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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/23/?d=1</link><description>Neue Studien: Europe PMC</description><language>de</language><item><title>PIEZO1 promotes psoriasis-like skin inflammation in mice via NF-&#x3BA;B/IL-17 signaling pathway activation.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/piezo1-promotes-psoriasis-like-skin-inflammation-in-mice-via-nf-%CE%BAbil-17-signaling-pathway-activation-r81/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/40495117?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">81</guid><pubDate>Sat, 14 Jun 2025 05:52:56 +0000</pubDate></item><item><title>Comorbid psoriasis in systemic lupus erythematosus: a cohort study from a tertiary referral centre and the National Patient Register in Sweden.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/comorbid-psoriasis-in-systemic-lupus-erythematosus-a-cohort-study-from-a-tertiary-referral-centre-and-the-national-patient-register-in-sweden-r80/</link><description><![CDATA[<h4>Objectives</h4>To investigate the prevalence of psoriasis in SLE using a Swedish regional cohort and a nationwide cohort from the National Patient Register (NPR). Furthermore, we compared clinical features between patients with and without comorbid psoriasis.<h4>Methods</h4>In total, 351 patients diagnosed with SLE based on the 1982 American College of Rheumatology and/or the 2012 Systemic Lupus International Collaborating Clinics criteria from Linköping University Hospital were evaluated. We obtained patient-reported and relevant clinical data extracted in 2024. Individuals with coexisting psoriasis were identified via the International Classification of Diseases code L40 and subsequent confirmation through chart review in the regional cohort. In the NPR, 7490 subjects with SLE living in Sweden in 2022 were identified, as well as therapies obtained from the Prescribed Drug Register.<h4>Results</h4>We identified 12 subjects with SLE and coexisting psoriasis (3.4%) in the regional cohort and 367 patients (4.9%) in the nationwide cohort. Men were proportionally more common in the group with comorbid psoriasis in both cohorts. Patients with psoriasis reported more pain on a visual analogue scale (median 45.5/100 mm, IQR 23.3-58.3) compared with those without coexisting psoriasis (median 27.0/100 mm, IQR 7.0-50.5, p&lt;0.04). We observed no differences in damage accrual or clinical phenotypes between the two groups. Subjects with psoriasis were more frequently prescribed methotrexate in the nationwide cohort.<h4>Conclusion</h4>The prevalence of coexisting psoriasis in patients with SLE in Sweden was estimated to be 3.4-4.9%. Individuals with comorbid psoriasis reported more pain and were more likely to be prescribed methotrexate than those without psoriasis.<p><a href="http://europepmc.org/article/MED/40473266?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">80</guid><pubDate>Sat, 14 Jun 2025 05:52:56 +0000</pubDate></item><item><title>"Full-na&#xEF;ve" patients: the impact of previous methotrexate, cyclosporine, and acitretin on first-line biologics response in the treatment of moderate-to-severe psoriasis - a monocentric retrospective study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/full-na%C3%AFve-patients-the-impact-of-previous-methotrexate-cyclosporine-and-acitretin-on-first-line-biologics-response-in-the-treatment-of-moderate-to-severe-psoriasis-a-monocentric-retrospective-study-r79/</link><description><![CDATA[<h4>Background</h4>The impact of traditional systemic drugs to treat psoriasis (ciclosporin, methotrexate, and acitretin) in a subsequent response to biologics, has not been adequately addressed in the literature. In clinical practice it is increasingly necessary to initiate, due to concomitant comorbidities, biologics in patients with psoriasis or psoriatic arthritis (PsA) who have not undergone prior treatment with systemics, i.e. full-naive.<h4>Objectives and methods</h4>This study analyzed the possible impact of non-biological systemic therapies on the effectiveness and drug survival of first-line biologic drug up to 12 months in bio-naive psoriatic and PsA patients consecutively enrolled from January 2017 to March 2021.<h4>Results</h4>95 patients with severe psoriasis (13.5%) were full-naive. Being full-naive and having or not having undergone methotrexate or cyclosporine therapy did not impact response to subsequent years of biologic therapy. Only acitretin promotes faster response to subsequent biologic drugs with 59.6% and 74.2% of patients achieving Psoriasis Area Severity Index (PASI) 90 at 16 and 28 Week, respectively, vs. 50.5% and 65% (<i>p</i> = 0.034 and 0.026). In multivariate analysis, the advantage given by acitretin was lost.<h4>Conclusion</h4>Previous systemic therapy in bio-naive patients does not appear to result in a differential response to biologics during the first year of treatment.<p><a href="http://europepmc.org/article/MED/40485370?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">79</guid><pubDate>Sat, 14 Jun 2025 05:52:56 +0000</pubDate></item><item><title>Gender differences in psychological features and determinates of quality of life in axial spondyloarthritis and psoriatic arthritis: a cross-sectional study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/gender-differences-in-psychological-features-and-determinates-of-quality-of-life-in-axial-spondyloarthritis-and-psoriatic-arthritis-a-cross-sectional-study-r78/</link><description><![CDATA[<h4>Background</h4>Investigating gender-specific differences in rheumatology is crucial for improving personalized treatment. The present study aimed to explore gender differences in psychological characteristics and features associated with impaired physical and mental quality of life in male and female patients affected by axial spondyloarthritis or psoriatic arthritis.