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<rss version="2.0"><channel><title>Neue Studien: Europe PMC</title><link>https://www.psoriasis-news.de/articles.html/1_articles/page/17/?d=1</link><description>Neue Studien: Europe PMC</description><language>de</language><item><title>Human Dermal Fibroblast-derived Spheroids Demonstrate Efficacious Immune Modulation in a Psoriasis Mouse Model</title><link>https://www.psoriasis-news.de/articles.html/1_articles/human-dermal-fibroblast-derived-spheroids-demonstrate-efficacious-immune-modulation-in-a-psoriasis-mouse-model-r176/</link><description><![CDATA[<h4>Background: </h4> Psoriasis is a chronic inflammatory disease associated with high morbidity and few cases of sustained remission. Innovative immunomodulatory therapies, including fibroblast-based cell therapies, offer promising alternatives. This study investigates the therapeutic potential of human dermal fibroblasts (HDFs) organized into three-dimensional (3D) spheroids in a mouse model of imiquimod (IMQ)-induced psoriasis. Methods HDF spheroids were cultured using Elplasia microcavity plates, and their size, viability, and phenotype were compared with single cells in 2D monolayer cultures. Cellular responses in whole blood and acute inflammatory responses were evaluated at various time points following intravenous injection of HDFs. The therapeutic efficacy of HDF spheroids was assessed using an IMQ-induced psoriasis mouse model, with disease severity scored using the Psoriasis Area and Severity Index (PASI). Optimized HDF spheroids (~150 um, 1x106 cells/mouse) were administered intravenously in a single dose for mild psoriasis or multiple doses for moderate-to-severe psoriasis. The efficacy of HDF spheroids was compared to a pre-clinical monoclonal antibody targeting interleukin 23 (anti-IL-23). Results Spheroid cultures of HDFs showed reduced cell size, enhanced viability, and distinct phenotypic changes compared to monolayer cultures. Intravenous injection of HDF spheroids resulted in less thrombocytopenia and reduced acute inflammatory responses compared to single-cell injection. A single dose of HDF spheroids reduced the severity of mild psoriasis by 35%, while repeated doses resulted in a 36% reduction in moderate-to-severe psoriasis. Single-dose administration normalized blood cell counts, alleviated spleen enlargement, and improved cytokine dysregulation. Although HDF spheroids and anti-IL-23 reduced epidermal thickening and immune cell infiltration, HDF spheroids uniquely inhibited monocyte production and infiltration, a benefit not observed with anti-IL-23. No acute or chronic toxicity was observed. Conclusions HDF spheroids offer comparable therapeutic efficacy to anti-IL-23 in treating psoriasis, with a distinct mechanism involving inhibiting monocyte production and infiltration. Their safety profile and broader immunomodulatory potential support their development as a novel therapeutic strategy for psoriasis and other inflammatory diseases.<p><a href="http://europepmc.org/article/PPR/PPR1063923?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">176</guid><pubDate>Sun, 10 Aug 2025 12:04:09 +0000</pubDate></item><item><title>Composite Outcome Measures for Psoriatic Arthritis: Project Updates 2024.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/composite-outcome-measures-for-psoriatic-arthritis-project-updates-2024-r175/</link><description><![CDATA[The Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA)-Outcome Measures in Rheumatology (OMERACT) psoriatic arthritis (PsA) working group provided updates at the GRAPPA 2024 annual meeting on their assessment of composite outcome measures for PsA. The group presented the progress of a systematic literature review on the psychometric properties of the following candidate composite outcome measures using the OMERACT filter 2.2: (1) minimal disease activity (MDA), (2) Disease Activity for Psoriatic Arthritis (DAPSA), (3) American College of Rheumatology (ACR) response criteria, (4) Psoriatic Arthritis Disease Activity Score (PASDAS), (5) Composite Psoriatic Disease Activity Index (CPDAI), (6) 3-item visual analog scale (3VAS), and (7) 4VAS. A Delphi exercise for patient research partners (PRPs) on domain match and feasibility is ongoing. Following analysis and endorsement of domain match and feasibility by PRPs, the working group will seek endorsement from the GRAPPA community. In addition, the group illustrated a new research proposal for using network metaanalysis to quantitatively compare the responsiveness of these various composite outcome measures.<p><a href="http://europepmc.org/article/MED/40763944?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">175</guid><pubDate>Sun, 10 Aug 2025 12:04:09 +0000</pubDate></item><item><title>Representation of Psoriasis on the Web for Patients With Skin of Color.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/representation-of-psoriasis-on-the-web-for-patients-with-skin-of-color-r174/</link><description><![CDATA[<h4>Unlabelled</h4>This study analyzed over 2000 images of psoriasis across major web-based platforms and found a significant underrepresentation of darker skin tones, highlighting a critical gap in dermatologic representation that may contribute to misdiagnoses and health disparities among patients with skin of color.<p><a href="http://europepmc.org/article/MED/40764051?