PMID- 33660212 OWN - NLM STAT- MEDLINE DCOM- 20211209 LR - 20220119 IS - 1559-0267 (Electronic) IS - 1080-0549 (Print) IS - 1080-0549 (Linking) VI - 61 IP - 1 DP - 2021 Aug TI - How Angioedema Quality of Life Questionnaire Can Help Physicians in Treating C1-Inhibitor Deficiency Patients? PG - 50-59 LID - 10.1007/s12016-021-08850-9 [doi] AB - The Angioedema Quality of Life Questionnaire (AE-QoL) is an angioedema (AE)-specific validated questionnaire, which surveys the quality of life of diagnosed patients. The questionnaire has been used in multiple clinical trials. Our aim was to investigate how the questionnaire can assist physicians in the everyday practice of following up and managing C1-inhibitor deficiency patients. In a prospective trial conducted in our center between 2016 and 2018, 125 hereditary angioedema and 10 diagnosed with acquired angioedema completed an AE-QoL during their annual follow-up visit. Laboratory indices (i.e., complement levels) were obtained for each patient. Statistical analysis comparing clinical data with QoL parameters was performed. Results of the analysis show that AE-QoL total score and number of AE attacks per year correlated well (r = 0.47; p < 0.0001). Women reached higher AE-QoL total score values than men, over a 3-year period (p = 0.0014). The highest AE-QoL total scores were reached by the 41-60-year age group; we obtained a similar result, when analyzing the four domains. No correlation was found between the AE-QoL total score and complement parameters. Patients with a negative correlation between AE-QoL total score and number of AE attacks had a positive correlation with psychologic attributes like fatigue/mood and fears/shame domains. Patients that acquired HAE showed a significant correlation between the annual number of AE attacks and the AE-QoL total scores (r = 0.46; p < 0.0001). The study establishes the use of AE-QoL as a clinical tool for follow-up which can help in the complex assessment of both hereditary and acquired HAE patients, and help to develop better therapeutic strategies. CI - (c) 2021. The Author(s). FAU - Balla, Zsuzsanna AU - Balla Z AUID- ORCID: 0000-0002-9041-5036 AD - Hungarian Angioedema Center of Reference and Excellence, Department of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary. AD - School of PhD Studies, Semmelweis University, Budapest, Hungary. FAU - Ignacz, Bettina AU - Ignacz B AD - Department of Laboratory Medicine, Semmelweis University, Budapest, Hungary. FAU - Varga, Lilian AU - Varga L AUID- ORCID: 0000-0002-5484-364X AD - Hungarian Angioedema Center of Reference and Excellence, Department of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary. FAU - Kohalmi, Kinga Viktoria AU - Kohalmi KV AUID- ORCID: 0000-0002-7381-6866 AD - Department of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary. AD - Department of Rheumatology and Clinical Immunology, Semmelweis University, Budapest, Hungary. AD - Department of Rheumatology, Hospital of the Hospitaller Brothers of Saint John of God, Budapest, Hungary. FAU - Farkas, Henriette AU - Farkas H AUID- ORCID: 0000-0003-2929-1721 AD - Hungarian Angioedema Center of Reference and Excellence, Department of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary. farkas.henriette@med.semmelweis-univ.hu. LA - eng GR - National Research, Development and Innovation Office grant N degrees K124557./OTKA/ PT - Journal Article DEP - 20210303 PL - United States TA - Clin Rev Allergy Immunol JT - Clinical reviews in allergy & immunology JID - 9504368 SB - IM MH - *Angioedema/diagnosis/epidemiology MH - *Angioedemas, Hereditary/diagnosis/therapy MH - Female MH - Humans MH - Male MH - *Physicians MH - Prospective Studies MH - Quality of Life MH - Surveys and Questionnaires PMC - PMC8282561 OTO - NOTNLM OT - Acquired angioedema OT - C1-inhibitor deficiency OT - Complement OT - Hereditary angioedema OT - Quality of life OT - Questionnaire COIS- KVK-has received honoraria and travel grants from CSL Behring and Shire and has participated in clinical trials of BioCryst, CSL Behring, Pharming and Shire. LV-has received travel grants from CSL Behring and Shire Human Genetic Therapies Inc. HF-received research grants from CSL Behring, Shire/Takeda and Pharming and served as an advisor for these companies and Biocryst, and has participated in clinical trials/registries for BioCryst, CSL Behring, Pharming, Kalvista and Shire/Takeda. The other authors have declared that no conflict of interest exists. EDAT- 2021/03/05 06:00 MHDA- 2021/12/15 06:00 PMCR- 2021/03/03 CRDT- 2021/03/04 06:00 PHST- 2021/02/05 00:00 [accepted] PHST- 2021/03/05 06:00 [pubmed] PHST- 2021/12/15 06:00 [medline] PHST- 2021/03/04 06:00 [entrez] PHST- 2021/03/03 00:00 [pmc-release] AID - 10.1007/s12016-021-08850-9 [pii] AID - 8850 [pii] AID - 10.1007/s12016-021-08850-9 [doi] PST - ppublish SO - Clin Rev Allergy Immunol. 2021 Aug;61(1):50-59. doi: 10.1007/s12016-021-08850-9. Epub 2021 Mar 3.