<h4>Methods</h4>The present study is cross-sectional. Quality of life was evaluated using a Medical Outcome Study 36-item Short Form health survey (SF-36), and physical and mental component scores were presented. Data about disease activity, anxiety and depression, fatigue, perceived stress, and coping strategies were collected. The patients were stratified by gender, and clinical and psychological data were compared.<h4>Results</h4>A total of 119 patients with axial spondyloarthritis [age 49.0 (SD 11.7); 45.4% F] and 198 patients with psoriatic arthritis [age 56.9 (SD 11.6); 62.6% F] were included. Female patients with axial spondyloarthritis and psoriatic arthritis had worse scores on fatigue, pain, perceived stress, physical quality of life, dysfunctional coping strategies, mental quality of life (only in axial spondyloarthritis), and anxiety (only in psoriatic arthritis) than men. In multivariable analysis, physical quality of life is mainly explained by fatigue and pain, and mental quality of life by fatigue, anxiety and stress in women with axial spondyloarthritis and psoriatic arthritis. Fatigue, pain and anxiety were significant variables across the models with male patients.<h4>Conclusions</h4>The study indicates that female patients with axial spondyloarthritis and psoriatic arthritis experience worse scores in psychological variables compared to men. Additionally, women's quality of life is significantly lower when compared to men's one, primarily due to factors such as fatigue, stress, pain, and anxiety. To enhance patient well-being, therapeutic strategies should be tailored to address the unique clinical and psychological needs that arise from gender differences.<p><a href="http://europepmc.org/article/MED/40481599?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">78</guid><pubDate>Sat, 14 Jun 2025 05:52:56 +0000</pubDate></item><item><title>Long-term air pollutants exposure on risk of psoriasis: the mediating role of accelerated biological aging among 284,544 participants.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/long-term-air-pollutants-exposure-on-risk-of-psoriasis-the-mediating-role-of-accelerated-biological-aging-among-284544-participants-r77/</link><description><![CDATA[Psoriasis burdens children and adults, but the impact of air pollution and aging is unclear. This study examines the association between air pollution exposure and psoriasis risk, considering the mediating role of biological aging. A prospective cohort study of 284,544 adults (51.3% female, mean age 56.26 ± 8.10 years) from the UK Biobank examined long-term exposure to air pollutants (PM2.5, PM10, PM2.5-10, NO2, and NOX). Biological aging was assessed using phenotypic age algorithms. Cox proportional hazards models were constructed to analyze the relationships with the risk of psoriasis, adjusting for demographic, socioeconomic, and health-related factors. Mediation analysis explored the role of biological aging. During a median follow-up of 15.58 years, 3,446 (1.21%) participants developed psoriasis. After adjusting for all confounders, each ten-unit increase (10 μg/m³) in PM2.5, PM10, NO2, and NOx, corresponded to the significantly increased risk of psoriasis by 95.7% (HR = 1.957, 95% CI 1.435-2.671), 19.7% (HR = 1.197, 95% CI 1.006-1.426), 9.0% (HR = 1.090, 95% CI 1.043-1.138) and 4.4% (HR = 1.044, 95% CI 1.024-1.066), respectively. Moreover, all air pollutants are significantly associated with biologically aging, while each one-year increase in PhenoAge was associated with a 5.0% higher risk of psoriasis (HR = 1.050, 95% CI 1.045-1.056). Finally, accelerated biological aging partially mediated 5.96%-13.86% of these air pollutants. Long-term exposure to air pollution significantly affects psoriasis risk, with biological aging as a partial mediator. Reducing pollution may lower the risk of psoriasis by slowing biological aging.<p><a href="http://europepmc.org/article/MED/40493780?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">77</guid><pubDate>Sat, 14 Jun 2025 05:52:56 +0000</pubDate></item><item><title>The Association of Psoriasis and Bacterial Infections in&#xA0;Pediatric Patients: A Retrospective Review.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/the-association-of-psoriasis-and-bacterial-infections-in%C2%A0pediatric-patients-a-retrospective-review-r76/</link><description><![CDATA[<h4>Background/objectives</h4>Guttate psoriasis onset and plaque psoriasis flares are associated with streptococcal pharyngitis. Literature regarding the relationship between anogenital bacterial dermatitis and psoriasis in pediatric patients is limited. We aimed to evaluate the clinical characteristics, microbiology, and treatment course of patients with psoriasis/psoriasiform dermatitis and concomitant pharyngeal and/or anogenital bacterial infections.<h4>Methods</h4>A multicenter retrospective review of patients ≤ 18 years of age with psoriasis/psoriasiform dermatitis and bacterial infection, defined by positive culture results, was performed. Demographic characteristics, clinical features, microbiology, treatment recommendations, and outcomes were evaluated. Comparisons were made between pharyngeal and anogenital culture groups.<h4>Results</h4>A total of 166 unique patients with psoriasis/psoriasiform dermatitis and suspected pharyngeal and/or anogenital infection were evaluated between 2011 and 2021. Staphylococcus sp. and Streptococcus sp. were isolated in anogenital cultures. Inverse psoriasis was associated with a positive anogenital culture (p = 0.0356). Guttate psoriasis was more common in patients with a positive pharyngeal culture (p &lt; 0.0001). Treatment of a positive bacterial culture did not correlate with the treatment response of psoriasis/psoriasiform dermatitis.<h4>Conclusions</h4>Investigations for anogenital and pharyngeal infections should be considered in pediatric patients presenting with new-onset or worsening psoriasis. A high clinical suspicion should be maintained for anogenital infection in patients with inverse psoriasis, specifically.<p><a href="http://europepmc.org/article/MED/40503759?