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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/8/?d=1</link><description>Neue Studien: Europe PMC</description><language>de</language><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><item><title>Role of real-world evidence from patient registries for psoriasis in decision-making: a systematic review.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/role-of-real-world-evidence-from-patient-registries-for-psoriasis-in-decision-making-a-systematic-review-r409/</link><description><![CDATA[<h4>Introduction</h4>Treatment of moderate to severe psoriasis typically requires the use of multiple systemic therapies over a patient's lifetime. The efficacy and safety of systemic treatments are typically evaluated in clinical trials; however, patient registries are increasingly used to monitor long-term outcomes of systemic therapies for psoriasis in real-world settings. Psoriasis registries also generate important real-world evidence about psoriasis treatment that may facilitate a greater understanding of outcomes outside of a controlled clinical trial setting. This study thus characterises the design and measures used in real-world studies of psoriasis treatment from patient registries and assesses its use in informing clinical guidelines and reimbursement decisions.<h4>Methods and analysis</h4>A systematic literature review was conducted to identify real-world observational studies that used psoriasis registry data. PubMed and Embase were searched for English-language studies published between January 2018 and January 2023. To assess how real-world studies, clinical guidelines, and reimbursement and coverage reports have informed practice, treatment, and reimbursement guidelines, a narrative review of recommendations was conducted. All results were screened by two independent reviewers (LP and TAS) using prespecified inclusion and exclusion criteria. Outcomes of interest were extracted into Excel, with all conflicts resolved through discussion/consensus. Tables displayed outcomes and research topics first by year, then by registry.<h4>Prospero registration number</h4>CRD42023402431.<p><a href="http://europepmc.org/article/MED/41526088?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">409</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item><item><title>Network pharmacology-based elucidation of the regulatory mechanism of Solanum lyratum (Bai Ying) against psoriasis via the IL-17A/STAT3 axis: Molecular docking and HaCaT cell validation.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/network-pharmacology-based-elucidation-of-the-regulatory-mechanism-of-solanum-lyratum-bai-ying-against-psoriasis-via-the-il-17astat3-axis-molecular-docking-and-hacat-cell-validation-r408/</link><description><![CDATA[<h4>Background</h4>Psoriasis affects approximately 2% of the global population, with the IL-17A-STAT3 pathway mediating abnormal keratinocyte proliferation and inflammatory amplification. Solanum lyratum (Bai Ying) has long been used for skin disorders, and its steroidal alkaloids have anti-inflammatory potential, though the mechanisms remain unclear.<h4>Objective</h4>To elucidate the molecular basis and cytological efficacy of S. lyratum steroidal alkaloids in exerting anti-psoriatic effects via the IL-17A/STAT3 axis.<h4>Methods</h4>HPLC-MS-QTOF, network pharmacology, molecular simulation, and a HaCaT cell model with STAT3-siRNA assays were employed.<h4>Results</h4>Eighteen components were identified; steroidal alkaloids showed high affinity for STAT3 and IL17RA. S. lyratum (5-40 μg/mL) enhanced cell viability, inhibited p-STAT3 (IC50 = 14.30 μg/mL), and attenuated inflammatory responses and keratinocyte proliferation.<h4>Conclusion</h4>S. lyratum steroidal alkaloids exert dual-targeted blocking effects on the IL-17A/STAT3 axis, supporting it as a potential therapeutic candidate for psoriasis.<p><a href="http://europepmc.org/article/MED/41546581?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">408</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item><item><title>Beyond the skin: Lived experiences and coping strategies of psoriasis patients in Malaysia.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/beyond-the-skin-lived-experiences-and-coping-strategies-of-psoriasis-patients-in-malaysia-r407/</link><description><![CDATA[<h4>Background</h4>Psoriasis is a chronic autoimmune skin condition that significantly impacts an individual's quality of life, resulting in physical discomfort, psychological distress, and compromised social well-being. However, there is limited understanding regarding the challenges faced by patients in Malaysia. This study examines the lived experiences of patients with psoriasis in Malaysia, focusing on the emotional, social, financial, and treatment-related challenges they face, as well as the coping mechanisms they employ.<h4>Methods</h4>A qualitative, phenomenological approach was employed among members of the Psoriasis Association Malaysia. Purposive sampling was used to recruit adult participants who were capable of participating in the online interview. Data collection involved the use of Google Forms, which included the Malay version of the Dermatology Life Quality Index questionnaire, supplementing the qualitative findings. This was followed by semi-structured online interviews conducted via video conferencing. Thematic analysis was conducted using NVivo version 14, and descriptive analysis was performed using SPSS version 28.