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Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant

The rapid advancement of next-generation sequencing (NGS) technology and the decrease in costs for whole-exome sequencing (WES) and whole-genome sequening (WGS), has prompted its clinical application in several fields of medicine. Currently, there are no specific guidelines for the use of NGS in the...

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Autores principales: Borghesi, Alessandro, Mencarelli, Maria Antonietta, Memo, Luigi, Ferrero, Giovanni Battista, Bartuli, Andrea, Genuardi, Maurizio, Stronati, Mauro, Villani, Alberto, Renieri, Alessandra, Corsello, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670717/
https://www.ncbi.nlm.nih.gov/pubmed/29100554
http://dx.doi.org/10.1186/s13052-017-0418-0
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author Borghesi, Alessandro
Mencarelli, Maria Antonietta
Memo, Luigi
Ferrero, Giovanni Battista
Bartuli, Andrea
Genuardi, Maurizio
Stronati, Mauro
Villani, Alberto
Renieri, Alessandra
Corsello, Giovanni
author_facet Borghesi, Alessandro
Mencarelli, Maria Antonietta
Memo, Luigi
Ferrero, Giovanni Battista
Bartuli, Andrea
Genuardi, Maurizio
Stronati, Mauro
Villani, Alberto
Renieri, Alessandra
Corsello, Giovanni
author_sort Borghesi, Alessandro
collection PubMed
description The rapid advancement of next-generation sequencing (NGS) technology and the decrease in costs for whole-exome sequencing (WES) and whole-genome sequening (WGS), has prompted its clinical application in several fields of medicine. Currently, there are no specific guidelines for the use of NGS in the field of neonatal medicine and in the diagnosis of genetic diseases in critically ill newborn infants. As a consequence, NGS may be underused with reduced diagnostic success rate, or overused, with increased costs for the healthcare system. Most genetic diseases may be already expressed during the neonatal age, but their identification may be complicated by nonspecific presentation, especially in the setting of critical clinical conditions. The differential diagnosis process in the neonatal intensive care unit (NICU) may be time-consuming, uncomfortable for the patient due to repeated sampling, and ineffective in reaching a molecular diagnosis during NICU stay. Serial gene sequencing (Sanger sequencing) may be successful only for conditions for which the clinical phenotype strongly suggests a diagnostic hypothesis and for genetically homogeneous diseases. Newborn screenings with Guthrie cards, which vary from country to country, are designed to only test for a few dozen genetic diseases out of the more than 6000 diseases for which a genetic characterization is available. The use of WES in selected cases in the NICU may overcome these issues. We present an intersociety document that aims to define the best indications for the use of WES in different clinical scenarios in the NICU. We propose that WES is used in the NICU for critically ill newborn infants when an early diagnosis is desirable to guide the clinical management during NICU stay, when a strong hypothesis cannot be formulated based on the clinical phenotype or the disease is genetically heterogeneous, and when specific non-genetic laboratory tests are not available. The use of WES may reduce the time for diagnosis in infants during NICU stay and may eventually result in cost-effectiveness.
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spelling pubmed-56707172017-11-15 Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant Borghesi, Alessandro Mencarelli, Maria Antonietta Memo, Luigi Ferrero, Giovanni Battista Bartuli, Andrea Genuardi, Maurizio Stronati, Mauro Villani, Alberto Renieri, Alessandra Corsello, Giovanni Ital J Pediatr Review The rapid advancement of next-generation sequencing (NGS) technology and the decrease in costs for whole-exome sequencing (WES) and whole-genome sequening (WGS), has prompted its clinical application in several fields of medicine. Currently, there are no specific guidelines for the use of NGS in the field of neonatal medicine and in the diagnosis of genetic diseases in critically ill newborn infants. As a consequence, NGS may be underused with reduced diagnostic success rate, or overused, with increased costs for the healthcare system. Most genetic diseases may be already expressed during the neonatal age, but their identification may be complicated by nonspecific presentation, especially in the setting of critical clinical conditions. The differential diagnosis process in the neonatal intensive care unit (NICU) may be time-consuming, uncomfortable for the patient due to repeated sampling, and ineffective in reaching a molecular diagnosis during NICU stay. Serial gene sequencing (Sanger sequencing) may be successful only for conditions for which the clinical phenotype strongly suggests a diagnostic hypothesis and for genetically homogeneous diseases. Newborn screenings with Guthrie cards, which vary from country to country, are designed to only test for a few dozen genetic diseases out of the more than 6000 diseases for which a genetic characterization is available. The use of WES in selected cases in the NICU may overcome these issues. We present an intersociety document that aims to define the best indications for the use of WES in different clinical scenarios in the NICU. We propose that WES is used in the NICU for critically ill newborn infants when an early diagnosis is desirable to guide the clinical management during NICU stay, when a strong hypothesis cannot be formulated based on the clinical phenotype or the disease is genetically heterogeneous, and when specific non-genetic laboratory tests are not available. The use of WES may reduce the time for diagnosis in infants during NICU stay and may eventually result in cost-effectiveness. BioMed Central 2017-11-03 /pmc/articles/PMC5670717/ /pubmed/29100554 http://dx.doi.org/10.1186/s13052-017-0418-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Review
Borghesi, Alessandro
Mencarelli, Maria Antonietta
Memo, Luigi
Ferrero, Giovanni Battista
Bartuli, Andrea
Genuardi, Maurizio
Stronati, Mauro
Villani, Alberto
Renieri, Alessandra
Corsello, Giovanni
Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant
title Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant
title_full Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant
title_fullStr Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant
title_full_unstemmed Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant
title_short Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant
title_sort intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670717/
https://www.ncbi.nlm.nih.gov/pubmed/29100554
http://dx.doi.org/10.1186/s13052-017-0418-0
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