<?xml version="1.0"?>
<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>Disentangling Nicotine vs Non-Nicotine Components of Tobacco Exposure in Psoriasis and Psoriatic Arthritis: A Multivariable and Trans-Ethnic Mendelian Randomization Study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/disentangling-nicotine-vs-non-nicotine-components-of-tobacco-exposure-in-psoriasis-and-psoriatic-arthritis-a-multivariable-and-trans-ethnic-mendelian-randomization-study-r536/</link><description><![CDATA[<h4>Objective</h4>To disentangle tobacco constituents in psoriasis, we contrasted nicotine exposure-proxied by the nicotine metabolite ratio (NMR)-with smoking intensity (cigarettes per day, CPD) and evaluated cross-ancestry effects.<h4>Methods</h4>This study applied multivariable Mendelian randomization (MR) jointly modeling genetically proxied NMR (instrumented using variants from a European-ancestry GWAS) and CPD to estimate their independent effects on liability to psoriasis and psoriatic arthritis (PsA). Chronic obstructive pulmonary disease (COPD) served as a positive control. Cross-ancestry generalizability was tested using a trans-ethnic MR (TEMR) framework under conditional likelihood with Nelder-Mead optimization. Sensitivity analyses assessed pleiotropy, heterogeneity, directionality (Steiger), MRLap, RadialMR, and multiple testing (Benjamini-Hochberg).<h4>Results</h4>NMR showed an independent association with higher PsA risk irrespective of CPD (OR = 1.104, 95% CI: 1.039-1.174). CPD retained an independent effect on overall psoriasis after conditioning on NMR (OR = 1.305, 95% CI: 1.082-1.573), while the NMR effect on psoriasis attenuated (P &gt; 0.05). In univariable MR, genetically predicted NMR increased psoriasis risk in Europeans (EUR; OR = 1.032, 95% CI: 1.013-1.051). CPD associated with psoriasis in EUR (OR = 1.130, 95% CI: 1.031-1.239) and strongly in Hispanics (HIS; OR = 1.448, 95% CI: 1.434-1.463), with suggestive evidence in East Asians. Reverse-direction MR indicated psoriasis liability correlated with lower CPD across EUR, EAS, AFR, and HIS (β &lt; 0, <i>P<sub>adj</sub></i> &lt; 0.05).<h4>Conclusion</h4>This study supports ancestry-specific differences and suggests distinct roles of nicotine-related versus non-nicotine tobacco smoke constituents in psoriasis and its subtypes, while the underlying biological mechanisms remain to be clarified.<p><a href="http://europepmc.org/article/MED/41890444?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">536</guid><pubDate>Mon, 30 Mar 2026 08:02:12 +0000</pubDate></item><item><title>A Study on Lifestyle and Dietary Factors in Psoriasis: Global Prevalence Trends in Working-Age Populations, Association with LE4 Lifestyle Factors, and Mendelian Randomization Analysis of Dietary Causal Effects.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/a-study-on-lifestyle-and-dietary-factors-in-psoriasis-global-prevalence-trends-in-working-age-populations-association-with-le4-lifestyle-factors-and-mendelian-randomization-analysis-of-dietary-causal-effects-r535/</link><description><![CDATA[<h4>Background</h4>Psoriasis is a chronic immune-mediated skin disease influenced by genetic, environmental, and lifestyle factors, with increasing burden among working-age adults.<h4>Objective</h4>To examine global trends in psoriasis prevalence among working-age adults, evaluate associations with lifestyle factors using a simplified Life's Essential 4 (LE4) index, and explore potential dietary causal relationships through Mendelian randomization (MR).<h4>Methods</h4>Global prevalence trends from 1990 to 2021 were analyzed using GBD 2021 data, calculating age-standardized rates (ASR) and estimated annual percentage changes (EAPC), with projections to 2031. Regional variations across SDI levels were also assessed. The LE4 index, derived from core lifestyle components of the Life's Essential 8 framework using NHANES data, was evaluated via survey-weighted logistic regression and restricted cubic spline analysis. Two-sample MR analyses were conducted using the inverse-variance weighted (IVW) method to assess dietary traits.<h4>Results</h4>The global prevalence of psoriasis among working-age adults increased from 555.7 to 600.6 per 100,000 (EAPC: 0.22%), with projections reaching 631.6 by 2031; Notably, upward trends were consistently observed across all SDI regions. Higher LE4 scores (≥81.2) were associated with lower odds of psoriasis (OR: 0.518, P=0.040). MR analyses suggested that genetically predicted fizzy drink consumption increased risk (OR: 1.57, P=0.0215), whereas salad vegetable intake showed a protective association (OR: 0.85, P=0.0224).<h4>Conclusion</h4>The burden of psoriasis among working-age adults shows a modest global increase with regional heterogeneity. Healthier lifestyle patterns and favorable dietary factors were associated with reduced risk, highlighting the importance of modifiable behaviors in prevention strategies.<p><a href="http://europepmc.org/article/MED/41890443?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">535</guid><pubDate>Mon, 30 Mar 2026 08:02:12 +0000</pubDate></item><item><title>Sensitive skin in patients with inflammatory chronic cutaneous disorders: results from an observational study on psoriasis, atopic dermatitis and hand eczema.