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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/6/?d=1</link><description>Neue Studien: Europe PMC</description><language>de</language><item><title>Observation on The Formation of Neutrophil Extracellular Traps in Psoriatic Peripheral Blood</title><link>https://www.psoriasis-news.de/articles.html/1_articles/observation-on-the-formation-of-neutrophil-extracellular-traps-in-psoriatic-peripheral-blood-r462/</link><description><![CDATA[Abstract  <p>Objective  To explore the clinical application value of Neutrophil extracellular traps (NETs) in evaluating psoriasis. Methods  2ml peripheral blood of 63 patients with psoriasis and 27 healthy controls were collected. Neutrophils were isolated by density gradient method, and the formation of NETs was observed by immunofluorescence staining. We then calculated the proportion and fluorescence intensity of NETs and analyzed their correlation with clinical classification, severity, and serological indicators. Furthermore, the skin lesions of 5 patients with psoriasis were collected, and the NETs were observed by immunofluorescence method. Results  The proportion and fluorescence intensity of spontaneous NETs in patients with psoriasis were significantly higher than those in healthy controls and were positively correlated with the PASI scores. The generation of NETs in psoriasis patients with metabolic syndrome (MetS) or high-TNF-α was higher than in psoriasis patients without metabolic abnormalities or normal-TNF-α. NETs were also observed in most psoriatic skin specimens. Conclusions  The levels of NETs are correlated with the disease severity of psoriasis and patients with metabolic abnormalities and may be used as a clinical indicator to reflect the inflammatory state of psoriasis and metabolic comorbidity of psoriasis for disease evaluation.</p><p><a href="http://europepmc.org/article/PPR/PPR1155392?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">462</guid><pubDate>Sun, 22 Feb 2026 17:38:20 +0000</pubDate></item><item><title>Psychological Well-Being of Patients with Moderate-to-Severe Plaque Psoriasis Treated with Tildrakizumab: 28-Week Interim Results from a Multicenter Observational Study in Italy Using the DASS-21 Questionnaire, the BLUE Study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/psychological-well-being-of-patients-with-moderate-to-severe-plaque-psoriasis-treated-with-tildrakizumab-28-week-interim-results-from-a-multicenter-observational-study-in-italy-using-the-dass-21-questionnaire-the-blue-study-r461/</link><description><![CDATA[<h4>Introduction</h4>Psoriasis is a chronic inflammatory skin disease associated with significant physical and psychological burden. Tildrakizumab, an interleukin-23 p19 inhibitor, has demonstrated efficacy in treating moderate-to-severe plaque psoriasis both in clinical trials and real-world setting. However, limited data are available on the impact of the effective treatment of psoriasis on the psychological health of patients. The aim of this study was to assess changes in psychological well-being, as well as clinical and quality-of-life outcomes, in patients with moderate-to-severe plaque psoriasis treated with tildrakizumab in routine clinical practice in Italy.<h4>Methods</h4>This was an interim analysis (IA) of a 52-week multicenter, prospective, observational study. Adults with moderate-to-severe plaque psoriasis initiating tildrakizumab were enrolled. Endpoints focused on well-being and psychological health and included changes, from baseline to week 28, in Depression, Anxiety, and Stress Scale-21 (DASS-21) scores, Dermatology Life Quality Index (DLQI), European Social Survey (ESS) items, and World Health Organization-Five Well-Being Index (WHO-5). Effectiveness was also monitored via Psoriasis Area and Severity Index (PASI), and safety via treatment-emergent adverse event reporting.<h4>Results</h4>A total of 115 patients were included (mean age 52.5 years, 60.8% male), 102 receiving ≥ 1 dose of tildrakizumab and completing DASS-21 evaluations at baseline and week 28. At week 28, improvements were observed in DASS-21 subscales [depression (- 2.6, 95% CI - 2.0 to - 1.0), anxiety (- 2.3, 95% CI - 2.0 to - 1.0), and stress (- 3.4, 95% CI - 4.0 to - 2.0)], accompanied by marked PASI reduction (- 13.7, 95% CI - 12.8 to - 10.1). DLQI, ESS, and WHO-5 scores also improved. Adverse events were generally mild or moderate, with no unexpected safety signals.<h4>Conclusion</h4>In this real-world IA, tildrakizumab was observed to improve the psychological well-being of patients, reflected by a reduction in all items of the DASS-21 scale and, in parallel, confirmed its effectiveness in managing physical symptoms of psoriasis, establishing its role in the holistic management of psoriasis.<p><a href="http://europepmc.org/article/MED/41712057?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">461</guid><pubDate>Sun, 22 Feb 2026 17:38:20 +0000</pubDate></item><item><title>Exploring the risk association between psoriasis and chronic obstructive pulmonary disease, and asthma using the NHIS database.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/exploring-the-risk-association-between-psoriasis-and-chronic-obstructive-pulmonary-disease-and-asthma-using-the-nhis-database-r459/</link><description><![CDATA[<h4>Background</h4>Asthma (AS) and chronic obstructive pulmonary disease (COPD) are prevalent chronic airway disorders with shared inflammatory pathways. Considering the systemic inflammatory nature of psoriasis, this study utilized the National Health Interview Survey (NHIS) to investigate its potential association with COPD and AS.