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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/9/?d=1</link><description>Neue Studien: Europe PMC</description><language>de</language><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><item><title>In vivo multiphoton microscopy of psoriasis: A new diagnosis and therapeutic monitoring technique.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/in-vivo-multiphoton-microscopy-of-psoriasis-a-new-diagnosis-and-therapeutic-monitoring-technique-r431/</link><description><![CDATA[<h4>Background and objectives</h4>Psoriasis is a chronic inflammatory skin disease, and noninvasive diagnostic tools are essential for accurate diagnosis and treatment monitoring. Multiphoton microscopy (MPM) enables real-time, noninvasive skin imaging with submicron resolution. This study evaluated the diagnostic accuracy of MPM in psoriasis and its potential application in therapeutic monitoring.<h4>Patients and methods</h4>This prospective observational study enrolled 34 patients with psoriasis. It comprised three parts: (1) analysis of imaging features of lesional and nonlesional skin using multiphoton microscopy (MPM; Transcend Vivoscope); (2) evaluation of the diagnostic performance of MPM parameters compared with reflectance confocal microscopy (RCM); and (3) prospective monitoring of 24 patients treated with Benvitimod (Tapinarof) cream for 8 weeks (T0/T1/T2).<h4>Results</h4>MPM detected psoriasis characteristics (including hyperkeratosis, parakeratosis, an absent stratum granulosum, enlarged nucleus diameter, and absent bright rimming) with comparable diagnostic efficiency to RCM (AUC = 0.838, p &lt; 0.001 vs. 0.824, p &lt; 0.001). Psoriatic lesions showed significant perinuclear fluorescence accumulation compared to healthy skin (p &lt; 0.001). All imaging features improved significantly after 8 weeks of treatment (p &lt; 0.001). PASI/TLS scores showed correlations with the epidermal thickness (r = 0.403/0.492, p &lt; 0.001), nuclear diameter (r = 0.4/0.375, p &lt; 0.001), and fluorescence intensity (r = -0.419/-0.492, p &lt; 0.001).<h4>Conclusions</h4>MPM is a novel and non-invasive imaging technique for psoriasis evaluation and treatment monitoring.<p><a href="http://europepmc.org/article/MED/41580911?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">431</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item><item><title>Clinical proof of concept for small molecule mediated inhibition of IL-17 in psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/clinical-proof-of-concept-for-small-molecule-mediated-inhibition-of-il-17-in-psoriasis-r430/</link><description><![CDATA[Efficacious and well-tolerated systemic, oral treatments for psoriasis are needed. We report preclinical and phase 1c (NCT06808815) results for DC-806, a small molecule interleukin (IL)-17 inhibitor, for the treatment of mild-to-moderate psoriasis. Preclinical results demonstrated DC-806 targets IL-17AA and IL-17AF with secukinumab-like therapeutic efficacy. In the phase 1c trial, 32 patients consented to receive twice daily (BID) doses of placebo or DC-806 (200 mg or 800 mg) for 28 days. No serious adverse events (SAEs) or discontinuations due to treatment-related adverse events (TRAEs) occurred. In an exploratory analysis, adjusted mean percentage reductions from baseline in psoriasis area and severity indices (PASI) at Day 29 were 43.7%, 15.1%, and 13.3% for 800 mg BID, 200 mg BID, and placebo arms, respectively (800 mg BID vs placebo, P value = 0.0008). DC-806 was found to be well tolerated with an acceptable safety profile and preliminary signals of clinical efficacy in mild-to-moderate psoriasis. EudraCT Identifier: 2021-002888-21.<p><a href="http://europepmc.org/article/MED/41575986?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">430</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item><item><title>Early maladaptive schemas, emotion regulation, coping with stress, quality of life, and psychological symptoms in psoriasis disease.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/early-maladaptive-schemas-emotion-regulation-coping-with-stress-quality-of-life-and-psychological-symptoms-in-psoriasis-disease-r429/</link><description><![CDATA[This study examined relationships between Early Maladaptive Schemas (EMS), emotion regulation, coping styles, and psoriasis outcomes in Istanbul, Turkey. Participants included 100 psoriasis patients (ages 25-45) and 107 healthy controls. Data were analyzed using structural equation modeling. Psoriasis patients scored significantly higher on six schemas: Emotional Deprivation, Approval Seeking, Pessimism, Self-Sacrifice, Punitiveness, and Unrelenting Standards (Cohen's d = 0.42-0.89). They also demonstrated greater emotion regulation difficulties and reduced adaptive coping. Mediation analyses revealed that maladaptive emotion-focused coping fully mediated relationships between EMS and quality of life deterioration (β = .11, 95% CI (.04, .19]) and psoriasis severity (β = .08, 95% CI [.02, .15]). Pessimism and Punitiveness schemas, impulse control difficulties, and maladaptive emotion-focused coping predicted general psychological symptom severity (measured by validated scales) (R<sup>2</sup> = .46). Findings suggest maladaptive emotion-focused coping as a key mechanism linking schemas to psoriasis outcomes, supporting integrated dermatological and psychological interventions.