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">76</guid><pubDate>Sat, 14 Jun 2025 05:52:56 +0000</pubDate></item><item><title>Exploring the association between relative fat mass and psoriasis risk: insights from the NHANES data.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/exploring-the-association-between-relative-fat-mass-and-psoriasis-risk-insights-from-the-nhanes-data-r75/</link><description><![CDATA[<h4>Background</h4>Patients' quality of life is greatly impacted by psoriasis, a prevalent chronic inflammatory skin condition that is frequently linked to a number of systemic disorders. Recent research shows that obesity is a major risk factor for psoriasis. Since Relative Fat Mass (RFM), an innovative way to measure obesity, offers a more precise estimate of body fat percentage, this study aims to investigate the connection between RFM and psoriasis and its potential as a disease predictor.<h4>Methods</h4>The analysis included 6,006 people the National Health and Nutrition Examination Survey (NHANES) conducted between 2003 and 2006, 151 of whom had psoriasis. Weighted multivariable logistic regression, restricted cubic splines (RCS), subgroup analysis, and interaction tests were employed to assess the link between RFM and psoriasis. ROC curves were used to compare RFM with conventional measures of obesity (WWI, BRI). Furthermore, LASSO regression and multivariable regression based on AIC were used to create a psoriasis risk prediction model that included RFM and additional clinical factors.<h4>Results</h4>RFM and psoriasis risk were revealed to be significantly positively correlated. The chance of developing psoriasis increased by 7% for every unit rise in RFM (95% CI: 1.03 to 1.12). RFM showed better predictive ability than conventional markers including BMI, WWI, and BRI (AUC = 0.573). The RFM-psoriasis relationship and diabetes status significantly interacted, with the association being weaker in diabetic individuals, according to subgroup analysis and interaction tests. Promising results were obtained from the created psoriasis risk prediction model that included RFM, age, total dietary sugar, education level, history of heart disease, and hypertension.<h4>Conclusion</h4>This research demonstrates that RFM outperforms traditional anthropometric methods in predicting risk. It also presents the initial evidence establishing a positive link between RFM and the likelihood of developing psoriasis.The psoriasis risk prediction model underscores RFM's effectiveness as a valuable approach in both clinical and public health domains, aiming to alleviate the impact of psoriasis-related issues by offering a practical instrument for early risk assessment and personalized clinical strategies.<p><a href="http://europepmc.org/article/MED/40490769?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">75</guid><pubDate>Sat, 14 Jun 2025 05:52:56 +0000</pubDate></item><item><title>Effects of Adalimumab on Mitochondria of Psoriatic Mesenchymal Stem Cells</title><link>https://www.psoriasis-news.de/articles.html/1_articles/effects-of-adalimumab-on-mitochondria-of-psoriatic-mesenchymal-stem-cells-r74/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12143177?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">74</guid><pubDate>Wed, 11 Jun 2025 06:56:28 +0000</pubDate></item><item><title>Understanding Psoriasis Patient Preferences for Biologic Dosing Frequencies: Insights From a Patient Survey</title><link>https://www.psoriasis-news.de/articles.html/1_articles/understanding-psoriasis-patient-preferences-for-biologic-dosing-frequencies-insights-from-a-patient-survey-r73/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12133784?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">73</guid><pubDate>Sat, 07 Jun 2025 16:48:48 +0000</pubDate></item><item><title>Are psoriasis severity and comorbidities associated with diet quality? A cross-sectional analysis using UK Biobank.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/are-psoriasis-severity-and-comorbidities-associated-with-diet-quality-a-cross-sectional-analysis-using-uk-biobank-r72/</link><description><![CDATA[Psoriasis has been linked to various diet-related comorbidities such as metabolic syndrome, type 2 diabetes, and cardiovascular disease. Evidence is lacking on the role of diet in the management of psoriasis and its comorbidities. We aimed to characterise the dietary patterns and quality of diet in individuals living with psoriasis and to assess whether psoriasis severity and comorbidities are associated with diet quality. Using the UK Biobank cohort, individuals identified with psoriasis via self-report and/or linked health records at baseline were compared with participants without psoriasis. Dietary intake was assessed through online 24 h-recalls (Oxford WebQ) conducted every 3-4 months over one year. Average nutrient and food group intakes were calculated from at least two 24 h dietary recalls to determine adherence to national food-based dietary guidelines (Eatwell Score (EWS), range: 0-9) and the Mediterranean-style diet (alternative Mediterranean diet (aMED) score, range: 0-9). Associations between psoriasis severity (using treatment category as a proxy), the presence of major comorbidities and diet quality scores were evaluated using regression models adjusting for covariates. Among 2613 people with psoriasis (mean age 56.5, 49.6 % women) and 120,555 people without psoriasis (mean age 56.2, 56.2 % women), both groups had similar average scores for EWS (3.9 ± 1.7 for both groups). The psoriasis group had a slightly higher aMED score (4.4 ± 1.8 and 3.8 ± 1.7, P &lt; 0.001). However, participants with psoriasis also reported higher intake of red and processed meat, sodium, free sugars, and alcohol (all P &lt; 0.05) compared to the non-psoriasis group. Within the psoriasis group, no significant difference in diet quality was found between different clinical severities of psoriasis, but participants with the highest severity had lower odds of meeting guidelines for daily fruit and vegetable intakes (odds ratio (OR) 95 % confidence interval (CI): 0.69 (0.48, 0.98), P = 0.040) and scoring on nuts intake (OR (95 % CI): 0.66 (0.44, 1.00), P = 0.050) compared to those not receiving treatment. Participants in the psoriasis group with at least one comorbidity had significantly lower diet quality scores (EWS, beta (95%CI): -0.184 (-0.354, -0.014), P = 0.034; aMED beta (95%CI): -0.266 (-0.442, -0.089), P = 0.003). Participants with psoriasis showed slightly better adherence to a Mediterranean-style diet but also consumed more processed meat, sodium, free sugars, and alcohol. Those with the most severe psoriasis or comorbidities had poorer diet quality, highlighting the opportunity for dietary interventions in this population.