<h4>Methods</h4>Data from the 2023 NHIS were analyzed, with participants selected based on specific inclusion criteria. A baseline table was constructed, and multivariate logistic regression models, along with risk stratification analysis, were employed to examine the correlations between psoriasis and COPD and AS. Receiver operating characteristic (ROC) analysis was conducted to assess the predictive value for both conditions.<h4>Results</h4>A total of 27,106 participants were included in the study. Significant differences were observed in the baseline characteristics of psoriasis, age, race, region, gender, education, marital status, employment, income, smoking habits, health status, mental health, disability, heart attack history, BMI, prediabetes, cancer, hypertension, hypercholesterolemia, arthritis, coronary heart disease, stroke, health insurance, anxiety, and depression (P &lt; 0.001). Multivariate logistic regression revealed a strong association between psoriasis and COPD (model 1: OR 2.63, 95% CI: 2.13-3.23, P &lt; 0.001; model 2: OR 2.43, 95% CI: 1.95-2.99, P &lt; 0.001; model 3: OR 1.54, 95% CI: 1.21-1.96, P &lt; 0.001). A similar association was found between psoriasis and AS (model 1: OR 1.68, 95% CI: 1.42-1.97, P &lt; 0.001; model 2: OR 1.74, 95% CI: 1.47-2.05, P &lt; 0.001; model 3: OR 1.32, 95% CI: 1.11-1.56, P &lt; 0.01). The ROC analysis based on model 3 demonstrated substantial predictive power of psoriasis for COPD, with an AUC of 0.881.<h4>Conclusion</h4>Psoriasis was identified to have a strong association with COPD and AS, which provided valuable insights into understanding the pathogenesis of these diseases.<p><a href="http://europepmc.org/article/MED/41686756?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">459</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>Investigating the role of serum human beta defensin-2 in psoriasis and psoriatic arthritis: a case-control study on hBD-2 and CRP, ESR.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/investigating-the-role-of-serum-human-beta-defensin-2-in-psoriasis-and-psoriatic-arthritis-a-case-control-study-on-hbd-2-and-crp-esr-r458/</link><description><![CDATA[<h4>Introduction</h4>Human beta-defensin 2 (hBD-2) is an antimicrobial peptide upregulated by IL-17A and TNF-α, important in skin immunity and inflammation. While hBD-2 is elevated in psoriatic skin, its systemic expression and clinical significance remain unclear, particularly in psoriatic arthritis (PsA).<h4>Objectives</h4>To compare serum hBD-2 levels among patients with psoriasis vulgaris, PsA, and healthy controls, and to evaluate its correlation with disease severity and inflammatory markers.<h4>Methods</h4>This case-control study included 66 patients with psoriasis, 30 with PsA, and 67 healthy controls. Serum hBD-2, C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR) were measured. Psoriasis severity was assessed using the Psoriasis Area and Severity Index (PASI). A <i>p</i> value &lt; 0.05 was considered statistically significant.<h4>Results</h4>Median serum hBD-2 levels were significantly higher in psoriasis and PsA groups compared to controls (<i>p</i> &lt; 0.001), but no significant difference was found between the two patient groups (p: 0.223). In the psoriasis group, hBD-2 showed no significant correlation with PASI (r: 0.218, p: 0.095), CRP (r: 0.158, p: 0.277), or ESR (r: 0.129, p: 0.369). CRP and ESR were significantly higher in the PsA group than in other groups (<i>p</i> &lt; 0.001 and p: 0.002, respectively).<h4>Conclusions</h4>Although serum hBD-2 is elevated in psoriasis and PsA, it does not correlate with clinical or laboratory disease activity in psoriasis. These findings suggest that hBD-2 may reflect local cutaneous immune activation rather than systemic inflammation.<p><a href="http://europepmc.org/article/MED/41689371?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">458</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>Increased risk of inflammatory bowel disease in ankylosing spondylitis compared to psoriasis</title><link>https://www.psoriasis-news.de/articles.html/1_articles/increased-risk-of-inflammatory-bowel-disease-in-ankylosing-spondylitis-compared-to-psoriasis-r457/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12920575?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">457</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>Nail Amino Acid and Trace Element Profiles and Their Association with Clinical Severity in Nail Psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/nail-amino-acid-and-trace-element-profiles-and-their-association-with-clinical-severity-in-nail-psoriasis-r456/</link><description><![CDATA[<h4>Background</h4>Nail involvement is common in psoriasis, yet objective and non-invasive biomarkers of nail disease activity are limited. The biochemical composition of the nail plate may reflect local pathophysiological changes and could provide measurable indicators of disease severity.<h4>Objective</h4>To compare the nail biochemical composition between psoriatic patients with and without nail involvement, and to examine its associations with nail severity.<h4>Methods</h4>In this case-control study, nail clippings from adults with psoriasis were analyzed for trace elements (Cr, Cu, Fe, Mn, Mg, Se, Zn) by ICP-OES and for amino acids by LC-MS/MS. Group comparisons and correlation analyses with the Nail Psoriasis Severity Index (NAPSI) were conducted, and multivariable logistic regression identified independent predictors of nail involvement.<h4>Results</h4>Fifty-seven patients were included (30 with nail involvement; 27 without). Compared with patients without nail involvement, those with nail psoriasis showed significantly lower nail levels of several trace elements and amino acids, whereas histidine was higher (all p &lt; 0.05). NAPSI correlated negatively with selenium, zinc, glycine, and proline, and positively with histidine. In multivariable analysis, lower nail selenium and asparagine and higher histidine independently predicted nail involvement.