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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/7/?d=1</link><description>Neue Studien: Europe PMC</description><language>de</language><item><title>TLR9/MyD88/NF-&#x3BA;B signaling mediates mental stress-induced exacerbation of psoriasis through immune dysregulation in a mouse model.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/tlr9myd88nf-%CE%BAb-signaling-mediates-mental-stress-induced-exacerbation-of-psoriasis-through-immune-dysregulation-in-a-mouse-model-r498/</link><description><![CDATA[<h4>Objective</h4>Psoriasis is a chronic inflammatory autoimmune disease that affects physical and mental health. Mental stress has been shown to exacerbate human psoriasis by unknown mechanism.<h4>Methods</h4>Peripheral blood mononuclear cells (PBMCs) were collected from patients with psoriasis and mental stress-treated psoriatic mice. The expression levels of TLR9/MyD88/NF-κB pathway-related molecules were analyzed by qRT-PCR and western blotting. Histological examination of skin lesions was examined using hematoxylin-eosin staining. The ratios of Treg/CD4+T cells and Th17/Treg cells were determined by flow cytometry. The associations among mental stress, the TLR9/MyD88/NF-κB pathway, and psoriasis were explored using pharmacological inhibitors and lentiviral transfection.<h4>Results</h4>Our findings demonstrated a significant upregulation of TLR9/MyD88/NF-κB pathway-associated molecules in the PBMCs of psoriasis patients, accompanied by elevated expression of inflammatory factors. These observations were validated using a mouse model of psoriasis. Notably, mental stress was shown to activate the TLR9/MyD88/NF-κB pathway and enhance inflammatory factor production, while simultaneously increasing the Th17/Treg ratio and decreasing the Treg/CD4+T ratio. Therapeutic interventions including antipsychotic sertraline, pathway-specific inhibitors, and lentiviral transfection significantly ameliorated inflammatory markers and improved psoriasis severity grading.<h4>Conclusion</h4>The results of this study demonstrates that mental stress induces inflammation and immune dysregulation, exacerbating psoriasis progression. These findings provide valuable insights into the pathophysiological mechanisms underlying psoriasis progression, particularly the mental stress-mediated immunoregulatory axis.<p><a href="http://europepmc.org/article/MED/41790734?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">498</guid><pubDate>Wed, 11 Mar 2026 05:52:24 +0000</pubDate></item><item><title>Bimekizumab efficacy in scalp, nail and palmoplantar psoriasis versus comparators and over 4 years.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/bimekizumab-efficacy-in-scalp-nail-and-palmoplantar-psoriasis-versus-comparators-and-over-4-years-r497/</link><description><![CDATA[To investigate bimekizumab efficacy in scalp, nail and palmoplantar psoriasis.In this analysis, data are included from the BE SURE, BE VIVID, BE READY, and BE RADIANT phase 3/3b trials (48-56 weeks) and BE BRIGHT open-label extension (144 weeks). Adults with moderate to severe plaque psoriasis and scalp/palmoplantar Investigator's Global Assessment (IGA) score ≥3 or modified Nail Psoriasis Severity Index (mNAPSI) &gt;10 at baseline were randomized to bimekizumab or comparators (adalimumab, ustekinumab, secukinumab, placebo). Higher rates of complete clearance of scalp and palmoplantar psoriasis were generally observed at Week 4 with bimekizumab than comparators.At Week 24, rates of complete resolution of scalp/nail/palmoplantar psoriasis were 77.7%/39.8%/78.7% with bimekizumab and 58.1%/24.5%/73.3% with adalimumab; at Week 52, 71.9%/54.0%/85.2% with bimekizumab and 51.8%/30.6%/75.0% with ustekinumab; and at Week 48, 80.6%/69.5%/82.4% with bimekizumab and 71.6%/52.5%/76.8% with secukinumab. Complete scalp/nail/palmoplantar clearance rates were sustained through 4 years' bimekizumab treatment (79.5%/61.6%/88.7%). Bimekizumab consistently showed higher rates of complete clearance of psoriasis in high-impact areas along with greater patient-reported health-related quality of life benefits than comparators. Responses were sustained over 4 years, which may lead to improvements in patients' quality of life.<h4>Trial registration</h4>BE SURE (NCT03412747), BE VIVID (NCT03370133), BE RADIANT (NCT03536884), BE READY (NCT03410992), BE BRIGHT (NCT03598790).<p><a href="http://europepmc.org/article/MED/41800601?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">497</guid><pubDate>Wed, 11 Mar 2026 05:52:24 +0000</pubDate></item><item><title>Psoriasis-like disease prevents squamous skin tumor development by neutrophil-driven inflammation.