Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/35104
Conference/Presentation Title: A demonstration of the diagnostic and clinical utility of genomic sequencing in primary immunodeficiency diseases in Australia.
Authors: Gaff C.;Lynch E.;Masters S.;Bryant V.L.;Douglass J.A.;Slade C.;Moghaddas F.;Lunke S.;Stark Z.;Winship I.;West K.;Trainer A.;Ojaimi S. ;Hunter M. ;Prawer Y.;Nicholls K.;Patel M.;Auyeung P.;Spriggs K.;McComish J.;Unglik G.;De Luca J.;Chan S.;Valente G.;Jarmolowicz A.;Hosking L.;Van Dort B.;Cole T.;Smart J.;Choo S.
Monash Health Department(s): Genetics
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 Institute
Presentation/Conference Date: 21-Jul-2020
Copyright year: 2020
Publisher: Springer
Publication information: Journal 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.
Journal: Journal of Clinical Immunology
Abstract: Primary 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.
Conference Start Date: 2019-04-04
Conference End Date: 2019-04-07
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1007/s10875-019-00597-5
ISSN: 1573-2592
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/35104
Type: Conference Abstract
Subjects: diagnostic test accuracy study
genetic counseling
genomics
human
immunology
major clinical study
male
medical genetics
molecularly targeted therapy
outcome assessment
patient care
practice guideline
*whole exome sequencing
female
adult
*angioneurotic edema
*Australia
autoinflammatory disease
child
clinical outcome
conference abstract
controlled study
diagnosis
diagnostic test accuracy study
genetic counseling
genomics
immunology
medical genetics
molecularly targeted therapy
patient care
practice guideline
whole exome sequencing
angioneurotic edema
Australia
autoinflammatory disease
human
immunology
major clinical study
male
medical genetics
molecularly targeted therapy
outcome assessment
patient care
practice guideline
child
autoinflammatory disease
*Australia
*angioneurotic edema
adult
*whole exome sequencing
clinical outcome
conference abstract
controlled study
diagnosis
diagnostic test accuracy study
female
genetic counseling
genomics
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