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/sensitive-skin-in-patients-with-inflammatory-chronic-cutaneous-disorders-results-from-an-observational-study-on-psoriasis-atopic-dermatitis-and-hand-eczema-r534/</link><description><![CDATA[<h4>Background</h4>Data on the prevalence of sensitive skin in patients with chronic inflammatory skin diseases are lacking. The aim of this study was to address this gap.<h4>Methods</h4>This observational study included patients with psoriasis, atopic dermatitis or chronic hand eczema who attended the Unit of Dermatology of Ferrara and Messina, Italy, between June and December 2023. All participants completed a 10-item questionnaire for the diagnosis of sensitive skin (score range: 0-10). Participants were classified as having sensitive skin if they scored ≥4.<h4>Results</h4>A total of 188 subjects were included, of whom 82 had psoriasis (mean Psoriasis Area and Severity Index [PASI] 4.2±5.1), 59 had atopic dermatitis (Eczema Area and Severity Index [EASI] 3.5±6.7) and 47 had hand eczema (Hand Eczema Severity Index [HECSI] 39.3±3.26). The mean questionnaire scores were 2.6±2.4 for psoriasis, 4.7±2.9 for atopic dermatitis, and 3.0±2.1 for hand eczema, with significant differences observed between atopic dermatitis and both psoriasis (P&lt;0.001) and hand eczema (P&lt;0.001). The prevalence of sensitive skin was higher among atopic dermatitis patients compared to those with psoriasis (P&lt;0.001) and hand eczema (P&lt;0.01).<h4>Conclusions</h4>In the present study, which should be regarded as a pilot due to the relatively small number of cases included, sensitive skin was both more prevalent and more severe in patients with atopic dermatitis compared to those with psoriasis and hand eczema. Atopic dermatitis appears to promote skin sensitivity, independently of its clinical severity.<p><a href="http://europepmc.org/article/MED/41891834?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">534</guid><pubDate>Mon, 30 Mar 2026 08:02:12 +0000</pubDate></item><item><title>IL-17A Inhibitors Therapy Affect Oral Fungal and Bacterial Microbiome in Psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/il-17a-inhibitors-therapy-affect-oral-fungal-and-bacterial-microbiome-in-psoriasis-r533/</link><description><![CDATA[Psoriasis is a chronic inflammatory skin disease in which the IL-23/Th17/IL-17 axis plays a central pathogenic role while also contributing to antifungal defence. IL-17-targeting biologics such as secukinumab and ixekizumab are increasingly used in its management. This study aimed to characterize changes in the diversity and composition of oral fungal and bacterial communities in psoriasis patients before and after treatment with IL-17 inhibitors. Oral swabs were collected from psoriasis patients at baseline and after 3 months of IL-17 inhibitor therapy, as well as from healthy controls. Direct microscopy and fungal culture were performed. Microbial DNA was extracted and subjected to amplicon sequencing of the fungal ITS1 region and the bacterial 16S rRNA V3-V4 region using the Illumina HiSeq platform. A total of 36 patients and 38 healthy controls were enrolled in this study. Fungal microbiome analysis revealed significantly increased alpha diversity after treatment compared with baseline (p &lt; 0.05), accompanied by markedly elevated beta diversity (p &lt; 0.001). The dominant fungal genera were Blumeria, Pichia and Aspergillus. The relative abundance of Candida was significantly higher in psoriasis patients at baseline than in controls (16.00% vs. 6.43%, p &lt; 0.05) and decreased significantly after therapy (6.12%, p &lt; 0.05). In the bacterial microbiome, beta diversity decreased significantly following treatment (p &lt; 0.001), whereas alpha diversity increased (p &lt; 0.05). The predominant bacterial genera were Streptococcus, Neisseria and Rothia. After treatment, the relative abundance of Haemophilus was significantly lower than at baseline (9.18% vs. 10.14%, p &lt; 0.05). Streptococcus showed a higher trend in patients versus controls (29.74% vs. 16.48%) and declined post-treatment (23.71%). In conclusion, IL-17 inhibitor therapy in psoriasis alters the oral fungal and bacterial microbiota, with notable shifts in Candida, Haemophilus and Streptococcus. These findings provide new insights into the oral microbial changes associated with biologic therapy and may inform clinical monitoring of mucocutaneous microbial imbalance during treatment.<p><a href="http://europepmc.org/article/MED/41888636?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">533</guid><pubDate>Mon, 30 Mar 2026 08:02:12 +0000</pubDate></item><item><title>Spatial transcriptomic profiling reveals body site-specific inflammatory differences in psoriasis lesions</title><link>https://www.psoriasis-news.de/articles.html/1_articles/spatial-transcriptomic-profiling-reveals-body-site-specific-inflammatory-differences-in-psoriasis-lesions-r532/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC13017802?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">532</guid><pubDate>Mon, 30 Mar 2026 08:02:12 +0000</pubDate></item><item><title>Machine learning meets psoriasis: identifying key lactylation biomarkers as potential targets for diagnosis and therapies</title><link>https://www.psoriasis-news.de/articles.html/1_articles/machine-learning-meets-psoriasis-identifying-key-lactylation-biomarkers-as-potential-targets-for-diagnosis-and-therapies-r531/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC13021890?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">531</guid><pubDate>Mon, 30 Mar 2026 08:02:12 +0000</pubDate></item><item><title>Long-term safety and efficacy in paediatric psoriasis: Remaining challenges.