<h4>Conclusion</h4>Psoriatic nail dystrophy is associated with a distinct biochemical profile in the nail plate. Selected trace elements and amino acids correlate with clinical severity and may represent potential biochemical indicators of nail disease activity. Prospective studies are warranted to validate these findings.<p><a href="http://europepmc.org/article/MED/41710526?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">456</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>[Moderate-severe psoriasis and associated comorbidity in patients on biologic therapy: implications for primary care].</title><link>https://www.psoriasis-news.de/articles.html/1_articles/moderate-severe-psoriasis-and-associated-comorbidity-in-patients-on-biologic-therapy-implications-for-primary-care-r455/</link><description><![CDATA[<h4>Objective</h4>To describe the comorbidity profile in patients with moderate-to-severe psoriasis treated with biologics and their association with clinical phenotype and therapeutic choice.<h4>Material and methods</h4>This was an observational, cross-sectional, single-center study conducted at the Lozano Blesa University Clinical Hospital (Zaragoza, Spain). Consecutive patients with moderate-to-severe psoriasis receiving biologic treatment were included. Data were collected during the Dermatology consultation and reviewed from medical records. The variables analyzed included demographic data, clinical phenotype, previous and current treatments, cardiometabolic comorbidities, neoplasia, infections, and lifestyle habits. Statistical analysis employed means and proportions comparison tests, and logistic regression to explore associations between phenotype, comorbidities, and biologic type.<h4>Results</h4>350 patients were included (median age 54.1years; 57% men; 84% plaque psoriasis). The most prevalent comorbidities were dyslipidemia (55%), hypertension (42%), and obesity (36%). Among patients with liver elastography, 58% met MASLD criteria. Significant associations were observed between clinical phenotype and comorbidities: plaque psoriasis with hypertension and vitaminD deficiency, erythrodermic psoriasis with alcoholism and neoplasia, pustular psoriasis with dyslipidemia and kidney disease, and guttate psoriasis with a lower prevalence of cardiovascular factors. Guselkumab was the most commonly used biologic (15%).<h4>Conclusions</h4>Patients with moderate-to-severe psoriasis have a high burden of comorbidities, with differential profiles according to phenotype. These results reinforce the need for a multidisciplinary approach and the role of primary care in screening and managing comorbidities to improve disease control and overall prognosis.<p><a href="http://europepmc.org/article/MED/41707582?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">455</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>Three-Year Patient-Reported Outcomes From Bimekizumab for Plaque Psoriasis: The BE RADIANT Randomized Clinical Trial With Open-Label Extension.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/three-year-patient-reported-outcomes-from-bimekizumab-for-plaque-psoriasis-the-be-radiant-randomized-clinical-trial-with-open-label-extension-r454/</link><description><![CDATA[<h4>Importance</h4>Patient-reported outcome (PRO) assessments alongside clinical parameters help to holistically determine treatment benefits.<h4>Objective</h4>To assess PROs among bimekizumab-treated patients with moderate to severe plaque psoriasis.<h4>Design, setting, and participants</h4>The BE RADIANT multicenter, phase 3b randomized clinical trial and open-label extension (OLE) had a 48-week double-blinded period and 96-week OLE (3 years' total treatment). Patients initially received bimekizumab or secukinumab. At year 1 (week 48/OLE entry), bimekizumab-randomized patients continued bimekizumab treatment (continuous bimekizumab-treated patients) and secukinumab-randomized patients switched to bimekizumab (secukinumab/bimekizumab-treated patients).<h4>Interventions</h4>Continuous bimekizumab-treated patients received bimekizumab, 320 mg, every 4 weeks to week 16, then every 4 weeks or every 8 weeks to 1 year and into the OLE. Secukinumab/bimekizumab-treated patients received secukinumab, 300 mg, every 4 weeks to 1 year, then switched to bimekizumab, 320 mg, every 4 weeks or every 8 weeks. All received bimekizumab every 8 weeks by week 64.<h4>Main outcomes and measures</h4>Patient-reported itching/skin pain/scaling (Psoriasis Symptoms and Impacts Measure [P-SIM]) and concurrent achievement of Psoriasis Area and Severity Index (PASI) and Dermatology Life Quality Index (DLQI) scores are reported (nonresponder imputation to 1 year; modified nonresponder imputation to 1-3 years).<h4>Results</h4>A total of 373 bimekizumab-treated and 370 secukinumab-treated patients were randomized at baseline; 336 and 318, respectively, entered the OLE. Among bimekizumab-randomized and secukinumab-randomized patients, 127 (34.0%) and 93 (25.1%) reported no itching; 278 (74.5%) and 222 (60.0%) no skin pain; and 172 (46.1%) and 80 (21.6%) no scaling at week 4, respectively; at year 1, rates remained higher in bimekizumab-randomized vs secukinumab-randomized patients (itching: 227 [60.9%] vs 178 [48.1%]; nominal P &lt; .001; skin pain: 293 [78.6%] vs 262 [70.8%]; nominal P = .01; scaling: 263 [70.5%] vs 184 [49.7%]; nominal P &lt; .001). Bimekizumab-randomized patients had greater concurrent achievement rates of PASI = 0 and DLQI 0/1 vs secukinumab-randomized patients (week 4: 43 [11.5%] vs 17 [4.6%]; nominal P &lt; .001; year 1: 230 [61.7%] vs 158 [42.7%]; nominal P &lt; .001). In patients entering the OLE, high P-SIM = 0 rates were maintained to year 3. At OLE entry, concurrent achievement of PASI = 0 and DLQI 0/1 was reported in 69.2% continuous bimekizumab-treated and 48.5% secukinumab/bimekizumab-treated patients. After switching, secukinumab/bimekizumab responses increased, and high rates were maintained to year 3 for both continuous bimekizumab and secukinumab/bimekizumab (62.2% and 63.8%, respectively).