Association of Plasma miRNA-7-5p and miRNA-214-5p With Rheumatoid Arthritis Associated Interstitial Lung Disease

MakaleAçık ErişimScopus SJRQ3

Özet

Objective: Rheumatoid arthritis–associated interstitial lung disease (RA-ILD) is a major extra-articular complication contributing to increased morbidity and mortality. Circulating microRNAs (miRNAs) have emerged as potential non-invasive biomarkers in autoimmune diseases. This study aimed to evaluate whether plasma miRNA-7-5p and miRNA-214-5p are associated with the presence of RA-ILD and with radiological and functional indicators of pulmonary involvement. Methods: In this cross-sectional study, 58 RA patients (29 RA-ILD, 29 without ILD) and 30 matched healthy controls were included. RA-ILD was diagnosed by multidisciplinary assessment (HRCT and pulmonary function tests). Plasma miRNA levels were measured by qRT-PCR and analyzed using the 2^−ΔΔCT method. Diagnostic performance was evaluated by ROC analysis. Results: Plasma miRNA-7-5p and miRNA-214-5p levels were significantly higher in RA patients compared with healthy controls (p < 0.05 for both). Among RA patients, both miRNAs were significantly lower in those with ILD (p < 0.05). miRNA-7-5p demonstrated promising discriminatory performance for identifying RA-ILD (AUC = 0.87, 95% CI: 0.760–0.947; p < 0.001), whereas miRNA-214-5p showed modest accuracy (AUC = 0.676, 95% CI: 0.539–0.794; p = 0.01). In multivariable analysis, ILD presence was independently associated with decreased levels of both miRNAs. Neither miRNA correlated significantly with DAS28-CRP, disease duration, nor with radiological or functional severity parameters. Conclusion: Circulating miRNA-7-5p and miRNA-214-5p are associated with the presence of RA-ILD but do not reflect disease severity in this cohort. Larger prospective studies are required to validate their potential role as adjunctive biomarkers for RA-ILD detection and risk stratification.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/bayburt/12685Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1111/1756-185x.70820Yayıncı resmi DOI adresi
İndeks kayıtları
Kaydın indeks veri tabanlarındaki sayfası (aktarımda alınan kayıt numarasıyla). Erişim, indeksin kendi koşullarına bağlıdır.
Atıflar
Scopus
0
WoS
0
Her kaynağın kendi saydığı toplam atıf; aktarım ve zenginleştirme sırasında alındı.
Tam Kayıt
AlanDeğerDil
dc.contributor.authorSahinoğlu, Irem
dc.contributor.authorKarakas, Umit
dc.contributor.authorUslu, Sadettin
dc.contributor.authorKizilirmak, Deniz
dc.contributor.authorAcar, Emre Ali
dc.contributor.authorTasgöz, Filiz Cemre
dc.contributor.authorKacar, Mevlüt
dc.contributor.authorSülükcü, Seref
dc.contributor.authorSengül, Merve Türkegün
dc.contributor.authorErdal, Mehmet Emin
dc.contributor.authorGündüz, Ozgül Soysal
dc.date.accessioned2026-10-29T19:09:54.382211766Z
dc.date.available2026-10-29T19:09:54.382211766Z
dc.date.issued2026
dc.description.abstractObjective: Rheumatoid arthritis–associated interstitial lung disease (RA-ILD) is a major extra-articular complication contributing to increased morbidity and mortality. Circulating microRNAs (miRNAs) have emerged as potential non-invasive biomarkers in autoimmune diseases. This study aimed to evaluate whether plasma miRNA-7-5p and miRNA-214-5p are associated with the presence of RA-ILD and with radiological and functional indicators of pulmonary involvement. Methods: In this cross-sectional study, 58 RA patients (29 RA-ILD, 29 without ILD) and 30 matched healthy controls were included. RA-ILD was diagnosed by multidisciplinary assessment (HRCT and pulmonary function tests). Plasma miRNA levels were measured by qRT-PCR and analyzed using the 2^−ΔΔCT method. Diagnostic performance was evaluated by ROC analysis. Results: Plasma miRNA-7-5p and miRNA-214-5p levels were significantly higher in RA patients compared with healthy controls (p < 0.05 for both). Among RA patients, both miRNAs were significantly lower in those with ILD (p < 0.05). miRNA-7-5p demonstrated promising discriminatory performance for identifying RA-ILD (AUC = 0.87, 95% CI: 0.760–0.947; p < 0.001), whereas miRNA-214-5p showed modest accuracy (AUC = 0.676, 95% CI: 0.539–0.794; p = 0.01). In multivariable analysis, ILD presence was independently associated with decreased levels of both miRNAs. Neither miRNA correlated significantly with DAS28-CRP, disease duration, nor with radiological or functional severity parameters. Conclusion: Circulating miRNA-7-5p and miRNA-214-5p are associated with the presence of RA-ILD but do not reflect disease severity in this cohort. Larger prospective studies are required to validate their potential role as adjunctive biomarkers for RA-ILD detection and risk stratification.