<p><a href="http://europepmc.org/article/MED/40449291?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">72</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>Immunoglobulin A vasculitis and pustular psoriasis precipitated by Tawon Liar: a case report.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/immunoglobulin-a-vasculitis-and-pustular-psoriasis-precipitated-by-tawon-liar-a-case-report-r71/</link><description><![CDATA[Unregulated herbal supplements can pose significant health risks due to undisclosed ingredients. Tawon Liar, an Indonesian product marketed as an "all-natural" remedy, claims to alleviate pain and boost immunity but lacks stringent regulatory oversight. We report a unique case of Tawon Liar-induced Immunoglobulin A (IgA) vasculitis and exacerbation of psoriasis, highlighting the potential dangers associated with misadvertised supplements. A 53-year-old migrant worker from Mexico with a history of psoriasis and ankylosing spondylitis, effectively managed with adalimumab, presented with new-onset rashes on his extremities. Physical examination revealed palpable purpura on the lower legs and erythematous papules and plaques with pustules on the upper extremities. Dermoscopic analysis suggested IgA vasculitis and pustular psoriasis. The patient denied recent infections, new medications, or over-the-counter drug use. However, after thorough questioning, it was revealed that he had been intermittently ingesting Tawon Liar for chronic musculoskeletal pain. The supplement, obtained from a coworker, contained undisclosed ingredients including meloxicam, ketorolac, and dexamethasone. Laboratory tests ruled out renal involvement, and biopsies were not performed due to financial constraints. The patient was advised to discontinue Tawon Liar and was treated with topical corticosteroids, leading to substantial improvement and resolution of symptoms within one week. This case underscores the potential dangers of herbal supplements containing hidden pharmacologic agents. It highlights the need for clinicians to diligently inquire about supplement use during patient evaluations, especially for vulnerable populations facing language barriers and limited access to healthcare. Public health authorities should enhance efforts to disseminate drug safety information across diverse languages and platforms to mitigate health risks associated with such products.<p><a href="http://europepmc.org/article/MED/40448236?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">71</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>Effectiveness of Tildrakizumab 200&#xA0;mg in Moderate-to-Severe Plaque Psoriasis: A Multicenter Real-World Study Analyzing Patient Outcomes by Weight, PASI, BMI, and Previous Therapies.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/effectiveness-of-tildrakizumab-200%C2%A0mg-in-moderate-to-severe-plaque-psoriasis-a-multicenter-real-world-study-analyzing-patient-outcomes-by-weight-pasi-bmi-and-previous-therapies-r70/</link><description><![CDATA[<h4>Introduction</h4>Psoriasis is a chronic immune-mediated disease with significant systemic implications. Tildrakizumab, an IL-23p19 inhibitor, has demonstrated efficacy in moderate-to-severe plaque psoriasis. Higher doses may be beneficial for patients with elevated body weight or greater disease burden. This study evaluates the effectiveness of tildrakizumab 200 mg in a real-world setting, analyzing outcomes based on weight, Psoriasis Area Severity Index (PASI), body mass index (BMI), and prior biologic exposure.<h4>Methods</h4>A multicenter retrospective study was conducted across 10 Italian hospitals. Adult patients (≥ 18 years) with moderate-to-severe plaque psoriasis treated with tildrakizumab 200 mg for ≥ 36 weeks were included. Patients were stratified by weight (≥ 90 kg vs. &lt; 90 kg), BMI (≥ 30 vs. &lt; 30), PASI (≥ 15 vs. &lt; 15), and biologic history (naïve vs. biologic (bio)-experienced). PASI100 response rates at 36 weeks were assessed. Statistical analyses included Fisher's exact test (p &lt; 0.05 significant).<h4>Results</h4>Among 137 patients, PASI100 response rates were 67.1% for patients &lt; 90 kg vs. 49.2% for ≥ 90 kg (p = 0.04), 61.5% for PASI &lt; 15 vs. 50% for PASI ≥ 15 (p = 0.03), and 60.8% for bio-naïve vs. 57.1% for bio-experienced (p = 0.08). BMI ≥ 30 was associated with lower PASI100 (44.2%) compared to BMI &lt; 30 (61.4%) (p = 0.05). Despite subgroup differences, all patients exhibited clinical improvement.<h4>Conclusion</h4>Tildrakizumab 200 mg effectively treated moderate-to-severe psoriasis across diverse patient subgroups. While higher weight and PASI were associated with slightly lower PASI100 rates, significant improvements were observed, supporting its role in difficult-to-treat patients.<p><a href="http://europepmc.org/article/MED/40413278?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">70</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>Multimodal Function of Mesenchymal Stem Cells in Psoriasis Treatment.