<p><a href="http://europepmc.org/article/MED/41581208?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">429</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item><item><title>The path to interception in psoriatic disease: from conceptual clarity to clinical translation.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/the-path-to-interception-in-psoriatic-disease-from-conceptual-clarity-to-clinical-translation-r428/</link><description><![CDATA[Psoriatic arthritis develops in up to one-third of individuals with psoriasis, typically following a prolonged subclinical phase. Diagnostic delays are common, often exceeding 2 years, and can result in irreversible joint damage. The growing recognition of this latent period has fuelled interest in earlier identification and interception. However, efforts are hampered by inconsistent definitions of early or subclinical psoriatic arthritis, insufficient prognostic tools, and an absence of consensus on the outcome for interception studies. This Review synthesises a rapidly evolving field, offering a framework organised around four crucial questions: first, what defines progression from psoriasis to psoriatic arthritis? Second, who is most at risk of transition? Third, how can progression be reliably measured using imaging, molecular biomarkers, or digital health technologies? Fourth, when should preventive intervention be considered? We critically examine new conceptual models, the limitations of existing classification criteria, advances in imaging and biomarker research, and the promise of digital phenotyping. Addressing the current challenges in definitions, risk stratification, measurement, and trial design is essential for the development of biologically grounded, ethically robust interception strategies.<p><a href="http://europepmc.org/article/MED/41587560?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">428</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item><item><title>Systemic Treatment Strategies for Patients with Psoriasis and Psoriatic Arthritis in the Setting of ANA Positivity or Lupus Spectrum Disease: A Comprehensive Systematic Review.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/systemic-treatment-strategies-for-patients-with-psoriasis-and-psoriatic-arthritis-in-the-setting-of-ana-positivity-or-lupus-spectrum-disease-a-comprehensive-systematic-review-r427/</link><description><![CDATA[Psoriasis and psoriatic arthritis (PsA) occasionally coexist with antinuclear antibody (ANA) positivity, cutaneous lupus erythematosus (CLE), or systemic lupus erythematosus (SLE), creating one of the most challenging therapeutic overlap scenarios in immunodermatology. Divergent immune pathways-IL-23/Th17-driven psoriatic inflammation versus type I interferon-mediated autoimmunity-generate unique vulnerabilities when systemic treatments are used. To synthesize treatment outcomes, lupus-related safety signals, and mechanistic insights across systemic therapies in patients with psoriasis or PsA who also exhibit ANA positivity, CLE, or SLE. A systematic review following PRISMA 2020 guidelines was conducted across PubMed/MEDLINE, Embase, the Cochrane Library, Scopus, and ClinicalTrials.gov from database inception through 31 October 2025. Thirty-three eligible reports (29 unique clinical studies; 1429 patients) were included and organized into six prespecified overlap subgroups. Mechanistic and translational studies-including ustekinumab and deucravacitinib SLE trial data and reports of IL-17 inhibitor-associated CLE-were reviewed separately to provide contextual interpretation. IL-23 inhibitors were consistently associated with a favorable cross-disease safety profile, with no clear signal for CLE worsening, SLE flares, or drug-induced autoimmunity. IL-17 inhibitors maintained strong psoriatic efficacy but were associated with an increased frequency of de novo or exacerbated CLE. TNF-α inhibitors showed the strongest association with ANA seroconversion, anti-dsDNA induction, drug-induced lupus, and lupus flares. Ustekinumab demonstrated a stable safety profile across lupus-spectrum disease despite variable efficacy in formal SLE trials. TYK2 inhibition provided