<h4>Result</h4>This study involved 30 respondents with a mean age of 44 years diagnosed with psoriasis. The mean (SD) for the duration of illness is 21.3 (11.8) years. About 70% respondents reported that psoriasis had a moderate to very high impact on their quality of life. Thematic analysis has identified six major themes, including physical devastation, emotional burden, disruption in social functioning, treatment hurdles and advancements, financial barriers, and behavioral adaptation.<h4>Conclusion</h4>Psoriasis imposes complex challenges that extend beyond physical symptoms, affecting emotional well-being, social interactions, financial stability, and treatment struggles. In response to the various challenges that arose, respondents developed behavioral adaptations to achieve a better quality of life. Framed within the biopsychosocial model, the findings emphasize the need for a holistic, patient-centred approach to psoriasis care that integrates medical treatment with psychological support and social interventions to improve overall quality of life.<p><a href="http://europepmc.org/article/MED/41544022?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">407</guid><pubDate>Sun, 25 Jan 2026 18:42:10 +0000</pubDate></item><item><title>Unsaturated Fatty Acid Metabolic Reprogramming in Psoriatic Skin Drives Inflammation and Predicts Response to Biologic Therapy.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/unsaturated-fatty-acid-metabolic-reprogramming-in-psoriatic-skin-drives-inflammation-and-predicts-response-to-biologic-therapy-r406/</link><description><![CDATA[<h4>Purpose</h4>Psoriasis is frequently associated with dyslipidemia, yet the role of specific unsaturated fatty acid (UFA) metabolic pathways in disease pathogenesis and treatment response remains poorly understood. This study aimed to characterize the landscape of UFA metabolic reprogramming in psoriasis and evaluate its clinical relevance for predicting response to biologic therapy.<h4>Patients and methods</h4>We performed an integrated multi-omics analysis incorporating transcriptomic data from human psoriatic lesions, single-cell RNA sequencing, and lipidomic profiling. Gene set variation analysis (GSVA) was used to evaluate UFA pathway activity. Logistic regression and LASSO were employed for biomarker selection and predictive modeling.<h4>Results</h4>We identified eight significantly dysregulated UFA metabolic pathways in psoriatic lesions, six of which were associated with key pathogenic processes in psoriasis. All pathways were reversibly modulated by biologic agents targeting TNF-α, IL-12/23, and IL-17A. We derived a three-gene biomarker signature (PLA2G4D, PLA2G4A, and FADS2) that robustly predicts response to IL-12/23 inhibition prior to treatment initiation (AUC = 0.902). Single-cell RNA sequencing revealed keratinocytes as the primary cellular contributors to UFA metabolism and identified an expanded PLA2G4D-high keratinocyte subpopulation in psoriatic skin, which was associated with the accumulation of Lysophosphatidylcholine (LysoPC) and Lysophosphatidylethanolamine (LysoPE).<h4>Conclusion</h4>Our findings elucidate the pathway-level metabolic basis of psoriasis inflammation and provide a clinically applicable tool for predicting response to biologic therapy. The results highlight the importance of UFA metabolic reprogramming in psoriatic pathogenesis and offer new avenues for treatment personalization.<p><a href="http://europepmc.org/article/MED/41445854?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">406</guid><pubDate>Mon, 29 Dec 2025 19:17:49 +0000</pubDate></item><item><title>Preparation of Tanshinone IIA and glycyrrhetinic acid emulsion and preliminary study on its anti-psoriasis efficacy.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/preparation-of-tanshinone-iia-and-glycyrrhetinic-acid-emulsion-and-preliminary-study-on-its-anti-psoriasis-efficacy-r405/</link><description><![CDATA[<h4>Aim</h4>The current work highlighted the preparation method of Tanshinone IIA, Glycyrrhetinic acid Emulsion with eutectic (GT-eEmu) and investigated its effectiveness in the internal and external treatment of psoriasis.<h4>Materials &amp; methods</h4>The optimal prescription ratios of the emulsions were screened based on single-factor and orthogonal experiments, in which the appearance, particle size, centrifugal stability, and placement stability of the emulsion were used as indicators. On this basis, the maximum drugs loading was determined and optimized by D-optimal. Then the gloss, consistency, uniformity, spreading, and centrifugal stability of the emulsion gel were used as indicators to screen the best preparation method of the emulsion gel. The gastrointestinal stability of GT-eEmu and the original drug was evaulated by the artificial gastrointestinal fluid test, while the irritation to the the gastrointestinal mucosa was investigated after treatment. In addition, the skin permeability and skin side effects of the preparation were studied. Finally, the therapeutic effects of various preparations on psoriasis in mice were studied based on PASI scores, HE pathological sections and the expression of SOCS1 and STAT3.