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/multimodal-function-of-mesenchymal-stem-cells-in-psoriasis-treatment-r69/</link><description><![CDATA[Psoriasis is a chronic inflammatory disease mediated by the innate and adaptive immune systems, and its pathogenesis involves multiple aspects, including abnormal interleukin (IL)-23-Th17 axis, dysfunction of Tregs and other immune cells, and a complex relationship between keratinocytes and the vascular endothelium. Dysfunction of mesenchymal stem cells in psoriatic skin may also be the main reason for the dysregulated inflammatory response. Mesenchymal stem cells, a type of adult stem cells with multidifferentiation potential, are involved in the regulation of multiple links and targets in the pathogenesis of psoriasis. Thus, a detailed exploration of these mechanisms may lead to the development of new therapeutic strategies for the treatment of psoriasis. In this paper, the role of mesenchymal stem cells in skin homeostasis, the pathogenesis of psoriasis, and the multimodal function of using mesenchymal stem cells in the treatment of psoriasis are reviewed.<p><a href="http://europepmc.org/article/MED/40427630?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">69</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>Tratamiento t&#xF3;pico de la psoriasis: recomendaciones de expertos del Grupo Espa&#xF1;ol de Psoriasis (GPS).</title><link>https://www.psoriasis-news.de/articles.html/1_articles/tratamiento-t%C3%B3pico-de-la-psoriasis-recomendaciones-de-expertos-del-grupo-espa%C3%B1ol-de-psoriasis-gps-r68/</link><description><![CDATA[Justification and objectives: Topical therapy is vital in the management of psoriasis. In recent years there have been multiple advances and changes in the management of psoriatic patients that justify a review and update of the use of topical therapy. Experts from the Spanish Psoriasis Working Group (GPS) of the Spanish Academy of Dermatology Venereology (AEDV) have developed a set of recommendations for the treatment of psoriasis based on the best available evidence and experts' opinion. Methodology: We followed the methodology of nominal groups, with the help from a systematic review. A coordinator was designated, and a group of experts was selected based on their experience and knowledge on topical therapies for the management of psoriasis. Afterwards, the objectives and key points of the document were defined and agreed upon, and with help from a documentary specialist, a systematic review was conducted across Medline, Embase and Cochrane Library. Systematic reviews, meta-analyses, clinical trials, as well as observational studies were selected. Published clinical practice guidelines and related documents were also reviewed. With this information, the coordinator generated a series of recommendations that would be later evaluated and modified by the experts themselves. After several review processes and an external evaluation, the final document was drafted. Results: Practical recommendations on the use of topical therapies for the management of psoriasis are presented in line with other documents of the AEDV, including the use of topical treatment as the main therapy, their adjuvant role when using systemic therapies, treatment selection, treatment strategies, their use in special locations and severe psoriasis, and the patients adherence and preferences to the topical therapy. The document critically evaluates the safety and efficacy profile of topical therapy.<p><a href="http://europepmc.org/article/MED/40446915?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">68</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>Deucravacitinib in Patients with Plaque Psoriasis Who Screened Positive for Psoriatic Arthritis: Improvements in Joint Pain and the Impact of Musculoskeletal Symptoms.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/deucravacitinib-in-patients-with-plaque-psoriasis-who-screened-positive-for-psoriatic-arthritis-improvements-in-joint-pain-and-the-impact-of-musculoskeletal-symptoms-r67/</link><description><![CDATA[For patients with psoriasis, psoriatic arthritis can be a painful comorbid condition that is often undiagnosed. It is therefore essential that more research is done to understand which treatments for psoriasis relieve both dermatologic and joint symptoms. This analysis aimed to compare the effects of deucravacitinib vs. placebo or apremilast on joint pain and the impact of musculoskeletal symptoms at weeks 16 and 24 in patients from the POETYK psoriasis (PSO-1; NCT03624127) and POETYK PSO second (PSO-2; NCT03611751) trials who self-reported joint symptoms. During screening in each trial, patients with psoriasis who reported musculoskeletal complaints completed the self-administered Psoriatic Arthritis Screening and Evaluation (PASE) questionnaire. Scores of ≥ 47 constituted positive screens (PASE positive). Joint pain and the impact of musculoskeletal symptoms were measured using a visual analog scale (VAS), with higher scores denoting worse disease burden. This pooled analysis included 185 patients who screened as PASE-positive in the combined POETYK PSO-1 and PSO-2 trials. Improvement from baseline was greater in patients treated with deucravacitinib vs. placebo at week 16 for joint pain VAS (- 15.2 vs. - 3.2) and joint disease VAS (- 17.4 vs. - 3.8). Improvements from baseline were also greater for patients treated with deucravacitinib vs. apremilast for joint pain VAS (- 22.8 vs. - 8.6) and joint disease VAS (- 19.6 vs. - 8.8) scores at week 24. Greater proportions of deucravacitinib-treated patients also achieved 30%, 50%, and 70% improvements in joint pain and musculoskeletal symptoms and impact VAS scores at weeks 16 and 24 than those who received placebo or apremilast. Findings from this pooled analysis suggest that deucravacitinib may be used in patients with psoriasis to effectively treat both dermatologic and joint symptoms. Graphical abstract available for this article.<p><a href="http://europepmc.org/article/MED/40445270?