Predictors of Quality of Life in Psoriasis Patients: Insights from a Cross-Sectional Study.

IF 5.2 Q1 DERMATOLOGY
Psoriasis (Auckland, N.Z.) Pub Date : 2025-04-24 eCollection Date: 2025-01-01 DOI:10.2147/PTT.S516109
Patrycja Walniczek, Malgorzata Ponikowska, Ewelina Barbara Kolarczyk, Paulina Spaleniak, Katarzyna Mróz-Kijowska, Michał Czapla, Izabella Uchmanowicz
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Abstract

Background: Psoriasis significantly impacts patients' mental health and social relationships, often leading to feelings of stigmatization and shame due to the visibility of skin lesions. This study aimed to identify factors influencing the quality of life in patients with psoriasis.

Methods: A cross-sectional study was conducted from November 2018 to December 2020, involving 100 patients treated for psoriasis. The research utilized the WHO Quality of Life Questionnaire (WHOQoL-Bref), the Psoriasis Area and Severity Index (PASI), the Acceptance of Illness Scale (AIS), the Hospital Anxiety and Depression Scale (HADS), and the Mini Nutritional Assessment (MNA). The analysis included demographic, clinical, and psychological variables to evaluate their impact on quality of life.

Results: The multivariate linear regression model revealed that significant independent predictors of quality of life included age (p=0.001), duration of disease (p=0.004), and nutritional status (p=0.002). In the physical domain, factors such as phototherapy (r=2.46) and anxiety levels assessed by the HADS anxiety subscale (r=-0.23) were particularly relevant. In the psychological domain, the presence of psoriatic arthritis (r=1.978), hand and foot psoriasis (r=2.34), and scores on the HADS anxiety (r=-0.212) and depression subscales (r=-0.226) were significant. Male gender (r=1.632) and depressive symptoms (r=-0.352) impacted the social domain. In the environmental domain, predictors included erythrodermic psoriasis (r=1.98), hand and foot psoriasis (r=2.312), phototherapy (r=1.877), PASI score (r=-0.04), and depression as measured by HADS (r=-0.228).

Conclusion: The primary predictors of quality of life in patients with psoriasis are the type of psoriasis, the presence of anxiety and depressive disorders, and treatment with phototherapy. However, the study's single-center design and relatively small sample size may limit the generalizability of the findings. Further multi-center studies are needed to confirm these results and broaden their applicability.

银屑病患者生活质量的预测因素:来自横断面研究的见解。
背景:牛皮癣严重影响患者的心理健康和社会关系,由于皮肤病变的可见性,经常导致污名化和羞耻感。本研究旨在确定影响牛皮癣患者生活质量的因素。方法:2018年11月至2020年12月,对100例银屑病患者进行横断面研究。研究采用世界卫生组织生活质量问卷(WHOQoL-Bref)、银屑病面积及严重程度指数(PASI)、疾病接受度量表(AIS)、医院焦虑抑郁量表(HADS)和迷你营养评估量表(MNA)。分析包括人口统计学、临床和心理变量,以评估它们对生活质量的影响。结果:多变量线性回归模型显示,生活质量的显著独立预测因子包括年龄(p=0.001)、病程(p=0.004)和营养状况(p=0.002)。在物理领域,光疗(r=2.46)和HADS焦虑子量表评估的焦虑水平(r=-0.23)等因素尤其相关。在心理领域,银屑病关节炎(r=1.978)、手足牛皮癣(r=2.34)、HADS焦虑(r=-0.212)和抑郁(r=-0.226)得分显著。男性性别(r=1.632)和抑郁症状(r=-0.352)影响社会领域。在环境领域,预测因子包括红皮病型牛皮癣(r=1.98)、手足牛皮癣(r=2.312)、光疗(r=1.877)、PASI评分(r=-0.04)和HADS测量的抑郁(r=-0.228)。结论:银屑病患者生活质量的主要预测因素是银屑病的类型、焦虑和抑郁障碍的存在以及光疗的治疗。然而,该研究的单中心设计和相对较小的样本量可能限制了研究结果的普遍性。需要进一步的多中心研究来证实这些结果并扩大其适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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