Clinical symptoms in adults with selective IgA deficiency: a case-control study.

To access publisher's full text version of this article. Please click on the hyperlink in Additional Links field. Selective IgA deficiency (SIgAD) is the most common primary immunodeficiency in Caucasians with a prevalence of 1/600 and is generally considered a mild disorder. In this study, the...

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Published in:Journal of Clinical Immunology
Main Authors: Jorgensen, G H, Gardulf, A, Sigurdsson, M I, Sigurdardottir, S Th, Thorsteinsdottir, I, Gudmundsson, S, Hammarström, L, Ludviksson, B R
Other Authors: Landspitali University Hospital, Reykjavik Iceland
Format: Article in Journal/Newspaper
Language:English
Published: Springer Verlag 2013
Subjects:
Online Access:http://hdl.handle.net/2336/312350
https://doi.org/10.1007/s10875-012-9858-x
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spelling ftlandspitaliuni:oai:www.hirsla.lsh.is:2336/312350 2023-05-15T16:50:57+02:00 Clinical symptoms in adults with selective IgA deficiency: a case-control study. Jorgensen, G H Gardulf, A Sigurdsson, M I Sigurdardottir, S Th Thorsteinsdottir, I Gudmundsson, S Hammarström, L Ludviksson, B R Landspitali University Hospital, Reykjavik Iceland 2013-05 http://hdl.handle.net/2336/312350 https://doi.org/10.1007/s10875-012-9858-x en eng Springer Verlag http://dx.doi.org/10.1007/s10875-012-9858-x http://link.springer.com/article/10.1007%2Fs10875-012-9858-x J. Clin. Immunol. 2013, 33(4):742-7 1573-2592 23389234 doi:10.1007/s10875-012-9858-x http://hdl.handle.net/2336/312350 Journal of clinical immunology Archived with thanks to Journal of clinical immunology Adult Aged Autoimmune Diseases Case-Control Studies Female Humans Hypersensitivity Iceland IgA Deficiency Male Middle Aged Questionnaires Respiratory Function Tests Respiratory Tract Infections Risk Article 2013 ftlandspitaliuni https://doi.org/10.1007/s10875-012-9858-x 2022-05-29T08:21:55Z To access publisher's full text version of this article. Please click on the hyperlink in Additional Links field. Selective IgA deficiency (SIgAD) is the most common primary immunodeficiency in Caucasians with a prevalence of 1/600 and is generally considered a mild disorder. In this study, the clinical status of 32 adults with SIgAD was investigated and compared to 63 age- and gender matched controls, randomly selected from a population database. The SIgAD individuals reported significantly more often contracting various upper and lower respiratory infections, with 8 (25.0 %) having been diagnosed with ≥1 pneumonia in the preceding two years, compared to one (1.6 %) control (p < 0.001). Furthermore, the SIgAD individuals were found to have increased proneness to infections and increased prevalence of allergic diseases and autoimmunity, with a total of 84.4 % being affected by any of these diseases, compared to 47.6 % of the controls (p < 0.01). This study challenges the common statement of SIgAD being a mild form of immunodeficiency. It also highlights the importance of using matched controls in PID clinical research to better detect clinically important manifestations. Landspitali University Hospital Research FundIcelandic Research Fund Karolinska Institutet (KI Fonder), Stockholm Sweden and Division of Research and Development Primary Care County Council of Uppsala, Sweden Article in Journal/Newspaper Iceland Hirsla - Landspítali University Hospital research archive Journal of Clinical Immunology 33 4 742 747
institution Open Polar
collection Hirsla - Landspítali University Hospital research archive
op_collection_id ftlandspitaliuni
language English
topic Adult
Aged
Autoimmune Diseases
Case-Control Studies
Female
Humans
Hypersensitivity
Iceland
IgA Deficiency
Male
Middle Aged
Questionnaires
Respiratory Function Tests
Respiratory Tract Infections
Risk
spellingShingle Adult
Aged
Autoimmune Diseases
Case-Control Studies
Female
Humans
Hypersensitivity
Iceland
IgA Deficiency
Male
Middle Aged
Questionnaires
Respiratory Function Tests
Respiratory Tract Infections
Risk
Jorgensen, G H
Gardulf, A
Sigurdsson, M I
Sigurdardottir, S Th
Thorsteinsdottir, I
Gudmundsson, S
Hammarström, L
Ludviksson, B R
Clinical symptoms in adults with selective IgA deficiency: a case-control study.
