Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/3723
Title: A Multi-Disciplinary Team Approach to Genomic Testing for Drug-Resistant Epilepsy Patients-The GENIE Study
Authors: Lau, C.
Abdulrasool, G.
Brion, K.
Lundie, B.
Aung, H.
Rodgers, J.
Gordon, L.
Riney, K.
Vadlamudi, L.
Bennett, C. M.
Tom, M.
Issue Date: 2022
Source: Jul 21 11, (14), 2022
Journal: J Clin Med
Abstract: BACKGROUND: The genomic era has led to enormous progress in clinical care and a multi-disciplinary team (MDT) approach is imperative for integration of genomics into epilepsy patient care. METHODS: The MDT approach involved patient selection, genomic testing choice, variant discussions and return of results. Genomics analysis included cytogenomic testing and whole exome sequencing (WES). Neurologist surveys were undertaken at baseline and after genomic testing to determine if genomic diagnoses would alter their management, and if there was a change in confidence in genomic testing and neurologist perceptions of the MDT approach. RESULTS: The total diagnostic yield from all genomic testing was 17% (11/66), with four diagnoses from cytogenomic analyses. All chromosomal microarray (CMA) diagnoses were in patients seen by adult neurologists. Diagnostic yield for WES was 11% (7/62). The most common gene with pathogenic variants was DCX, reported in three patients, of which two were mosaic. The genomic diagnosis impacted management in 82% (9/11). There was increased confidence with integrating genomics into clinical care (Pearson chi square = 83, p = 0.004) and qualitative comments were highly supportive of the MDT approach. CONCLUSIONS: We demonstrated diagnostic yield from genomic testing, and the impact on management in a cohort with drug-resistant epilepsy. The MDT approach increased confidence in genomic testing and neurologists valued the input from this approach. The utility of CMA was demonstrated in epilepsy patients seen by adult neurologists as was the importance of considering mosaicism for previously undiagnosed patients.2077-0383Vadlamudi, Lata
Orcid: 0000-0002-8742-0125
Bennett, Carmen Maree
Tom, Melanie
Abdulrasool, Ghusoon
Brion, Kristian
Lundie, Ben
Aung, Hnin
Lau, Chiyan
Orcid: 0000-0002-9129-8783
Rodgers, Jonathan
Riney, Kate
Gordon, Louisa
Orcid: 0000-0002-3159-4249
not applicable/Queensland Genomics/
Not applicable/Metro North Clinician Research Fellowship/
Journal Article
J Clin Med. 2022 Jul 21;11(14):4238. doi: 10.3390/jcm11144238.
DOI: 10.3390/jcm11144238
Keywords: the content of this manuscript. K.R. has received speaker honoraria, advisory;genomics;board payments and/or research funding from: UCB, Eisai, Novartis, Zogenix Inc.,;epilepsy;diagnosisdrug-resistant
Type: Article
Appears in Sites:Children's Health Queensland Publications

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