Implementationof a genomic medicine multi-disciplinary team approach for rare diseasein the clinical setting: a prospective exome sequencingcase series

被引:24
|
作者
Taylor, John [1 ]
Craft, Jude [1 ]
Blair, Edward [1 ]
Wordsworth, Sarah [2 ,7 ]
Beeson, David [3 ]
Chandratre, Saleel [4 ]
Cossins, Judith [3 ]
Lester, Tracy [1 ]
Nemeth, Andrea H. [1 ,5 ]
Ormondroyd, Elizabeth [6 ,7 ]
Patel, Smita Y. [7 ,8 ]
Pagnamenta, Alistair T. [7 ,8 ]
Taylor, Jenny C. [7 ,9 ]
Thomson, Kate L. [1 ]
Watkins, Hugh [6 ,7 ,9 ]
Wilkie, Andrew O. M. [1 ,3 ,7 ]
Knight, Julian C. [7 ,9 ]
机构
[1] Oxford Univ Hosp NHS Fdn Trust, Oxford Ctr Genom Med, Oxford, England
[2] Univ Oxford, Nuffield Dept Populat Hlth, Oxford, England
[3] Univ Oxford, MRC Weatherall Inst Mol Med, Oxford, England
[4] Oxford Univ Hosp NHS Fdn Trust, Childrens Hosp, Oxford, England
[5] Oxford Univ Hosp NHS Fdn Trust, Nuffield Dept Clin Neurosci, Oxford, England
[6] Univ Oxford, Radcliffe Dept Med, Div Cardiovasc Med, Oxford, England
[7] Natl Inst Hlth Res, Biomed Res Ctr, Oxford, England
[8] Oxford Univ Hosp NHS Fdn Trust, Dept Clin Immunol, Oxford, England
[9] Univ Oxford, Wellcome Ctr Human Genet, Oxford, England
基金
英国惠康基金;
关键词
Genetic disease; Genome sequencing; Exome; Multidisciplinary team; Next-generation sequencing; SYNTHASE; 1; DEFICIENCY; MUTATIONS; VARIANTS; ATAXIA; GENE; IDENTIFICATION; EXPERIENCE;
D O I
10.1186/s13073-019-0651-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
BackgroundA 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.MethodsWe 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.ResultsIn 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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页数:12
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