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Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series.
Taylor, John; Craft, Jude; Blair, Edward; Wordsworth, Sarah; Beeson, David; Chandratre, Saleel; Cossins, Judith; Lester, Tracy; Németh, Andrea H; Ormondroyd, Elizabeth; Patel, Smita Y; Pagnamenta, Alistair T; Taylor, Jenny C; Thomson, Kate L; Watkins, Hugh; Wilkie, Andrew O M; Knight, Julian C.
Afiliación
  • Taylor J; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Craft J; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Blair E; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Wordsworth S; Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Beeson D; National Institute for Health Research Biomedical Research Centre, Oxford, UK.
  • Chandratre S; MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Cossins J; Children's Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Lester T; MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
  • Németh AH; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Ormondroyd E; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Patel SY; Nuffield Department of Clinical Neurosciences, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Pagnamenta AT; Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Taylor JC; National Institute for Health Research Biomedical Research Centre, Oxford, UK.
  • Thomson KL; National Institute for Health Research Biomedical Research Centre, Oxford, UK.
  • Watkins H; Department of Clinical Immunology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Wilkie AOM; National Institute for Health Research Biomedical Research Centre, Oxford, UK.
  • Knight JC; Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Genome Med ; 11(1): 46, 2019 07 25.
Article en En | MEDLINE | ID: mdl-31345272
ABSTRACT

BACKGROUND:

A multi-disciplinary approach to promote engagement, inform decision-making and support clinicians and patients is increasingly advocated to realise the potential of genome-scale sequencing in the clinic for patient benefit. Here we describe the results of establishing a genomic medicine multi-disciplinary team (GM-MDT) for case selection, processing, interpretation and return of results.

METHODS:

We report a consecutive case series of 132 patients (involving 10 medical specialties with 43.2% cases having a neurological disorder) undergoing exome sequencing over a 10-month period following the establishment of the GM-MDT in a UK NHS tertiary referral hospital. The costs of running the MDT are also reported.

RESULTS:

In total 76 cases underwent exome sequencing following triage by the GM-MDT with a clinically reportable molecular diagnosis in 24 (31.6%). GM-MDT composition, operation and rationale for whether to proceed to sequencing are described, together with the health economics (cost per case for the GM-MDT was £399.61), the utility and informativeness of exome sequencing for molecular diagnosis in a range of traits, the impact of choice of sequencing strategy on molecular diagnostic rates and challenge of defining pathogenic variants. In 5 cases (6.6%), an alternative clinical diagnosis was indicated by sequencing results. Examples were also found where findings from initial genetic testing were reconsidered in the light of exome sequencing including TP63 and PRKAG2 (detection of a partial exon deletion and a mosaic missense pathogenic variant respectively); together with tissue-specific mosaicism involving a cytogenetic abnormality following a normal prenatal array comparative genomic hybridization.

CONCLUSIONS:

This consecutive case series describes the results and experience of a multidisciplinary team format that was found to promote engagement across specialties and facilitate return of results to the responsible clinicians.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Genómica / Enfermedades Raras / Investigación Interdisciplinaria / Estudios de Asociación Genética / Genética Médica Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Genome Med Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Genómica / Enfermedades Raras / Investigación Interdisciplinaria / Estudios de Asociación Genética / Genética Médica Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Genome Med Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido