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

The 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 c...

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Autores principales: Janssen, Lisanne M. A., van Hout, Roeland W. N. M., de Vries, Esther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850338/
https://www.ncbi.nlm.nih.gov/pubmed/30887554
http://dx.doi.org/10.1111/sji.12763
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author Janssen, Lisanne M. A.
van Hout, Roeland W. N. M.
de Vries, Esther
author_facet Janssen, Lisanne M. A.
van Hout, Roeland W. N. M.
de Vries, Esther
author_sort Janssen, Lisanne M. A.
collection PubMed
description The 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.
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spelling pubmed-68503382019-11-18 Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study Janssen, Lisanne M. A. van Hout, Roeland W. N. M. de Vries, Esther Scand J Immunol Human Immunology The 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. John Wiley and Sons Inc. 2019-04-25 2019-06 /pmc/articles/PMC6850338/ /pubmed/30887554 http://dx.doi.org/10.1111/sji.12763 Text en © 2019 The Authors. Scandinavian Journal of Immunology published by John Wiley & Sons Ltd on behalf of The Foundation for the Scandinavian Journal of Immunology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Human Immunology
Janssen, Lisanne M. A.
van Hout, Roeland W. N. M.
de Vries, Esther
Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study
title Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study
title_full Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study
title_fullStr Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study
title_full_unstemmed Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study
title_short Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study
title_sort challenges in investigating patients with isolated decreased serum igm: the simcal study
topic Human Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850338/
https://www.ncbi.nlm.nih.gov/pubmed/30887554
http://dx.doi.org/10.1111/sji.12763
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