<h4>Conclusions and relevance</h4>In this randomized clinical trial and OLE, bimekizumab rapidly and durably improved symptoms/health-related quality of life to 3 years, demonstrating that clinical efficacy translates to quality of life improvements. Secukinumab-randomized patients reported improvements on switching to bimekizumab.<h4>Trial registration</h4>ClinicalTrials.gov Identifier: NCT03536884.<p><a href="http://europepmc.org/article/MED/41706476?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">454</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>Guttate Psoriasis Triggered by Streptococcal Pharyngitis in Older Patients: A Case Report.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/guttate-psoriasis-triggered-by-streptococcal-pharyngitis-in-older-patients-a-case-report-r453/</link><description><![CDATA[BACKGROUND Guttate psoriasis is a form of psoriasis that often occurs following infections and is most commonly triggered by group A Streptococcus. The link between streptococcal pharyngitis and the development of guttate psoriasis is well documented in younger populations; however, this presentation in older adults is less common. Additionally, older adult populations can have multiple comorbidities that could influence the development and clinical course of guttate psoriasis. CASE REPORT We report the case of a 66-year-old woman with multiple comorbidities, including type 2 diabetes mellitus, vitamin D deficiency, colon cancer treated with surgical resection, and endometriosis, who developed guttate psoriasis following a confirmed episode of streptococcal pharyngitis. Initially, the patient's condition was misdiagnosed as tinea versicolor, leading to delays in appropriate treatment. After further dermatologic evaluation and laboratory investigations, the diagnosis of guttate psoriasis was more firmly established, allowing for more tailored treatment decisions. CONCLUSIONS This case highlights guttate psoriasis as a rare post-streptococcal complication in a 66-year-old woman, emphasizing the importance of clinical awareness and accurate diagnosis in older adults with recent upper respiratory infections. Although the exact mechanism of guttate psoriasis development remains unclear, its distinct clinical features allow for its recognition in patients of all ages. Guttate psoriasis also contributes to the understanding of the varied clinical manifestations of streptococcal pharyngitis, particularly in patients with complex medical histories.<p><a href="http://europepmc.org/article/MED/41709535?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">453</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>Real-World Predictors of Relapse-Free Duration After Narrowband UVB in Pediatric Psoriasis: A Multicenter Study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/real-world-predictors-of-relapse-free-duration-after-narrowband-uvb-in-pediatric-psoriasis-a-multicenter-study-r452/</link><description><![CDATA[<h4>Background</h4>Narrowband ultraviolet B (NB-UVB) phototherapy is a well-established, safe, and effective treatment for pediatric psoriasis; however, relapse after therapy remains a major challenge. Data regarding prognostic factors influencing remission durability in children are limited.<h4>Objectives</h4>To evaluate treatment response, relapse patterns, and predictors of relapse-free duration in pediatric psoriasis patients treated with NB-UVB phototherapy, with a particular focus on concomitant topical corticosteroid and calcipotriol use, and clinical features such as nail involvement.<h4>Methods</h4>This multicenter retrospective study included 114 pediatric psoriasis patients treated with NB-UVB across six tertiary dermatology centers in Türkiye. Treatment response was defined as ≥ 75% improvement in the Psoriasis Area and Severity Index (PASI75). Relapse was defined as clinically significant recurrence requiring renewed NB-UVB or systemic therapy within 6 months after treatment completion. Multivariable linear regression identified independent predictors of relapse-free duration.<h4>Results</h4>Of 114 patients (mean age 12.2 ± 3.6 years; 52.6% male), 65.8% achieved PASI75 and 42.1% PASI90. Responders received significantly higher cumulative doses and more sessions than nonresponders (p &lt; 0.001). Relapse occurred in 24.0% of responders within 6 months. In multivariate analysis, concomitant topical corticosteroid use independently predicted longer relapse-free duration (β = 0.578, p = 0.001), whereas nail involvement predicted shorter remission (β = -0.520, p = 0.002). Topical calcipotriol and disease subtype were not significant predictors. NB-UVB was well tolerated, with mild erythema and pruritus as the most frequent adverse events (16.7%).<h4>Conclusion</h4>NB-UVB phototherapy provides high efficacy and an acceptable safety profile in pediatric psoriasis. Concomitant topical corticosteroid use may prolong remission, while nail involvement identifies patients at higher relapse risk, supporting closer monitoring and individualized follow-up and maintenance strategies.<p><a href="http://europepmc.org/article/MED/41678732?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">452</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>Macronutrient intakes and associations with psoriasis severity: a cross-sectional analysis of the asking people with psoriasis about lifestyle and eating (APPLE) study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/macronutrient-intakes-and-associations-with-psoriasis-severity-a-cross-sectional-analysis-of-the-asking-people-with-psoriasis-about-lifestyle-and-eating-apple-study-r451/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/41711966?