Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study.

dc.contributor.authorJanssen, Lisanne M A
dc.contributor.authorvan Hout, Roeland W N M
dc.contributor.authorde Vries, Esther
dc.contributor.authorSIMcal Consortium
dc.date.accessioned2025-01-07T14:19:43Z
dc.date.available2025-01-07T14:19:43Z
dc.date.issued2019-04-25
dc.description.abstractThe clinical consequences of isolated decreased serum immunoglobulin (Ig)M are not sufficiently known. Therefore, it is difficult to determine the clinical policy following such a finding. Only few reported IgM-deficient patients fulfil the European Society for Immunodeficiencies (ESID) diagnostic criteria for selective IgM deficiency (true sIgMdef), or their diagnosis is uncertain due to insufficient laboratory data (possible sIgMdef). Decreased serum IgM is often incidentally found in asymptomatic adults. The objective of our study was to further characterize true sIgMdef and to compare the European data collected through the ESID Registry community (tertiary centres) to our previously published Dutch cohort (secondary centre). Fifteen centres (12 countries) participated with 98 patients. Patients were excluded if serum IgM was only determined once (n = 14), had normalized (n = 8), or if they also had other immunological abnormalities (n = 15). Ten patients (5 adults) completely fulfilled the ESID criteria for true sIgMdef. Age-matched cut-off values varied widely between centres; when using the ESID diagnostic protocol reference values, only six patients (five adults) had true sIgMdef. Because of these small numbers, further analyses were performed in patients with true or possible sIgMdef (13 adults, 48 children). Respiratory infections were commonly reported at presentation (adults 54%, children 60%). Symptomatic adults had lower serum IgM levels (mean 0.27 g/L, 95% CI 0.22-0.31) than those without symptoms (mean 0.33 g/L, 95% CI 0.30-0.36; P = 0.02). To be able to explore the clinical consequences of true sIgMdef, we should fully analyse and accurately describe those patients in whom a decreased serum IgM is found.
dc.identifier.doi10.1111/sji.12763
dc.identifier.essn1365-3083
dc.identifier.pmcPMC6850338
dc.identifier.pmid30887554
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC6850338/pdf
dc.identifier.unpaywallURLhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/sji.12763
dc.identifier.urihttps://hdl.handle.net/10668/26290
dc.issue.number6
dc.journal.titleScandinavian journal of immunology
dc.journal.titleabbreviationScand J Immunol
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.page.numbere12763
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectprimary immunodeficiency
dc.subjectprimary selective IgM deficiency
dc.subjectunclassified antibody deficiency
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAsymptomatic Diseases
dc.subject.meshB-Lymphocyte Subsets
dc.subject.meshChild
dc.subject.meshChild, Preschool
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshImmunoglobulin M
dc.subject.meshImmunologic Deficiency Syndromes
dc.subject.meshInfant
dc.subject.meshInfant, Newborn
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshRespiratory Tract Infections
dc.subject.meshT-Lymphocyte Subsets
dc.subject.meshYoung Adult
dc.titleChallenges in investigating patients with isolated decreased serum IgM: The SIMcal study.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number89

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