Quality of life, sleep, and psychological well-being in chronic spontaneous urticaria patients receiving omalizumab: a case–control study

IF 1.8 4区 医学 Q3 DERMATOLOGY
Mustafa Esen, Abdullah Demirbaş, Esin Diremsizoglu
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Abstract

Chronic spontaneous urticaria (CSU) impacts both physical and mental well-being, causing distress and sleep disturbances. While omalizumab reduces disease activity, its effects on mental health and quality of life remain unclear. This study assesses the psychosocial burden and sleep disturbances in CSU patients receiving omalizumab compared to healthy controls and explores their relationship with disease parameters. This case––control study included 210 CSU patients receiving omalizumab for at least three months and 210 age- and sex-matched healthy controls. Disease severity was assessed using the Urticaria Activity Score over 7 Days (UAS7) and Urticaria Control Test (UCT), while quality of life was evaluated with the Chronic Urticaria Quality of Life Questionnaire (CU-Q₂oL). Psychological distress and sleep disturbances were measured using validated scales, including the Perceived Stress Scale (PSS), Beck Depression Inventory (BDI), Beck Anxiety Inventory (BAI), Pittsburgh Sleep Quality Index (PSQI), and Epworth Sleepiness Scale (ESS). CSU patients had significantly higher scores for perceived stress, depression, anxiety, and daytime sleepiness compared to controls (p < 0.001). Patients with a good response to omalizumab also showed significantly higher psychological distress and poorer sleep quality than controls (p < 0.001). Omalizumab response was good in 29.5%, moderate in 38.6%, and limited in 31.9% of patients. Despite treatment, 32.9% reported no change in quality of life, while 35.7% had mild and 31.4% had moderate improvement. A history of atopic disease was present in 55.7% of patients, who had significantly higher daytime sleepiness scores than those without (p = 0.045). In CSU patients, while omalizumab improves symptoms and quality of life, psychological distress persists in substantial subsets, highlighting the need to address mental health and lifestyle factors.

接受奥玛珠单抗治疗的慢性自发性荨麻疹患者的生活质量、睡眠和心理健康:一项病例对照研究
慢性自发性荨麻疹(CSU)影响身体和精神健康,引起痛苦和睡眠障碍。虽然omalizumab可减少疾病活动,但其对心理健康和生活质量的影响尚不清楚。本研究评估了接受omalizumab治疗的CSU患者与健康对照组相比的心理社会负担和睡眠障碍,并探讨了它们与疾病参数的关系。该病例对照研究包括210名接受omalizumab治疗至少3个月的CSU患者和210名年龄和性别匹配的健康对照。使用7天荨麻疹活动评分(UAS7)和荨麻疹控制测试(UCT)评估疾病严重程度,使用慢性荨麻疹生活质量问卷(CU-Q₂oL)评估生活质量。采用有效的压力感知量表(PSS)、贝克抑郁量表(BDI)、贝克焦虑量表(BAI)、匹兹堡睡眠质量指数(PSQI)和Epworth嗜睡量表(ESS)测量心理困扰和睡眠障碍。与对照组相比,CSU患者在感知压力、抑郁、焦虑和白天嗜睡方面得分显著较高(p < 0.001)。与对照组相比,对omalizumab反应良好的患者也表现出明显更高的心理困扰和更差的睡眠质量(p < 0.001)。29.5%的患者Omalizumab反应良好,38.6%的患者反应中等,31.9%的患者反应有限。尽管接受了治疗,32.9%的人报告生活质量没有改变,35.7%的人有轻度改善,31.4%的人有中度改善。55.7%的患者有特应性疾病史,白天嗜睡评分明显高于无特应性疾病史的患者(p = 0.045)。在CSU患者中,虽然omalizumab可以改善症状和生活质量,但心理困扰在大量亚群中持续存在,这突出了解决心理健康和生活方式因素的必要性。
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来源期刊
CiteScore
4.10
自引率
3.30%
发文量
30
审稿时长
4-8 weeks
期刊介绍: Archives of Dermatological Research is a highly rated international journal that publishes original contributions in the field of experimental dermatology, including papers on biochemistry, morphology and immunology of the skin. The journal is among the few not related to dermatological associations or belonging to respective societies which guarantees complete independence. This English-language journal also offers a platform for review articles in areas of interest for dermatologists and for publication of innovative clinical trials.
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