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">67</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>Long term outcomes among patients with pre-existing psoriasis undergoing immune checkpoint inhibitor therapy: a case series and literature review</title><link>https://www.psoriasis-news.de/articles.html/1_articles/long-term-outcomes-among-patients-with-pre-existing-psoriasis-undergoing-immune-checkpoint-inhibitor-therapy-a-case-series-and-literature-review-r66/</link><description><![CDATA[Abstract  <p>Psoriasiform adverse cutaneous reactions to immune checkpoint inhibitor (ICI) therapy for cancer are potentially treatment-limiting. Few studies have investigated long-term outcomes related to exacerbations of pre-existing psoriasis and their impact on the efficacy of cancer treatment. Understanding outcomes in patients with autoimmune disease is important to guide management of these reactions and avoid unnecessary exclusion from ICI therapy. We conducted a retrospective cohort study using the University of Kansas Cancer Center database. We identified 20 adult patients with pre-existing psoriasis who were treated with ICIs between 2013 and 2022 and had at least one year of follow-up. Of these, 15 experienced exacerbation of their psoriasis during ICI therapy. Patients with exacerbation completed a higher median number of ICI cycles than those with unaffected psoriasis (16 vs. 9 cycles). Rates of ICI discontinuation due to side effects were similar between the two groups (26% vs. 20%). Kaplan-Meier analysis showed that patients with psoriasis exacerbation had significantly better progression-free survival compared to unaffected patients (p = 0.015). Although overall mortality was lower in the exacerbation group (40% vs. 60%), this difference was not statistically significant. Two patients with severe flares discontinued ICIs and initiated systemic therapy for psoriasis. One continued to show tumor remission, while the other maintained stable tumor burden, highlighting the variability and chronicity of flare responses. Overall, ICIs appear to be tolerable in patients with pre-existing psoriasis. Despite the high rate of exacerbation, most flares were mild and manageable with topical therapy, and most patients were able to complete their treatment. The comparable discontinuation rates and greater number of ICI cycles among those with flares suggest that psoriasis exacerbation does not necessarily impede cancer therapy. These findings support the inclusion of patients with psoriasis in ICI treatment protocols and suggest that cutaneous irAEs may be associated with improved therapeutic outcomes. Although limited by small sample size and retrospective design, this study contributes to the growing body of evidence supporting safe ICI use in patients with pre-existing autoimmune skin disease.</p><p><a href="http://europepmc.org/article/PPR/PPR1030166?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">66</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>Practical Recommendations on Cardiovascular Risk Evaluation in Patients With Psoriasis and Psoriatic Arthritis for Dermatologists, Rheumatologists, and Primary Care Physicians by the Psoriasis and Psoriatic Arthritis Clinics Multicenter Advancement Networ</title><link>https://www.psoriasis-news.de/articles.html/1_articles/practical-recommendations-on-cardiovascular-risk-evaluation-in-patients-with-psoriasis-and-psoriatic-arthritis-for-dermatologists-rheumatologists-and-primary-care-physicians-by-the-psoriasis-and-psoriatic-arthritis-clinics-multicenter-advancement-network-r65/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12119537?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">65</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>All-Cause Mortality is Higher in Generalized Pustular Psoriasis (GPP) than Plaque Psoriasis and the General Population: A US-Based Claims Analysis</title><link>https://www.psoriasis-news.de/articles.html/1_articles/all-cause-mortality-is-higher-in-generalized-pustular-psoriasis-gpp-than-plaque-psoriasis-and-the-general-population-a-us-based-claims-analysis-r64/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12125009?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">64</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>Unraveling Psoriasis Flare-up and Dengue Infection</title><link>https://www.psoriasis-news.de/articles.html/1_articles/unraveling-psoriasis-flare-up-and-dengue-infection-r63/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12119508?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">63</guid><pubDate>Thu, 05 Jun 2025 13:21:39 +0000</pubDate></item><item><title>Prevalence of Psychiatric and Addictive Disorders in Patients with Psoriasis: A Cross-Sectional Study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/prevalence-of-psychiatric-and-addictive-disorders-in-patients-with-psoriasis-a-cross-sectional-study-r61/</link><description><![CDATA[<b>Background/Objectives:</b> Psoriasis is a chronic inflammatory skin disease increasingly linked to psychiatric and behavioral comorbidities, including depression, anxiety, and substance use disorders. Shared inflammatory pathways, including elevated IL-6, TNF-α, and IL-17, may link psoriasis with psychiatric disorders such as depression and anxiety. The bidirectional interaction between systemic inflammation and mental health may exacerbate the disease burden and affect treatment outcomes. The objective of this study was to determine the prevalence of psychiatric and behavioral comorbidities in patients with psoriasis and to explore potential demographic and clinical correlations. Assessing these correlations contributes to a better understanding of the mental health status of psoriasis patients, potentially influencing both therapeutic efficacy and quality of life. <b>Methods:</b> We conducted a cross-sectional observational study on 316 patients with clinically and histopathologically confirmed psoriasis, evaluated between January 2021 and March 2025 at the Clinical Railway Hospital in Iași, Romania. Psychiatric and behavioral comorbidities were assessed through clinical interviews, medical record reviews, and standardized tools including AUDIT-C, Fagerström Test for Nicotine Dependence, and the Binge Eating Scale. Psoriasis severity was evaluated using the Psoriasis Area and Severity Index (PASI). <b>Results:</b> Of 316 participants, 88 (27.8%) had psychiatric/behavioral comorbidities. The most frequent conditions were tobacco use disorder (11.1% overall; 39.8% among comorbid patients), alcohol use disorder (9.2%; 32.9%), binge eating (7.9%; 28.4%), anxiety (6.3%; 22.7%), and depression (4.1%; 14.8%). Additional diagnoses included personality disorders, dementia, PTSD, and sleep disorders. <b>Conclusions:</b> Psychiatric and behavioral comorbidities, particularly substance use disorders, are relatively common in patients with psoriasis. These findings support the need for regular mental health screening and integrated care approaches in psoriasis management.