dual modulation of IL-23 and type I interferon pathways and showed emerging utility in psoriasis or PsA coexisting with CLE or SLE. Apremilast, methotrexate, and mycophenolate mofetil remained reliable non-biologic systemic options. Phototherapy was associated with potential risk in ANA-positive or lupus-susceptible populations and therefore requires careful consideration. Interpretation is limited by the predominantly observational nature and heterogeneity of the available evidence. IL-23 inhibition and TYK2 inhibition appear to offer a balanced profile of efficacy and lupus-related safety in psoriatic disease complicated by lupus-spectrum autoimmunity. IL-17 inhibitors and TNF-α inhibitors may be associated with higher risk in CLE- or SLE-prone patients and therefore warrant particular caution. Personalized treatment strategies should integrate the relative dominance of psoriatic versus lupus disease, ANA/ENA profile, CLE subtype, and underlying mechanistic considerations. Prospective, biomarker-driven studies are needed to guide therapy in this increasingly recognized overlap population (PROSPERO registration: CRD420251241279).<p><a href="http://europepmc.org/article/MED/41596733?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">427</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item><item><title>Differential clinical factors influencing the effectiveness of distinct biologic agents in psoriasis: insights from a prospective cohort study in China.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/differential-clinical-factors-influencing-the-effectiveness-of-distinct-biologic-agents-in-psoriasis-insights-from-a-prospective-cohort-study-in-china-r426/</link><description><![CDATA[<h4>Objective and design</h4>This prospective multicenter cohort study was conducted to identify and compare clinical factors associated with the effectiveness of commonly used biologics in Chinese patients with moderate-to-severe psoriasis.<h4>Subjects</h4>Patients from the SPEECH registry initiating treatment with ixekizumab, secukinumab, guselkumab, or ustekinumab were included.<h4>Treatment</h4>Guideline-recommended dosing; 3-month follow-up.<h4>Methods</h4>The primary endpoint was PASI90 response at 3 months. Multivariable logistic regression estimated adjusted odds ratios (aORs) and 95% confidence intervals (CIs) for clinical predictors of treatment response.<h4>Results</h4>A total of 717 patients were included in the analysis. In guselkumab-treated patients, obesity (aOR 0.22, 95% CI 0.06-0.78) and prior biologic exposure (aOR 0.22, 95% CI 0.06-0.75) were independently associated with reduced PASI90 response. Psoriatic arthritis predicted poorer response to ustekinumab (aOR 0.16, 95% CI 0.03-0.78). For secukinumab, male sex reduced the likelihood of PASI90 (aOR 0.47, 95% CI 0.23-0.96), whereas family history of psoriasis improved outcomes (aOR 2.20, 95% CI 1.10-4.42). In ixekizumab-treated patients, obesity (aOR 0.38, 95% CI 0.18-0.80) was a negative predictor, while family history (aOR 2.79, 95% CI 1.22-6.38) enhanced treatment response.<h4>Conclusions</h4>Predictors of biologic effectiveness differ by agent, supporting personalized treatment based on patient characteristics.<p><a href="http://europepmc.org/article/MED/41591532?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">426</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item><item><title>Impact of treatment interruption on the efficacy and safety of vunakizumab in patients with moderate-to-severe plaque psoriasis: a post-hoc analysis of a phase 3 trial</title><link>https://www.psoriasis-news.de/articles.html/1_articles/impact-of-treatment-interruption-on-the-efficacy-and-safety-of-vunakizumab-in-patients-with-moderate-to-severe-plaque-psoriasis-a-post-hoc-analysis-of-a-phase-3-trial-r425/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12855095?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">425</guid><pubDate>Tue, 03 Feb 2026 08:49:23 +0000</pubDate></item><item><title>Do Nails Tell a Pulmonary Tale? A Cross-Sectional Study on Psoriasis and Pulmonary Hypertension Risk.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/do-nails-tell-a-pulmonary-tale-a-cross-sectional-study-on-psoriasis-and-pulmonary-hypertension-risk-r416/</link><description><![CDATA[<h4>Background</h4>Psoriasis is a systemic inflammatory disease associated with cardiopulmonary comorbidities. Nail psoriasis, quantified by the Nail Psoriasis Severity Index (NAPSI), is a marker of severe disease. While pulmonary arterial hypertension (PAH) is reported more frequently in psoriasis, the specific correlation between nail psoriasis severity and PAH remains underexplored.<h4>Objective</h4>To investigate the correlation between NAPSI scores and the presence or severity of PAH in patients with psoriasis.