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...
Published in: | Journal of Clinical Immunology |
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Online Access: | http://hdl.handle.net/2336/312350 https://doi.org/10.1007/s10875-012-9858-x |
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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 |
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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 |
_version_ |
1766041070568734720 |