Your browser doesn't support javascript.
loading
ClinGen's Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents.
Hunter, Jessica Ezzell; Jenkins, Charisma L; Bulkley, Joanna E; Gilmore, Marian J; Lee, Kristy; Pak, Christine M; Wallace, Kathleen E; Buchanan, Adam H; Foreman, Ann Katherine M; Freed, Amanda S; Goehringer, Scott; Manickam, Kandamurugu; Meeks, Naomi J L; Ramos, Erin M; Shah, Neethu; Steiner, Robert D; Subramanian, Sai Lakshmi; Trotter, Tracy; Webber, Elizabeth M; Williams, Marc S; Goddard, Katrina A B; Powell, Bradford C.
Afiliação
  • Hunter JE; Genomics, Ethics, and Translational Research Program, RTI International, ResearchTriangle Park, NC. Electronic address: jehunter@rti.org.
  • Jenkins CL; Department of Translational and Applied Genomics (TAG), Kaiser Permanente Center for Health Research, Portland, OR.
  • Bulkley JE; Department of Translational and Applied Genomics (TAG), Kaiser Permanente Center for Health Research, Portland, OR.
  • Gilmore MJ; Department of Translational and Applied Genomics (TAG), Kaiser Permanente Center for Health Research, Portland, OR.
  • Lee K; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Pak CM; Department of Translational and Applied Genomics (TAG), Kaiser Permanente Center for Health Research, Portland, OR.
  • Wallace KE; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Buchanan AH; Genomic Medicine Institute, Geisinger, Danville, PA.
  • Foreman AKM; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Freed AS; Department of Clinical Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, CA.
  • Goehringer S; Genomic Medicine Institute, Geisinger, Danville, PA.
  • Manickam K; Division of Genetic and Genomic Medicine, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH; The Ohio State University College of Medicine, Columbus, OH.
  • Meeks NJL; Section of Genetics and Metabolism, Department of Pediatrics, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO.
  • Ramos EM; Division of Genomic Medicine, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD.
  • Shah N; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
  • Steiner RD; School of Medicine and Public Health, University of Wisconsin, Madison, WI.
  • Subramanian SL; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
  • Trotter T; John Muir Health, Walnut Creek, CA.
  • Webber EM; Kaiser Permanente Center for Health Research, Portland, OR.
  • Williams MS; Genomic Medicine Institute, Geisinger, Danville, PA.
  • Goddard KAB; Department of Translational and Applied Genomics (TAG), Kaiser Permanente Center for Health Research, Portland, OR.
  • Powell BC; Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Genet Med ; 24(6): 1328-1335, 2022 06.
Article em En | MEDLINE | ID: mdl-35341655
ABSTRACT

PURPOSE:

Synthesis and curation of evidence regarding the clinical actionability of secondary findings (SFs) from genome-scale sequencing are needed to support decision-making on reporting of these findings. To assess actionability of SFs in children and adolescents, the Clinical Genome Resource established the Pediatric Actionability Working Group (AWG).

METHODS:

The Pediatric AWG modified the framework of the existing Adult AWG, which included production of summary reports of actionability for genes and associated conditions and consensus actionability scores for specific outcome-intervention pairs. Modification of the adult framework for the pediatric setting included accounting for special considerations for reporting presymptomatic or predictive genetic findings in the pediatric context, such as maintaining future autonomy by not disclosing conditions not actionable until adulthood. The Pediatric AWG then applied this new framework to genes and associated conditions with putative actionability.

RESULTS:

As of September 2021, the Pediatric AWG applied the new framework to 70 actionability topics representing 143 genes. Reports and scores are publicly available at www.clinicalgenome.org.

CONCLUSION:

The Pediatric AWG continues to curate gene-condition topics and build an evidence-based resource, supporting clinical communities and decision-makers with policy development on the return of SFs in pediatric populations.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Relatório de Pesquisa Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Adult / Child / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Relatório de Pesquisa Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Adult / Child / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article