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">451</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>Sex hormone&#x2013;psoriasis interactions: from sex-specific clinical features to immunoregulatory mechanisms</title><link>https://www.psoriasis-news.de/articles.html/1_articles/sex-hormonepsoriasis-interactions-from-sex-specific-clinical-features-to-immunoregulatory-mechanisms-r450/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12920573?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">450</guid><pubDate>Sun, 22 Feb 2026 17:23:03 +0000</pubDate></item><item><title>S3&#x2010;Leitlinie zur Therapie der Psoriasis vulgaris, adaptiert von EuroGuiDerm &#x2013; Teil 2: Hilfestellungen f&#xFC;r besondere klinische Situationen und bei Vorliegen von Komorbidit&#xE4;ten</title><link>https://www.psoriasis-news.de/articles.html/1_articles/s3%E2%80%90leitlinie-zur-therapie-der-psoriasis-vulgaris-adaptiert-von-euroguiderm-teil-2-hilfestellungen-f%C3%BCr-besondere-klinische-situationen-und-bei-vorliegen-von-komorbidit%C3%A4ten-r445/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12875179?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">445</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>Real-World Efficacy and Drug Survival of Adalimumab in Australian Patients With Psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/real-world-efficacy-and-drug-survival-of-adalimumab-in-australian-patients-with-psoriasis-r444/</link><description><![CDATA[<h4>Background</h4>Although adalimumab has shown strong efficacy and safety in clinical trials, real-world evidence in Australian patients with moderate-to-severe chronic plaque psoriasis is limited. This study assessed adalimumab efficacy and drug survival in routine clinical practice, comparing outcomes with the Phase 3 REVEAL trial and its open-label extension.<h4>Methods</h4>Data were extracted from the Australasian Psoriasis Registry for adults meeting Pharmaceutical Benefits Scheme criteria to be prescribed adalimumab for chronic plaque psoriasis. Baseline demographics, Psoriasis Area and Severity Index (PASI) scores and treatment history between June 2006 and March 2022 were analysed. Drug survival was evaluated using Kaplan-Meier and Cox regression.<h4>Results</h4>A total of 306 patients were included; 59.8% had prior biologic exposure compared to 12.8% in REVEAL. The mean baseline PASI was 24.1 and at 3 months, 63.5% achieved PASI75 while 33.6% achieved PASI90. PASI90 responses remained stable through 3 years and exceeded REVEAL extension rates beyond 18 months. Median drug survival was 27.9 months; survival was 97.7%, 78.6%, 63.7% and 51.0% at 3, 9, 15 and 27 months, respectively. Male sex and achieving PASI ≤ 2 predicted longer drug survival.<h4>Conclusions</h4>In Australian real-world practice, adalimumab demonstrated sustained effectiveness and drug survival in patients with chronic plaque psoriasis comparable to RCTs, despite higher baseline disease severity and greater prior biologic exposure.<p><a href="http://europepmc.org/article/MED/41629766?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">444</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>Management of Obesity in Psoriasis Consultations.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/management-of-obesity-in-psoriasis-consultations-r443/</link><description><![CDATA[<h4>Introduction</h4>Psoriasis and obesity often occur together, with up to 50% of patients with psoriasis being classified as obese. This increases systemic inflammation, cardiovascular risk, and disease severity while reducing the efficacy of biologic treatments. Despite this overlap, dermatology lacks obesity-specific guidance. This review evaluates lifestyle, pharmacological (glucagon-like peptide 1 receptor agonists [GLP-1 RAs] and tirzepatide) and surgical strategies, as well as clinic-level algorithms, to inform dermatological practice.<h4>Methods</h4>We performed a narrative synthesis of epidemiology, randomized trials, real-world studies, and guideline recommendations. Our focus was on the pathophysiology and the efficacy of GLP-1 RAs and tirzepatide, providing a practical algorithm pathway for triage, pharmacotherapy escalation, and referral criteria to a multidisciplinary unit.<h4>Results</h4>Although there are no psoriasis-specific guidelines for obesity treatment, the strong link between the two conditions and the poorer therapeutic response observed in obese patients make addressing excess weight essential for people with psoriasis. The proposed algorithms emphasize universal lifestyle counseling and dermatology-led management for patients with a BMI (body mass index) &lt; 35 kg/m<sup>2</sup> and without major metabolic complications. GLP-1 RAs are considered the first-line treatment, given the available scientific evidence about their efficacy in terms of weight loss and management of comorbidities, as well as their safety profile. If weight loss with these drugs is insufficient, the next proposed treatment step is tirzepatide. Bariatric surgery, including bypass procedures, should be reserved for patients with a BMI ≥ 40 kg/m<sup>2</sup>, or with a BMI ≥ 35 kg/m<sup>2</sup> when earlier measures have failed and/or comorbidities are not adequately controlled.<h4>Conclusion</h4>Dermatologists should integrate obesity assessment and patient-centered interventions into psoriasis care. A structured, multidisciplinary approach could meaningfully enhance dermatological, metabolic, and cardiovascular outcomes in patients with psoriasis and obesity.<p><a href="http://europepmc.org/article/MED/41627722?