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">174</guid><pubDate>Sun, 10 Aug 2025 12:04:09 +0000</pubDate></item><item><title>Gender differences in the association between adverse childhood experiences and early onset psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/gender-differences-in-the-association-between-adverse-childhood-experiences-and-early-onset-psoriasis-r173/</link><description><![CDATA[Psoriasis, a chronic autoimmune skin disease, arises from both genetic predisposition and environmental factors, including Adverse Childhood Experiences (ACEs). This cross-sectional study investigated the association between ACEs, family history, and early-onset psoriasis (≤ 18 years), with particular attention to gender differences. Among 102 psoriasis patients (54 early-onset, 48 late-onset), the early-onset group demonstrated a higher proportion of females, greater prevalence of parental psoriasis, and elevated anxiety levels compared to the late-onset group. However, multivariable regression analysis revealed that parental psoriasis was not significantly associated with early-onset psoriasis. Exposure to three or more ACEs significantly associated with early-onset psoriasis (adjusted OR = 2.61, p = 0.014), with specific associations observed for emotional neglect, domestic violence, and loneliness. Gender-stratified analysis showed a stronger association in females (adjusted OR = 6.609, p = 0.016) than in males (adjusted OR = 2.494, p = 0.115), though no significant gender-ACEs interaction was detected (p = 0.289). These findings demonstrate a gender differences, dose-response relationship between ACEs and early-onset psoriasis, highlighting the potential value of early psychological interventions for at-risk individuals, particularly females with high ACE exposure.<p><a href="http://europepmc.org/article/MED/40764339?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">173</guid><pubDate>Sun, 10 Aug 2025 12:04:09 +0000</pubDate></item><item><title>Non-communicable diseases comorbidities negatively impact the treatment outcomes among psoriasis patients: a longitudinal study in Shanghai, China.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/non-communicable-diseases-comorbidities-negatively-impact-the-treatment-outcomes-among-psoriasis-patients-a-longitudinal-study-in-shanghai-china-r172/</link><description><![CDATA[<h4>Background</h4>Psoriasis is frequently associated with non-communicable disease (NCD) comorbidities, prompting interest in how these concurrent conditions may influence psoriasis treatment outcomes.<h4>Objectives</h4>To assess NCD prevalence and their influence on psoriasis treatment outcomes.<h4>Methods</h4>From 2022 to 2024, we recruited psoriasis patients in Shanghai Skin Disease Hospital. Data on demographic features, NCD comorbidities and treatment outcomes at week 4 and week 8 were systematically collected through questionnaire, physical examination, and clinical severity assessment (psoriasis area and severity index [PASI], body surface area [BSA], physician's global assessment [PGA]).<h4>Results</h4>Among 1116 patients, 48.4% had at least one NCD comorbidity. NCD-free patients exhibited higher PASI<sub>50</sub> response rates at both week 4 (46.5 <i>vs.</i> 39.1%) and week 8 (72.2 <i>vs.</i> 70.9%). Log binomial regression revealed that NCDs significantly reduced the likelihood of achieving PASI<sub>50</sub> at week 4 (relative risk [RR] = 0.84, 95% confidence interval [CI]: 0.73-0.96), with a similar but non-significant trend at week 8 (RR = 0.98, 95% CI: 0.92-1.06).<h4>Conclusion</h4>NCDs negatively impact early treatment outcomes in psoriasis patients. So we propose that dermatologists should integrate systematic NCD management into psoriasis treatment regimen.<p><a href="http://europepmc.org/article/MED/40709738?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">172</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>Real-World Effectiveness of Bimekizumab in Predominantly Difficult-to-Treat Patients with Psoriatic Arthritis Followed in a Combined Dermatology-Rheumatology Clinic: A 24-Week Multicenter Study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/real-world-effectiveness-of-bimekizumab-in-predominantly-difficult-to-treat-patients-with-psoriatic-arthritis-followed-in-a-combined-dermatology-rheumatology-clinic-a-24-week-multicenter-study-r171/</link><description><![CDATA[<h4>Introduction</h4>Bimekizumab (BKZ), a monoclonal antibody targeting interleukin (IL)-17A and IL-17F, has shown high efficacy in clinical trials. However, real-world data on its use in psoriatic arthritis (PsA) are limited. This study aimed to evaluate the effectiveness and safety of BKZ over 24 weeks in a real-world setting.<h4>Methods</h4>A retrospective, multicenter study was conducted at two Italian rheumatology centers, enrolling adult patients with PsA who initiated BKZ treatment between January 2023 and February 2025. Clinical data were collected at baseline, week 12, and week 24.<h4>Results</h4>Forty patients with PsA were included. Of these, 75% had failed at least two biologic and/or targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs) prior to BKZ and 25/40 (62.5%) had failed at least one IL-17A inhibitor (IL-17Ai). Among these 25 patients, 32% experienced a primary failure and 68% a secondary failure. The median baseline Disease Activity in Psoriatic Arthritis (DAPSA) score was 22.9 (17.5-27.2), decreasing to 6.0 (3.1-12.8) at week 24 (p &lt; 0.001). By week 24, 72.5% achieved DAPSA low disease activity (LDA), and 25% achieved DAPSA remission. The median swollen joint count (SJC) decreased from 3.0 (0.8-5.3) to 0.0 (IQR 0.0-1.0), and median tender joint count (TJC) decreased from 4.5 (3.0-7.3) to 1.0 (0.0-2.0) (both p &lt; 0.001). Pain visual analog scale (VAS) and Patient Global Assessment (PGA) improved significantly, from 7.0 (6.0-8.0) and 7.5 (6.5-8.0) at baseline to 2.0 (1.0-5.0) and 2.0 (1.0-4.5) at week 24 (both p &lt; 0.001). Skin involvement also improved, with 51.5% achieving Psoriasis Area and Severity Index (PASI) 100 by week 24. The safety profile was favorable; 15% of patients developed mild oral candidiasis, none of which required treatment discontinuation.