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Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions
BACKGROUND: Angioedema without wheals (AE) is a symptom characterised by localised episodes of oedema presumably caused by kinin release from kininogen cleavage. It can result from a hereditary deficiency in C1 Inhibitor (C1Inh), but it can present with normal level of C1Inh. These forms are typical...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042432/ https://www.ncbi.nlm.nih.gov/pubmed/27685806 http://dx.doi.org/10.1371/journal.pone.0163958 |
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author | Baroso, Rémi Sellier, Pauline Defendi, Federica Charignon, Delphine Ghannam, Arije Habib, Mohammed Drouet, Christian Favier, Bertrand |
author_facet | Baroso, Rémi Sellier, Pauline Defendi, Federica Charignon, Delphine Ghannam, Arije Habib, Mohammed Drouet, Christian Favier, Bertrand |
author_sort | Baroso, Rémi |
collection | PubMed |
description | BACKGROUND: Angioedema without wheals (AE) is a symptom characterised by localised episodes of oedema presumably caused by kinin release from kininogen cleavage. It can result from a hereditary deficiency in C1 Inhibitor (C1Inh), but it can present with normal level of C1Inh. These forms are typically difficult to diagnose although enhanced kinin production is suspected or demonstrated in some cases. OBJECTIVES: We wanted to investigate bradykinin overproduction in all AE condition with normal C1Inh, excluding cases with enhanced kinin catabolism, and to propose this parameter as a disease biomarker. METHODS: We retrospectively investigated high molecular weight kininogen (HK) cleavage pattern, using gel electrophoresis and immunorevelation. Plasma samples were drawn using the same standardised procedure from blood donors or AE patients with normal C1Inh conditions, normal kinin catabolism, and without prophylaxis. RESULTS: Circulating native HK plasma concentrations were similar in the healthy men (interquartile range: 98–175μg/mL, n = 51) and in healthy women (90–176μg/mL, n = 74), while HK cleavage was lower (p<0.001) in men (0–5%) than women (3–9%). Patients exhibited lower native HK concentration (p<10(−4); 21–117μg/mL, n = 31 for men; 0–84μg/mL, n = 41 for women) and higher HK cleavage (p<10(−4); 10–30% and 14–89%, respectively) than healthy donors. Pathological thresholds were set at: <72μg/mL native HK, >14.4% HK cleavage for men; <38μg/mL; native HK, >33.0% HK cleavage for women, with >98% specificity achieved for all parameters. In plasma from patients undergoing recovery two months after oestrogen/progestin combination withdrawal (n = 13) or two weeks after AE attack (n = 2), HK cleavage was not fully restored, suggesting its use as a post-attack assay. CONCLUSION: As a diagnostic tool, HK cleavage can offer physicians supportive arguments for kinin production in suspected AE cases and improve patient follow-up in clinical trials or prophylactic management. |
format | Online Article Text |
id | pubmed-5042432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50424322016-10-27 Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions Baroso, Rémi Sellier, Pauline Defendi, Federica Charignon, Delphine Ghannam, Arije Habib, Mohammed Drouet, Christian Favier, Bertrand PLoS One Research Article BACKGROUND: Angioedema without wheals (AE) is a symptom characterised by localised episodes of oedema presumably caused by kinin release from kininogen cleavage. It can result from a hereditary deficiency in C1 Inhibitor (C1Inh), but it can present with normal level of C1Inh. These forms are typically difficult to diagnose although enhanced kinin production is suspected or demonstrated in some cases. OBJECTIVES: We wanted to investigate bradykinin overproduction in all AE condition with normal C1Inh, excluding cases with enhanced kinin catabolism, and to propose this parameter as a disease biomarker. METHODS: We retrospectively investigated high molecular weight kininogen (HK) cleavage pattern, using gel electrophoresis and immunorevelation. Plasma samples were drawn using the same standardised procedure from blood donors or AE patients with normal C1Inh conditions, normal kinin catabolism, and without prophylaxis. RESULTS: Circulating native HK plasma concentrations were similar in the healthy men (interquartile range: 98–175μg/mL, n = 51) and in healthy women (90–176μg/mL, n = 74), while HK cleavage was lower (p<0.001) in men (0–5%) than women (3–9%). Patients exhibited lower native HK concentration (p<10(−4); 21–117μg/mL, n = 31 for men; 0–84μg/mL, n = 41 for women) and higher HK cleavage (p<10(−4); 10–30% and 14–89%, respectively) than healthy donors. Pathological thresholds were set at: <72μg/mL native HK, >14.4% HK cleavage for men; <38μg/mL; native HK, >33.0% HK cleavage for women, with >98% specificity achieved for all parameters. In plasma from patients undergoing recovery two months after oestrogen/progestin combination withdrawal (n = 13) or two weeks after AE attack (n = 2), HK cleavage was not fully restored, suggesting its use as a post-attack assay. CONCLUSION: As a diagnostic tool, HK cleavage can offer physicians supportive arguments for kinin production in suspected AE cases and improve patient follow-up in clinical trials or prophylactic management. Public Library of Science 2016-09-29 /pmc/articles/PMC5042432/ /pubmed/27685806 http://dx.doi.org/10.1371/journal.pone.0163958 Text en © 2016 Baroso et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are credited. |
spellingShingle | Research Article Baroso, Rémi Sellier, Pauline Defendi, Federica Charignon, Delphine Ghannam, Arije Habib, Mohammed Drouet, Christian Favier, Bertrand Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions |
title | Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions |
title_full | Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions |
title_fullStr | Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions |
title_full_unstemmed | Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions |
title_short | Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions |
title_sort | kininogen cleavage assay: diagnostic assistance for kinin-mediated angioedema conditions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042432/ https://www.ncbi.nlm.nih.gov/pubmed/27685806 http://dx.doi.org/10.1371/journal.pone.0163958 |
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