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">443</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>Erectile dysfunction and associated factors in males with psoriasis: a case-control study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/erectile-dysfunction-and-associated-factors-in-males-with-psoriasis-a-case-control-study-r442/</link><description><![CDATA[Psoriasis is a chronic inflammatory skin disease associated with multiple comorbidities, including erectile dysfunction (ED). Data on the sexual health of male psoriasis patients in Vietnam are limited. We investigated the prevalence and severity of ED in male psoriasis patients compared with healthy individuals and explored potential associations between ED and psoriasis-related clinical characteristics. This case-control study included 135 male psoriasis patients and 166 healthy individuals aged ≥18 years and limited to those sexually active within the last 6 months. The 5-item version of the International Index of Erectile Function (IIEF) was used to assess ED risk and severity. Psoriasis patients demonstrated a higher prevalence of ED than controls (80.7% vs. 67.5%, p=0.01), with increased risk of moderate-to-severe ED. Age, obesity, age of psoriasis onset, Dermatology Life Quality Index (DLQI), Psoriasis Area Severity Index (PASI), and genital lesions were associated with ED. Advanced age and elevated PASI scores were independent risk factors for ED (p&lt;0.05). Hence, psoriasis is a risk factor for ED. Additionally, ED may serve as an early indicator of cardiovascular risk in male patients with psoriasis.<p><a href="http://europepmc.org/article/MED/41614235?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">442</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>Infliximab-induced paradoxical psoriasis successfully treated with secukinumab: A case report.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/infliximab-induced-paradoxical-psoriasis-successfully-treated-with-secukinumab-a-case-report-r441/</link><description><![CDATA[Psoriasis is a chronic, autoinflammatory skin disease. Tumor necrosis factor-alpha inhibitors are commonly used for the treatment of moderate-to-severe psoriasis; however, paradoxical psoriatic eruptions are a well-recognized adverse effect. There are no validated guidelines to manage this. We present the case of a 48-year-old woman with severe pustular psoriasis who developed acute paradoxical reactions after her first two infusions of infliximab, requiring hospitalization. She achieved disease control after transitioning to secukinumab, an interleukin-17 inhibitor. This case highlights the importance of early monitoring for paradoxical reactions in patients with severe psoriasis after initiating tumor necrosis factor-alpha inhibitor therapy and the value of transitioning to an alternative biologic class for effective management.<p><a href="http://europepmc.org/article/MED/41608230?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">441</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>S3 Guideline for the Treatment of Psoriasis vulgaris, adapted from EuroGuiDerm &#x2013; part 2: Specific clinical and comorbid situations</title><link>https://www.psoriasis-news.de/articles.html/1_articles/s3-guideline-for-the-treatment-of-psoriasis-vulgaris-adapted-from-euroguiderm-part-2-specific-clinical-and-comorbid-situations-r440/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12875186?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">440</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>Differences in the Expression of Insulin-Like Growth Factor Signaling Pathway Members in Patients With Psoriasis Vulgaris and Controls.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/differences-in-the-expression-of-insulin-like-growth-factor-signaling-pathway-members-in-patients-with-psoriasis-vulgaris-and-controls-r439/</link><description><![CDATA[Insulin-like growth factors (IGFs) and IGF-binding proteins (IGFBPs) regulate cell proliferation, differentiation, metabolic processes, and immune activities. Psoriasis is a systemic inflammatory disease with metabolic disorders as an important comorbidity in the pathogenesis of which members of the IGF family could also play a role. Therefore, we decided to evaluate the levels of members of the IGF signaling pathway in patients with psoriasis. Sixty-nine people were enrolled in our study: 34 patients with psoriasis and 35 controls. The following parameters were evaluated in serum obtained from peripheral blood: total cholesterol, triglycerides, high-density lipoprotein, fasting glucose, IGF-1, IGF-1R, IGF-2, IGF-2R, IGFBP1, IGFBP2, IGFBP3, IGFBP4, IGFBP6, and insulin. The levels of several parameters differed between groups. The levels of fasting glucose, insulin, IGFBP3, and IGFBP6 were higher in patients with psoriasis, while the levels of IGF-1, IGF-1R, and IGBP4 were higher in controls. The results suggested that the IGF-1 signaling pathway can be involved in the pathogenesis of psoriasis and its comorbidities, especially metabolic disorders such as insulin resistance, diabetes, and metabolic syndrome. The novelty of our study is in its comprehensive assessment of the involvement of the IGF-1 signaling pathway in the pathogenesis of psoriasis and advances the understanding of the pathogenesis of psoriasis and its comorbidities.<p><a href="http://europepmc.org/article/MED/41635444?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">439</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>Advancements in psoriasis classification using custom transfer learning algorithms.