<h4>Conclusion</h4>BKZ demonstrated rapid and sustained improvements in PsA symptoms in a challenging real-world population, with a favorable safety profile.<p><a href="http://europepmc.org/article/MED/40720055?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">171</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>The Burden of Pediatric Psoriasis: A Systematic Review.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/the-burden-of-pediatric-psoriasis-a-systematic-review-r170/</link><description><![CDATA[<h4>Background</h4>The approach to pediatric psoriasis requires special considerations, given the potential for negative consequences on overall physical and psychosocial health.<h4>Objective</h4>The aim of this study was to systematically review the literature to characterize the burden of pediatric psoriasis.<h4>Methods</h4>Papers assessing associations between pediatric psoriasis (in children &lt;18 years old) and quality of life, physical symptoms (e.g., skin pain, itch, sleep disruption), and adverse psychological, social, and financial effects were searched with no date restrictions through July 2023. Databases searched included Ovid MEDLINE<sup><span class="ipsEmoji">®</span></sup>, CENTRAL, the Cochrane Database of Systematic Reviews, and PsycInfo. Articles were excluded if they focused on comorbidities (including psoriatic arthritis/enthesitis), were of low quality, or were not in English.<h4>Results</h4>64 publications met eligibility criteria. Composite quality of life was the most frequently reported domain (40 publications) and was negatively impacted by psoriasis as a function of severity. Physical burdens, especially itch, occurred in 44.1-96.3% of children with psoriasis, while skin pain was less common. Psychosocial and family burdens were less frequently assessed and often with non-validated tools. Children with psoriasis participated less in social activities, but there were no clear associations between psoriasis and school performance or interpersonal relationships. Psoriasis was associated with a higher mental health burden on caregivers and greater family financial burden.<h4>Conclusions</h4>Psoriasis leads to high burden for pediatric patients and caregivers. Evaluation and management decisions should include and incorporate a thorough assessment of burden. Additional studies using validated tools are necessary to fully assess psychosocial and family burdens of psoriasis.<p><a href="http://europepmc.org/article/MED/40694272?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">170</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>Dietary Principles, Interventions and Oxidative Stress in Psoriasis Management: Current and Future Perspectives.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/dietary-principles-interventions-and-oxidative-stress-in-psoriasis-management-current-and-future-perspectives-r169/</link><description><![CDATA[Psoriasis is a chronic inflammatory autoimmune disease that causes significant deterioration of the quality of life, and due to its multifactorial causes, it is often difficult to manage. Apart from genetic and environmental components, an important part of its pathophysiology comprises an oxidative stress induction that the standard antioxidative mechanisms of the human body cannot compensate for. Moreover, in many psoriatic patients, there is a documented imbalance between antioxidant and pro-oxidative factors. Usually, psoriasis is evaluated using the Psoriasis Area and Severity Index (PASI) score. It has been demonstrated that dietary choices can lead to significant modification of PASI scores. Hypocaloric diets that are rich in antioxidants are highly effective in this regard, especially when focusing on vegetables and restricting consumption of animal-derived protein. Specific dietary regimens, namely the Mediterranean diet and potentially the ketogenic diet, are very beneficial, in the former case owing in large part to the omega-three fatty acids it provides and its ability to alter gut microbiome, a factor which seems to play a notable role in the pathogenesis of the disease. Another option is the topical application of vitamin D and its analogues, combined with corticosteroids, which can ameliorate the manifestations of psoriasis at the level of the skin. Finally, oral vitamin D supplementation has a positive impact on psoriatic arthritis and can mitigate the risk of associated comorbidities.<p><a href="http://europepmc.org/article/MED/40731925?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">169</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>Psoriasis Beyond the Skin: A Disease With Cardiovascular Risk.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/psoriasis-beyond-the-skin-a-disease-with-cardiovascular-risk-r168/</link><description><![CDATA[Psoriasis is a chronic immune-mediated skin disease that is increasingly understood as a systemic inflammatory condition with implications that extend far beyond the skin. Among its most serious associations is an elevated risk of cardiovascular disease, which has emerged as a leading cause of morbidity and mortality in affected patients. The persistent immune activation characteristic of psoriasis, driven by cytokines such as tumor necrosis factor α (TNFα), interleukin (IL)-17, and IL-23, contributes to endothelial dysfunction, oxidative stress, and atherogenesis. This shared pathophysiology helps explain the increased prevalence of coronary artery calcification, impaired microvascular function, and early-onset myocardial infarction observed in this population. Traditional risk assessment tools often fail to capture the actual cardiovascular burden in patients with moderate to severe disease. Evidence suggests that biologic therapies targeting key inflammatory pathways not only improve dermatologic outcomes but may also mitigate vascular risk, offering systemic benefits that extend beyond skin clearance. Recognizing psoriasis as a multisystem disorder reinforces the need for a more integrated approach to risk assessment and long-term management.