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/long-term-safety-and-efficacy-in-paediatric-psoriasis-remaining-challenges-r530/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/41879060?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">530</guid><pubDate>Mon, 30 Mar 2026 08:02:12 +0000</pubDate></item><item><title>Paediatric psoriasis and biologics: An evidence gap in plain sight.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/paediatric-psoriasis-and-biologics-an-evidence-gap-in-plain-sight-r529/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/41879075?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">529</guid><pubDate>Mon, 30 Mar 2026 08:02:12 +0000</pubDate></item><item><title>Development of transdermal nanofilm containing fluticasone propionate: In-vitro, in-vivo correlation.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/development-of-transdermal-nanofilm-containing-fluticasone-propionate-in-vitro-in-vivo-correlation-r528/</link><description><![CDATA[<h4>Background</h4>Psoriasis is one of the chronic inflammatory skin conditions, affecting about 2-3% of the world population. Steroidal treatment are only best choice of treatments, but it is often associated with side effects due to higher lipophilicity.<h4>Objectives</h4>In this work, a nanoparticle-loaded transdermal film was developed to maintain nanoparticle integrity in the skin.<h4>Methods</h4>Fluticasone propionate loaded chitosan nanoparticles (NPs) were developed, and their particle size, zeta potential, drug loading, entrapment efficiency and scanning electron microscope (SEM) images were determined. The NPs-loaded film was further characterized for appearance, thickness and Fourier Transform Infrared (FTIR) spectra, and an in vitro and in vivo permeation study was conducted.<h4>Results</h4>The particle size of FSNPs was found to be 250nm with +32.4 ±1.5 mV zeta potential, great entrapment efficiency and spherical in shape. In vivo dermato-kinetic studies showed long-term, confined drug release from the NP-formulated film in the epidermal layers, compared with the film containing free drug.<h4>Conclusion</h4>The study demonstrated that the FSNPs-loaded film showed higher skin permeation, which is effective for managing psoriasis and warrants further evaluation.<p><a href="http://europepmc.org/article/MED/41879408?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">528</guid><pubDate>Mon, 30 Mar 2026 08:02:12 +0000</pubDate></item><item><title>Hibiscetin-Loaded Nanogel Ameliorated the Severity of IMQ-Induced Psoriasis-Like Inflammation in Mice via Down-Regulating Interleukins/TNF-&#x3B1;/NF-&#x3BA;B.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/hibiscetin-loaded-nanogel-ameliorated-the-severity-of-imq-induced-psoriasis-like-inflammation-in-mice-via-down-regulating-interleukinstnf-%CE%B1nf-%CE%BAb-r527/</link><description><![CDATA[<h4>Introduction</h4>The rising incidence of inflammatory skin diseases, including psoriasis, has necessitated new treatment approaches. This paper focuses on the development of a hibiscetin-impregnated nanogel that reduces the severity of skin inflammation.<h4>Methods</h4>Imiquimod (IMQ) was used to induce psoriasis-like inflammation in animal models, and the nanogel's worthiness was compared. Nanogel was prepared in different concentrations of hibiscetin, namely F1 (1) and F2 (2), and characterized in terms of appearance, size, charge, spreadability, pH, release kinetics of the drug, skin penetration and stability.<h4>Results</h4>Lab analyses showed that the nanogel possessed desirable characteristics, with an average particle size of 205 nm, a polydispersity index (PDI) of 0.385, and a surface charge of -69.5 mV. Its morphology was confirmed to be spherical by scanning electron microscopy (SEM). The nanogel demonstrated powerful anti-inflammatory properties, including the disappearance of redness and skin thickening, reduced pro-inflammatory cytokine concentrations, reduced oxidative stress markers, and apoptosis-mediated cell death in vivo. Hibiscetin, as an effect of IMQ, also had a reparative effect on damaged skin as evidenced by histopathological studies.<h4>Conclusion</h4>The results imply that hibiscetin-conjugated nanogels offer an option for improving the delivery and therapeutic efficacy of inherent compounds in the management of skin inflammation.<p><a href="http://europepmc.org/article/MED/41809764?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">527</guid><pubDate>Thu, 12 Mar 2026 13:34:20 +0000</pubDate></item><item><title>Letter From the New Editor-in-Chief.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/letter-from-the-new-editor-in-chief-r526/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/41816260?