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/advancements-in-psoriasis-classification-using-custom-transfer-learning-algorithms-r438/</link><description><![CDATA[Psoriasis is a skin disorder which mainly occurs as a rash, scaly areas and an itchy skin. The symptoms usually occur on the chest, elbows, and the scalp. World Health Organization (WHO) reports that about 125 million individuals in the world, that is about two to three% of the world population, live with psoriasis. Moreover, approximately 30% of psoriasis patients can have psoriatic arthritis. Psoriasis can have a detrimental effect on the quality of life of the affected people. They can also deal with several chronic diseases, such as depression, metabolic syndrome, cardiovascular diseases, such as atherosclerosis, heart attacks, and strokes. The psoriasis may develop at any age of life, but this disease is most prevalent in the ages between 20 and 30 and 50-60. Psoriasis is caused by different aspects, such as hereditary aspects, lifestyle habits of modern people, diet, use of drugs, skin trauma, stress, or abnormalities in the immune system, and hormonal fluctuations. Regrettably, the available conventional measures of determining the type of psoriasis are not always accurate with human errors. In order to overcome these problems, our study would attempt to develop a new dataset classified into seven classes of psoriasis diseases. We make use of publicly accessible data like SKIN LESION, ISIC and DEMANET. To overcome the problem of class imbalances, we will use the method of image augmentation to make the number of imageries in each class close to each other.To identify the presence of psoriasis in skin disease images, we employ transfer learning algorithms. Specifically, our proposed methodology utilizes ResNet50, InceptionResNetV2, and InceptionV3 with Adam and RMSprop optimizers for psoriasis classification. During training and validation, the ResNet50 model achieved good accuracy rates with values of 92.36, 84.59, and 83.55, respectively. The InceptionV2 model demonstrated impressive accuracy during training, validation, and testing, with values of 99.07, 96.65, and 97.20, respectively. Similarly, the InceptionV3 model achieved superior accuracy rates during training, validation, and testing, with values of 99.57, 96.82, and 98.68, respectively.When compared to all the models, InceptionV3 consistently demonstrates superior accuracy.<p><a href="http://europepmc.org/article/MED/41629591?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">438</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>Delayed Diagnosis of Psoriatic Arthritis Presenting with Infection-like Finger Inflammation: A Case Report.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/delayed-diagnosis-of-psoriatic-arthritis-presenting-with-infection-like-finger-inflammation-a-case-report-r437/</link><description><![CDATA[Psoriatic arthritis is a chronic inflammatory disease associated with psoriasis, and its diagnosis can be challenging owing to nonspecific symptoms, absence of reliable biomarkers, and occasional delay in skin manifestations. Herein, we report a case of psoriatic arthritis that initially presented as an acute finger inflammation mimicking infection. A 46-year-old woman developed sudden swelling and pain in the left ring finger during chemotherapy for cervical cancer. Based on the results of the physical examination, laboratory tests, and magnetic resonance imaging, pyogenic flexor tenosynovitis was suspected, and synovectomy was performed; however, bacterial and mycobacterial cultures yielded negative results. Despite the administration of antibiotics, the inflammation persisted, and she was referred to the Rheumatology Department, where she was diagnosed with reactive arthritis secondary to Chlamydia infection. Although the inflammation improved after antimicrobial therapy, the finger swelling persisted. Follow-up magnetic resonance imaging and serological testing were performed, and the patient was diagnosed of seronegative rheumatoid arthritis. Four years after onset, erythematous skin lesions appeared, and dermatological evaluation confirmed plaque psoriasis; thus, a definitive diagnosis of psoriatic arthritis was established. Disease-modifying antirheumatic drug adjustments improved symptoms, but residual 'pencil-in-cup' deformity and limited finger motion remained. This case highlights the difficulty in diagnosing psoriatic arthritis when arthritis precedes skin lesions. Clinicians should consider psoriatic arthritis in persistent or refractory arthritis and carefully monitor skin and nail changes to achieve an earlier diagnosis and prevent irreversible joint damage.<p><a href="http://europepmc.org/article/MED/41626754?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">437</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>Single-cell transcriptomics reveals keratinocyte dynamic processes associated with S100a4 expression in psoriasiform dermatitis</title><link>https://www.psoriasis-news.de/articles.html/1_articles/single-cell-transcriptomics-reveals-keratinocyte-dynamic-processes-associated-with-s100a4-expression-in-psoriasiform-dermatitis-r436/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12876221?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">436</guid><pubDate>Tue, 10 Feb 2026 08:00:25 +0000</pubDate></item><item><title>Transcriptomic profiling and machine learning uncover gene signatures of psoriasis endotypes and disease severity.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/transcriptomic-profiling-and-machine-learning-uncover-gene-signatures-of-psoriasis-endotypes-and-disease-severity-r434/</link><description><![CDATA[<h4>Background</h4>Despite increased understanding of psoriasis pathogenesis, molecular classification of clinical phenotypes and disease severity is poorly defined. Knowledge gaps include whether molecular endotypes of psoriasis underlie distinct clinical phenotypes and the positive and negative molecular regulators of disease severity across tissue compartments.