<p><a href="http://europepmc.org/article/MED/40698258?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">168</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>Family planning and pregnancy among patients with psoriasis: incorporating the patients' voice in healthcare practice and information provision.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/family-planning-and-pregnancy-among-patients-with-psoriasis-incorporating-the-patients-voice-in-healthcare-practice-and-information-provision-r167/</link><description><![CDATA[<b>Aim:</b> Having psoriasis and being treated with medication could raise concerns regarding family planning and pregnancy (FPP), and no guidelines are available on healthcare practice and information provision regarding FPP for these patients. This study aims to gain insight in the perspectives of patients with psoriasis on this important subject.<b>Methods:</b> A cross-sectional questionnaire study including adult female and male patients with psoriasis, independent of their treatment type.<b>Results:</b> A total of 102 patients responded to the questionnaire (70% females, 30% males), of whom 47.1% have ever used biologic therapy. Respondents preferred dermatologists or general practitioners (GPs) as information provider. Patients would like to receive FPP information on fertility, heredity of psoriasis, use of psoriasis medication, and - specifically for females- the course of psoriasis during and after pregnancy and breastfeeding. Timing of FPP information provision was preferable at moment of diagnosis and medication changes or upon explicit request.<b>Conclusion:</b> Dermatologists and GPs have a crucial role in providing FPP information. The findings of this study have provided hands-on guidance for healthcare professionals to improve healthcare for both female and male patients with psoriasis in the reproductive age.<p><a href="http://europepmc.org/article/MED/40739803?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">167</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>Greater topical corticosteroid quantity applied reduces severity of psoriasis: Results from two randomized controlled trials.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/greater-topical-corticosteroid-quantity-applied-reduces-severity-of-psoriasis-results-from-two-randomized-controlled-trials-r166/</link><description><![CDATA[<h4>Background</h4>Topical drugs containing corticosteroids are recommended first-line treatment for patients with mild-moderate psoriasis. However, the optimal recommended dosage of topical drugs has not been well established.<h4>Objectives</h4>To investigate the effect of topical drug application quantity and treatment duration on psoriasis treatment outcome.<h4>Methods</h4>We conducted a post-hoc analysis of two randomized controlled trials investigating 214 patients with psoriasis using topical drugs containing corticosteroids and/or calcipotriol for up to 48 weeks. We measured the amount of topical drugs used during the study period and calculated the mean amount of applied drugs per 1% affected body surface area (BSA) divided by number of days in the study period. Improvement in severity of psoriasis was measured by Lattice-System Physician's Global Assessment (LS-PGA) (where affected BSA was divided into seven categories) from baseline to last study visit. Descriptive results were reported as counts with proportions, and as means with normality-based confidence intervals (CI). Associations were analyzed using linear regressions.<h4>Results</h4>Most study participants had a duration of psoriasis greater than 20 years, moderate psoriasis, and no history of using systemic psoriasis treatment. They had applied a mean of 1.0 g per 1% BSA per day (95% CI 0.9; 1.2). Daily use of topical drugs for four-weeks reduced severity of psoriasis. However, extended daily use for up to 48 weeks provided further reduction in disease severity (coefficient --0.30 (95% CI -0.51, -0.09)) and -0.73 (95% CI -1.09; -0.38) (P= 0.028). Greater amount of applied topical drugs reduced severity of psoriasis in a linear manner. Every increase of 1 g of topical drugs applied per 1% BSA per day reduced LS-PGA by 0.43 (95% CI 0.24; 0.61). Finally, patients who had never used systemic drugs experienced a greater reduction in psoriasis when applying the same mean amount of topical drugs (coefficient -0.7 (95% CI -1.1, -0.4) compared to those who had a history of taking systemic treatment (-0.3 (95% CI -0.5; -0.1), P=0.026).<h4>Conclusions</h4>A mean application amount of at least 1.0 g of topical drugs per 1% BSA per day seems safe and effective and can be used daily until clearance.<p><a href="http://europepmc.org/article/MED/40737510?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">166</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>Apremilast in Psoriasis: Current Landscape and Perspectives.