Hereditary Angioedema Type 1 and 2 in Finland: Incidence, Prevalence, and Preceding Diagnoses
DOI:
https://doi.org/10.2340/actadv.v104.24176Keywords:
Hereditary angioedema, HAE, Incidence, Prevalence, Patient characteristicsAbstract
Abstract is missing (Short communication)
Downloads
References
Bork K, Hardt J, Witzke G. Fatal laryngeal attacks and mortality in hereditary angioedema due to C1-INH deficiency. J Allergy Clin Immunol 2012; 130: 692-697.
https://doi.org/10.1016/j.jaci.2012.05.055 DOI: https://doi.org/10.1016/j.jaci.2012.05.055
Busse PJ, Christiansen SC, Riedl MA, Banerji A, Bernstein JA, Castaldo AJ, et al. US HAEA Medical Advisory Board 2020 guidelines for the management of hereditary angioedema. J Allergy Clin Immunol Pract 2021; 9: 132-150.e3.
https://doi.org/10.1016/j.jaip.2020.08.046 DOI: https://doi.org/10.1016/j.jaip.2020.08.046
Bork K, Hardt J, Schicketanz KH, Ressel N. Clinical studies of sudden upper airway obstruction in patients with hereditary angioedema due to C1 esterase inhibitor deficiency. Arch Intern Med 2003; 163: 1229-1235.
https://doi.org/10.1001/archinte.163.10.1229 DOI: https://doi.org/10.1001/archinte.163.10.1229
Maurer M, Magerl M, Betschel S, Aberer W, Ansotegui IJ, Aygören-Pürsün E, et al. The international WAO/EAACI guideline for the management of hereditary angioedema: the 2021 revision and update. Allergy 2022; 77: 1961-1990.
https://doi.org/10.1111/all.15214 DOI: https://doi.org/10.1111/all.15214
Lumry WR, Settipane RA. Hereditary angioedema: epidemiology and burden of disease. Allergy Asthma Proc 2020; 41: S08-S13.
https://doi.org/10.2500/aap.2020.41.200050 DOI: https://doi.org/10.2500/aap.2020.41.200050
Zanichelli A, Magerl M, Longhurst HJ, Aberer W, Caballero T, Bouillet L, et al. Improvement in diagnostic delays over time in patients with hereditary angioedema: findings from the Icatibant Outcome Survey. Clin Transl Allergy 2018; 8: 42.
https://doi.org/10.1186/s13601-018-0229-4 DOI: https://doi.org/10.1186/s13601-018-0229-4
Aygören-Pürsün E, Magerl M, Maetzel A, Maurer M. Epidemiology of bradykinin-mediated angioedema: a systematic investigation of epidemiological studies. Orphanet J Rare Dis 2018; 13: 73.
https://doi.org/10.1186/s13023-018-0815-5 DOI: https://doi.org/10.1186/s13023-018-0815-5
Bygum A. Hereditary angio-oedema in Denmark: a nationwide survey. Br J Dermatol 2009; 161: 1153-1158.
https://doi.org/10.1111/j.1365-2133.2009.09366.x DOI: https://doi.org/10.1111/j.1365-2133.2009.09366.x
Nordenfelt P, Nilsson M, Björkander J, Mallbris L, Lindfors A, Wahlgren C. Hereditary angioedema in Swedish adults: report from the national cohort. Acta Derm Venereol 2016; 96: 540-545.
https://doi.org/10.2340/00015555-2274 DOI: https://doi.org/10.2340/00015555-2274
Stray-Pedersen A. Primary immunodeficiency diseases in Norway. J Clin Immunol 2000; 20: 477-485.
https://doi.org/10.1023/A:1026416017763 DOI: https://doi.org/10.1023/A:1026416017763
Laitinen I, Jokelainen J, Tasanen K, Huilaja L. Comorbidities of alopecia areata in Finland between 1987 and 2016. Acta Derm Venereol 2020; 100: adv00063.
https://doi.org/10.2340/00015555-3412 DOI: https://doi.org/10.2340/00015555-3412
Heiskanen SL, Niskala J, Jokelainen J, Tasanen K, Huilaja L, Sinikumpu SP. Hyperhidrosis comorbidities and treatments: a register-based study among 511 subjects. Acta Derm Venereol 2022; 102: adv00656.
https://doi.org/10.2340/actadv.v102.1061 DOI: https://doi.org/10.2340/actadv.v102.1061
Kurki M, Sinikumpu SP, Kiviniemi E, Jokelainen J, Huilaja L. Validation of diagnoses of atopic dermatitis in hospital registries: a cross-sectional database study from Finland. Acta Derm Venereol 2023; 103: adv7266.
https://doi.org/10.2340/actadv.v103.7266 DOI: https://doi.org/10.2340/actadv.v103.7266
Haverinen S, Vihervaara A, Löyttyniemi E, Peltonen S, Koulu L, Tasanen K, et al. Validation of psoriasis diagnoses recorded in Finnish biobanks. Acta Derm Venereol 2020; 100: adv00297.
https://doi.org/10.2340/00015555-3656 DOI: https://doi.org/10.2340/00015555-3656
Leisti P, Pankakoski A, Jokelainen J, Varpuluoma O, Huilaja L, Panelius J, et al. Accurate diagnosis of bullous pemphigoid requires multiple health care visits. Front Immunol 2023; 14: 1281302.
https://doi.org/10.3389/fimmu.2023.1281302 DOI: https://doi.org/10.3389/fimmu.2023.1281302
Published
How to Cite
Issue
Section
Categories
License
Copyright (c) 2024 Andreas Sandberg, Mariann Lassenius, Ville Vihervaara, Iiro Toppila, Laura Huilaja
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
All digitalized ActaDV contents is available freely online. The Society for Publication of Acta Dermato-Venereologica owns the copyright for all material published until volume 88 (2008) and as from volume 89 (2009) the journal has been published fully Open Access, meaning the authors retain copyright to their work.
Unless otherwise specified, all Open Access articles are published under CC-BY-NC licences, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for non-commercial purposes, provided proper attribution to the original work.