Challenges Psoriasis and Its Impact on Quality of Life: Challenges in Treatment and Management.

IF 5.2 Q1 DERMATOLOGY
Psoriasis (Auckland, N.Z.) Pub Date : 2025-05-01 eCollection Date: 2025-01-01 DOI:10.2147/PTT.S519420
Małgorzata Ponikowska, Ercole Vellone, Michał Czapla, Izabella Uchmanowicz
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Abstract

Psoriasis, a chronic inflammatory disease affecting approximately 3% of the global population, presents complex challenges that extend beyond its physical manifestations. This comprehensive review examines the multidimensional impact of psoriasis on patients' lives, encompassing physical, psychological, and social aspects. We analyze current therapeutic approaches, from traditional systemic treatments to cutting-edge biological therapies and emerging oral medications, evaluating their efficacy, limitations, and accessibility. The review explores how disease severity correlates with quality of life measures and psychological burden, noting the high prevalence of depression (20%), anxiety (21%), and suicidal ideation (0.77%) among affected individuals. However, emerging evidence suggests that clinical severity, as measured by PASI or BSA, does not always correlate with the psychoemotional burden experienced by patients, highlighting the need for a more comprehensive assessment of disease impact. We discuss the evolution of treatment strategies, highlighting recent developments in targeted therapies, including JAK inhibitors, particularly selective TYK2 inhibitors, and PDE4 inhibitors, which offer promising alternatives to traditional treatments. Additionally, we examine the role of various assessment tools and quality of life measures in evaluating treatment outcomes. The analysis emphasizes the need for a holistic approach to patient care that integrates medical interventions with psychological support, addressing both the visible and invisible burdens of the disease. This review underscores the importance of personalized treatment strategies that consider not only clinical efficacy but also patient preferences, accessibility, and long-term safety profiles.

牛皮癣及其对生活质量的影响:治疗和管理的挑战。
牛皮癣是一种影响全球约3%人口的慢性炎症性疾病,它带来的复杂挑战超出了其身体表现。这篇综合综述探讨了牛皮癣对患者生活的多方面影响,包括身体、心理和社会方面。我们分析了目前的治疗方法,从传统的全身治疗到尖端的生物治疗和新兴的口服药物,评估了它们的疗效、局限性和可及性。该综述探讨了疾病严重程度如何与生活质量指标和心理负担相关,注意到受影响个体中抑郁(20%)、焦虑(21%)和自杀意念(0.77%)的高患病率。然而,新出现的证据表明,PASI或BSA测量的临床严重程度并不总是与患者所经历的心理情绪负担相关,这突出了对疾病影响进行更全面评估的必要性。我们讨论了治疗策略的演变,重点介绍了靶向治疗的最新进展,包括JAK抑制剂,特别是选择性TYK2抑制剂和PDE4抑制剂,它们为传统治疗提供了有希望的替代方案。此外,我们研究了各种评估工具和生活质量措施在评估治疗结果中的作用。分析强调需要对病人护理采取综合办法,将医疗干预与心理支持结合起来,解决这种疾病的有形和无形负担。这篇综述强调了个性化治疗策略的重要性,不仅要考虑临床疗效,还要考虑患者的偏好、可及性和长期安全性。
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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