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/apremilast-in-psoriasis-current-landscape-and-perspectives-r165/</link><description><![CDATA[Psoriasis is an immune-mediated skin disease manifested in more than 3% of Americans and over 125 million people worldwide. The inflammatory skin condition with an increased rate of keratinocyte turnover involves every level of the skin and exhibits various forms of the disease, including plaque, guttate, inverse, pustular, and erythrodermic psoriasis, as well as disease-associated conditions, such as psoriatic arthritis and nail psoriasis. Innovative treatment has highlighted the importance of Apremilast, an oral drug that belongs to the phosphodiesterase- 4 (PDE4) class, which was approved by the FDA in 2014. Apremilast works by increasing the presence of cyclic adenosine monophosphate (cAMP) within cells, thereby affecting inflammatory processes and reducing the production of pathological cytokines. Randomized controlled trials have shown that it effectively treats moderately to severely affected plaque psoriasis and psoriatic arthritis, and it is safer than traditional systemic agents. The new perspective on the usage of ethosomes, niosomes, liposomes, and nanostructured lipid carriers in psoriasis treatment is based on emerging nanotechnology in drug delivery systems. These new formulations are designed to enhance the solubility and targeted release of Apremilast, thus providing an enhanced therapeutic effect. This review will discuss the basic mechanisms of the disease known as psoriasis, as well as the mode of operation, pharmacological properties, clinical trials, and pharmacokinetics of apremilast, particularly in relation to nanocarrier modification of this promising drug.<p><a href="http://europepmc.org/article/MED/40739686?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">165</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>Therapeutic Potential of Mesenchymal Stem Cells in Psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/therapeutic-potential-of-mesenchymal-stem-cells-in-psoriasis-r164/</link><description><![CDATA[Psoriasis is a chronic immune-mediated disease mainly affecting the skin with different clinical manifestations. As patients with psoriasis may also suffer from psoriatic arthritis and the skin lesions of psoriasis are disfiguring, their quality of life is often impaired. Many environmental and genetic factors have been implicated in psoriasis development. Currently, there is no cure for the disease and long-term drug treatment is usually necessary, especially in moderate to severe cases. Mesenchymal stem cells (MSCs) are popular candidates for cell-based treatment in many immune-mediated diseases due to their ability to secrete a wide array of cytokines and growth factors and their immunomodulatory properties. MSCs from various sources administered via different routes have been shown to ameliorate psoriasis. This review gives an overview of psoriasis and MSCs and examine preclinical and clinical studies concerning the application of MSCs in the treatment of psoriasis, as well as consolidate major findings in this area of research.<p><a href="http://europepmc.org/article/MED/40748586?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">164</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>Copay Accumulators: A Legislative Issue in Dermatology.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/copay-accumulators-a-legislative-issue-in-dermatology-r163/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/40741379?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">163</guid><pubDate>Mon, 04 Aug 2025 07:43:04 +0000</pubDate></item><item><title>Real-World Effectiveness and Safety of Risankizumab in Psoriasis: A Comprehensive Analysis from the Saudi Arabia Psoriasis Registry (PSORSA).</title><link>https://www.psoriasis-news.de/articles.html/1_articles/real-world-effectiveness-and-safety-of-risankizumab-in-psoriasis-a-comprehensive-analysis-from-the-saudi-arabia-psoriasis-registry-psorsa-r154/</link><description><![CDATA[<h4>Introduction</h4>Psoriasis is a chronic immune-mediated skin condition that has a substantial impact on patients' quality of life. The Saudi Arabia Psoriasis Registry (PSORSA) was established to address long-term real-world data (RWD) on systemic and biologic therapies in the region. This observational cohort study provides a comprehensive analysis of baseline disease characteristics, comorbidities, and treatment efficacy among patients enrolled in PSORSA, with an emphasis on risankizumab.<h4>Methods</h4>Data were sourced from a governmental online database covering multiple healthcare centers. Patients eligible for biologics were followed at baseline and at weeks 16, 28, 40, and 52 to evaluate disease severity, quality of life, and adherence. Statistical analyses were conducted using Jamovi and R. Descriptive statistics were performed for categorical and continuous variables. p-Values &lt; 0.05 were considered significant.<h4>Results</h4>The study cohort included 313 patients. Plaque psoriasis was the most prevalent clinical type (93.9%). An analysis of treatment history revealed that 39.6% of patients had prior therapy exposure, and all patients received risankizumab as a biologic therapy. At baseline, the mean Psoriasis Area and Severity Index (PASI) score was 25.49. By week 52, it had decreased to 0.358, indicating complete clearance. PASI scores showed a steady and substantial reduction over time, with an 88% reduction at week 16, 96% at week 28, 97.5% at week 40, and 98.5% by week 52, demonstrating a strong and sustained treatment effect (p &lt; 0.001). Additionally, risankizumab exhibited a favorable drug survival profile, with many patients maintaining treatment beyond 122 weeks.