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/psoriasis-like-disease-prevents-squamous-skin-tumor-development-by-neutrophil-driven-inflammation-r496/</link><description><![CDATA[Psoriasis is a chronic inflammatory skin disease affecting millions of people worldwide. Although growing evidence links chronic inflammation with increased cancer risk, the association between psoriasis and cutaneous squamous cell carcinoma (cSCC) is still elusive. Using cell transplantation and chemical-induced models of cSCC combined with inducible genetically engineered mouse models of psoriasis, we investigated how chronic skin and systemic inflammation affects squamous skin tumor initiation and progression. Here we show that in the context of severe psoriasis-like disease, neutrophil-dependent inflammation prevents squamous skin tumor development. Cellular and molecular analyses of psoriasis-like skin at the tumor initiation stage revealed a marked infiltration of CD54-expressing neutrophils, associated with the release of cytotoxic granules and neutrophil extracellular traps (NETs), as well as enhanced senescence and the expression of senescence-associated secretory phenotype in keratinocytes. Furthermore, single-cell RNA sequencing demonstrated that inflammatory N1-like neutrophils mediate reprogramming of the cell-cell communication networks, while keratinocytes displayed diminished responsiveness to mitogenic signals, including epidermal growth factor and Wnt/β-catenin. Importantly, neutrophil depletion ameliorated psoriasis-like inflammation, abolished the senescence-like phenotype in keratinocytes and restored tumor growth. We propose that the release of neutrophil granules and NETs in psoriasis-like skin eliminate tumor cells and/or mediate oxidative and inflammatory stress-induced senescence in keratinocytes, thereby preventing tumor growth. Taken together, we have defined an innate control of skin tumorigenesis in psoriasis-like disease, which will be relevant for developing cancer prevention strategies.<p><a href="http://europepmc.org/article/MED/41802042?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">496</guid><pubDate>Wed, 11 Mar 2026 05:52:24 +0000</pubDate></item><item><title>Biological Treatment of Psoriasis-Data So Far.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/biological-treatment-of-psoriasis-data-so-far-r495/</link><description><![CDATA[Psoriasis is a chronic, inflammatory skin disease occurring worldwide that significantly affects patients' quality of life. This common skin condition is characterized by abnormal hyperplasia of keratinocytes, which leads to the formation of raised, scaly plaques, typically located on the head, elbows, knees, and lumbar region. Psoriasis usually requires long-term drug therapy, which aims not only to combat skin symptoms but also to improve quality of life. Although topical treatments, systemic treatments (methotrexate, cyclosporine, acitretin), and phototherapy play a role, biologic agents have improved the efficacy of treatment of moderate-to-severe psoriasis. The purpose of this article is to comprehensively review the clinical trial data and evaluate and compare the key features of the currently approved biologic drugs for the treatment of psoriasis.<p><a href="http://europepmc.org/article/MED/41754879?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">495</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>'Thousand counties, no psoriasis': A public-health pathway to early psoriasis care in China.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/thousand-counties-no-psoriasis-a-public-health-pathway-to-early-psoriasis-care-in-china-r494/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/41758086?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">494</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>Increased Risk of Incident Uveitis Among Patients with Psoriasis: A Nationwide Population-Based Cohort Study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/increased-risk-of-incident-uveitis-among-patients-with-psoriasis-a-nationwide-population-based-cohort-study-r493/</link><description><![CDATA[<b>Background:</b> Psoriasis is a chronic systemic inflammatory disease with established extra-cutaneous manifestations. While the association between uveitis and spondyloarthritis (SpA)-related disorders is well recognized, the incident risk of uveitis among broader psoriasis populations remains inadequately defined due to methodological limitations and inconsistent findings across previous studies. We aimed to estimate the incidence of uveitis in a large, nationwide population-based cohort and identify specific clinical and treatment-related predictors of ocular inflammation. <b>Methods:</b> This retrospective cohort study utilised electronic health records from Clalit Health Services, Israel's largest health maintenance organization (2002-2024). We identified 157,360 patients with dermatologist-confirmed psoriasis and 156,927 age- and sex-matched controls. The primary outcome was incident uveitis, with risk estimated using Cox proportional hazards models. Within the psoriasis cohort, multivariable logistic regression was employed to identify predictors of uveitis, ensuring appropriate temporal sequencing between psoriasis treatment exposure and outcome. <b>Results:</b> Over a median follow-up of 12.6 years, psoriasis was associated with a significantly higher risk of incident uveitis (adjusted Hazard Ratio [aHR] 1.80; 95% CI, 1.50-2.15). Stratified analysis revealed a graded risk pattern: mild psoriasis showed no increased risk (aHR 1.01; 95% CI, 0.91-1.13), whereas severe disease (aHR 1.59; 95% CI, 1.25-2.03) and concomitant SpA (aHR 2.21; 95% CI, 1.87-2.61) demonstrated markedly elevated risks. Within the psoriasis cohort, independent predictors included SpA, diabetes mellitus, systemic lupus erythematosus, and sarcoidosis. Exposure to biologics, particularly etanercept (OR 3.37; 95% CI, 2.42-4.54), was associated with higher odds of uveitis, potentially reflecting higher disease severity. <b>Conclusions:</b> Incident uveitis risk in psoriasis is primarily driven by the magnitude of systemic inflammatory burden, with the highest risk observed in severe disease and those with concomitant SpA. Clinicians should maintain heightened vigilance for ocular symptoms in these high-risk subgroups to ensure timely intervention.