<p><a href="http://europepmc.org/article/MED/40428224?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">61</guid><pubDate>Sun, 01 Jun 2025 05:56:38 +0000</pubDate></item><item><title>Myeloid PGGT1B Deficiency Promotes Psoriasiform Dermatitis by Promoting the Secretion of Inflammatory Factors.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/myeloid-pggt1b-deficiency-promotes-psoriasiform-dermatitis-by-promoting-the-secretion-of-inflammatory-factors-r60/</link><description><![CDATA[Psoriasis pathogenesis involves dysregulated immune responses, yet the role of protein prenylation (particularly PGGT1B-mediated geranylgeranylation) in macrophage-driven inflammation remains poorly understood. This study aims to explore the role and molecular mechanism of protein geranylgeranyltransferase type I subunit beta (PGGT1B) in the development of psoriasis. Myeloid cell-specific PGGT1B gene knockout mice were generated, and a mouse psoriasis model was established with imiquimod to study the role and mechanism of PGGT1B gene downregulation-induced macrophage activation in the pathogenesis of psoriasis. Bone marrow-derived macrophages (BMDMs) from wild-type and PGGT1B knockout mice were cultured and stimulated with resiquimod (R848) to simulate the immune microenvironment of psoriasis. In addition, the differentially expressed genes induced by PGGT1B knockout were analyzed using RNA-seq, and bioinformatics analysis was carried out to study the possible biological process of PGGT1B regulation. Finally, PMA-THP-1 was co-cultured with HaCaT cells to study the effect of PGGT1B deletion in macrophages on the proliferation and differentiation of keratinocytes. Bone marrow PGGT1B deficiency aggravated the psoriasis-like lesions induced by imiquimod in mice. In BMDMs with PGGT1B deficiency, the NF-κB signaling pathway was over-activated by R848, and the expressions of proinflammatory cytokines IL-1β, IL-6, and TNF-α were significantly increased. Activation of cell division cycle 42 (CDC42) may mediate the activation of the NF-κB pathway in PGGT1B-deficient BMDMs. PGGT1B deletion can promote the proliferation and inhibit the differentiation of HaCaT cells. Reduced PGGT1B levels can increase the expression of CDC42, which further activates NLRP3 inflammation in macrophages through NF-κB signaling, further aggravating the inflammatory state of psoriasis. Psoriasis-like lesions induced by IMQ are aggravated when PGGT1B expression is reduced in mouse bone marrow cells. A possible mechanism for this is that PGGT1B-deficient macrophages migrate to the epidermis more easily during psoriasis, which leads to the activation of Cdc42, NF-κB signaling, and NLRP3 inflammatory corpuscles.<p><a href="http://europepmc.org/article/MED/40430037?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">60</guid><pubDate>Sun, 01 Jun 2025 05:56:38 +0000</pubDate></item><item><title>Novel ribosome biogenesis-related biomarkers and therapeutic targets identified in psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/novel-ribosome-biogenesis-related-biomarkers-and-therapeutic-targets-identified-in-psoriasis-r59/</link><description><![CDATA[Psoriasis is an immune-mediated chronic inflammatory disease. Increasing evidence suggests a close association between ribosome biogenesis (RiboSis) and the pathogenesis of psoriasis. However, the precise mechanisms remain unclear. We first obtained bulk transcriptome and single-cell RNA sequencing datasets from the GEO database. Subsequently, differential expression analysis (DEG) and weighted gene co-expression network analysis (WGCNA) were performed, preliminarily identifying 11 candidate biomarkers. Protein-protein interaction (PPI) analysis revealed that these biomarkers are primarily involved in protein synthesis, regulation of gene expression, and control of the cell cycle and growth. Consensus clustering analysis combined with immune infiltration analysis revealed that the candidate biomarkers were strongly associated with innate immune cells, such as NK cells, mast cells, and monocytes, and were more closely linked to signaling pathways related to cell proliferation, cell cycle, inflammation, and glycolysis. From the 11 candidate biomarkers, we selected MPHOSPH6 and ISG20 (exhibiting the highest fold-changes) for external dataset validation, scRNA-seq analysis, and in vivo expression verification. Subsequently, potential therapeutic compounds targeting these biomarkers were predicted and validated via molecular docking. Collectively, our findings not only substantiate the critical role of RiboSis in psoriasis pathogenesis but also provide a framework for developing targeted therapeutic strategies.<p><a href="http://europepmc.org/article/MED/40425712?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">59</guid><pubDate>Sun, 01 Jun 2025 05:56:38 +0000</pubDate></item><item><title>Treatment with spesolimab in patients with generalized pustular psoriasis: A review of real-world experience.