IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0328249.html
   My bibliography  Save this article

Diagnostic value of long noncoding RNAs as biomarkers for Ankylosing Spondylitis: A systematic review and meta-analysis

Author

Listed:
  • Ermiyas Alemayehu
  • Sintayehu Ambachew
  • Daniel Asmelash
  • Melaku Ashagrie Belete

Abstract

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.

Suggested Citation

  • Ermiyas Alemayehu & Sintayehu Ambachew & Daniel Asmelash & Melaku Ashagrie Belete, 2025. "Diagnostic value of long noncoding RNAs as biomarkers for Ankylosing Spondylitis: A systematic review and meta-analysis," PLOS ONE, Public Library of Science, vol. 20(7), pages 1-15, July.
  • Handle: RePEc:plo:pone00:0328249
    DOI: 10.1371/journal.pone.0328249
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0328249
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0328249&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0328249?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0328249. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.