<p><a href="http://europepmc.org/article/MED/41750775?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">493</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>Long-term osteoprotective effects of IL-17A blockade with secukinumab in psoriatic arthritis: data from the PSARTROS-II study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/long-term-osteoprotective-effects-of-il-17a-blockade-with-secukinumab-in-psoriatic-arthritis-data-from-the-psartros-ii-study-r492/</link><description><![CDATA[<h4>Objective</h4>To evaluate the long-term efficacy of interleukin (IL)-17A inhibition with secukinumab on structural bone changes and clinical outcomes in psoriatic arthritis (PsA).<h4>Methods</h4>We conducted a phase-IV non-interventional study on adult patients with active PsA using high-resolution peripheral quantitative CT (HR-pQCT) and MRI of the hand over 48 months. All participants received secukinumab treatment and were followed up according to clinical practice, with repeated HR-pQCT and MRI. Number and volume of erosions, bone density, cortical and trabecular microarchitecture and bone biomechanical properties were assessed based on HR-pQCT scans. MRI synovitis, tenosynovitis, osteitis, periarticular inflammation, erosions and osteoproliferation were quantified by Psoriatic Arthritis MRI Score (PsAMRIS)-Outcome Measures in Rheumatology (OMERACT) score. Study outcomes included drug survival and changes from baseline in disease activity, functional status and imaging-detected inflammation and damage.<h4>Results</h4>32 patients with PsA (40.6% female, mean age 56±7.5 years) were enrolled. Drug survival rate was 68.8% at 48 months. Secukinumab was highly effective in all PsA disease domains, with significant improvements in Disease Activity Score 28 (p&lt;0.001), Leeds Enthesitis Index (p=0.027), Psoriasis Area and Severity Index (p=0.001), C reactive protein (p=0.09), Psoriatic Arthritis Impact of Disease (p&lt;0.001) and pain (p&lt;0.001). Functional status measured by the Health Assessment Questionnaire remained stable. On HR-pQCT, bone density, microarchitecture and biomechanics were preserved. There was no progression of bone erosions (all changes were not significant). On MRI, PsAMRIS erosion and osteoproliferation subitems increased marginally (+1.4 and +0.8, respectively), while inflammatory changes remained stably low. No major safety signals emerged.<h4>Conclusion</h4>Multimodal imaging with HR-pQCT and MRI showed no relevant progression of structural bone damage over 48 months in patients with PsA treated with secukinumab, suggesting that anti-IL-17A therapy induces sustained osteoprotective effects in PsA.<p><a href="http://europepmc.org/article/MED/41741168?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">492</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>Photosensitive psoriasis mimicking cutaneous lupus erythematosus: a case report.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/photosensitive-psoriasis-mimicking-cutaneous-lupus-erythematosus-a-case-report-r491/</link><description><![CDATA[Photosensitive presentations of psoriasis are often under-recognized and may closely mimic other photodistributed dermatoses. We report the case of a 39-year-old male patient with no history of other photodermatoses who developed a progressive, non-pruritic rash, localized in sun-exposed skin areas, with marked exacerbation after phototherapy. Pronounced photosensitivity and atypical lesion distribution, involving the malar and nasal regions, complicated the initial differential diagnosis between photosensitive plaque psoriasis and cutaneous lupus erythematosus (CLE). Only further clinical evaluation, alongside histopathological analysis and immunological testing, helped to confirm the final diagnosis of photosensitive plaque psoriasis. Treatment with systemic and topical corticosteroids, vitamin D analogues, and calcineurin inhibitors resulted in gradual clinical improvement. This case report highlights photosensitive psoriasis as an important cause of photodistributed eruptions and a rare but significant mimic of CLE.<p><a href="http://europepmc.org/article/MED/41755625?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">491</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>Assessing Targeted Proteomics in Inflammatory Skin Diseases with the Tape-stripping Method.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/assessing-targeted-proteomics-in-inflammatory-skin-diseases-with-the-tape-stripping-method-r490/</link><description><![CDATA[This cross-sectional study aimed to determine the detectability of a panel of 92 inflammatory biomarkers in tape strips from the skin of patients with inflammatory skin diseases, and whether this depended on the number of tape strips taken. Furthermore, the biomarker levels in the patients were compared with those in healthy controls. Eight consecutive uniform tape strips (each 3.8 cm²) were obtained from 2 adjacent skin sites from 8 atopic dermatitis, contact dermatitis, and psoriasis patients, respectively, and 5 controls. Three separate analyses were carried out using the Olink<span class="ipsEmoji">®</span> Target Inflammation panel: (i) all 8 tape strips (1-8) from 1 skin site and from the other skin site, (ii) the first 4 tape strips (1-4), and (iii) the next 4 tape strips (5-8). Biomarkers were above the detection limit for 65.7% of atopic dermatitis, 70.2% of psoriasis, and 45.1% of contact dermatitis samples. There were no significant differences in biomarker levels between the use of 4 or 8 tape strips, or between the first and last 4 tape strips. In general, atopic dermatitis and psoriasis patients were distinguishable from controls, whereas contact dermatitis patients were not. Based on the overall data quality, analysing protein signatures in tape strips with the targeted inflammatory panel is feasible.