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">526</guid><pubDate>Thu, 12 Mar 2026 13:34:20 +0000</pubDate></item><item><title>The Impact of Tobacco Smoking on Treatment Response Among Patients With Psoriasis Undergoing Biologic Treatment: Prospective Observational Study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/the-impact-of-tobacco-smoking-on-treatment-response-among-patients-with-psoriasis-undergoing-biologic-treatment-prospective-observational-study-r525/</link><description><![CDATA[Tobacco smoking is viewed as a behavioral risk factor for psoriasis initiation and progress, even among those undergoing biologic treatment. However, evidence regarding the association between tobacco smoking and treatment response to biologics among patients with psoriasis is limited. This study aimed to explore the impact of tobacco smoking on the efficacy of biologic treatment in patients with psoriasis. Patients with psoriasis undergoing biologic treatment were recruited from 2022 to 2024 at the Shanghai Skin Disease Hospital. Demographic characteristics and smoking habits were collected using a structured questionnaire. Clinical features and treatment efficacy were assessed and recorded by dermatologists at baseline and weeks 4, 8, 12, 24, and 48 after treatment, and the Psoriasis Area and Severity Index (PASI) 75 and PASI 90 measures were calculated for treatment efficacy evaluation. A total of 192 patients with psoriasis were included, of whom 78 (40.6%) were tobacco smokers, with a higher smoking prevalence observed in male patients (74/154, 48.1%). The PASI 75 response rates at weeks 4, 8, 12, 24, and 48 were 29.2% (56/192), 54.2% (104/192), 78.6% (151/192), 84.5% (153/181), and 82.7% (134/162), respectively. The PASI 90 response rates increased from 13.0% (25/192) at week 4 to 62.4% (113/181) at week 24 and 59.9% (97/162) at week 48. Logistic regression analysis indicated that nonsmoking patients with psoriasis had a high PASI 75 response rate. The adjusted odds ratios were 2.57 (95% CI 1.19-5.53), 2.61 (95% CI 1.34-5.08), 2.62 (95% CI 1.13-6.04), 2.27 (95% CI 0.89-5.75), and 2.75 (95% CI 1.01-7.49) at weeks 4, 8, 12, 24, and 48, respectively. Moreover, nonsmoking patients with psoriasis also had a higher PASI 90 response rate than those who smoked. The odds ratios ranged from 1.32 (95% CI 0.49-3.54) to 2.59 (95% CI 1.21-5.55). Correlation analysis showed that both tobacco smoking duration and daily cigarette consumption were negatively correlated with the reduction in PASI score at weeks 4 to 48 after treatment (P&lt;.05). Tobacco smoking was negatively associated with treatment response among patients with psoriasis undergoing biologic treatment, especially among patients with longer tobacco smoking duration and higher daily cigarette consumption.<p><a href="http://europepmc.org/article/MED/41813109?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">525</guid><pubDate>Thu, 12 Mar 2026 13:34:20 +0000</pubDate></item><item><title>Correction to "Successful Treatment With Spesolimab in a Haemodialysis Patient With Acutely Flaring Generalised Pustular Psoriasis".</title><link>https://www.psoriasis-news.de/articles.html/1_articles/correction-to-successful-treatment-with-spesolimab-in-a-haemodialysis-patient-with-acutely-flaring-generalised-pustular-psoriasis-r524/</link><description><![CDATA[[This corrects the article DOI: 10.1002/jvc2.70093.].<p><a href="http://europepmc.org/article/MED/41809917?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">524</guid><pubDate>Thu, 12 Mar 2026 13:34:20 +0000</pubDate></item><item><title>Establishing a Generalizable Early Improvement Cutoff in Psoriasis Area and Severity Index for Outcome Prediction Across Systemic Treatments</title><link>https://www.psoriasis-news.de/articles.html/1_articles/establishing-a-generalizable-early-improvement-cutoff-in-psoriasis-area-and-severity-index-for-outcome-prediction-across-systemic-treatments-r523/</link><description><![CDATA[Abstract  <p>Background  Early identification of treatment response is clinically important in psoriasis management, as it may facilitate timely treatment modification and reduce exposure to ineffective therapies. Although early improvement in the Psoriasis Area and Severity Index (PASI) has been associated with long term outcomes for individual therapies, a broadly applicable early PASI threshold across different treatment modalities in real-world practice remains unclear. Objectives  To evaluate the predictive value of early PASI improvement for subsequent PASI90 achievement across multiple psoriasis treatment modalities and to identify a clinically meaningful early PASI response threshold applicable in routine clinical practice. Methods  This prospective, multicenter real-world cohort study included adult patients with moderate-to-severe plaque psoriasis receiving methotrexate, phototherapy, IL-17 inhibitors, or IL-23 inhibitors. Receiver operating characteristic (ROC) curve analyses were used to evaluate the predictive performance of week-4 PASI improvement for achieving PASI90 at 3 months and 6 months. The optimal early response threshold was identified using the Youden Index. Multivariable logistic regression analyses were conducted to assess the independent association between early PASI response and subsequent PASI90 achievement. Results  A total of 2,023 patients were included in the analysis. The optimal week-4 PASI improvement threshold for predicting PASI90 at 3 months was 62% for IL-17 inhibitors, 62% for IL-23 inhibitors, 59% for methotrexate and 61% for phototherapy. Multivariable logistic regression analyses further demonstrated that a PASI improvement of approximately 60% at week 4 was independently associated with a higher likelihood of achieving PASI90 at 3 months. Conclusions  Achieving PASI60 at week 4 serves as a consistent and broadly applicable early indicator of subsequent PASI90 response across multiple psoriasis treatment modalities. Incorporating this threshold into early treatment assessment may help inform individualized treatment decisions and optimize outcomes in real-world management of moderate-to-severe psoriasis.