Exploring the impact of chronic urticaria profile as a key predictor of alexithymia: A cross-sectional study

IF 4.6 2区 医学 Q2 ALLERGY
Ivan Cherrez Ojeda, Simon Francis Thomsen, Ana M. Gimenez-Arnau, Jennifer Astrup Sørensen, Hermenio Lima, Kiran Godse, Carole Guillet, Luis Escalante, Astrid Maldonado, Gonzalo Federico Chorzepa, Blanca Morfin-Maciel, Jose Ignacio Larco Sousa, Erika de Arruda-Chaves, Abhishek De, Daria Fomina, Anant Patil, Roberta Jardim Criado, Luis Felipe Ensina, Solange O. R. Valle, Rosana Câmara Agondi, Herberto Chong Neto, Nelson Rosario, German Dario Ramon, Marco Faytong-Haro, Isabel Ogueta, Ivan Tinoco Moran, Jennifer Donnelly, Emek Kocatürk, Anna Zalewska-Janowska, Karla Robles-Velasco
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引用次数: 0

Abstract

Introduction

The relationship between chronic urticaria (CU) and alexithymia, a cognitive-affective impairment characterized by difficulty in identifying and expressing emotions, is complex and underexplored. This study aimed to identify predictors of alexithymia in CU patients by focusing on the impact of coexisting mental illnesses and antihistamine use.

Methods

An online survey was distributed to specialized allergy and dermatology centers from 2021 to 2022. The survey included the TAS-20, UAS-7, UCT, CU-Q2oL, and demographic information. Participants were 18–80 years old, diagnosed with CU, and had no prior diagnosis of alexithymia. The final analysis included a total of 332 respondents from various countries. Regression models were used to investigate the relationship between clinical and demographic factors of patients with CU as key predictors of alexithymia.

Results

Among CU patients, the main predictors of having alexithymia were: presenting mental (OR = 2.406, p < 0.05) and cardiovascular comorbidities (OR = 2.085, p < 0.05), active urticaria (as opposed to being urticaria-free), OR = 1.989, p < 0.05, severe impact on quality of life (OR = 1.973, p < 0.01), and the use of oral first-generation antihistamines (OR = 2.340, p < 0.05). The duration of chronic urticaria diagnosis and other types of treatments (sg-AH use, omalizumab use, and corticosteroid use) do not appear to be significantly associated with alexithymia.

Conclusions

Alexithymia is closely linked to clinical and demographic variables among patients with CU. These findings suggest that comprehensive management of CU should include psychological assessment and support, especially for patients with alexithymia and those using fg-AH. Reducing the reliance on fg-AH and addressing mental health issues may improve outcomes for these patients.

Abstract Image

探讨慢性荨麻疹作为述情障碍关键预测因子的影响:一项横断面研究
慢性荨麻疹(CU)与述情障碍(一种以难以识别和表达情绪为特征的认知情感障碍)之间的关系是复杂的,尚未得到充分研究。本研究旨在通过关注共存精神疾病和抗组胺药物使用的影响,确定CU患者述情障碍的预测因素。方法于2021 - 2022年在专业过敏和皮肤病学中心进行在线调查。该调查包括TAS-20、UAS-7、UCT、CU-Q2oL和人口统计信息。参与者年龄在18-80岁之间,诊断为CU,之前没有述情障碍的诊断。最终的分析包括来自不同国家的332名受访者。采用回归模型探讨作为述情障碍关键预测因素的CU患者临床与人口学因素之间的关系。结果CU患者述情障碍的主要预测因素为:出现精神障碍(OR = 2.406, p <;0.05)和心血管合并症(OR = 2.085, p <;0.05),活动性荨麻疹(相对于无荨麻疹),OR = 1.989, p <;0.05,严重影响生活质量(OR = 1.973, p <;0.01)和口服第一代抗组胺药的使用(OR = 2.340, p <;0.05)。慢性荨麻疹诊断和其他类型治疗的持续时间(使用sg-AH,使用omalizumab和使用皮质类固醇)似乎与述情障碍没有显着相关。结论CU患者述情障碍与临床及人口学变量密切相关。这些发现表明,CU的综合管理应包括心理评估和支持,特别是对述情障碍患者和使用fg-AH的患者。减少对fg-AH的依赖和解决心理健康问题可能会改善这些患者的预后。
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来源期刊
Clinical and Translational Allergy
Clinical and Translational Allergy Immunology and Microbiology-Immunology
CiteScore
7.50
自引率
4.50%
发文量
117
审稿时长
12 weeks
期刊介绍: Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience. Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.
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