<p><a href="http://europepmc.org/article/MED/41725456?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">490</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>Perspectives and Real-World Clinical Practice of Portuguese Dermatologists on Biologic Dose Spacing in Psoriasis: Results from a Nationwide Survey.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/perspectives-and-real-world-clinical-practice-of-portuguese-dermatologists-on-biologic-dose-spacing-in-psoriasis-results-from-a-nationwide-survey-r489/</link><description><![CDATA[<h4>Introduction</h4>Biologic therapies have transformed the management of moderate-to-severe psoriasis but are associated with long-term treatment burden and substantial healthcare costs. Dose spacing, defined as extending dosing intervals in patients with controlled disease, has emerged as a potential optimization strategy. However, data on real-world implementation and clinician perspectives remain limited.<h4>Methods</h4>We conducted a national, cross-sectional survey among Portuguese dermatologists experienced in prescribing biologic therapies for psoriasis. An anonymous, web-based questionnaire assessed clinicians' perspectives and real-world practices regarding biologic dose spacing, including eligibility criteria, preferred biologic classes, implementation strategies, outcomes after loss of disease control, and limiting clinical factors.<h4>Results</h4>Seventy-five dermatologists completed the survey (response rate 48.4%). All respondents considered dose spacing feasible. The most frequently cited eligibility criteria were absolute Psoriasis Area and Severity Index (PASI) ≤ 1, body surface area (BSA) ≤ 1%, and a 90% improvement in PASI (PASI 90). Interleukin-23 (IL-23) inhibitors were perceived as the most suitable class for dose spacing (93.3%). In routine practice, dose spacing was applied frequently by 30.7% of respondents and occasionally by 48.0%. Most clinicians (69.3%) required more than 12 months of sustained disease control before initiating dose spacing, predominantly using progressive extension of dosing intervals (96.0%). IL-23 inhibitors were the biologics most frequently dose-spaced in current practice. Following loss of disease control, 86.7% reported successful recapture of response after reintroduction of standard dosing. The main factors limiting dose spacing were a history of difficult-to-control psoriasis (77.3%) and concomitant psoriatic arthritis (72.0%).<h4>Conclusion</h4>Biologic dose spacing is already integrated into clinical practice in Portugal. Further prospective studies are needed to establish standardized criteria and guide safe implementation.<p><a href="http://europepmc.org/article/MED/41758325?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">489</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>From static pathology to dynamic immunity: immunological plasticity and histopathological remodeling in atopic dermatitis and psoriasis</title><link>https://www.psoriasis-news.de/articles.html/1_articles/from-static-pathology-to-dynamic-immunity-immunological-plasticity-and-histopathological-remodeling-in-atopic-dermatitis-and-psoriasis-r488/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12945763?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">488</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>From skin clearance to psychological wellbeing: real-world outcomes of biologic therapy in psoriasis</title><link>https://www.psoriasis-news.de/articles.html/1_articles/from-skin-clearance-to-psychological-wellbeing-real-world-outcomes-of-biologic-therapy-in-psoriasis-r487/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12946107?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">487</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>Ambient air pollution and psoriasis: a nationwide cross-sectional study of 149&#x2009;744 Chinese patients in 31 provinces.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/ambient-air-pollution-and-psoriasis-a-nationwide-cross-sectional-study-of-149%E2%80%89744-chinese-patients-in-31-provinces-r486/</link><description><![CDATA[<h4>Background</h4>Skin is the largest organ of the human body. It continuously encounters environmental toxicants, including airborne pollutants, which may induce many skin disorders, such as psoriasis. However, evidence on the association between airborne pollutants and psoriasis prevalence in China remains limited.<h4>Methods</h4>We used nationwide inpatient diagnostic data on psoriasis from 2021 to 2023, encompassing 149 744 cases across 31 provinces, municipalities, and autonomous regions in China, along with corresponding air pollution data. We analysed the spatial distribution and clustering patterns of psoriasis using the spatial autocorrelation analysis. We employed Pearson correlation analysis and Geodetector to explore the spatial heterogeneity of psoriasis and its association with airborne pollutants at the provincial level. We assessed the explanatory power of individual airborne pollutants and their combined effects on psoriasis prevalence.