<h4>Methods</h4>A prospective, cross-sectional study was conducted at a tertiary care centre involving 100 patients with chronic plaque psoriasis (50 with and 50 without nail psoriasis). All participants underwent dermatological evaluation [Psoriasis Area and Severity Index (PASI) and NAPSI scoring], transthoracic echocardiography to estimate pulmonary artery systolic pressure (PASP), and measurement of inflammatory markers [C-reactive protein (CRP), IL-17, TNF-α]. PAH was defined as PASP &gt; 35 mmHg. Statistical analyses included correlation tests, comparative analyses, and multivariate logistic regression.<h4>Results</h4>PAH was identified in 29% (n = 29) of patients, with a significantly higher prevalence in the nail psoriasis group (40% vs 18%, <i>P</i> = .01). Patients with PAH had higher mean NAPSI scores than those without (29.5 ± 13.4 vs 18.2 ± 10.6, <i>P</i> = .001). A moderate positive correlation was found between NAPSI scores and PASP (<i>r</i> = 0.44, <i>P</i> &lt; .001). PASI scores and CRP levels were also significantly elevated in patients with PAH and correlated with PASP (<i>r</i> = 0.38, <i>P</i> = .001 and <i>r</i> = 0.41, <i>P</i> &lt; .001, respectively).Multivariate analysis confirmed NAPSI score as an independent predictor of PAH [odds ratio (OR): 1.07/unit increase, 95% CI: 1.03-1.11, <i>P</i> = .002], after adjusting for confounders including PASI score and comorbidities. PASI (OR: 1.05, <i>P</i> = .01) and CRP (OR: 1.13, <i>P</i> = .008) were also independent predictors. Nail matrix involvement was more strongly associated with PAH than nail bed involvement (<i>P</i> = .03). Inflammatory markers (CRP, IL-17, TNF-α) were significantly elevated in patients with PAH.<h4>Conclusion</h4>NAPSI scores, PASI scores, and CRP levels are all significantly correlated with and independently predict PAH in patients with psoriasis. Assessment of nail psoriasis severity may serve as a valuable, noninvasive clinical tool to identify psoriasis patients at increased risk of pulmonary vascular complications, warranting further cardiological evaluation.<p><a href="http://europepmc.org/article/MED/41526803?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">416</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item><item><title>Outcomes in Patients with Psoriasis Following Apremilast Treatment: Results from the German Psoriasis Registry PsoBest.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/outcomes-in-patients-with-psoriasis-following-apremilast-treatment-results-from-the-german-psoriasis-registry-psobest-r415/</link><description><![CDATA[<h4>Introduction</h4>The German national psoriasis registry PsoBest collects long-term data on the effectiveness, safety, and tolerability of systemic treatments for psoriatic disease. Here, we describe patient characteristics and the safety and effectiveness of apremilast for the treatment of psoriatic disease in Germany based on data from PsoBest.<h4>Methods</h4>This was a descriptive analysis of observational data collected from PsoBest using cross-sectional (baseline characteristics) and longitudinal (outcomes, safety) designs. PsoBest recruits patients with moderate to severe plaque psoriasis or psoriatic arthritis who initiate a new systemic psoriasis treatment. Adverse events (AEs) and sociodemographic descriptors were reported for patients exposed to apremilast during the study period (safety cohort). Clinical and patient-reported outcomes were collected 3, 6, and 12 months after the initiation of apremilast monotherapy (outcomes cohort).<h4>Results</h4>From January 15, 2015 to June 30, 2020, 595 registry patients were exposed to apremilast; 417 were treated with apremilast monotherapy. Patients taking apremilast had a higher mean age and higher proportions of comorbidities such as cardiovascular or metabolic disease compared with those taking other nonbiologic systemic or biologic drugs. The most common nonserious AEs were drug ineffectiveness (14.1%), diarrhea (9.4%), nausea (7.1%), and headache (6.1%). The highest incidence rates of nonserious and serious AEs of special interest were for infections and infestations per system organ class (8.03/100 patient-years) and malignant or unspecified tumors (2.50/100 patient-years), respectively. Improvements in Dermatology Life Quality Index, patient-defined treatment benefits (Patient Benefit Index), body surface area, and Psoriasis Area and Severity Index were observed after 3, 6, and 12 months of apremilast treatment.<h4>Conclusions</h4>Patients in routine care treated with apremilast in the German PsoBest registry experienced treatment benefits and improved skin, psoriasis severity, and quality of life. Safety was consistent with the established safety profile. Apremilast is safe and effective for treating moderate to severe psoriatic disease.