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The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema?
BACKGROUND: C1 inhibitor (C1-INH) and complement 4 (C4) have historically been referred to as positive acute phase reactants, however this has never been evaluated in hereditary angioedema (HAE) patients. Low function of C1-INH and low levels of C4 are important in the diagnosis of HAE type 1 and 2....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501576/ https://www.ncbi.nlm.nih.gov/pubmed/34627363 http://dx.doi.org/10.1186/s13223-021-00607-5 |
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author | Stepaniuk, Peter Bosonea, Ana-Maria Pourshahnazari, Persia Roos, Adrienne Kanani, Amin |
author_facet | Stepaniuk, Peter Bosonea, Ana-Maria Pourshahnazari, Persia Roos, Adrienne Kanani, Amin |
author_sort | Stepaniuk, Peter |
collection | PubMed |
description | BACKGROUND: C1 inhibitor (C1-INH) and complement 4 (C4) have historically been referred to as positive acute phase reactants, however this has never been evaluated in hereditary angioedema (HAE) patients. Low function of C1-INH and low levels of C4 are important in the diagnosis of HAE type 1 and 2. If C1-INH and/or C4 are significant acute phase reactants, their levels may be falsely “normal” in patients with HAE when measured during times of infection or inflammation resulting in missed or delayed diagnosis. CASE PRESENTATION: We present a case series of four HAE patients who had C4, C1-INH, c-reactive protein (CRP) and ferritin measured at baseline and again during a self-reported upper respiratory tract infection (URTI) or flu-like illness. We did not identify any HAE patients who had a significant change in their C1-INH functional level in the context of a mild infection. However, the C4 level did increase into the normal range on three occasions (2 patients, with 1 patient having elevation during two separate illnesses). CONCLUSIONS: C1 inhibitor may not be a clinically significant acute phase protein and appears to still be a reliable diagnostic marker of hereditary angioedema, even in times of modest acute inflammation, unlike complement C4 which can be elevated in this setting. |
format | Online Article Text |
id | pubmed-8501576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85015762021-10-20 The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema? Stepaniuk, Peter Bosonea, Ana-Maria Pourshahnazari, Persia Roos, Adrienne Kanani, Amin Allergy Asthma Clin Immunol Case Report BACKGROUND: C1 inhibitor (C1-INH) and complement 4 (C4) have historically been referred to as positive acute phase reactants, however this has never been evaluated in hereditary angioedema (HAE) patients. Low function of C1-INH and low levels of C4 are important in the diagnosis of HAE type 1 and 2. If C1-INH and/or C4 are significant acute phase reactants, their levels may be falsely “normal” in patients with HAE when measured during times of infection or inflammation resulting in missed or delayed diagnosis. CASE PRESENTATION: We present a case series of four HAE patients who had C4, C1-INH, c-reactive protein (CRP) and ferritin measured at baseline and again during a self-reported upper respiratory tract infection (URTI) or flu-like illness. We did not identify any HAE patients who had a significant change in their C1-INH functional level in the context of a mild infection. However, the C4 level did increase into the normal range on three occasions (2 patients, with 1 patient having elevation during two separate illnesses). CONCLUSIONS: C1 inhibitor may not be a clinically significant acute phase protein and appears to still be a reliable diagnostic marker of hereditary angioedema, even in times of modest acute inflammation, unlike complement C4 which can be elevated in this setting. BioMed Central 2021-10-09 /pmc/articles/PMC8501576/ /pubmed/34627363 http://dx.doi.org/10.1186/s13223-021-00607-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Stepaniuk, Peter Bosonea, Ana-Maria Pourshahnazari, Persia Roos, Adrienne Kanani, Amin The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema? |
title | The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema? |
title_full | The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema? |
title_fullStr | The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema? |
title_full_unstemmed | The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema? |
title_short | The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema? |
title_sort | role of c1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema? |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501576/ https://www.ncbi.nlm.nih.gov/pubmed/34627363 http://dx.doi.org/10.1186/s13223-021-00607-5 |
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