</p><p><a href="http://europepmc.org/article/PPR/PPR1164412?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">523</guid><pubDate>Thu, 12 Mar 2026 13:34:20 +0000</pubDate></item><item><title>Determinants of Quality of Life and Mental Health in Kenyan Psoriasis Patients: A Cross-Sectional Analysis from the Kenyan Psoriasis Registry.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/determinants-of-quality-of-life-and-mental-health-in-kenyan-psoriasis-patients-a-cross-sectional-analysis-from-the-kenyan-psoriasis-registry-r522/</link><description><![CDATA[Psoriasis is a chronic immune-mediated disease with global prevalence of 2-3% that is associated with significantly reduced quality of life (QoL) and worsened mental health. Despite this, there is a lack of research in African psoriasis populations, with no modern epidemiological studies conducted in Kenya to examine these factors. This study aims to identify demographic and clinical features associated with dermatology-related QoL and mental health among psoriasis patients enrolled in the newly established Kenyan Psoriasis Registry (KPR), based at Moi Teaching and Referral Hospital in Eldoret, Kenya. In a cross-sectional analysis of 97 adult psoriasis patients enrolled in the KPR, we evaluated associations of demographic and disease characteristics with independent outcomes of dermatology-associated QoL (Dermatology Life Quality Index, DLQI), anxiety (Generalized Anxiety Disorder 7-item, GAD-7), and depression (Patient Health Questionnaire 9-item, PHQ-9). Univariate and multivariate linear regression models were used to identify associations, with P &lt; 0.05 considered statistically significant. In univariate analyses, age, female gender, marital status, certain subethnicities, high-impact body sites, itch and pain, sleep disturbance, and disease severity were factors associated with worse QoL, anxiety, and depression scores. In multivariate analyses, younger age, Itch Numeric Rating Scale, and Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep Disturbance T-score remained significantly associated with worse DLQI. Both PROMIS Sleep Disturbance and separated marital status were associated with worse GAD-7 and PHQ-9. Kenyan psoriasis patients experience significant QoL and mental health burden, with younger age, itch, sleep disturbance, and separated marital status associated with worse outcomes.<p><a href="http://europepmc.org/article/MED/41816259?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">522</guid><pubDate>Thu, 12 Mar 2026 13:34:20 +0000</pubDate></item><item><title>&#x391;-Hederin alleviates psoriasiform skin inflammation by inhibiting NF-&#x3BA;B p65/CXCL2 Axis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/%CE%B1-hederin-alleviates-psoriasiform-skin-inflammation-by-inhibiting-nf-%CE%BAb-p65cxcl2-axis-r521/</link><description><![CDATA[<h4>Background</h4>Psoriasis is a chronic, inflammatory and systemic skin disease. Currently, none of the treatment can effectively prevent the recurrent of psoriasis. α-Hederin is the main active ingredient of the traditional Chineses medicine Ivy, which has been proven to have anti-inflammatory effects. However, its effects on psoriasis and mechanisms of action remain unclear.<h4>Objective</h4>This study aimed to investigate the effects of α-Hederin on murine psoriasis and its underlying mechanisms.<h4>Methods</h4>This study firstly evaluated the therapeutic effects of α-Hederin on psoriasis using imiquimod-induced psoriatic mice. H&amp;E and Ki67 immunohistochemical stainings were used to observe the pathological changes and proliferation of the skin lesions. The expression of inflammatory cytokines in skin lesions was analyzed by ELISA. Subsequently, the network pharmacology was employed to predict the molecular targets of α-Hederin in psoriasis. CXCL2 expression and neutrophil infiltration in skin lesions were evaluated via immunohistochemical staining, immunofluorescent staining and flow cytometry. Finally, the effects of α-Hederin on NF-κB p65 pathway were evaluated. The binding of α-Hederin to NF-κB p65 protein was verified through molecular docking, molecular dynamics simulation, CETSA and DARTS.<h4>Results</h4>α-Hederin significantly improved IMQ-induced psoriasiform skin lesions and inflammation in mice. It also reduced the expression of CXCL2 and infiltration of CD11b<sup>+</sup>Ly6G<sup>+</sup> neutrophils in the skin of psoriatic mice. Importantly, administration of recombinant CXCL2 protein aggravated the skin lesions and increased CD11b<sup>+</sup>Ly6G<sup>+</sup> neutrophil infiltration in psoriatic mice previously treated with α-Hederin. Furthermore, α-Hederin inhibited the production of CXCL2 in HaCaT cells and migration of neutrophils to HaCaT cells. But these effects were completely reversed by the CU-T12-9, an NF-κB p65 agonist. Similarly, α-Hederin failed to further alleviate psoriasiform skin lesions and inflammation in mice treated with SC75741 (NF-κB p65 inhibitor). Finally, based on molecular docking, molecular dynamics simulation, CETSA and DARTS, NF-κB p65 was revealed as the direct target of α-Hederin in treating psoriasis.<h4>Conclusion</h4>This study has provided the first evidence that α-Hederin may be a promising anti-psoriatic drug by inhibiting NF-κB p65/CXCL2 axis.<p><a href="http://europepmc.org/article/MED/41797086?