<h4>Results</h4>Pearson correlation analysis revealed that PM10 (r = 0.604), PM2.5 (r = 0.429), air quality index (AQI) (r = 0.542), and NO<sub>2</sub> (r = 0.476) have significant positive correlations with psoriasis prevalence. Psoriasis and its subtypes exhibited significant spatial heterogeneity and diverse clustering patterns across regions. Geodetector identified PM10 (q = 0.357; P = 0.000), AQI (q = 0.315; P = 0.000), and O<sub>3</sub> (q = 0.264; P = 0.000) as key contributors to this spatial heterogeneity. Interactive detection analysis further revealed that the combined effects of specific pollutant pairs, including PM2.5 and SO<sub>2</sub> (q = 0.790), PM10 and SO<sub>2</sub> (q = 0.727), as well as O<sub>3</sub> and SO<sub>2</sub> (q = 0.704), played a pivotal role in explaining the prevalence of psoriasis. The other combinations also showed an important impact on psoriasis subtypes, including psoriasis vulgaris (PM2.5 and SO<sub>2</sub>) (q = 0.792), psoriasis erythematous (PM2.5 and SO<sub>2</sub>) (q = 0.852), psoriatic arthritis (PM10 and O<sub>3</sub>) (q = 0.840), and nail psoriasis (PM10 and O<sub>3</sub>) (q = 0.789).<h4>Conclusions</h4>The airborne pollutants influence psoriasis prevalence and its subtypes. With the largest global study of the Asian population, we provide novel insights into the impact of air pollution on psoriasis, guiding future public health policies and clinical interventions.<p><a href="http://europepmc.org/article/MED/41747084?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">486</guid><pubDate>Sat, 28 Feb 2026 14:57:08 +0000</pubDate></item><item><title>Development and optimization of sulfasalazine loaded microemulsion for improved topical treatment of psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/development-and-optimization-of-sulfasalazine-loaded-microemulsion-for-improved-topical-treatment-of-psoriasis-r485/</link><description><![CDATA[<h4>Background</h4>Psoriasis is a persistent, chronic autoimmune skin disease that affects around 2% of the global population. Conventional therapies often exhibit limited efficacy, systemic side effects, and poor patient compliance due to long-term treatment needs.<h4>Materials &amp; methods</h4>This study focused to develop and optimize a sulfasalazine-loaded microemulsion (SSZ-ME) for topical delivery to enhance skin penetration and therapeutic efficacy in psoriasis. Pseudo-ternary phase diagrams were prepared to identify the optimal surfactant mixture, with Tween 80 and Polyethylene Glycol 400 selected in a 2:1 ratio. A 2<sup>3</sup> factorial design was used to optimize formulation parameters, focusing on oil and surfactant mixture effects on globule size and viscosity.<h4>Results and conclusions</h4>The resulting microemulsions showed globule sizes between 60 ± 0.42 to 349 ± 0.13 nm, with optimal viscosity. In vitro release studies confirmed sustained drug release over 24 hours, following first-order kinetics. Skin permeation studies demonstrated enhanced drug penetration with SSZ-ME, while histopathological analysis revealed significant improvements in psoriatic symptoms in mice treated with 4% SSZ-ME compared to 2% SSZ-ME and marketed formulation. Blood analysis confirmed minimal systemic absorption and localized action. These results suggest that SSZ-ME offers a promising, patient-compliant, and effective topical therapy for psoriasis with improved therapeutic outcomes and minimal systemic exposure.<p><a href="http://europepmc.org/article/MED/41705797?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">485</guid><pubDate>Thu, 26 Feb 2026 20:10:42 +0000</pubDate></item><item><title>Beyond cytokine blockade: could CAR-Tregs open a new era of tissue-targeted immune tolerance in psoriatic arthritis?</title><link>https://www.psoriasis-news.de/articles.html/1_articles/beyond-cytokine-blockade-could-car-tregs-open-a-new-era-of-tissue-targeted-immune-tolerance-in-psoriatic-arthritis-r484/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12932465?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">484</guid><pubDate>Thu, 26 Feb 2026 20:10:42 +0000</pubDate></item><item><title>The Psoriatic Disease Assessment Index (PSODAI) Score to Evaluate Systemic Involvement of Psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/the-psoriatic-disease-assessment-index-psodai-score-to-evaluate-systemic-involvement-of-psoriasis-r483/</link><description><![CDATA[<h4>Background</h4>To the best of our knowledge, no validated scoring instrument currently exists that comprehensively evaluates both cutaneous manifestations and systemic comorbidities of psoriasis. This multicenter study aimed to develop and validate a novel multidimensional scoring system addressing this clinical gap.<h4>Methods</h4>Under the guidance of the Shenzhen Psoriasis Academy, we conducted seven expert meetings to analyze existing evidence from PubMed, Wanfang, and CNKI databases. Through iterative Delphi consensus processes involving 26 specialists across 10 disciplines, we established the Psoriasis Disease Assessment Index (PSODAI). This 60-point composite instrument evaluates cutaneous involvement and nine key organ/system comorbidities. An accompanying online calculator (http://www.psodai.com.cn/) was developed for clinical implementation. Validation involved 254 psoriasis patients from six tertiary centers, with comparative analyses against PASI and DLQI metrics.