topic_facet Adult
Aged
Autoimmune Diseases
Case-Control Studies
Female
Humans
Hypersensitivity
Iceland
IgA Deficiency
Male
Middle Aged
Questionnaires
Respiratory Function Tests
Respiratory Tract Infections
Risk
description To access publisher's full text version of this article. Please click on the hyperlink in Additional Links field. Selective IgA deficiency (SIgAD) is the most common primary immunodeficiency in Caucasians with a prevalence of 1/600 and is generally considered a mild disorder. In this study, the clinical status of 32 adults with SIgAD was investigated and compared to 63 age- and gender matched controls, randomly selected from a population database. The SIgAD individuals reported significantly more often contracting various upper and lower respiratory infections, with 8 (25.0 %) having been diagnosed with ≥1 pneumonia in the preceding two years, compared to one (1.6 %) control (p < 0.001). Furthermore, the SIgAD individuals were found to have increased proneness to infections and increased prevalence of allergic diseases and autoimmunity, with a total of 84.4 % being affected by any of these diseases, compared to 47.6 % of the controls (p < 0.01). This study challenges the common statement of SIgAD being a mild form of immunodeficiency. It also highlights the importance of using matched controls in PID clinical research to better detect clinically important manifestations. Landspitali University Hospital Research FundIcelandic Research Fund Karolinska Institutet (KI Fonder), Stockholm Sweden and Division of Research and Development Primary Care County Council of Uppsala, Sweden
author2 Landspitali University Hospital, Reykjavik Iceland
format Article in Journal/Newspaper
author Jorgensen, G H
Gardulf, A
Sigurdsson, M I
Sigurdardottir, S Th
Thorsteinsdottir, I
Gudmundsson, S
Hammarström, L
Ludviksson, B R
author_facet Jorgensen, G H
Gardulf, A
Sigurdsson, M I
Sigurdardottir, S Th
Thorsteinsdottir, I
Gudmundsson, S
Hammarström, L
Ludviksson, B R
author_sort Jorgensen, G H
title Clinical symptoms in adults with selective IgA deficiency: a case-control study.
title_short Clinical symptoms in adults with selective IgA deficiency: a case-control study.
title_full Clinical symptoms in adults with selective IgA deficiency: a case-control study.
title_fullStr Clinical symptoms in adults with selective IgA deficiency: a case-control study.
title_full_unstemmed Clinical symptoms in adults with selective IgA deficiency: a case-control study.
title_sort clinical symptoms in adults with selective iga deficiency: a case-control study.
publisher Springer Verlag
publishDate 2013
url http://hdl.handle.net/2336/312350
https://doi.org/10.1007/s10875-012-9858-x
genre Iceland
genre_facet Iceland
op_relation http://dx.doi.org/10.1007/s10875-012-9858-x
http://link.springer.com/article/10.1007%2Fs10875-012-9858-x
J. Clin. Immunol. 2013, 33(4):742-7
1573-2592
23389234
doi:10.1007/s10875-012-9858-x
http://hdl.handle.net/2336/312350
Journal of clinical immunology
op_rights Archived with thanks to Journal of clinical immunology
op_doi https://doi.org/10.1007/s10875-012-9858-x
container_title Journal of Clinical Immunology
container_volume 33
container_issue 4
container_start_page 742
op_container_end_page 747
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