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">521</guid><pubDate>Wed, 11 Mar 2026 16:16:46 +0000</pubDate></item><item><title>Nanocarriers, Smart Biomaterials and Emerging Therapeutics for Psoriasis: Current Progress and Future Directions.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/nanocarriers-smart-biomaterials-and-emerging-therapeutics-for-psoriasis-current-progress-and-future-directions-r520/</link><description><![CDATA[Psoriasis is a chronic, immune-mediated inflammatory skin disorder characterized by keratinocyte hyperproliferation, dysregulated immune signaling and systemic comorbidities, affecting nearly 2-3% of the global population. Although conventional therapies have improved disease management, they remain limited by poor drug penetration, systemic toxicity, adverse effects, high costs and relapse after discontinuation. The distinctive pathophysiology of psoriatic skin, with its thickened stratum corneum and aberrant immune microenvironment, poses persistent challenges to achieving targeted, sustained drug delivery. To address these limitations, emerging drug delivery systems and devices are being engineered to optimize therapeutic outcomes. Nanocarrier-based platforms are enabling enhanced drug localization, improved bioavailability and modulation of key inflammatory pathways. In parallel, microneedle-assisted delivery, hydrogel scaffolds and nanofiber matrices are establishing themselves as versatile technologies for localized, sustained and patient-friendly administration. Furthermore, stimuli-responsive and bio-inspired systems, incorporating plant-derived bioactives or extracellular vesicles, are advancing the paradigm of personalized and precision medicine in dermatology. This review critically evaluates recent progress in advanced therapeutics, nanotechnology-driven platforms and bioengineered systems for psoriasis therapy, with emphasis on their mechanisms, drug targeting, translational potential and future integration into clinical practice. Additionally, this review provides insight into how advanced delivery systems may redefine the future landscape of psoriasis management.<p><a href="http://europepmc.org/article/MED/41807739?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">520</guid><pubDate>Wed, 11 Mar 2026 16:16:46 +0000</pubDate></item><item><title>Correction to &#x201C;Successful Treatment With Spesolimab in a Haemodialysis Patient With Acutely Flaring Generalised Pustular Psoriasis&#x201D;</title><link>https://www.psoriasis-news.de/articles.html/1_articles/correction-to-successful-treatment-with-spesolimab-in-a-haemodialysis-patient-with-acutely-flaring-generalised-pustular-psoriasis-r519/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12969770?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">519</guid><pubDate>Wed, 11 Mar 2026 16:16:46 +0000</pubDate></item><item><title>Screening practice of cardiovascular risk and psoriatic arthritis among patients with psoriasis in primary care.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/screening-practice-of-cardiovascular-risk-and-psoriatic-arthritis-among-patients-with-psoriasis-in-primary-care-r518/</link><description><![CDATA[<h4>Background</h4>General Practitioners (GPs) act as primary gatekeepers for patients with psoriasis and their screening practice for cardiovascular disease (CVD) and psoriastic arhtiris (PsA) y. This study aimed to assess the awareness and screening routines of Danish GPs regarding CVD and PsA in patients with psoriasis.<h4>Methods</h4>A nationwide cross-sectional survey on screening practice was conducted involving 490 randomly selected Danish GPs. Data were analyzed descriptively based on 101 responses (21% response rate).<h4>Results</h4>The survey revealed a high level of awareness regarding CVD risk (84%), with 60% of GPs reporting routine screening for cardiovascular issues. Commonly assessed parameters included blood pressure (93%) and cholesterol (67%). Conversely, screening for PsA was notably less frequent, with only 32% of GPs actively screening for PsA.<h4>Conclusion</h4>While screening and awareness of CVD risk among primary care professionals, PsA screening remains suboptimal. The findings suggest an urgent need for updated guidelines endorsing simple, validated PsA screening tools and targeted education to prevent missed opportunities for early diagnosis.<p><a href="http://europepmc.org/article/MED/41774672?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">518</guid><pubDate>Wed, 11 Mar 2026 15:51:58 +0000</pubDate></item><item><title>Choice of Biologic Immunotherapy for Psoriasis or Psoriatic Arthritis and Its Association With Risk of Major Adverse Cardiac Events.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/choice-of-biologic-immunotherapy-for-psoriasis-or-psoriatic-arthritis-and-its-association-with-risk-of-major-adverse-cardiac-events-r517/</link><description><![CDATA[<h4>Objective</h4>Individuals with psoriasis (PsO) or psoriatic arthritis (PsA) have an elevated risk of major adverse cardiac events (MACE), which include congestive heart failure (CHF), myocardial infarction (MI), and cerebrovascular accident (CVA). Biologic disease-modifying antirheumatic drugs (bDMARDs) may reduce cardiovascular risk; however, whether MACE risk differs by bDMARD class for this population is unknown.