<h4>Results</h4>The PSODAI framework stratifies disease severity as mild (0-20), moderate (21-40), and severe (41-60). Comparative analysis revealed comparable proportions of moderate-to-severe cases between PSODAI and conventional tools (PASI/DLQI) (p&gt;0.05). Notably, 11 patients (4.3%) classified as severe by PASI were re-categorized as mild through PSODAI's systemic evaluation, primarily due to limited extracutaneous manifestations.<h4>Conclusion</h4>As the first comorbidity-integrated assessment tool, PSODAI enables cross-specialty collaboration for holistic patient management. Its clinical adoption may facilitate timely comorbidity detection and preventive interventions. Further multicenter validation is warranted to confirm these preliminary findings.<p><a href="http://europepmc.org/article/MED/41737997?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">483</guid><pubDate>Thu, 26 Feb 2026 07:51:29 +0000</pubDate></item><item><title>On-label persistence in psoriasis after switching to guselkumab, tumor necrosis factor inhibitors, interleukin-17 inhibitors, or apremilast from other advanced therapies.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/on-label-persistence-in-psoriasis-after-switching-to-guselkumab-tumor-necrosis-factor-inhibitors-interleukin-17-inhibitors-or-apremilast-from-other-advanced-therapies-r482/</link><description><![CDATA[<h4>Objective</h4>To compare on-label persistence among adults with psoriasis who switched from other advanced therapies to guselkumab versus subcutaneous tumor necrosis factor inhibitors (SC TNFi), subcutaneous interleukin-17 inhibitors (SC IL-17i), or apremilast.<h4>Materials and methods</h4>This retrospective cohort study used U.S. claims data from the IQVIA PharMetrics<span class="ipsEmoji">®</span> Plus database (2016- 2023). Overlap propensity score weights were used to balance cohorts on baseline characteristics. On-label persistence was defined as the absence of drug discontinuation (event) and any dose change relative to the U.S. label (censoring). Survival analyses were used to assess on-label persistence from the start of the maintenance phase.<h4>Results</h4>At 12, 18, and 24 months after the start of the maintenance phase, respectively, on-label persistence was 190%, 180%, and 179% more likely on guselkumab versus SC TNFi; 78%, 87%, and 91% more likely on guselkumab versus SC IL-17i; and 187%, 199%, and 193% more likely on guselkumab versus apremilast (all <i>p</i> &lt; 0.001).<h4>Conclusions</h4>Patients experiencing suboptimal outcomes with other psoriasis-indicated advanced therapies achieved higher on-label persistence after switching to guselkumab, raising the potential for improved disease control relative to other treatment options.<p><a href="http://europepmc.org/article/MED/41732098?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">482</guid><pubDate>Thu, 26 Feb 2026 07:51:29 +0000</pubDate></item><item><title>Activation of NF-&#x3BA;B signaling in tissue-resident memory T cells promotes recurrent psoriasis in mice</title><link>https://www.psoriasis-news.de/articles.html/1_articles/activation-of-nf-%CE%BAb-signaling-in-tissue-resident-memory-t-cells-promotes-recurrent-psoriasis-in-mice-r481/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12926151?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">481</guid><pubDate>Thu, 26 Feb 2026 07:51:29 +0000</pubDate></item><item><title>Toward the definition of moderate psoriasis: an expert opinion.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/toward-the-definition-of-moderate-psoriasis-an-expert-opinion-r480/</link><description><![CDATA[<h4>Background</h4>The clinical definition of moderate psoriasis is debated, affecting treatment eligibility and patient outcomes.<h4>Objective</h4>A panel of Italian dermatologists aimed to propose practical criteria to define moderate psoriasis, based on a comprehensive literature review and clinical experience.<h4>Methods</h4>The panel reviewed publications between 2016 and 2024 focusing on key severity scores, including the Psoriasis Area and Severity Index (PASI), Body Surface Area (BSA), Dermatology Life Quality Index (DLQI), and Physician's Global Assessment (PGA), along with special area involvement and patient-reported outcomes.<h4>Results</h4>Despite variability among studies, and the lack of universally accepted thresholds, the panel defined moderate psoriasis as a BSA of 5%-10%, DLQI of 5-10, a PGA score of 3, and involvement of at least two special areas (e.g. scalp, face, genitals, nails, hands, or feet). Distressing itch and psychosocial impact were also recognized as critical elements influencing perceived disease burden. A composite PGA-based approach, integrating objective measures with patient-centered criteria, is proposed for identifying patients with moderate psoriasis who may benefit from systemic therapy.<h4>Conclusion</h4>This pragmatic approach may help bridge the gap between guidelines and real-world clinical practice, ensuring more accurate treatment allocation and reducing undertreatment of psoriasis.<p><a href="http://europepmc.org/article/MED/41725608?