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/treatment-with-spesolimab-in-patients-with-generalized-pustular-psoriasis-a-review-of-real-world-experience-r58/</link><description><![CDATA[Generalized pustular psoriasis (GPP) is a potentially life-threatening infrequent immune-mediated disease characterized by rapid-onset of erythematous plaques, sterile pustules, and systemic inflammation. Spesolimab, a monoclonal antibody targeting the interleukin-36 receptor, is a novel treatment for GPP. However, GPP's low incidence and limited evidence represents a challenge in determining its real-world efficacy. This review aims to explore the clinical use of spesolimab in a real-world setting. We conducted a review on PubMed, SCOPUS, EMBASE, and ScienceDirect of case series and reports of patients with GPP treated with spesolimab. Review articles and clinical trials were excluded. A total of 62 patients with GPP were included. Age ranged from 4 to 88 years. A total of 48 reported comorbidities of which 30 patients had plaque psoriasis. Spesolimab 900 mg IV was administered in 1 to 4 doses. Follow-up periods ranged from 2 weeks to 15 months. Complete GPP remission was observed in 35 (56.4%, 35/62) patients, 21 of them achieving it within a week. Partial remission was defined in 27 (43.5%) patients. GPP recurrence after treatment was observed in seven patients. After spesolimab administration, plaque psoriasis recurrence was reported in six (20%, 6/30) patients, three (10%, 3/30) reported improvement, and 21 (70%, 21/30) didn't report information about their outcome. Eight patients reported adverse effects including laboratory abnormalities, infections, and erythema multiforme. Spesolimab demonstrates a low prevalence of adverse events and clinical efficacy for GPP treatment including patients with comorbidities, infections, and over 75 years of age. Its effect on plaque psoriasis remains unclear.<p><a href="http://europepmc.org/article/MED/40444369?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">58</guid><pubDate>Sat, 31 May 2025 17:47:51 +0000</pubDate></item><item><title>Oral Peptide Therapeutics as an Emerging Treatment Modality in Immune-Mediated Inflammatory Diseases: A Narrative Review.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/oral-peptide-therapeutics-as-an-emerging-treatment-modality-in-immune-mediated-inflammatory-diseases-a-narrative-review-r57/</link><description><![CDATA[Immune-mediated inflammatory diseases (IMIDs), such as psoriasis, psoriatic arthritis, and inflammatory bowel disease, encompass a heterogenous group of conditions associated with chronic inflammation. Systemic treatments for patients with IMIDs include parenterally delivered monoclonal antibodies (mAbs) that disrupt specific cytokine and cytokine receptor binding interactions, and orally delivered small molecules that inhibit certain enzymes involved in the regulation of inflammatory signaling. Many patients prefer oral alternatives to injectables, but currently available oral advanced therapies are less effective than mAbs and/or have tolerability concerns. Thus, an unmet need exists for additional oral treatment options for patients with IMIDs. Therapeutic peptides can be designed to possess characteristics that provide both the target selectivity typically associated with parenterally delivered mAbs and an oral route of administration. Oral peptide therapeutics are an area of intense research in several therapeutic areas, and, although some oral peptides are available for certain indications, such as diabetes, there are currently no targeted oral peptides available for the treatment of patients with IMIDs. Icotrokinra (JNJ-77242113), which is currently in development to treat patients with various IMIDs, is the first targeted oral peptide designed to selectively inhibit interleukin (IL)-23 signaling by blocking the IL-23 receptor on human immune cells. In a phase 2b study in adults with moderate-to-severe psoriasis, icotrokinra showed a significant dose-response effect versus placebo, and a tolerable safety profile at Week 16. Sustained skin clearance and no safety signals were observed through Week 52 in the extension study to the phase 2b study. Ongoing phase 2 and phase 3 clinical studies in patients with psoriasis, psoriatic arthritis, and ulcerative colitis will provide data to inform the therapeutic potential of icotrokinra to address the unmet need in these diseases.<p><a href="http://europepmc.org/article/MED/40439953?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">57</guid><pubDate>Sat, 31 May 2025 17:47:51 +0000</pubDate></item><item><title>Early Peripheral Psoriatic Arthritis: Baseline Features of the First 186 Patients in the French Nationwide APACHE Cohort.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/early-peripheral-psoriatic-arthritis-baseline-features-of-the-first-186-patients-in-the-french-nationwide-apache-cohort-r56/</link><description><![CDATA[To describe the design and methodology of APACHE, a cohort of patients with early peripheral psoriatic arthritis (pPsA), and to assess the main baseline clinical characteristics of the first included patients. APACHE is an ongoing prospective multicentre national cohort (NCT03768271) with a planned follow-up of 10 years. Included patients have recent-onset (&lt;12 months) peripheral arthritis, a personal and/or family history of psoriasis, pPsA diagnosed by a rheumatologist, and no history of targeted disease-modifying antirheumatic drug therapy. At inclusion, demographic data, disease activity, comorbidities, and imaging results (not reported here) are collected. A descriptive analysis of these data was performed. The 186 study patients had a mean age of 44±11 years and mean arthritis duration of 6±4 months; 84 (45%) were women; 169 (91%) had a history of psoriasis (mean duration, 14 years) and 71 (38%) were receiving methotrexate. Disease activity was moderate with a mean DAPSA score of 19±14 and mean swollen and tender joint counts of 2.1±3.2 and 6.0±8.0, respectively. The initially involved joints were mainly the hands (40%) and knees (28%). Entheseal pain (39%) was more prevalent than dactylitis (27%). Comorbidities were common, with obesity in 27% and at least one cardiovascular risk factor or disease in 49% of patients. Patients with early peripheral PsA had moderate disease activity, a predominant oligoarticular profile, and a high prevalence of entheseal pain.<p><a href="http://europepmc.org/article/MED/40441347?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">56</guid><pubDate>Sat, 31 May 2025 17:47:51 +0000</pubDate></item></channel></rss>
