Literature DB >> 29760485

Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature.

Hadley Stevens Smith1, J Michael Swint2, Seema R Lalani3, Jose-Miguel Yamal4, Marcia C de Oliveira Otto4, Stephan Castellanos5, Amy Taylor6, Brendan H Lee7, Heidi V Russell8.   

Abstract

PURPOSE: Availability of clinical genomic sequencing (CGS) has generated questions about the value of genome and exome sequencing as a diagnostic tool. Analysis of reported CGS application can inform uptake and direct further research. This scoping literature review aims to synthesize evidence on the clinical and economic impact of CGS.
METHODS: PubMed, Embase, and Cochrane were searched for peer-reviewed articles published between 2009 and 2017 on diagnostic CGS for infant and pediatric patients. Articles were classified according to sample size and whether economic evaluation was a primary research objective. Data on patient characteristics, clinical setting, and outcomes were extracted and narratively synthesized.
RESULTS: Of 171 included articles, 131 were case reports, 40 were aggregate analyses, and 4 had a primary economic evaluation aim. Diagnostic yield was the only consistently reported outcome. Median diagnostic yield in aggregate analyses was 33.2% but varied by broad clinical categories and test type.
CONCLUSION: Reported CGS use has rapidly increased and spans diverse clinical settings and patient phenotypes. Economic evaluations support the cost-saving potential of diagnostic CGS. Multidisciplinary implementation research, including more robust outcome measurement and economic evaluation, is needed to demonstrate clinical utility and cost-effectiveness of CGS.

Entities:  

Keywords:  Clinical implementation; Medical genomics; Review; exome sequencing; genome sequencing

Mesh:

Year:  2018        PMID: 29760485     DOI: 10.1038/s41436-018-0024-6

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  171 in total

1.  Right test, right time, right patient.

Authors:  Karl W Thomas
Journal:  Crit Care Med       Date:  2014-01       Impact factor: 7.598

2.  Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.

Authors:  Laurel K Willig; Josh E Petrikin; Laurie D Smith; Carol J Saunders; Isabelle Thiffault; Neil A Miller; Sarah E Soden; Julie A Cakici; Suzanne M Herd; Greyson Twist; Aaron Noll; Mitchell Creed; Patria M Alba; Shannon L Carpenter; Mark A Clements; Ryan T Fischer; J Allyson Hays; Howard Kilbride; Ryan J McDonough; Jamie L Rosterman; Sarah L Tsai; Lee Zellmer; Emily G Farrow; Stephen F Kingsmore
Journal:  Lancet Respir Med       Date:  2015-04-27       Impact factor: 30.700

3.  Convergence of Implementation Science, Precision Medicine, and the Learning Health Care System: A New Model for Biomedical Research.

Authors:  David A Chambers; W Gregory Feero; Muin J Khoury
Journal:  JAMA       Date:  2016-05-10       Impact factor: 56.272

4.  Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.

Authors:  Hussein Daoud; Stephanie M Luco; Rui Li; Eric Bareke; Chandree Beaulieu; Olga Jarinova; Nancy Carson; Sarah M Nikkel; Gail E Graham; Julie Richer; Christine Armour; Dennis E Bulman; Pranesh Chakraborty; Michael Geraghty; Matthew A Lines; Thierry Lacaze-Masmonteil; Jacek Majewski; Kym M Boycott; David A Dyment
Journal:  CMAJ       Date:  2016-05-30       Impact factor: 8.262

5.  Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.

Authors:  Linyan Meng; Mohan Pammi; Anirudh Saronwala; Pilar Magoulas; Andrew Ray Ghazi; Francesco Vetrini; Jing Zhang; Weimin He; Avinash V Dharmadhikari; Chunjing Qu; Patricia Ward; Alicia Braxton; Swetha Narayanan; Xiaoyan Ge; Mari J Tokita; Teresa Santiago-Sim; Hongzheng Dai; Theodore Chiang; Hadley Smith; Mahshid S Azamian; Laurie Robak; Bret L Bostwick; Christian P Schaaf; Lorraine Potocki; Fernando Scaglia; Carlos A Bacino; Neil A Hanchard; Michael F Wangler; Daryl Scott; Chester Brown; Jianhong Hu; John W Belmont; Lindsay C Burrage; Brett H Graham; Vernon Reid Sutton; William J Craigen; Sharon E Plon; James R Lupski; Arthur L Beaudet; Richard A Gibbs; Donna M Muzny; Marcus J Miller; Xia Wang; Magalie S Leduc; Rui Xiao; Pengfei Liu; Chad Shaw; Magdalena Walkiewicz; Weimin Bi; Fan Xia; Brendan Lee; Christine M Eng; Yaping Yang; Seema R Lalani
Journal:  JAMA Pediatr       Date:  2017-12-04       Impact factor: 16.193

Review 6.  Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing.

Authors:  Yuan Xue; Arunkanth Ankala; William R Wilcox; Madhuri R Hegde
Journal:  Genet Med       Date:  2014-09-18       Impact factor: 8.822

7.  The economic value of personalized medicine tests: what we know and what we need to know.

Authors:  Kathryn A Phillips; Julie Ann Sakowski; Julia Trosman; Michael P Douglas; Su-Ying Liang; Peter Neumann
Journal:  Genet Med       Date:  2013-10-17       Impact factor: 8.822

Review 8.  Issues surrounding the health economic evaluation of genomic technologies.

