Literature DB >> 28488681

Practices and views of neurologists regarding the use of whole-genome sequencing in clinical settings: a web-based survey.

Iris Jaitovich Groisman1, Thierry Hurlimann1, Amir Shoham2, Béatrice Godard1.   

Abstract

The use of Whole-Genome Sequencing (WGS) in clinical settings has brought up a number of controversial scientific and ethical issues. The application of WGS is of particular relevance in neurology, as many conditions are difficult to diagnose. We conducted a worldwide, web-based survey to explore neurologists' views on the benefits of, and concerns regarding, the clinical use of WGS, as well as the resources necessary to implement it. Almost half of the 204 neurologists in the study treated mostly adult patients (48%), while the rest mainly children (37.3%), or both (14.7%). Epilepsy (73%) and headaches (57.8%) were the predominant conditions treated. Factor analysis brought out two profiles: neurologists who would offer WGS to their patients, and those who would not, or were not sure in which circumstances it should be offered. Neurologists considering the use of WGS as bringing more benefits than drawbacks currently used targeted genetic testing (P<0.05) or treated mainly children (P<0.05). WGS' benefits were directed towards the patients, while its risks were of a financial and legal nature. Furthermore, there was a correlation between respondents' current use of genetic tests and an anticipation of increased use in the future (P<0.001). However, over half of respondents did not feel sufficiently informed to use WGS in their practice (53.5%). Our results highlight gaps in education, organization, and funding to support the use of WGS in neurology, and draw attention to the need for resources that could strongly contribute to more straightforward diagnoses and possibly better treatment of neurological conditions.

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Year:  2017        PMID: 28488681      PMCID: PMC5520076          DOI: 10.1038/ejhg.2017.64

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  38 in total

1.  Reporting results from whole-genome and whole-exome sequencing in clinical practice: a proposal for Canada?

Authors:  Ma'n H Zawati; David Parry; Adrian Thorogood; Minh Thu Nguyen; Kym M Boycott; David Rosenblatt; Bartha Maria Knoppers
Journal:  J Med Genet       Date:  2013-09-27       Impact factor: 6.318

2.  The Future of Next-Generation Sequencing in Neurology.

Authors:  Jean-Baptiste LePichon; Carol J Saunders; Sarah E Soden
Journal:  JAMA Neurol       Date:  2015-09       Impact factor: 18.302

Review 3.  Movement disorders in 2014. Genetic advances spark a revolution in dystonia phenotyping.

Authors:  Tom J de Koning; Marina A J Tijssen
Journal:  Nat Rev Neurol       Date:  2015-01-06       Impact factor: 42.937

4.  Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing.

Authors:  Zoe Lohn; Shelin Adam; Patricia Birch; Anne Townsend; Jan Friedman
Journal:  Am J Med Genet A       Date:  2013-02-07       Impact factor: 2.802

Review 5.  Consortium on the Genetics of Schizophrenia (COGS) assessment of endophenotypes for schizophrenia: an introduction to this Special Issue of Schizophrenia Research.

Authors:  Neal R Swerdlow; Raquel E Gur; David L Braff
Journal:  Schizophr Res       Date:  2014-10-24       Impact factor: 4.939

6.  Managing incidental genomic findings in clinical trials: fulfillment of the principle of justice.

Authors:  Rafael Dal-Ré; Nicholas Katsanis; Sara Katsanis; Lisa S Parker; Carmen Ayuso
Journal:  PLoS Med       Date:  2014-01-14       Impact factor: 11.069

Review 7.  Neurodevelopmental disorders and genetic testing: current approaches and future advances.

Authors:  Elliott H Sherr; David J Michelson; Michael I Shevell; John B Moeschler; Andrea L Gropman; Stephen Ashwal
Journal:  Ann Neurol       Date:  2013-08       Impact factor: 11.274

8.  Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model.

Authors:  Andrea H Németh; Alexandra C Kwasniewska; Stefano Lise; Ricardo Parolin Schnekenberg; Esther B E Becker; Katarzyna D Bera; Morag E Shanks; Lorna Gregory; David Buck; M Zameel Cader; Kevin Talbot; Rajith de Silva; Nicholas Fletcher; Rob Hastings; Sandeep Jayawant; Patrick J Morrison; Paul Worth; Malcolm Taylor; John Tolmie; Mary O'Regan; Ruth Valentine; Emily Packham; Julie Evans; Anneke Seller; Jiannis Ragoussis
Journal:  Brain       Date:  2013-09-11       Impact factor: 13.501

9.  Mutations in HECW2 are associated with intellectual disability and epilepsy.

Authors:  Jonatan Halvardson; Jin J Zhao; Ammar Zaghlool; Christian Wentzel; Patrik Georgii-Hemming; Else Månsson; Helena Ederth Sävmarker; Göran Brandberg; Cecilia Soussi Zander; Ann-Charlotte Thuresson; Lars Feuk
Journal:  J Med Genet       Date:  2016-06-22       Impact factor: 6.318

10.  Ethical issues in consumer genome sequencing: Use of consumers' samples and data.

Authors:  Emilia Niemiec; Heidi Carmen Howard
Journal:  Appl Transl Genom       Date:  2016-02-01
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  7 in total

1.  Exploring neurologists' perspectives on the return of next generation sequencing results to their patients: a needed step in the development of guidelines.

Authors:  Thierry Hurlimann; Iris Jaitovich Groisman; Béatrice Godard
Journal:  BMC Med Ethics       Date:  2018-09-29       Impact factor: 2.652

Review 2.  Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy.

Authors:  Erin Crellin; Belinda McClaren; Amy Nisselle; Stephanie Best; Clara Gaff; Sylvia Metcalfe
Journal:  Front Genet       Date:  2019-09-11       Impact factor: 4.599

3.  Genetic testing offer for inherited neuromuscular diseases within the EURO-NMD reference network: A European survey study.

Authors:  Borut Peterlin; Francesca Gualandi; Ales Maver; Serenella Servidei; Silvère M van der Maarel; Francoise Lamy; Alexander Mejat; Teresinha Evangelista; Alessandra Ferlini
Journal:  PLoS One       Date:  2020-09-18       Impact factor: 3.240

4.  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

5.  Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education.

Authors:  Belinda J McClaren; Emily A King; Erin Crellin; Clara Gaff; Sylvia A Metcalfe; Amy Nisselle
Journal:  Front Genet       Date:  2020-03-03       Impact factor: 4.599

6.  Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics.

Authors:  Kushani Jayasinghe; Catherine Quinlan; Andrew J Mallett; Peter G Kerr; Belinda McClaren; Amy Nisselle; Amali Mallawaarachchi; Kevan R Polkinghorne; Chirag Patel; Stephanie Best; Zornitza Stark
Journal:  Kidney Int Rep       Date:  2020-11-10

7.  Measuring physician practice, preparedness and preferences for genomic medicine: a national survey.

Authors:  Amy Nisselle; Emily A King; Belinda McClaren; Monika Janinski; Sylvia Metcalfe; Clara Gaff
Journal:  BMJ Open       Date:  2021-07-09       Impact factor: 2.692

  7 in total

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