<p><a href="http://europepmc.org/article/MED/41537947?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">415</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item><item><title>Evaluating Risankizumab's Long-Term Effects in Psoriasis Using Optical Coherence Tomography.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/evaluating-risankizumabs-long-term-effects-in-psoriasis-using-optical-coherence-tomography-r414/</link><description><![CDATA[<h4>Introduction</h4>Psoriasis is a chronic inflammatory disease associated with multiple systemic comorbidities and reduced quality of life. Risankizumab, an interleukin (IL)-23 inhibitor, has demonstrated efficacy in achieving rapid and sustained skin clearance in moderate-to-severe psoriasis. However, its impact on chronic subclinical inflammation is less understood. Conventional clinical assessments like Psoriasis Area and Severity Index (PASI), Investigator's Global Assessment (IGA), and Body Surface Area (BSA) focus on evaluating visible symptoms and are limited in capturing underlying disease activity. Optical coherence tomography (OCT), a non-invasive imaging modality, offers real-time assessment of structural and vascular changes, providing valuable insights beyond the skin surface.<h4>Methods</h4>This sub-analysis of a prospective, single-center exploratory study included 22 patients with moderate-to-severe psoriasis treated with risankizumab. Clinical assessments (PASI, IGA, BSA) were conducted at baseline and weeks 2, 4, 16, 28, 40, and 52. OCT imaging performed at baseline and weeks 4, 16, and 52 evaluated epidermal thickness and vascular parameters (e.g., vessel density and diameter) in lesional and perilesional skin.<h4>Results</h4>By week 16, mean (95% confidence interval [CI]) PASI score decreased from 16.3 (11.6-21.1) at baseline to 3.5 (1.8-5.2), and BSA involvement from 24.7% (16.1-33.3) to 5.2% (1.9-8.4) (both p &lt; 0.001). By week 52, 86.7%, 73.3%, and 40.0% of patients achieved PASI 75, 90, and 100, respectively, and 93.3% achieved IGA 0/1. OCT showed lesional reductions in epidermal thickness (- 37.4%), vessel density (- 26.6% Δ area under the curve [AUC]), and vessel diameter (- 59.5% ΔAUC) over the 52-week period. Notably, vascular changes also occurred in uninvolved perilesional skin.<h4>Conclusion</h4>Risankizumab improved both clinical and OCT parameters over 52 weeks, emphasizing the importance of long-term therapy with benefits extending beyond visible improvement. OCT emerged as a valuable tool for assessing deep (vascular) treatment response, thereby supporting a more comprehensive understanding of therapeutic outcomes in psoriasis.<p><a href="http://europepmc.org/article/MED/41575605?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">414</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item><item><title>Dual biologic therapy in a patient with severe psoriasis and psoriatic arthritis, using guselkumab and bimekizumab: A case report and review of the literature.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/dual-biologic-therapy-in-a-patient-with-severe-psoriasis-and-psoriatic-arthritis-using-guselkumab-and-bimekizumab-a-case-report-and-review-of-the-literature-r413/</link><description><![CDATA[Dual biologic therapy is not often used in psoriasis and psoriatic arthritis due to cost and safety concerns, with limited literature supporting its use. We present a case of a 31-year-old man with severe plaque psoriasis and erosive psoriatic arthritis, refractory to multiple therapies. While guselkumab improved skin symptoms, joint inflammation persisted. Given the patient's reluctance to discontinue guselkumab and his poor response to prior therapies, bimekizumab was added. This combination led to near-complete skin clearance and significant joint improvement within 3 months, with sustained benefits and no adverse effects at 17 months. This case illustrates how targeting multiple points in the interleukin-23/interleukin-17 pathway can improve outcomes in patients unresponsive to monotherapy. Dual biologic therapy may be a viable option for select patients with complex disease, though further research is needed to evaluate its long-term safety and efficacy.<p><a href="http://europepmc.org/article/MED/41551112?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">413</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item><item><title>Exploration of shared gene signatures and molecular mechanisms between psoriasis and COVID-19: evidence from transcriptome data.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/exploration-of-shared-gene-signatures-and-molecular-mechanisms-between-psoriasis-and-covid-19-evidence-from-transcriptome-data-r412/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/41530290?