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Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings
BACKGROUND: Primary immunodeficiency diseases (PIDs) comprise a heterogeneous group of disorders mainly characterized by increased susceptibility to infections. The aims of this study were to estimate the occurrence rate of PID in the paediatric (age ≤ 18 years) population of southern Sweden (approx...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159572/ https://www.ncbi.nlm.nih.gov/pubmed/25318568 http://dx.doi.org/10.1186/s12865-014-0031-6 |
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author | Brodszki, Nicholas Jönsson, Göran Skattum, Lillemor Truedsson, Lennart |
author_facet | Brodszki, Nicholas Jönsson, Göran Skattum, Lillemor Truedsson, Lennart |
author_sort | Brodszki, Nicholas |
collection | PubMed |
description | BACKGROUND: Primary immunodeficiency diseases (PIDs) comprise a heterogeneous group of disorders mainly characterized by increased susceptibility to infections. The aims of this study were to estimate the occurrence rate of PID in the paediatric (age ≤ 18 years) population of southern Sweden (approx. 265,000 children) and to describe their demographic, clinical and immunological characteristics. During a period of 4 years, in four paediatric speciality clinics in Skåne County in southern Sweden, children being seen for infections and fulfilling specific criteria were evaluated according to a predefined examination schedule. The initial analysis consisted of complete blood counts with analysis of lymphocyte subpopulations (T, B, NK cells), measurement of immunoglobulins (IgG, IgA, IgM, IgE and IgG subclasses), and assessment of the complement system (classical, alternative and lectin pathways). In addition, results of these immunological analyses in other children from the same area and time period were evaluated. RESULTS: In total, 259 children (53.6% males) met the criteria and were included. The most common infection was recurrent otitis media. Immunological analyses results for about two thirds of the patients were outside age-related reference intervals. Further examination in this latter group identified 15 children with PID (9 males); 7 (2.7%) had genetically defined PID, representing 4 different diagnoses, and another 8 (3.1%) had a clinically defined PID - common variable immunodeficiency. No additional PID patient was identified from the evaluation of laboratory results in children not included in the study. The median age at diagnosis was 3.5 years (range 1–12 years). CONCLUSIONS: The occurrence rate of PID was about 4 new cases per year in this population. Several different PID diagnoses were found, and the application of specified criteria to identify PID patients was useful. In children who are prone to infection, the use of a predefined set of immunological laboratory analyses at their first examination was beneficial for early identification of patients with PID. |
format | Online Article Text |
id | pubmed-4159572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41595722014-09-11 Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings Brodszki, Nicholas Jönsson, Göran Skattum, Lillemor Truedsson, Lennart BMC Immunol Research Article BACKGROUND: Primary immunodeficiency diseases (PIDs) comprise a heterogeneous group of disorders mainly characterized by increased susceptibility to infections. The aims of this study were to estimate the occurrence rate of PID in the paediatric (age ≤ 18 years) population of southern Sweden (approx. 265,000 children) and to describe their demographic, clinical and immunological characteristics. During a period of 4 years, in four paediatric speciality clinics in Skåne County in southern Sweden, children being seen for infections and fulfilling specific criteria were evaluated according to a predefined examination schedule. The initial analysis consisted of complete blood counts with analysis of lymphocyte subpopulations (T, B, NK cells), measurement of immunoglobulins (IgG, IgA, IgM, IgE and IgG subclasses), and assessment of the complement system (classical, alternative and lectin pathways). In addition, results of these immunological analyses in other children from the same area and time period were evaluated. RESULTS: In total, 259 children (53.6% males) met the criteria and were included. The most common infection was recurrent otitis media. Immunological analyses results for about two thirds of the patients were outside age-related reference intervals. Further examination in this latter group identified 15 children with PID (9 males); 7 (2.7%) had genetically defined PID, representing 4 different diagnoses, and another 8 (3.1%) had a clinically defined PID - common variable immunodeficiency. No additional PID patient was identified from the evaluation of laboratory results in children not included in the study. The median age at diagnosis was 3.5 years (range 1–12 years). CONCLUSIONS: The occurrence rate of PID was about 4 new cases per year in this population. Several different PID diagnoses were found, and the application of specified criteria to identify PID patients was useful. In children who are prone to infection, the use of a predefined set of immunological laboratory analyses at their first examination was beneficial for early identification of patients with PID. BioMed Central 2014-08-14 /pmc/articles/PMC4159572/ /pubmed/25318568 http://dx.doi.org/10.1186/s12865-014-0031-6 Text en © Brodszki et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Brodszki, Nicholas Jönsson, Göran Skattum, Lillemor Truedsson, Lennart Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings |
title | Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings |
title_full | Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings |
title_fullStr | Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings |
title_full_unstemmed | Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings |
title_short | Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings |
title_sort | primary immunodeficiency in infection-prone children in southern sweden: occurrence, clinical characteristics and immunological findings |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159572/ https://www.ncbi.nlm.nih.gov/pubmed/25318568 http://dx.doi.org/10.1186/s12865-014-0031-6 |
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