<h4>Conclusion</h4>This study represents the first real-world assessment of risankizumab for moderate-to-severe psoriasis in Saudi Arabia. The findings demonstrate that risankizumab is an effective and well-tolerated treatment for moderate-to-severe psoriasis in this Saudi Arabian cohort. However, future studies should explore long-term safety outcomes and the comparative effectiveness of risankizumab and emerging biologics in diverse patient populations.<p><a href="http://europepmc.org/article/MED/40711523?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">154</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>Biologic and small molecule therapies for psoriasis in individuals with Down syndrome: Two cases and a systematic review.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/biologic-and-small-molecule-therapies-for-psoriasis-in-individuals-with-down-syndrome-two-cases-and-a-systematic-review-r153/</link><description><![CDATA[Down syndrome (DS), also known as trisomy 21, is a genetic condition linked to a higher prevalence of skin disorders, including psoriasis, which affects up to 8% of individuals. DS patients with psoriasis present unique management considerations, including a theoretical increased risk of infectious complications with immunosuppressive therapies. This report includes two cases and a systematic review summarizing available evidence on psoriasis characteristics and treatment outcomes in individuals with DS. We report two DS patients with psoriasis demonstrating variable therapeutic responses: one controlled with acitretin and another requiring secukinumab after multiple treatment failures. To contextualize these findings, we conducted a systematic review following PRISMA guidelines, identifying 10 studies comprising 37 DS patients with psoriasis. Methotrexate was the most frequently failed therapy. Biologics targeting IL-17 and IL-23 pathways achieved the highest rates of complete resolution. These findings reflect Th1/Th17-driven inflammation in DS and highlight the need for individualized, pathway-specific management strategies.<p><a href="http://europepmc.org/article/MED/40717838?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">153</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>Correction to "Impact of Delay of Treatment With Disease-Modifying Antirheumatic Drugs in Psoriatic Arthritis: The CorEvitas Psoriatic Arthritis/Spondyloarthritis Registry".</title><link>https://www.psoriasis-news.de/articles.html/1_articles/correction-to-impact-of-delay-of-treatment-with-disease-modifying-antirheumatic-drugs-in-psoriatic-arthritis-the-corevitas-psoriatic-arthritisspondyloarthritis-registry-r152/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/40728028?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">152</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>A Validated Quantitative LC-MS/MS Method for Determination of Deucravacitinib in Rat Plasma and Its Application to a Pharmacokinetic Study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/a-validated-quantitative-lc-msms-method-for-determination-of-deucravacitinib-in-rat-plasma-and-its-application-to-a-pharmacokinetic-study-r151/</link><description><![CDATA[We developed and validated a novel analytical methodology for the precise quantification of deucravacitinib, an oral TYK2 inhibitor for treating moderate-to-severe plaque psoriasis in adults. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was employed in this method for sensitive detection of the compound in rat plasma. Analytical separation was performed utilizing an ACE C18 column (4.6 × 100 mm, 5-μm particle size) with a carefully optimized mobile phase composition of methanol and 2-mM ammonium formate (90:10, v/v), maintained at a consistent flow rate of 0.9 mL/min. Detection was executed in positive ionization mode, targeting multiple reaction monitoring (MRM) transitions of m/z 426.8 → 358.4 for the analyte and m/z 394.1 → 363.2 for the internal standard. The validation of the analytical method encompassed an assessment of selectivity, linearity, accuracy, precision, recovery, and stability. This method demonstrated stability, specificity, and no matrix effect at three concentration levels (1.606, 267.600, 507.780 ng/mL). The method's lower limit of quantification (LLOQ) is 0.556 ng/mL. The calibration curve demonstrates linearity from the LLOQ up to 668.132 ng/mL, exhibiting a high correlation coefficient (r<sup>2</sup> = 0.9976). The intraday and interday precisions were less than 6.62% and 5.95%, respectively, with accuracies ranging from 90.68% to 103.80%. The recovery of deucravacitinib ranged from 95.34% to 103.80% and remained stable under different conditions. After successful validation, the method was used for pharmacokinetic profiling of deucravacitinib in rats following oral administration.<p><a href="http://europepmc.org/article/MED/40695726?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">151</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>Greater topical corticosteroid quantity applied reduces severity of psoriasis: Results from two randomized controlled trials.