<h4>Results</h4>The best optimized prescription of GT-eEmu was: oil phase 7%, emulsifier 4.5%, and emulsification temperature 60 ℃, where the drug loading of TSN IIA and GA were 0.17 and 0.70 g·L<sup>- 1</sup>. The best preparation method for GT-eEmu-Gel was to add carbomer 980 with 6% gel matrix to the emulsion prepared by the optimized method, followed by mixing with triethanolamine and adjusting the pH to 6.0-7.0 to prepare a 0.5% carbomer matrix emulsion. The gastrointestinal stability experiment showed that the addition of eutectic ingredients did not cause significant irritation to the gastrointestinal tract, while the good permeability and sustained release of GT-eEmu-Gel were shown by in vitro release assays and the emulsion gel form could further reduce the irritation of eutectic to the skin. Finally, imiquimod-induced psoriasis animal model experiments indicated that GT-eEmu and its gel could reduce the degree of skin lesions and histopathological changes in model mice, and decrease the average expression of SOCS1 and STAT3, which indicated these preparation had therapeutic effects on psoriasis. Additionally, the "internal and external treatment" group had the best effect compared with the oral-only group, while there was a significant difference (P &lt; 0.01) compared with the model group.<h4>Conclusion</h4>The preparation process of GT-eEmu and GT-eEmu-Gel is stable and quality-controlled, which can improve the oral bioavail ability of both drugs to different degrees and reduce the irritation to the skin. The results showed that they have certain therapeutic effects on psoriasi, which can be safely administered orally and applied externally on the skin. At the same time, compared with the single treatment, the "internal and external combined treatment" method was the most effective, which indicates the concept of "internal and external combined treatment" method has practical significance.<p><a href="http://europepmc.org/article/MED/41449306?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">405</guid><pubDate>Mon, 29 Dec 2025 19:17:49 +0000</pubDate></item><item><title>Prevalence of tobacco smoking and its association with disease severity and psoriatic arthritis among patients with nail psoriasis in China: a cross-sectional study.</title><link>https://www.psoriasis-news.de/articles.html/1_articles/prevalence-of-tobacco-smoking-and-its-association-with-disease-severity-and-psoriatic-arthritis-among-patients-with-nail-psoriasis-in-china-a-cross-sectional-study-r404/</link><description><![CDATA[<h4>Introduction</h4>Nail psoriasis is a common, treatment-refractory manifestation of psoriasis. Smoking is a key environmental factor implicated in nail and articular psoriasis. While smoking's association with cutaneous psoriasis is well-studied, its relationship with nail psoriasis remains less explored.<h4>Objective</h4>The primary objective of this study was to investigate the impact of smoking on the severity of nail psoriasis and arthritic psoriasis in patients with nail psoriasis.<h4>Methods</h4>Data from 1044 nail psoriasis patients within a population-based registry in China were analyzed. We assessed associations of smoking status and intensity with sociodemographics, disease severity and dermatology quality of life measures (including PASI, BSA, DLQI, and PEST scores), and PsA diagnosis. Analyses used SPSS 29.0; <i>p</i> &lt; 0.05 defined significance.<h4>Results</h4>The current smoking rate among patients with nail psoriasis is 34.6%, which is much higher than the current smoking rate among patients without nail psoriasis (20.2%). The proportions of the three different smoking intensities are also much higher than those among patients without nail psoriasis. Current smoking affects the total nail involvement count in patients with nail psoriasis, and severe smoking affects both the total nail involvement count and the nails with &gt; 90% area involvement count in these patients. However, we found that smoking intensity was negatively correlated with DLQI scores in nail psoriasis, which is contrary to previous studies on plaque psoriasis. Spearman's correlation analysis revealed that smoking intensity and smoking index were positively associated with total nail involvement count and individual nails &gt; 90% with area involvement count. In the regression analysis for PSA, the OR for current smokers was 0.57 (95% CI: 0.35-0.92) compared to non-smokers, and the OR for severe smokers was 0.37 (95% CI: 0.15-0.90) compared to mild smokers.<h4>Conclusion</h4>Patients with nail psoriasis have higher smoking rates and smoking intensity compared to those without nail psoriasis. The total nail involvement count was higher in current smokers than in non-smokers. Smoking intensity was positively associated with total nail involvement count and individual nails with &gt; 90% area involvement count. Current smoking was a negative associated factor for PEST risk level. Both current smoking and severe smoking were negative associations with the presence of psoriatic arthritis.<p><a href="http://europepmc.org/article/MED/41446844?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">404</guid><pubDate>Mon, 29 Dec 2025 19:17:49 +0000</pubDate></item></channel></rss>