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">480</guid><pubDate>Thu, 26 Feb 2026 07:51:29 +0000</pubDate></item><item><title>Perceptions over biologics for psoriasis after 5 years of access in Brazil: a cross-sectional study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/perceptions-over-biologics-for-psoriasis-after-5-years-of-access-in-brazil-a-cross-sectional-study-r479/</link><description><![CDATA[<h4>Background</h4>Biologic therapies have transformed psoriasis management, and their incorporation into Brazil's public healthcare system (SUS) in 2019 expanded access nationwide. However, real-world utilization and perceptions remain incompletely understood.<h4>Objectives</h4>To evaluate perceptions, barriers, and prescription patterns regarding biologic therapy among Brazilian dermatologists and patients five years after universal incorporation, while quantifying the prevalence of undertreatment.<h4>Methods</h4>We conducted two independent cross-sectional online surveys throughout 2024 among dermatologists (<i>n</i> = 225) and patients with psoriasis or psoriatic arthritis (<i>n</i> = 1,001). Data on demographics, clinical characteristics, and perceived barriers were analyzed.<h4>Results</h4>Overall, 64.9% of dermatologists prescribed biologics, with higher prescribing rates among younger physicians (<i>p</i> = 0.022), those with fewer years of practice (<i>p</i> = 0.013), higher patient volumes (<i>p</i> &lt; 0.001), and practice in tertiary centers (<i>p</i> = 0.001). Only 25.5% of patients were receiving biologics, strongly associated with psoriatic arthritis (<i>p</i> &lt; 0.001), with no difference between public and private care. Key barriers included perceptions that conventional therapies are sufficient (59.5%), insufficient training (38.0%), and administrative burden (45.5%), while patients mainly reported safety (45.7%) and cost (30.9%) concerns. Undertreatment was prevalent, affecting over 50% of patients with moderate-to-severe disease. While 71.3% of non-users were willing to start biologics, only 28.0% had received a medical recommendation.<h4>Conclusions</h4>Persistent educational and structural barriers continue to limit optimal biologic use despite formal availability, highlighting the need for targeted education, streamlined care pathways, and improved physician-patient communication to achieve equitable outcomes.<p><a href="http://europepmc.org/article/MED/41738157?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">479</guid><pubDate>Thu, 26 Feb 2026 07:51:29 +0000</pubDate></item><item><title>Cardiovascular Risk in Psoriasis Compared With Atopic Dermatitis: The Shizuoka Kokuho Database.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/cardiovascular-risk-in-psoriasis-compared-with-atopic-dermatitis-the-shizuoka-kokuho-database-r478/</link><description><![CDATA[Psoriasis is a chronic inflammatory skin disease, and previous studies among Western populations have suggested an increased risk of cardiovascular events in patients with psoriasis. However, evidence from Asian populations remains limited. We evaluated the risk of major adverse cardiovascular events (MACE) in patients with psoriasis compared with patients who have atopic dermatitis (AD) using a large-scale administrative claims database from Shizuoka, Japan. We conducted a cohort study using the Shizuoka Kokuho Database, including patients aged ≥ 40 years who were newly diagnosed with psoriasis or AD between April 2012 and September 2022. Propensity score matching was used to balance age, sex, and baseline cardiovascular risk factors. The primary outcome was hospitalization for MACE, defined as myocardial infarction (MI) or stroke. Survival analyses were conducted, treating death as a competing risk. After 1:1 propensity score matching (n = 2208 per group), the mean age was 70 years. During a follow-up period (median 4.5 years for psoriasis and 4.4 years for AD), the incidence of MACE was 2.7% in both groups (hazard ratio 0.96, 95% confidence interval 0.67-1.38; p = 0.84). When analyzed separately, the risks of MI and stroke did not differ significantly between groups. Results were consistent across subgroups by psoriasis severity and in two sensitivity analyses. We observed no excess risk of MACE in Japanese patients with psoriasis compared with those with AD over a median follow-up of approximately 4.5 years. These findings suggest that the cardiovascular risk specifically attributable to psoriasis may be limited in the Japanese population.<p><a href="http://europepmc.org/article/MED/41738586?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">478</guid><pubDate>Thu, 26 Feb 2026 07:51:29 +0000</pubDate></item><item><title>The Association Between the Aggregate Index of Systemic Inflammation (AISI) and Prevalence of Psoriasis: Cross Sectional NHANES Study 2003-2006 and 2009-2014.