Fino Edita, Russo Paolo Maria, Tengattini Vera, Bardazzi Federico, Patrizi Annalisa, Martoni Monica
Department of Experimental, Diagnostic and Specialty Medicine (DIMES), Alma Mater Studiorum Università di Bologna, St. Orsola-Malpighi Hospital, Via Massarenti 9, 40138 Bologna, Italy.
Dermatology Unit, Sant'Orsola-Malpighi Hospital, Via Massarenti 9, 40138 Bologna, Italy.
J Pers Med. 2021 Nov 21;11(11):1236. doi: 10.3390/jpm11111236.
A deeper understanding of how health-related quality of life relates to the clinical and individual characteristics of patients is essential for the delivery of patient-centered dermatological care. The current study aimed to examine the role of individual differences in emotion dysregulation and social anxiety in modulating quality of life in psoriatic patients. A total of 130 patients affected by psoriasis were consecutively enrolled in the study as they approached the Dermatology Unit of Sant'Orsola-Malpighi Hospital of Bologna. Clinical information gathered included illness severity, assessed with the Psoriasis Area and Severity Index (PASI) and the Body Surface Area (BSA); illness onset; familiarity; and prescribed treatment. The patient-reported outcome measures were the Dermatology Life Quality Index (DLQI), measuring the patient's quality of life; the Psoriasis Skin Appearance Bothersomeness scale (PSAB), measuring patient's perception of illness severity; the Difficulties in Emotion Regulation Scale (DERS), assessing emotion dysregulation traits; and the Social Interaction Anxiety Scale (SIAS), measuring anxiety about social interactions. Patients with moderate-to-severe psoriasis reported significantly lower quality of life compared to mildly affected patients. In addition, of the patients affected by mild psoriasis, those characterized by emotion dysregulation and social anxiety traits showed significantly lower levels of quality of life. Our findings suggest that individual differences in emotion dysregulation and social anxiety contribute to health-related quality of life in addition to illness severity. Therapeutic approaches that combine dermatological care with psychological support, especially focused on emotional regulation skills, may be useful to improve clinical outcomes in patients with psoriasis.
深入了解健康相关生活质量与患者临床及个体特征之间的关系,对于提供以患者为中心的皮肤科护理至关重要。本研究旨在探讨情绪调节障碍和社交焦虑方面的个体差异在调节银屑病患者生活质量中的作用。共有130名银屑病患者在前往博洛尼亚圣奥索拉 - 马尔皮基医院皮肤科就诊时连续纳入本研究。收集的临床信息包括疾病严重程度(用银屑病面积和严重程度指数(PASI)及体表面积(BSA)评估)、发病情况、家族史以及所开的治疗药物。患者报告的结局指标包括:皮肤病生活质量指数(DLQI),用于衡量患者的生活质量;银屑病皮肤外观困扰量表(PSAB),用于衡量患者对疾病严重程度的感知;情绪调节困难量表(DERS),用于评估情绪调节障碍特征;以及社交互动焦虑量表(SIAS),用于测量社交互动焦虑。与轻度银屑病患者相比,中度至重度银屑病患者报告的生活质量显著更低。此外,在轻度银屑病患者中,具有情绪调节障碍和社交焦虑特征的患者生活质量水平显著更低。我们的研究结果表明,除了疾病严重程度外,情绪调节障碍和社交焦虑方面的个体差异也会影响健康相关生活质量。将皮肤科护理与心理支持相结合,尤其是专注于情绪调节技能的治疗方法,可能有助于改善银屑病患者的临床结局。