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">412</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item><item><title>Psychometric Evaluation of Patients With Atopic Dermatitis and Comparison With Patients With Psoriasis</title><link>https://www.psoriasis-news.de/articles.html/1_articles/psychometric-evaluation-of-patients-with-atopic-dermatitis-and-comparison-with-patients-with-psoriasis-r411/</link><description><![CDATA[Abstract  <p>Atopic dermatitis and psoriasis are two dermatological diseases that affect the mental health of patients. The purpose of this research is to investigate the comparison of the psychometric characteristics of two groups of patients with psoriasis and atopic dermatitis respectively focusing on depression, personality, hostility and psychosomatic burden. Τhe sample was consisted by 100 patients with psoriasis and 40 patients with atopic dermatitis, respectively. Specific questionnaires were given for the psychometric evaluation of patients with atopic dermatitis and psoriasis. The Beck's Depression Inventory (BDI), the Eysenck Personality Questionnaire (EPQ) the Brief Symptom Inventory SCL-90 scale, and the HDHQ questionnaire (Psychometric Hostility and Direction of Hostility Questionnaire). Patients with atopic dermatitis have statistically significantly higher scores on the scale of somatization and paranoid ideation, while patients with psoriasis have statistically significantly higher scores on the scale of depression. On the personality scales, patients with atopic dermatitis have on average statistically significantly higher scores on the psychoticism scale and lower scores on the lying scale than the psoriatic patients. Patients with atopic dermatitis present statistically significantly higher scores on the scale of paranoid hostility than patients with psoriasis. Patients receiving medication as well as the interaction of disease group with receiving medication are statistically significantly related to the psychopathology index. Patients' scores on the psychotic scale of the EPQ are statistically significantly related to the duration of the illness and the patient group, gender and medication intake. The psychosocial effects of psoriasis and atopic dermatitis on patients' mental health are demonstrated in the present study based on patient scores on psychometric scales and psychopathology index.</p><p><a href="http://europepmc.org/article/PPR/PPR1146508?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">411</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item><item><title>Incidence rate and risk factors of arrhythmias in patients with psoriatic arthritis.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/incidence-rate-and-risk-factors-of-arrhythmias-in-patients-with-psoriatic-arthritis-r410/</link><description><![CDATA[<h4>Objectives</h4>To assess the incidence and risk factors for arrhythmias in patients with psoriatic arthritis (PsA).<h4>Methods</h4>We performed a cohort analysis of patients followed prospectively from 1994 to 2024. Participants were evaluated using standard protocols at 6-to-12-month intervals. The following events were assessed: (1) atrial tachyarrhythmia (including atrial fibrillation and supraventricular tachycardia); (2) ventricular tachyarrhythmia and (3) bradycardia/pacemaker. The cumulative incidence rate (CIR) of each arrhythmia was calculated. Cox proportional hazards models (reported as the current level HR (measured just prior to the event) and the adjusted mean HR) were fitted to assess the association between selected measures of PsA disease activity and the age of occurrence of arrhythmia events. Each model was adjusted for sex, PsA duration, cardiovascular risk factors and medications.<h4>Results</h4>A total of 1670 patients with PsA were analysed (80 atrial tachyarrhythmias, 17 bradyarrhythmias/pacemakers and 11 ventricular tachyarrhythmias). By age 70, the CIRs were 7.82%, 0.67% and 0.45% for atrial, ventricular and bradycardia, respectively. In multivariable analysis, remission/low versus high disease activity state was associated with lower risk of atrial tachyarrhythmia (current HR 0.49, 95% CI 0.26 to 0.92; adjusted mean HR 0.46, 95% CI 0.23 to 0.91). Similarly, a higher three-item Visual Analogue Scale (3-VAS) was associated with a higher risk of atrial tachyarrhythmia (current level HR 1.18, 95% CI 1.04 to 1.33; adjusted mean HR 1.22, 95% CI 1.04 to 1.44).<h4>Conclusions</h4>Higher PsA disease activity is associated with higher atrial tachyarrhythmia risk. These findings reinforce the importance of controlling inflammation in PsA to optimise cardiac health.<p><a href="http://europepmc.org/article/MED/41571321?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">410</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item></channel></rss>
