Cargando…
Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study
BACKGROUND: Registration of trigger factors, prodromal symptoms, swelling localization, therapeutic behavior and gender-specific differences of the largest cohort of patients with hereditary angioedema due to C1-Inhibitor deficiency (C1-INH-HAE) in Switzerland. METHODS: Questionnaire survey within a...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839073/ https://www.ncbi.nlm.nih.gov/pubmed/27101900 http://dx.doi.org/10.1186/s13023-016-0423-1 |
_version_ | 1782428085602222080 |
---|---|
author | Steiner, Urs C. Weber-Chrysochoou, Christina Helbling, Arthur Scherer, Kathrin Grendelmeier, Peter Schmid Wuillemin, Walter A. |
author_facet | Steiner, Urs C. Weber-Chrysochoou, Christina Helbling, Arthur Scherer, Kathrin Grendelmeier, Peter Schmid Wuillemin, Walter A. |
author_sort | Steiner, Urs C. |
collection | PubMed |
description | BACKGROUND: Registration of trigger factors, prodromal symptoms, swelling localization, therapeutic behavior and gender-specific differences of the largest cohort of patients with hereditary angioedema due to C1-Inhibitor deficiency (C1-INH-HAE) in Switzerland. METHODS: Questionnaire survey within a cohort study: Consenting eligible patients with diagnosed HAE according to clinical history, physical examination and laboratory results, including plasma values for C1-INH and C4 were selected. To each participant we sent a questionnaire assessing patients’ birthday, sex, date of first symptoms and diagnosis, trigger factors, prodromal symptoms, frequency and localization of angioedema, medication use and co-morbidities. Clinical information was collected in each center and then transmitted to the cohort database. Frequencies and distributions were summarized. Associations between gender and trigger factors or prodromal symptoms or localization of angioedema were assessed in multivariate analyses correcting for patients’ age. RESULTS: Of 135 patients, data from 104 patients (77 %) were available for analysis. Fifty- four percent were female, mean age at diagnosis was 19.5 years (SD 14.1), Mean age when completing the questionnaire was 44.0 (SD 19.8). More women than men were symptomatic (44/57 vs. 36/47; p = 0.005). This association remained when correcting for age at diagnosis (16.10. 95%CI (5.17 to 26.70); p = 0.004). Swelling episodes ranged between 1 and 136 episodes/year. Swelling was more common among female than among male (-13.15 (95 % CI; -23.10 to -3.22), p = 0.010). Age at diagnosis was inversely associated with the total number of attacks 0.50 (-0.88 to -.011); p = 0.012). One third of patients were on danazol prophylaxis. CONCLUSION: We found large differences of HAE in male and female both in terms of symptom number and swelling episodes. Women are more affected by intensity and frequency of angioedema episodes than men. Danazol treatment remains widely used as effective prophylaxis despite its side effects. New therapies which selectively influence the hormonal estrogen balance could open new therapeutic options mainly for women and maybe also for men. |
format | Online Article Text |
id | pubmed-4839073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48390732016-04-22 Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study Steiner, Urs C. Weber-Chrysochoou, Christina Helbling, Arthur Scherer, Kathrin Grendelmeier, Peter Schmid Wuillemin, Walter A. Orphanet J Rare Dis Research BACKGROUND: Registration of trigger factors, prodromal symptoms, swelling localization, therapeutic behavior and gender-specific differences of the largest cohort of patients with hereditary angioedema due to C1-Inhibitor deficiency (C1-INH-HAE) in Switzerland. METHODS: Questionnaire survey within a cohort study: Consenting eligible patients with diagnosed HAE according to clinical history, physical examination and laboratory results, including plasma values for C1-INH and C4 were selected. To each participant we sent a questionnaire assessing patients’ birthday, sex, date of first symptoms and diagnosis, trigger factors, prodromal symptoms, frequency and localization of angioedema, medication use and co-morbidities. Clinical information was collected in each center and then transmitted to the cohort database. Frequencies and distributions were summarized. Associations between gender and trigger factors or prodromal symptoms or localization of angioedema were assessed in multivariate analyses correcting for patients’ age. RESULTS: Of 135 patients, data from 104 patients (77 %) were available for analysis. Fifty- four percent were female, mean age at diagnosis was 19.5 years (SD 14.1), Mean age when completing the questionnaire was 44.0 (SD 19.8). More women than men were symptomatic (44/57 vs. 36/47; p = 0.005). This association remained when correcting for age at diagnosis (16.10. 95%CI (5.17 to 26.70); p = 0.004). Swelling episodes ranged between 1 and 136 episodes/year. Swelling was more common among female than among male (-13.15 (95 % CI; -23.10 to -3.22), p = 0.010). Age at diagnosis was inversely associated with the total number of attacks 0.50 (-0.88 to -.011); p = 0.012). One third of patients were on danazol prophylaxis. CONCLUSION: We found large differences of HAE in male and female both in terms of symptom number and swelling episodes. Women are more affected by intensity and frequency of angioedema episodes than men. Danazol treatment remains widely used as effective prophylaxis despite its side effects. New therapies which selectively influence the hormonal estrogen balance could open new therapeutic options mainly for women and maybe also for men. BioMed Central 2016-04-21 /pmc/articles/PMC4839073/ /pubmed/27101900 http://dx.doi.org/10.1186/s13023-016-0423-1 Text en © Steiner et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Steiner, Urs C. Weber-Chrysochoou, Christina Helbling, Arthur Scherer, Kathrin Grendelmeier, Peter Schmid Wuillemin, Walter A. Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study |
title | Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study |
title_full | Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study |
title_fullStr | Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study |
title_full_unstemmed | Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study |
title_short | Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study |
title_sort | hereditary angioedema due to c1 - inhibitor deficiency in switzerland: clinical characteristics and therapeutic modalities within a cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839073/ https://www.ncbi.nlm.nih.gov/pubmed/27101900 http://dx.doi.org/10.1186/s13023-016-0423-1 |
work_keys_str_mv | AT steinerursc hereditaryangioedemaduetoc1inhibitordeficiencyinswitzerlandclinicalcharacteristicsandtherapeuticmodalitieswithinacohortstudy AT weberchrysochoouchristina hereditaryangioedemaduetoc1inhibitordeficiencyinswitzerlandclinicalcharacteristicsandtherapeuticmodalitieswithinacohortstudy AT helblingarthur hereditaryangioedemaduetoc1inhibitordeficiencyinswitzerlandclinicalcharacteristicsandtherapeuticmodalitieswithinacohortstudy AT schererkathrin hereditaryangioedemaduetoc1inhibitordeficiencyinswitzerlandclinicalcharacteristicsandtherapeuticmodalitieswithinacohortstudy AT grendelmeierpeterschmid hereditaryangioedemaduetoc1inhibitordeficiencyinswitzerlandclinicalcharacteristicsandtherapeuticmodalitieswithinacohortstudy AT wuilleminwaltera hereditaryangioedemaduetoc1inhibitordeficiencyinswitzerlandclinicalcharacteristicsandtherapeuticmodalitieswithinacohortstudy |