<h4>Methods</h4>Using data from TriNetX database, we identified patients with PsO/PsA who were new bDMARD users, including tumor necrosis factor inhibitors (TNFi), interleukin (IL)-17A inhibitors (-i), IL-23i, or IL-12/23i. Time-dependent risk for MACE was calculated using weighted multinomial Cox proportional hazards regression with TNFi exposure as the referent. Additional analyses evaluated components of the primary outcome and baseline cardiovascular disease. A negative control outcome was used to assess bias.<h4>Results</h4>We identified 32,758 patients with PsO/PsA who were new bDMARD users. Patients had PsO/PsA for a mean of 3.5 (SD 4.5) years prior to starting a biologic, the most common being TNFi (62.9%), followed by IL-17i (15.4%), IL-23i (11%), and IL-12/23i (10.7%). In weighted multinomial Cox proportional hazards regression, the adjusted risk of MACE was similar for IL-17Ai (adjusted hazard ratio [aHR] 0.98, 95% CI 0.73-1.32), IL-23i (aHR 0.84, 95% CI 0.54-1.31), and IL-12/23i (aHR 1.08, 95% CI 0.80-1.47) as compared to TNFi. Subset analyses supported the primary analysis. Negative control outcomes suggested adequate control of bias confounding.<h4>Conclusion</h4>MACE risk does not significantly differ across bDMARD classes in patients with PsO/PsA. Therefore, cardiovascular risk should not guide biologic selection in this population.<p><a href="http://europepmc.org/article/MED/41033836?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">517</guid><pubDate>Wed, 11 Mar 2026 15:51:58 +0000</pubDate></item><item><title>Clinical characteristics, effectiveness, safety, and predictors of PASI75/90 responses to IL-17 biologics in psoriasis involving special sites: a large real-world cohort study revealing treatment response heterogeneity.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/clinical-characteristics-effectiveness-safety-and-predictors-of-pasi7590-responses-to-il-17-biologics-in-psoriasis-involving-special-sites-a-large-real-world-cohort-study-revealing-treatment-response-heterogeneity-r516/</link><description><![CDATA[Psoriasis affecting special anatomical sites (scalp, face, intertriginous areas, and genitals) poses unique treatment challenges and often shows inadequate responses. This study evaluates the real-world efficacy and safety of IL-17 inhibitors in treating psoriasis affecting special sites, and identifies clinical determinants for achieving PASI75 and PASI90 responses.A retrospective cohort of 1,469 patients receiving IL-17 therapy was analyzed.Generalized linear models, univariate and multivariate logistic regression analyses were used to identify clinical factors influencing the PASI75 and PASI90 response.At week 12, significant improvements were observed in various measures of disease severity and quality of life (BSA, IGA, PASI, DLQI), with all comparisons yielding <i>P</i> &lt; 0.0001. Treatment response rates were 74.0% for PASI50, 58.6% for PASI75, and 41.5% for PASI90, while adverse events were rare (0.75%). Prediction models for PASI75 and PASI90 responses exhibited moderate discriminative ability. Independent predictors for both PASI75 and PASI90 included clinical BMI, DLQI, BSA, and IGA (all <i>P</i> &lt; 0.05), while job status was an independent predictor for PASI90 only (<i>P</i> &lt; 0.05).Overall, IL-17 inhibitors show substantial efficacy and a favorable safety profile for psoriasis in special sites, with treatment response variability influenced primarily by baseline clinical characteristics such as BMI and disease severity indices.<p><a href="http://europepmc.org/article/MED/41782311?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">516</guid><pubDate>Wed, 11 Mar 2026 15:51:58 +0000</pubDate></item><item><title>Integrating network pharmacology and experimental validation to elucidate the mechanism of Xiao-bi decoction in psoriasis treatment: Inhibition of JAK2/STAT3 signaling and rebalancing Th17/Treg responses.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/integrating-network-pharmacology-and-experimental-validation-to-elucidate-the-mechanism-of-xiao-bi-decoction-in-psoriasis-treatment-inhibition-of-jak2stat3-signaling-and-rebalancing-th17treg-responses-r515/</link><description><![CDATA[<h4>Ethnopharmacological relevance</h4>The traditional Chinese herbal medicine called Xiao-bi decoction (XBD) has been used for decades to treat psoriasis, but its mechanism of action is poorly understood.<h4>Aim of the study</h4>To investigate the underlying mechanism of XBD against psoriasis using systematic pharmacological techniques.<h4>Materials and methods</h4>A psoriasis model was established in mice using imiquimod (IMQ). The efficacy of XBD was evaluated based on psoriasis severity scores and immune cell infiltration. Core components and targets were screened using UPLC-QE-MS/MS and network pharmacology. The mechanism was further explored via transcriptome sequencing, ELISA, western blotting, immunolocalization, and molecular docking.<h4>Results</h4>XBD treatment significantly alleviated IMQ-induced psoriatic symptoms like erythema, scaling, and thickening. It reduced CD4<sup>+</sup> T cell infiltration in skin and decreased serum levels of IL-17, IL-1β, IL-23, and IL-36. XBD specifically decreased CD4<sup>+</sup>-IL-17<sup>+</sup> cells while increasing CD4<sup>+</sup>-FoxP3<sup>+</sup> cells in both blood and skin. A total of 1223 chemical components were identified in XBD, including 78 blood-entering components. Network pharmacology and transcriptome analysis collectively demonstrate that XBD inhibits the activation of the JAK2/STAT3 signaling pathway, indicating its potential role in modulating this pathway. Our results also showed that XBD modulated Th17/Treg balance in serum and ameliorating skin inflammation in IMQ-induced psoriatic model.