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Introduction: Ankylosing spondylitis (AS) presents as a debilitating form of arthritis with potential for severe damage. In chronic cases, patients may experience progression to ankylosis and spinal immobility, significantly diminishing their quality of life. Given these challenges, there is a pressing need to explore novel diagnostic targets. Thus, this study aimed to evaluate the diagnostic potential of long non-coding RNAs (lncRNAs) for AS.
Methods: The search encompassed various databases including PubMed, Scopus, Embase, and Hinari. Analysis of pooled sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), and area under the curve (AUC) was carried out using Stata 17.0 software, employing a random effects model. Heterogeneity among studies was assessed through the Cochran-Q test and I2 statistic tests, followed by subgroup analyses to delve into primary sources of heterogeneity. Publication bias was assessed using Deeks' funnel plot, while Fagan's nomogram was used to evaluate the clinical utility of lncRNAs for AS. Furthermore, a sensitivity analysis was conducted to assess the robustness and reliability of the findings.
Results: This systematic review and meta-analysis synthesized data from 11 articles, of which 6 were included in the meta-analysis. The pooled sensitivity, specificity, PLR, NLR, DOR, and AUC of lncRNAs for diagnosing AS were calculated as 0.81 (95% CI, 0.73-0.88), 0.81 (95% CI, 0.55-0.93), 4.2 (95% CI, 1.64-10.77), 0.23 (95% CI, 0.17-0.32), 18.1 (95% CI, 6.39-51.24), and 0.86 (95% CI, 0.83-0.89), respectively. Furthermore, subgroup analysis revealed that lncRNAs identified in peripheral blood mononuclear cells (PMBCs), those showing upregulation, studies utilizing β-actin as the internal reference control, and research involving AS patients from China demonstrated enhanced diagnostic accuracy for AS.
Conclusions: In conclusion, the existing evidence indicates that lncRNAs have substantial diagnostic value in predicting AS and can serve as effective non-invasive markers for the condition. However, the results should undergo further validation through well-designed longitudinal studies with larger sample sizes in the future to enhance their reliability and generalizability.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12303277 | PMC |
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0328249 | PLOS |
J Neurosurg Spine
September 2025
1Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.
Objective: The evidence on ankylosing spinal disorders (ASDs), including ankylosing spondylitis (AS) and diffuse idiopathic skeletal hyperostosis (DISH), in the context of spinal fracture stems from studies with relatively small sample sizes. There are no studies addressing the patient-reported outcome measures (PROMs) and health-related quality of life (HRQOL) outcomes associated with spinal fracture in this population. The aim of this study was to investigate differences in complications, mortality, PROMs, and HRQOL in patients with and without ASD who had been treated for spinal fracture.
View Article and Find Full Text PDFInt Forum Allergy Rhinol
September 2025
Division of Otolaryngology Head & Neck Surgery, University of British Columbia, Vancouver, British Columbia, Canada.
Background: Emerging evidence suggests a possible link between rhinosinusitis and systemic rheumatic diseases; however, no meta-analysis has comprehensively examined this association to date. We aimed to investigate if patients with rhinosinusitis have a predisposition to unmasking rheumatic diseases compared to individuals without rhinosinusitis.
Methods: A comprehensive search in MEDLINE, Embase, Cochrane Library, and Web of Science was conducted until February 2025 for studies characterizing rheumatic disease incidence, prevalence, and risk in cohorts of rhinosinusitis patients.
Drugs
September 2025
Research Unit in Public Health, Epidemiology and Health Economics, University of Liege, Liege, Belgium.
Objectives: Our objective was to systematically synthesize and evaluate the existing evidence from meta-syntheses (systematic reviews and meta-analyses) reporting on the safety of celecoxib in adults with chronic musculoskeletal disorders.
Methods: We conducted a comprehensive literature search in November 2024 across MEDLINE, Cochrane Central, and Scopus databases, following Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2020 guidelines for umbrella reviews. Only systematic reviews and meta-analyses involving celecoxib safety in osteoarthritis, rheumatoid arthritis, or ankylosing spondylitis were included.
Acta Derm Venereol
September 2025
Evidence-based Medicine Center, Chung Shan Medical University Hospital, Taichung, Taiwan; Orthopedics Department, Chi-Mei Medical Center, Tainan, Taiwan; Institute of Allergology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin,
Prurigo nodularis (PN) has been associated with autoimmune diseases, though longitudinal data are limited. This study investigates the risk of autoimmune disease development in PN patients using a global electronic health record database. This retrospective cohort study analysed data from the Global Collaborative Network within the TriNetX research network.
View Article and Find Full Text PDFMicrob Cell
August 2025
Department of Biological and Morphofunctional Sciences, College of Medicine and Biological Science, Stefan cel Mare University of Suceava, 720229 Suceava, Romania.
Ankylosing spondylitis (AS) is a chronic inflammatory disease with complex pathogenesis influenced by genetic, immunological and environmental factors. Recent evidence suggests that gut microbiota significantly contributes to AS etiopathogenesis. Dysbiosis and altered immune responses in the gut potentially trigger or exacerbate the disease through intestinal barrier disruption, alteration of the IL-23/17 axis and metabolite production.
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