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/greater-topical-corticosteroid-quantity-applied-reduces-severity-of-psoriasis-results-from-two-randomized-controlled-trials-r150/</link><description><![CDATA[Topical drugs containing corticosteroids are recommended first-line treatment for patients with mild-moderate psoriasis. However, the optimal recommended dosage of topical drugs has not been well established. To investigate the effect of topical drug application quantity and treatment duration on psoriasis treatment outcome. We conducted a post-hoc analysis of two randomized controlled trials investigating 214 patients with psoriasis using topical drugs containing corticosteroids and/or calcipotriol for up to 48 weeks. We measured the amount of topical drugs used during the study period and calculated the mean amount of applied drugs per 1% affected body surface area (BSA) divided by number of days in the study period. Improvement in severity of psoriasis was measured by Lattice-System Physician's Global Assessment (LS-PGA) (where affected BSA was divided into seven categories) from baseline to last study visit. Descriptive results were reported as counts with proportions, and as means with normality-based confidence intervals (CI). Associations were analyzed using linear regressions. Most study participants had a duration of psoriasis greater than 20 years, moderate psoriasis, and no history of using systemic psoriasis treatment. They had applied a mean of 1.0 g per 1% BSA per day (95% CI 0.9; 1.2). Daily use of topical drugs for four-weeks reduced severity of psoriasis. However, extended daily use for up to 48 weeks provided further reduction in disease severity (coefficient --0.30 (95% CI -0.51, -0.09)) and -0.73 (95% CI -1.09; -0.38) (P= 0.028). Greater amount of applied topical drugs reduced severity of psoriasis in a linear manner. Every increase of 1 g of topical drugs applied per 1% BSA per day reduced LS-PGA by 0.43 (95% CI 0.24; 0.61). Finally, patients who had never used systemic drugs experienced a greater reduction in psoriasis when applying the same mean amount of topical drugs (coefficient -0.7 (95% CI -1.1, -0.4) compared to those who had a history of taking systemic treatment (-0.3 (95% CI -0.5; -0.1), P=0.026). A mean application amount of at least 1.0 g of topical drugs per 1% BSA per day seems safe and effective and can be used daily until clearance.<p><a href="http://europepmc.org/article/MED/40737510?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">150</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>IL-17A inhibitors modulate skin microbiome in psoriasis: implications for microbial homeostasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/il-17a-inhibitors-modulate-skin-microbiome-in-psoriasis-implications-for-microbial-homeostasis-r149/</link><description><![CDATA[<h4>Background</h4>The IL-17A inhibitors target aberrant immune responses in psoriasis but also impacts the host's defense against infections. The effects of this treatment on skin microorganisms and microbiome-encoded metabolic pathways remain unclear.<h4>Objectives</h4>This was an exploratory clinical study designed to investigate whether Psoriasis is associated with skin microbiota, as well as a longitudinal cohort study aimed at revealing the effects of IL-17A inhibitor treatment on skin microbiota in Psoriasis.<h4>Methods</h4>In this study, we recruited 26 patients with moderate to severe psoriasis and 15 healthy controls. We collected skin microbiome samples from both greasy and dry skin regions. All samples were analyzed using 16S rDNA gene sequencing to determine the microbial profiles.<h4>Results</h4>Compared with healthy controls, the composition and function of skin microbiome in psoriasis patients are heterogeneous. Treatment with IL-17A inhibitors significantly increases the alpha diversity of the skin microbiota in psoriasis patients, indicating potential restoration of microbial community richness and evenness. However, this treatment does not entirely alter the taxonomic composition of the skin microbiota; rather, it shifts the relative abundance of specific microbial species, indicating that certain core microbial features remain relatively stable. Moreover, IL-17A inhibitors help adjust the functional profile of the skin microbiome in psoriasis patients, bringing it closer to that of healthy individuals.<h4>Conclusions</h4>Psoriasis patients exhibit significant heterogeneity in both the composition and functionality of their skin microbiota. Although IL-17A inhibitor treatment fails to fundamentally alter its taxonomic composition, this therapy effectively enhances microbial community stability by increasing alpha diversity and modulating the relative abundance of various taxa. Additionally, it adjusts the functional profile of the skin microbiota towards a healthier state, thereby contributing to the restoration of microecological balance.<p><a href="http://europepmc.org/article/MED/40708005?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">149</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>Successful Treatment with Secukinumab in a Psoriasis Patient on Hemodialysis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/successful-treatment-with-secukinumab-in-a-psoriasis-patient-on-hemodialysis-r148/</link><description><![CDATA[Moderate to severe psoriasis has been reported as an independent risk factor for IgA nephropathy (IgAN). IgAN is characterized by episodic microscopic hematuria, which can progress to end-stage renal disease (ESRD). Managing therapeutic interventions for psoriasis patients requiring dialysis due to ESRD presents significant challenges. We present a case of severe plaque psoriasis in a patient concurrently diagnosed with IgAN who is dependent on hemodialysis. Over the past two months, his condition has worsened without any identifiable triggers. Physical examination revealed generalized scaly plaques on the scalp, trunk, and extremities, resulting in a Psoriasis Area Severity Index (PASI) score of 19.2. Laboratory tests confirmed end-stage renal insufficiency, with no other abnormalities detected. Consequently, the