<h4>Methods</h4>We performed comprehensive RNA sequencing of skin and blood (n = 718) from prospectively-recruited, deeply-phenotyped discovery and replication cohorts of 146 subjects with moderate-to-severe chronic plaque psoriasis initiating TNF-inhibitor (adalimumab) or IL-12/23-inhibitor (ustekinumab) therapy.<h4>Results</h4>Here we show, using two complementary dimensionality reduction methods, that co-expressed gene modules and factors within skin and blood are significantly associated with psoriasis phenotypes and disease severity. We identify a 14-gene signature negatively associated with BMI in nonlesional skin and with disease severity in lesional skin. Genotype integration reveals that HLA-DQA1*01 and HLA-DRB1*15 genotypes are positively associated with baseline psoriasis severity. Using explainable machine learning models, we define two disease severity-associated gene modules in lesional skin - one positive, one negatively-associated - and a 9-gene signature in lesional skin predictive of disease severity. Disease severity signatures in blood are only seen following adalimumab exposure, suggesting greater systemic impact of adalimumab compared to ustekinumab, in line with its side effect profile. In contrast, a gene signature in blood linked to HLA-C*06:02 status is independent of disease severity or drug.<h4>Conclusions</h4>These findings delineate gene-environmental and genetic effects on the psoriasis transcriptome linked to disease severity.<p><a href="http://europepmc.org/article/MED/41565778?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">434</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item><item><title>Accuracy Assessment of Chinese Large Language Models in Psoriasis Management: A Multicenter Expert Consensus Study</title><link>https://www.psoriasis-news.de/articles.html/1_articles/accuracy-assessment-of-chinese-large-language-models-in-psoriasis-management-a-multicenter-expert-consensus-study-r433/</link><description><![CDATA[Abstract  <p>Background  Psoriasis patients in China face significant challenges due to insufficient disease knowledge and limited access to medical resources, creating a need for reliable educational tools. Objectives  This multicenter consensus study aimed to systematically evaluate the consultation quality of mainstream Chinese large language models (LLMs) for psoriasis patient education. Methods  "365 Questions on Psoriasis" was jointly compiled by 109 Chinese psoriasis experts. Using an expert assessment methodology, nine dermatologists curated 40 high-frequency clinical questions from the book across five domains (etiology, triggers, treatment, management, psychosocial impact). Four Chinese LLMs (DeepSeek-R1, DeepSeek-V3, GLM-4, Qwen-3) were evaluated through double-blind scoring on a 10-point Likert scale assessing accuracy, completeness, clarity, and safety. Results  Performance varied significantly, with mean scores ranging from 5.95 to 9.88 (SD: 0-3.05). Qwen-3 achieved the highest average score (9.12), while GLM-4 showed the greatest inconsistency. All responses avoided dangerous content, and 87.5% proactively emphasized the necessity of consulting a physician. However, 12.5% of responses deviated from evidence-based guidelines, particularly on complex topics like biologics and management. Conclusions  Chinese LLMs show substantial potential for psoriasis education by providing generally safe information and appropriately directing users to doctors. However, current limitations exist, including performance inconsistency and occasional deviations from guidelines on specialized topics, indicating they are not yet replacements for professional medical.</p><p><a href="http://europepmc.org/article/PPR/PPR1147055?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">433</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item><item><title>Therapeutic approach with fatty acids in psoriasis: A systematic review.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/therapeutic-approach-with-fatty-acids-in-psoriasis-a-systematic-review-r432/</link><description><![CDATA[<h4>Objective</h4>This study aims to evaluate the clinical impacts of topical and/or oral administration of compounds rich in omega-3 fatty acids from various sources, such as oils and foods, on psoriatic lesions.<h4>Design</h4>A systematic review was carried out.<h4>Data sources</h4>Searches were conducted in six databases (PubMed, Cochrane, VHL, Scopus, Embase, and Web of Science) using descriptors related to fatty acids and psoriasis.<h4>Study selection</h4>Inclusion criteria were studies published in the last 10 years (2013-2023) that involved patients with psoriasis and provided quantitative clinical outcome data, such as psoriasis severity scale.<h4>Data extraction</h4>Two independent reviewers carried out the initial screening of the titles and abstracts identified in the search. The quality of studies was evaluated using the Newcastle-Ottawa Scale, the Risk of Bias in Randomized Studies of Interventions, and the Joanna Briggs Institute critical appraisal checklist.<h4>Results</h4>Out of 8570 articles identified, 9 met the inclusion criteria. The quality of randomized clinical trials and observational studies varied from low to high risk of bias, according to the respective parameters of each checklist.<h4>Conclusions</h4>Most studies demonstrated that the topical and/or oral administration of omega-3 fatty acids from different sources significantly improved clinical parameters, as measured by severity scales and the Psoriasis Area and Severity Index (PASI).<p><a href="http://europepmc.org/article/MED/41534196?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">432</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item></channel></rss>
