Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/35104
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGaff C.en
dc.contributor.authorLynch E.en
dc.contributor.authorMasters S.en
dc.contributor.authorBryant V.L.en
dc.contributor.authorDouglass J.A.en
dc.contributor.authorSlade C.en
dc.contributor.authorMoghaddas F.en
dc.contributor.authorLunke S.en
dc.contributor.authorStark Z.en
dc.contributor.authorWinship I.en
dc.contributor.authorWest K.en
dc.contributor.authorTrainer A.en
dc.contributor.authorOjaimi S.en
dc.contributor.authorHunter M.en
dc.contributor.authorPrawer Y.en
dc.contributor.authorNicholls K.en
dc.contributor.authorPatel M.en
dc.contributor.authorAuyeung P.en
dc.contributor.authorSpriggs K.en
dc.contributor.authorMcComish J.en
dc.contributor.authorUnglik G.en
dc.contributor.authorDe Luca J.en
dc.contributor.authorChan S.en
dc.contributor.authorValente G.en
dc.contributor.authorJarmolowicz A.en
dc.contributor.authorHosking L.en
dc.contributor.authorVan Dort B.en
dc.contributor.authorCole T.en
dc.contributor.authorSmart J.en
dc.contributor.authorChoo S.en
dc.date.accessioned2021-05-14T11:51:20Zen
dc.date.available2021-05-14T11:51:20Zen
dc.date.copyright2020en
dc.date.created20200721en
dc.date.issued2020-07-21en
dc.identifier.citationJournal of Clinical Immunology. Conference: 2019 CIS Annual Meeting: Immune Deficiency and Dysregulation North American Conference. Atlanta, GA United States. 39 (Supplement 1) (pp S74-S75), 2020. Date of Publication: 2020.en
dc.identifier.issn1573-2592en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/35104en
dc.description.abstractPrimary Immunodeficiency diseases (PID) are a heterogeneous group of conditions with variable clinical features that are frequently associated with significant diagnostic delay. Accurate diagnosis has significant therapeutic benefit and may lead to personalized therapies. We established the Immunology Flagship of Melbourne Genomics Health Alliance in Australia to determine the clinical utility of genomic sequencing for diagnosis and management of individuals with suspected and confirmed cases of PID. 198 adults and children with suspected or confirmed PID (n=153), autoinflammatory disease (n=33) and hereditary angioedema (HAE, n=11) were recruited to the Melbourne Genomics Immunology Flagship.Whole-exome sequencing (WES) was performed, with targeted gene analysis. Variant curation and reporting was performed according to the American Council of Medical Genetics guidelines. Overall, WES was diagnostic in 15% (30/198), confirming a preexisting diagnosis in 7% (14/198), and offering a new or more specific diagnosis in 8% (16/198). Variants of uncertain significance were identified in a further 28 patients (14%) in genes known to be associated with their clinical diagnosis, that warrant further functional validation. In the HAE group, diagnosis was confirmed in only 5 patients (45%), suggesting thatWES may not be the appropriate technique for genetic diagnosis in this condition. A higher diagnostic rate was observed for autoinflammatory disorders (20%; 8/40) compared to PID (12%; 18/146). Of those who received a diagnosis, immediate changes to patient management and treatment occurred for 17/29 patients (59%), including HSCT for 3 and specific targeted therapy for 11 (38%) individuals. We have demonstrated the utility ofWES for accurate diagnosis of complex immune diseases, with the potential to change diagnoses, guide therapeutic intervention and provide opportunities for genetic counseling. Further longitudinal analysis will determine clinical outcomes and health economic implications of genomic sequencing for diagnosis andmanagement of immunological conditions in Australia.en
dc.languageEnglishen
dc.languageenen
dc.publisherSpringeren
dc.relation.ispartofJournal of Clinical Immunology-
dc.subjectdiagnostic test accuracy studyen
dc.subjectgenetic counselingen
dc.subjectgenomicsen
dc.subjecthumanen
dc.subjectimmunologyen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectmedical geneticsen
dc.subjectmolecularly targeted therapyen
dc.subjectoutcome assessmenten
dc.subjectpatient careen
dc.subjectpractice guidelineen
dc.subject*whole exome sequencingen
dc.subjectfemaleen
dc.subjectadulten
dc.subject*angioneurotic edemaen
dc.subject*Australiaen
dc.subjectautoinflammatory diseaseen
dc.subjectchilden
dc.subjectclinical outcomeen
dc.subjectconference abstracten
dc.subjectcontrolled studyen
dc.subjectdiagnosisen
dc.subject.meshdiagnostic test accuracy study-
dc.subject.meshgenetic counseling-
dc.subject.meshgenomics-
dc.subject.meshimmunology-
dc.subject.meshmedical genetics-