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/the-association-between-the-aggregate-index-of-systemic-inflammation-aisi-and-prevalence-of-psoriasis-cross-sectional-nhanes-study-2003-2006-and-2009-2014-r477/</link><description><![CDATA[The aggregate index of systemic inflammation (AISI), calculated from monocyte, neutrophil, lymphocyte, and platelet counts, is a blood-count-derived composite marker of systemic inflammation. This cross-sectional study aimed to examine the association between AISI and the prevalence of psoriasis among U.S. adults. The dataset was obtained from the National Health and Nutrition Examination Survey (NHANES) database from 2003 to 2006 and from 2009 to 2014. The relevant covariates were adjusted during the analysis. We employed restricted cubic spline (RCS) regression and logistic regression frameworks to statistically assess the correlation between the AISI standard and psoriasis. The study also included subgroup analyses to determine whether the effectiveness of AISI varied among different categories. Compared with individuals without psoriasis, participants with psoriasis had higher AISI values. A total of 17 776 participants were included in the analysis. In multivariable logistic regression analyses, higher AISI levels were independently associated with higher odds of prevalent psoriasis after adjustment for potential confounders (p for trend &lt; 0.001). Restricted cubic spline analyses demonstrated an approximately linear positive association between ln-transformed AISI and psoriasis prevalence (p for non-linearity &gt; 0.05). Subgroup analyses showed no statistically significant interactions across most strata, suggesting overall consistency of the association. Receiver operating characteristic analysis indicated that AISI had limited discriminatory ability for prevalent psoriasis, with an AUC (95% CI) of 0.58 (0.55-0.60). In this large, population-based cross-sectional study, higher AISI levels were associated with the prevalence of psoriasis among U.S. adults. Given the cross-sectional design and the modest discriminatory ability (AUC = 0.58), AISI is best interpreted as a correlate of systemic inflammation rather than as a marker with predictive or causal utility for psoriasis.<p><a href="http://europepmc.org/article/MED/41732102?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">477</guid><pubDate>Thu, 26 Feb 2026 07:51:29 +0000</pubDate></item><item><title>Coexistence of MOG-IgG-associated bilateral optic neuritis with psoriasis vulgaris and psoriatic arthritis in an Asian patient: a rare case report.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/coexistence-of-mog-igg-associated-bilateral-optic-neuritis-with-psoriasis-vulgaris-and-psoriatic-arthritis-in-an-asian-patient-a-rare-case-report-r476/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/41723419?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">476</guid><pubDate>Mon, 23 Feb 2026 12:03:16 +0000</pubDate></item><item><title>Targeting the IL-36 Pathway: Spesolimab as a Therapeutic for Acute Flares of Pustular Psoriasis</title><link>https://www.psoriasis-news.de/articles.html/1_articles/targeting-the-il-36-pathway-spesolimab-as-a-therapeutic-for-acute-flares-of-pustular-psoriasis-r475/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12925328?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">475</guid><pubDate>Mon, 23 Feb 2026 12:03:16 +0000</pubDate></item><item><title>Effectiveness and Safety of Roflumilast in the Treatment of Psoriasis: A Systematic Review and Meta-Analysis...</title><link>https://www.psoriasis-news.de/articles.html/1_articles/effectiveness-and-safety-of-roflumilast-in-the-treatment-of-psoriasis-a-systematic-review-and-meta-analysis-r474/</link><description><![CDATA[<h4>Background</h4>Psoriasis, a chronic autoimmune condition, can severely impact patients' well-being. It is characterized by erythema, thickening, and scaling of the skin. Plaque psoriasis, the most prevalent type, affects 80%-90% of psoriasis patients, ranging from localized to severe cases. Although corticosteroids are commonly used to treat psoriasis, prolonged use poses risks. Therefore, alternative therapies are needed. Roflumilast, a potent phosphodiesterase 4 inhibitor, is currently being considered as a treatment for plaque psoriasis.<h4>Methods</h4>We searched four electronic databases (Cochrane Central Register of Controlled Trials, PubMed, Scopus, and Web of Science) up to March 2024 for relevant articles evaluating the efficacy and tolerability of roflumilast in the management of psoriasis. The quality of evidence from trials was assessed using the Cochrane Risk of Bias tool (RoB1). Data from the included studies were extracted into a standardized online sheet and analyzed using RevMan 5.4.<h4>Results</h4>Roflumilast significantly increased the proportion of patients achieving an Investigator's Global Assessment score of 0 or 1 and a 2-point improvement score at both weeks 4 and 8 compared to placebo (RR = 3.48, 95% CI [2.04 to 5.92], P &lt; 0.00001, and RR = 4.02, 95% CI [3.17 to 5.11], P &lt; 0.00001, respectively). The pooled studies demonstrated homogeneity at both weeks 4 (P = 0.17, I² = 38%) and 8 (P = 0.38, I² = 5%). Regarding the results of the Psoriasis Area and Severity Index, 75% favored roflumilast over placebo (RR = 2.72, 95% CI [1.18 to 6.28], P &lt; 0.00001, and RR = 3.41, 95% CI [2.19 to 5.32], P &lt; 0.00001, at weeks 4 and 8, respectively). Subgroup analysis addressed the observed heterogeneity in the results.<h4>Conclusion</h4>This meta-analysis represents the first investigation into the efficacy and safety of roflumilast for treating psoriasis. Results suggest that roflumilast is both effective and well-tolerated in managing psoriasis. However, additional robust clinical trials are needed to validate these observations..<p><a href="http://europepmc.org/article/MED/41691689?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">474</guid><pubDate>Sun, 22 Feb 2026 17:52:44 +0000</pubDate></item></channel></rss>