Authors:  James Buchanan; Sarah Wordsworth; Anna Schuh
Journal:  Pharmacogenomics       Date:  2013-11       Impact factor: 2.533

9.  The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders.

Authors:  Vandana Shashi; Allyn McConkie-Rosell; Bruce Rosell; Kelly Schoch; Kasturi Vellore; Marie McDonald; Yong-Hui Jiang; Pingxing Xie; Anna Need; David B Goldstein; David G Goldstein
Journal:  Genet Med       Date:  2013-08-29       Impact factor: 8.822

Review 10.  Implementing genomic medicine in the clinic: the future is here.

Authors:  Teri A Manolio; Rex L Chisholm; Brad Ozenberger; Dan M Roden; Marc S Williams; Richard Wilson; David Bick; Erwin P Bottinger; Murray H Brilliant; Charis Eng; Kelly A Frazer; Bruce Korf; David H Ledbetter; James R Lupski; Clay Marsh; David Mrazek; Michael F Murray; Peter H O'Donnell; Daniel J Rader; Mary V Relling; Alan R Shuldiner; David Valle; Richard Weinshilboum; Eric D Green; Geoffrey S Ginsburg
Journal:  Genet Med       Date:  2013-01-10       Impact factor: 8.822

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  33 in total

1.  The Genetic Landscape of Diamond-Blackfan Anemia.

Authors:  Jacob C Ulirsch; Jeffrey M Verboon; Shideh Kazerounian; Michael H Guo; Daniel Yuan; Leif S Ludwig; Robert E Handsaker; Nour J Abdulhay; Claudia Fiorini; Giulio Genovese; Elaine T Lim; Aaron Cheng; Beryl B Cummings; Katherine R Chao; Alan H Beggs; Casie A Genetti; Colin A Sieff; Peter E Newburger; Edyta Niewiadomska; Michal Matysiak; Adrianna Vlachos; Jeffrey M Lipton; Eva Atsidaftos; Bertil Glader; Anupama Narla; Pierre-Emmanuel Gleizes; Marie-Françoise O'Donohue; Nathalie Montel-Lehry; David J Amor; Steven A McCarroll; Anne H O'Donnell-Luria; Namrata Gupta; Stacey B Gabriel; Daniel G MacArthur; Eric S Lander; Monkol Lek; Lydie Da Costa; David G Nathan; Andrei A Korostelev; Ron Do; Vijay G Sankaran; Hanna T Gazda
Journal:  Am J Hum Genet       Date:  2018-11-29       Impact factor: 11.025

Review 2.  The clinical utility of exome and genome sequencing across clinical indications: a systematic review.

Authors:  Salma Shickh; Chloe Mighton; Elizabeth Uleryk; Petros Pechlivanoglou; Yvonne Bombard
Journal:  Hum Genet       Date:  2021-08-08       Impact factor: 4.132

3.  Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium.

Authors:  Joon-Ho Yu; Paul S Appelbaum; Kyle B Brothers; Steven Joffe; Tia L Kauffman; Barbara A Koenig; Anya Er Prince; Sarah Scollon; Susan M Wolf; Barbara A Bernhardt; Benjamin S Wilfond
Journal:  Per Med       Date:  2019-07-17       Impact factor: 2.512

4.  Diagnostic yield from routine metabolic screening tests in evaluation of global developmental delay and intellectual disability.

Authors:  Hilary Vallance; Graham Sinclair; Bojana Rakic; Sylvia Stockler-Ipsiroglu
Journal:  Paediatr Child Health       Date:  2020-12-19       Impact factor: 2.253

Review 5.  Data Science for Child Health.

Authors:  Tellen D Bennett; Tiffany J Callahan; James A Feinstein; Debashis Ghosh; Saquib A Lakhani; Michael C Spaeder; Stanley J Szefler; Michael G Kahn
Journal:  J Pediatr       Date:  2019-01-25       Impact factor: 4.406

6.  Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).

Authors:  Kandamurugu Manickam; Monica R McClain; Laurie A Demmer; Sawona Biswas; Hutton M Kearney; Jennifer Malinowski; Lauren J Massingham; Danny Miller; Timothy W Yu; Fuki M Hisama
Journal:  Genet Med       Date:  2021-07-01       Impact factor: 8.822

7.  Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test.

Authors:  Deanna G Brockman; Christina A Austin-Tse; Renée C Pelletier; Caroline Harley; Candace Patterson; Holly Head; Courtney Elizabeth Leonard; Kimberly O'Brien; Lisa M Mahanta; Matthew S Lebo; Christine Y Lu; Pradeep Natarajan; Amit V Khera; Krishna G Aragam; Sekar Kathiresan; Heidi L Rehm; Miriam S Udler
Journal:  Genet Med       Date:  2021-05-11       Impact factor: 8.822

8.  Genome-Wide Sequencing for Unexplained Developmental Disabilities or Multiple Congenital Anomalies: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2020-03-06

9.  Exome variant discrepancies due to reference-genome differences.

Authors:  He Li; Moez Dawood; Michael M Khayat; Jesse R Farek; Shalini N Jhangiani; Ziad M Khan; Tadahiro Mitani; Zeynep Coban-Akdemir; James R Lupski; Eric Venner; Jennifer E Posey; Aniko Sabo; Richard A Gibbs
Journal:  Am J Hum Genet       Date:  2021-06-14       Impact factor: 11.025

Review 10.  Paroxysmal Movement Disorders.

Authors:  Susan Harvey; Mary D King; Kathleen M Gorman
Journal:  Front Neurol       Date:  2021-06-11       Impact factor: 4.003

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