dc.description.sponsorshipManisa Celal Bayar Üniversitesi, CBU, (2024‐037)
dc.description.sponsorshipManisa Celal Bayar Üniversitesi, CBU
dc.identifier.articlenumbere70820
dc.identifier.doi10.1111/1756-185x.70820
dc.identifier.eissn1756-185X
dc.identifier.issn1756-1841
dc.identifier.issue8
dc.identifier.pmcidPMC13454854
dc.identifier.pmid42572845
dc.identifier.scopus2-s2.0-105046781690
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/bayburt/12685
dc.identifier.volume29
dc.identifier.wosWOS:001844525900001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofInternational Journal of Rheumatic Diseases
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectbiomarkers
dc.subjectinterstitial lung disease
dc.subjectmicroRNAs
dc.subjectrheumatoid arthritis
dc.subject.classificationRheumatology
dc.subject.otherAdult
dc.subject.otherAged
dc.subject.otherArea Under Curve
dc.subject.otherArthritis, Rheumatoid
dc.subject.otherBiomarkers
dc.subject.otherCase-Control Studies
dc.subject.otherCirculating MicroRNA
dc.subject.otherCross-Sectional Studies
dc.subject.otherFemale
dc.subject.otherGenetic Markers
dc.subject.otherHumans
dc.subject.otherLung Diseases, Interstitial
dc.subject.otherMale
dc.subject.otherMicroRNAs
dc.subject.otherMiddle Aged
dc.subject.otherPredictive Value of Tests
dc.subject.otherRisk Factors
dc.subject.otherROC Curve
dc.subject.otherTomography, X-Ray Computed
dc.subject.otherUp-Regulation
dc.subject.other2 propanol
dc.subject.othermicroRNA
dc.subject.otherrheumatoid factor
dc.subject.otherbiological marker
dc.subject.otherMIRN214 microRNA, human
dc.subject.otherMIRN7-1 microRNA, human
dc.subject.otherArticle
dc.subject.otherautoimmune disease
dc.subject.otherblood sampling
dc.subject.otherchronic lung disease
dc.subject.othercontrolled study
dc.subject.othercross-sectional study
dc.subject.otherdiagnostic test accuracy study
dc.subject.otherdisease activity
dc.subject.otherdisease duration
dc.subject.otherdisease severity
dc.subject.otherforced vital capacity
dc.subject.otherhuman
dc.subject.otherinterstitial lung disease
dc.subject.otherlung function test
dc.subject.othermajor clinical study
dc.subject.othermetabolic disorder
dc.subject.othermorbidity
dc.subject.othermortality
dc.subject.otherpulmonologist
dc.subject.otherreal time polymerase chain reaction
dc.subject.otherreceiver operating characteristic
dc.subject.otherrheumatoid arthritis
dc.subject.otherrheumatologist
dc.subject.otherRNA extraction
dc.subject.othersix minute walk test
dc.subject.otherarea under the curve
dc.subject.otherblood
dc.subject.othercase control study
dc.subject.othercomplication
dc.subject.otherdiagnosis
dc.subject.otheretiology
dc.subject.othergenetic marker
dc.subject.othergenetics
dc.subject.otherpredictive value
dc.subject.otherrisk factor
dc.subject.otherupregulation
dc.subject.otherx-ray computed tomography
dc.titleAssociation of Plasma miRNA-7-5p and miRNA-214-5p With Rheumatoid Arthritis Associated Interstitial Lung Disease
dc.typeArticle
rdl.citation.scopus0
rdl.citation.wos0
rdl.departmentDivision of Rheumatology, Department of Internal Medicine, Manisa Celal Bayar University School of Medicine, Manisa, Turkey
rdl.departmentDepartment of Pharmacy Services, Health Services Vocational School, Bayburt University, Bayburt, Turkey
rdl.departmentDepartment of Pulmonary Medicine, Manisa Celal Bayar University School of Medicine, Manisa, Turkey
rdl.departmentDepartment of Biostatistics and Medical Informatics, Alanya Alaaddin Keykubat University Faculty of Medicine, Antalya, Turkey
rdl.departmentDepartment of Medical Biology and Genetics, Mersin University Faculty of Medicine, Mersin, Turkey
rdl.oa.statusgreen
rdl.oa.statuspreprint
rdl.oa.urlhttps://pmc.ncbi.nlm.nih.gov/articles/PMC13454854/pdf/APL-29-e70820.pdf
rdl.scopus.quartileQ3
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)