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Immune Dysregulation in Monogenic Inborn Errors of Immunity in Oman: Over A Decade of Experience From a Single Tertiary Center

dc.contributor.authorAl Farsi, Tariq
dc.contributor.authorAhmed, Khwater
dc.contributor.authorAlshekaili, Jalila
dc.contributor.authorAl Kindi, Mahmood
dc.contributor.authorCook, Matthew
dc.contributor.authorAl-Hosni, Aliya
dc.contributor.authorAnsari, Zainab
dc.contributor.authorNasr, Iman
dc.contributor.authorAl Sukaiti, Nashat
dc.date.accessioned2024-05-13T23:12:40Z
dc.date.available2024-05-13T23:12:40Z
dc.date.issued2022
dc.date.updated2023-01-15T07:17:10Z
dc.description.abstractBackground: Inborn errors of immunity (IEIs) are being recognized as an important cause of morbidity and mortality in communities with a high frequency of consanguinity, such as Oman, and thus recessively inherited conditions. Various monogenic causes of IEI have been recently discovered; however, the disease phenotype may be variable and does not always include infection at presentation, leading to a delay in diagnosis and a poor outcome. It is now well recognized that immune dysregulation manifestations are observed in a significant proportion of patients with IEI and occasionally precede infection. Methods: Here, we retrospectively report the epidemiological, clinical, immunological, and molecular findings and outcomes from 239 patients with IEI who were diagnosed and managed at the Royal Hospital, Oman, from January 2010 to October 2021. Results: The estimated annual cumulative mean incidence of IEI was 25.5 per 100,000 Omani live births with a total prevalence of 15.5 per 100,000 Omani population. Both the high incidence and prevalence are attributed to the high rate of consanguinity (78.2%). Defects affecting cellular and humoral immunity including severe combined immunodeficiency (SCID), combined immunodeficiency (CID), and CID with syndromic features were the predominant defects in IEI (36%). Immune dysregulation was a prominent manifestation and occurred in approximately a third of all patients with IEI (32%), with a mean age of onset of 81 months and a mean diagnostic delay of 50.8 months. The largest percentage of patients who showed such clinical signs were in the category of diseases of immune dysregulation (41%), followed by predominantly antibody deficiency (18%). The overall mortality rate in our cohort was 25.1%, with higher death rates seen in CID including SCID and diseases of immune dysregulation. Conclusion: Immune dysregulation is a frequent manifestation of Omani patients with IEI. Early detection through raising awareness of signs of IEI including those of immune dysregulation and implementation of newborn screening programs will result in early intervention and improved overall outcome.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1664-3224en_AU
dc.identifier.urihttp://hdl.handle.net/1885/317488
dc.language.isoen_AUen_AU
dc.provenanceThis is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en_AU
dc.publisherFrontiers Research Foundationen_AU
dc.rights© 2022 The authorsen_AU
dc.rights.licenseCreative Commons Attribution licenceen_AU
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_AU
dc.sourceFrontiers in Immunologyen_AU
dc.subjectinborn errors of immunityen_AU
dc.subjectimmunodeficiencyen_AU
dc.subjectimmune dysregulationen_AU
dc.subjectphenotypeen_AU
dc.subjectgenotypeen_AU
dc.subjectchildrenen_AU
dc.subjectadultsen_AU
dc.subjectOmanien_AU
dc.titleImmune Dysregulation in Monogenic Inborn Errors of Immunity in Oman: Over A Decade of Experience From a Single Tertiary Centeren_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.lastpage12en_AU
local.bibliographicCitation.startpage1en_AU
local.contributor.affiliationAl Farsi, Tariq, The Royal Hospital, Omanen_AU
local.contributor.affiliationAhmed, Khwater, The Royal Hospital, Omanen_AU
local.contributor.affiliationAlshekaili, Jalila, Sultan Qaboos University Hospitalen_AU
local.contributor.affiliationAl Kindi, Mahmood, Sultan Qaboos University Hospitalen_AU
local.contributor.affiliationCook, Matthew, College of Health and Medicine, ANUen_AU
local.contributor.affiliationAl-Hosni, Aliya, National Genetics Centeren_AU
local.contributor.affiliationAnsari, Zainab, The Royal Hospitalen_AU
local.contributor.affiliationNasr, Iman, The Royal Hospitalen_AU
local.contributor.affiliationAl Sukaiti, Nashat, The Royal Hospital, Omanen_AU
local.contributor.authoruidCook, Matthew, u2572788en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor320406 - Immunogenetics (incl. genetic immunology)en_AU
local.identifier.ariespublicationa383154xPUB29902en_AU
local.identifier.citationvolume13en_AU
local.identifier.doi10.3389/fimmu.2022.849694en_AU
local.identifier.scopusID2-s2.0-85128647083
local.publisher.urlhttps://www.frontiersin.org/en_AU
local.type.statusPublished Versionen_AU

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