dc.subject.meshmolecularly targeted therapy-
dc.subject.meshpatient care-
dc.subject.meshpractice guideline-
dc.subject.meshwhole exome sequencing-
dc.subject.meshangioneurotic edema-
dc.subject.meshAustralia-
dc.subject.meshautoinflammatory disease-
dc.titleA demonstration of the diagnostic and clinical utility of genomic sequencing in primary immunodeficiency diseases in Australia.en
dc.typeConference Abstracten
dc.identifier.affiliationGeneticsen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1007/s10875-019-00597-5-
local.date.conferencestart2019-04-04en
dc.identifier.source632156909en
dc.identifier.institution(Slade) Walter and Eliza Hall Institute, Royal Melbourne Hospital (Moghaddas) Royal Melbourne Hospital (Lunke) Victorian Clinical Genetics Service (Stark) Victorian Clinical Genetics Service (Winship) Clinical Genetics, Royal Melbourne Hospital (West) Royal Melbourne Hospital (Trainer) Royal Melbourne Hospital (Ojaimi) Monash Health (Hunter) Monash Genetics Clinic, Monash Health (Prawer) Monash Health (Nicholls, Patel, Auyeung, Spriggs, McComish, Unglik, De Luca, Chan) Royal Melbourne Hospital (Valente) Austin Health (Jarmolowicz) Royal Children's Hosptial (Hosking, Cole, Choo) Royal Children's Hosptial (Van Dort) Royal Children's Hosptial (Smart) Clinical Immunology, Royal Children's Hosptial (Lynch) Melbourne Genomics Health Alliance (Gaff) Melbourne Genomics Health Alliance (Masters) Masters Lab, Walter and Eliza Hall Institute (Douglass) Clinical Immunology and Allergy, Royal Melbourne Hospital (Bryant) Immunogenetics Research Unit, Walter and Eliza Hall Instituteen
dc.description.addressC. Slade, Walter and Eliza Hall Institute, Royal Melbourne Hospitalen
dc.subject.keywordhumanen
dc.subject.keywordimmunologyen
dc.subject.keywordmajor clinical studyen
dc.subject.keywordmaleen
dc.subject.keywordmedical geneticsen
dc.subject.keywordmolecularly targeted therapyen
dc.subject.keywordoutcome assessmenten
dc.subject.keywordpatient careen
dc.subject.keywordpractice guidelineen
dc.subject.keywordchilden
dc.subject.keywordautoinflammatory diseaseen
dc.subject.keyword*Australiaen
dc.subject.keyword*angioneurotic edemaen
dc.subject.keywordadulten
dc.subject.keyword*whole exome sequencingen
dc.subject.keywordclinical outcomeen
dc.subject.keywordconference abstracten
dc.subject.keywordcontrolled studyen
dc.subject.keyworddiagnosisen
dc.subject.keyworddiagnostic test accuracy studyen
dc.subject.keywordfemaleen
dc.subject.keywordgenetic counselingen
dc.subject.keywordgenomicsen
dc.relation.libraryurlLibKey Linken
dc.description.publicationstatusCONFERENCE ABSTRACTen
local.date.conferenceend2019-04-07en
dc.rights.statementCopyright 2020 Elsevier B.V., All rights reserved.en
dc.identifier.affiliationext(Slade) Walter and Eliza Hall Institute, Royal Melbourne Hospital-
dc.identifier.affiliationext(Moghaddas) Royal Melbourne Hospital-
dc.identifier.affiliationext(Lunke) Victorian Clinical Genetics Service-
dc.identifier.affiliationext(Stark) Victorian Clinical Genetics Service-
dc.identifier.affiliationext(Winship) Clinical Genetics, Royal Melbourne Hospital-
dc.identifier.affiliationext(West) Royal Melbourne Hospital-
dc.identifier.affiliationext(Trainer) Royal Melbourne Hospital-
dc.identifier.affiliationext(Nicholls, Patel, Auyeung, Spriggs, McComish, Unglik, De Luca, Chan) Royal Melbourne Hospital-
dc.identifier.affiliationext(Valente) Austin Health-
dc.identifier.affiliationext(Jarmolowicz) Royal Children's Hosptial-
dc.identifier.affiliationext(Hosking, Cole, Choo) Royal Children's Hosptial-
dc.identifier.affiliationext(Van Dort) Royal Children's Hosptial-
dc.identifier.affiliationext(Smart) Clinical Immunology, Royal Children's Hosptial-
dc.identifier.affiliationext(Lynch) Melbourne Genomics Health Alliance-
dc.identifier.affiliationext(Gaff) Melbourne Genomics Health Alliance-
dc.identifier.affiliationext(Masters) Masters Lab, Walter and Eliza Hall Institute-
dc.identifier.affiliationext(Douglass) Clinical Immunology and Allergy, Royal Melbourne Hospital-
dc.identifier.affiliationext(Bryant) Immunogenetics Research Unit, Walter and Eliza Hall Institute-
dc.identifier.affiliationmh(Ojaimi) Monash Health (Hunter) Monash Genetics Clinic, Monash Health (Prawer) Monash Health-
item.openairetypeConference Abstract-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
crisitem.author.deptInfectious Diseases and Clinical Microbiology-
crisitem.author.deptGenetics-
Appears in Collections:Conferences
Show simple item record

Page view(s)

26
checked on Jun 30, 2024

Google ScholarTM

Check


Items in Monash Health Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.