diagnosis via genomic testing (diagnostic rate) compared with usual care. Secondary outcomes will include change in clinical diagnosis following genomic testing, change in clinical management following genomic testing and the cost-effectiveness of genomic testing compared with usual care. ETHICS AND DISSEMINATION: The project has received ethics approval from the Melbourne Health Human Research Ethics Committee as part of the Australian Genomics Health Alliance protocol: HREC/16/MH/251. All participants will provide written informed consent for data collection and to undergo clinically relevant genetic/genomic testing. The results of this study will be published in peer-reviewed journals and will also be presented at national and international conferences. BMJ Publishing Group 2019-08-05 /pmc/articles/PMC6687024/ /pubmed/31383705 http://dx.doi.org/10.1136/bmjopen-2019-029541 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Genetics and Genomics
Jayasinghe, Kushani
Stark, Zornitza
Patel, Chirag
Mallawaarachchi, Amali
McCarthy, Hugh
Faull, Randall
Chakera, Aron
Sundaram, Madhivanan
Jose, Matthew
Kerr, Peter
Wu, You
Wardrop, Louise
Goranitis, Ilias
Best, Stephanie
Martyn, Melissa
Quinlan, Catherine
Mallett, Andrew J
Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol
title Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol
title_full Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol
title_fullStr Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol
title_full_unstemmed Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol
title_short Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol
title_sort comprehensive evaluation of a prospective australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol
topic Genetics and Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687024/
https://www.ncbi.nlm.nih.gov/pubmed/31383705
http://dx.doi.org/10.1136/bmjopen-2019-029541
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