<h4>Conclusion</h4>The herbal medicine Xiao-bi decoction may regulate the JAK2/STAT3 pathway, thereby influencing the Th17 response and Treg differentiation, and thereby alleviating the skin inflammation of psoriasis.<p><a href="http://europepmc.org/article/MED/41785726?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">515</guid><pubDate>Wed, 11 Mar 2026 15:51:58 +0000</pubDate></item><item><title>Baseline Clinical and Metabolic Predictors of 52-Week Durability of Secukinumab Response in Moderate-to-Severe Plaque Psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/baseline-clinical-and-metabolic-predictors-of-52-week-durability-of-secukinumab-response-in-moderate-to-severe-plaque-psoriasis-r514/</link><description><![CDATA[<h4>Background</h4>Durability of response to IL-17A blockade (secukinumab) varies, representing a major clinical challenge. Psoriasis is inherently linked to immunometabolic dysfunction. We hypothesized that simple, routine metabolic indices could predict long-term treatment stability, offering crucial pre-treatment stratification tools.<h4>Methods</h4>This was a 52-week prospective, single-center cohort study of 118 patients with moderate-to-severe plaque psoriasis initiating secukinumab. We defined Durable Response (DR) as PASI90 at Week 12 maintained as absolute PASI ≤ 2 until Week 52. Multivariable logistic regression and Cox models were used to identify independent predictors of DR and drug survival.<h4>Results</h4>Independent predictors of durable response were biologic-naïve status (adjusted OR = 3.52, 95% CI: 1.58-7.85) and a lower baseline TG/HDL-C ratio (adjusted OR = 0.61, 95% CI: 0.47-0.79). Conversely, obesity (BMI≥30) (OR = 0.42) and higher baseline PASI (OR = 0.91) were associated with reduced odds of DR. Conventional systemic inflammatory markers (CRP, NLR) showed no significant difference. Drug survival was significantly higher in DRs (92.6% vs 78.3% at Week 52) and was independently reduced by psoriatic arthritis.<h4>Conclusion</h4>The routine baseline TG/HDL-C ratio is a strong, independent predictor of sustained secukinumab efficacy. These easily accessible clinical and metabolic features capture the immunometabolic milieu influencing IL-17A inhibition durability. Integrating the TG/HDL-C ratio into pre-treatment assessment can support patient stratification and optimize long-term management strategies for plaque psoriasis.<p><a href="http://europepmc.org/article/MED/41799428?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">514</guid><pubDate>Wed, 11 Mar 2026 15:51:58 +0000</pubDate></item><item><title>The Emerging Role of Gut Microbiota in Inflammatory Skin Diseases: A Systematic Review.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/the-emerging-role-of-gut-microbiota-in-inflammatory-skin-diseases-a-systematic-review-r513/</link><description><![CDATA[The human gut microbiota is involved in immune regulation, metabolism, and skin homeostasis. In recent years, gut microbiota alterations have been linked with several inflammatory skin disorders, such as atopic dermatitis (AD), psoriasis, and hidradenitis suppurativa (HS). This systematic review synthesises current evidence on gut microbiota composition and functional alterations in these dermatoses. A comprehensive literature search was conducted in the PubMed database, identifying studies from inception to January 2025. Eligible studies included human observational, interventional, and genetic studies investigating gut microbiota alterations in AD, psoriasis, or HS, using microbiome profiling or genetic causal-inference approaches. Studies lacking control groups or relying on culture-based techniques were excluded. Sixty-two studies were included: 38 on AD, 22 on psoriasis and 5 on HS, with three addressing more than one disease. In AD, most studies focused on paediatric populations, leaving a knowledge gap regarding adult-specific data. Reduced alpha-diversity and decreased abundance of Faecalibacterium prausnitzii, Bifidobacterium spp., and Akkermansia muciniphila were recurrent findings. In psoriasis, in addition to dysbiosis, microbial metabolic pathways were also found to be altered. In HS, data remain limited, but increased Ruminococcus gnavus and reduced alpha-diversity have been reported, mirroring findings in inflammatory bowel diseases. Gut microbiota has been increasingly implicated in skin inflammation. Despite advances in microbiota analysis, significant gaps remain-especially in adult AD and HS. Future research should prioritize standardised methodologies, larger and more diverse cohorts, and leverage emerging tools such as Mendelian randomization and AI-based models to develop precision medicine interventions.<p><a href="http://europepmc.org/article/MED/41795861?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">513</guid><pubDate>Wed, 11 Mar 2026 15:51:58 +0000</pubDate></item><item><title>PBMC transcriptomic signatures reflect immune dynamics and disease activity in psoriatic arthritis</title><link>https://www.psoriasis-news.de/articles.html/1_articles/pbmc-transcriptomic-signatures-reflect-immune-dynamics-and-disease-activity-in-psoriatic-arthritis-r512/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12971704?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">512</guid><pubDate>Wed, 11 Mar 2026 15:51:58 +0000</pubDate></item></channel></rss>