patient was prescribed subcutaneous secukinumab following a standard regimen. He achieved complete resolution of symptoms after eight weeks of treatment and experienced no recurrence during a one-year follow-up. His kidney-related parameters remained stable during secukinumab therapy. To summarize, this case report discusses a patient with severe psoriasis who also has concurrent IgAN and ESRD, successfully treated with secukinumab. It reinforces the rapid efficacy and enduring safety of secukinumab in managing psoriasis in hemodialysis-dependent patients with IgAN comorbidity. Zeno Fratton et al has reported that an interleukin (IL)-17A/F inhibitor effectively treats moderate-to-severe psoriasis in patients with chronic kidney disease (CKD). However, further studies are necessary to develop evidence-based guidelines for biologic selection within this vulnerable population.<p><a href="http://europepmc.org/article/MED/40718360?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">148</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>Copay Accumulators: A Legislative Issue in Dermatology</title><link>https://www.psoriasis-news.de/articles.html/1_articles/copay-accumulators-a-legislative-issue-in-dermatology-r147/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12303918?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">147</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>Treatment of severe psoriasis in a hospice care patient using secukinumab, an inhibitor of interleukin-17A expression: Treatment response and changes in quality of life.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/treatment-of-severe-psoriasis-in-a-hospice-care-patient-using-secukinumab-an-inhibitor-of-interleukin-17a-expression-treatment-response-and-changes-in-quality-of-life-r146/</link><description><![CDATA[Secukinumab, a fully human monoclonal antibody that antagonizes interleukin-17A (IL-17A), has proven efficacious in the management of moderate to severe plaque psoriasis. Secukinumab has established itself as an effective treatment for plaque psoriasis, offering rapid and sustained symptom improvement. However, more research is warranted to assess its efficacy and safety in elderly patients, where clinical data is currently lacking. We describe an 84-year-old female presented with stable angina pectoris needed to be hospice cared. She had more than 30 years history of plaque psoriasis. The patient underwent treatment with secukinumab for two weeks. The skin lesions had been decreased rapidly and this greatly improved quality life of this patient. We report the clinical use of secukinumab in the treatment of elderly psoriasis and biologicals may be a new strategy for hospice care of patients with psoriasis.<p><a href="http://europepmc.org/article/MED/40329840?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">146</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>Correction to &#x201C;Impact of Delay of Treatment With Disease&#x2010;Modifying Antirheumatic Drugs in Psoriatic Arthritis: The CorEvitas Psoriatic Arthritis/Spondyloarthritis Registry&#x201D;</title><link>https://www.psoriasis-news.de/articles.html/1_articles/correction-to-impact-of-delay-of-treatment-with-disease%E2%80%90modifying-antirheumatic-drugs-in-psoriatic-arthritis-the-corevitas-psoriatic-arthritisspondyloarthritis-registry-r145/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12305346?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">145</guid><pubDate>Thu, 31 Jul 2025 12:43:37 +0000</pubDate></item><item><title>Recent advancement of fisetin-based nanoformulations in the management of psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/recent-advancement-of-fisetin-based-nanoformulations-in-the-management-of-psoriasis-r143/</link><description><![CDATA[Psoriasis is a chronic inflammatory autoimmune skin disease with enhanced skin cell turnover. Despite the therapies currently available, better and target-oriented therapies are needed. Fisetin is a flavonoid with antioxidant, anti-inflammatory, and immunomodulatory properties. It shows therapeutic potential, but its poor bioavailability and penetration into the skin cannot be used effectively to treat psoriasis. While fisetin-loaded nanoformulations in cancer and other diseases have been explored, their potential as a therapy for psoriasis is unexplored. Most reviews detail the biological activities of fisetin or nanoformulations for psoriasis therapy but not their combination. The review here compiles fisetin's chemical and pharmacological properties along with the problems with conventional drug delivery and fisetin-loaded nanoformulations such as polymeric nanoparticles, liposomes, solid lipid nanoparticles, nanogels, and micelles. It also discusses their mechanisms, preclinical results, and potential for the clinic. Preclinical studies demonstrate fisetin nanoformulations to enhance penetration into the skin, reduce inflammation, promote skin regeneration in psoriasis models, and alleviate symptoms of redness and scaling. Clinical trials are lacking, and studies are needed to assess safety and efficacy. Fisetin nanoformulations are a potential target-oriented psoriasis therapy with better drug delivery and fewer side effects than conventional therapies. Despite formulation stability, scalability, and regulatory issues, the potential for fisetin-loaded nanoformulations is excellent and needs further exploration for their safety and efficacy in patients.<p><a href="http://europepmc.org/article/MED/40622453?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">143</guid><pubDate>Sat, 12 Jul 2025 18:34:11 +0000</pubDate></item></channel></rss>
