Association of circulating miR-223 and miR-16 with disease activity in patients with early rheumatoid arthritis
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
20088
Versus Arthritis - United Kingdom
20088
Arthritis Research UK - United Kingdom
19791
Versus Arthritis - United Kingdom
19791
Arthritis Research UK - United Kingdom
MR/K00414X/1
Medical Research Council - United Kingdom
PubMed
23897768
PubMed Central
PMC4173742
DOI
10.1136/annrheumdis-2012-202815
PII: S0003-4967(24)09867-4
Knihovny.cz E-zdroje
- Klíčová slova
- DAS28, Early Rheumatoid Arthritis, Rheumatoid Arthritis,
- MeSH
- antirevmatika terapeutické užití MeSH
- biologické markery krev metabolismus MeSH
- časná diagnóza MeSH
- dospělí MeSH
- exprese genu MeSH
- fibroblasty metabolismus MeSH
- kultivované buňky MeSH
- lidé středního věku MeSH
- lidé MeSH
- mikro RNA biosyntéza krev genetika MeSH
- následné studie MeSH
- počet leukocytů MeSH
- prognóza MeSH
- revmatoidní artritida diagnóza farmakoterapie genetika MeSH
- senioři MeSH
- studie případů a kontrol MeSH
- stupeň závažnosti nemoci MeSH
- synoviální membrána metabolismus patologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antirevmatika MeSH
- biologické markery MeSH
- mikro RNA MeSH
- MIRN16 microRNA, human MeSH Prohlížeč
- MIRN223 microRNA, human MeSH Prohlížeč
BACKGROUND: Identification of parameters for early diagnosis and treatment response would be beneficial for patients with early rheumatoid arthritis (ERA) to prevent ongoing joint damage. miRNAs have features of potential biomarkers, and an altered expression of miRNAs was shown in established rheumatoid arthritis (RA). OBJECTIVE: To analyse RA associated miRNAs in the sera of patients with ERA to find markers of early disease, clinical activity or predictors of disease outcome. METHODS: Total RNA was isolated from whole sera in ERA patients (prior to and after 3 and 12 months of therapy with disease modifying antirheumatic drugs), in patients with established RA and in healthy controls (HC) using phenol-chloroform extraction. Expression of miR-146a, miR-155, miR-223, miR-16, miR-203, miR-132 and miR-124a was analysed by TaqMan Real Time PCR. RESULTS: From all analysed miRNAs, levels of miR-146a, miR-155 and miR-16 were decreased in the sera of ERA patients in comparison with established RA. A change in circulating miR-16 in the first 3 months of therapy was associated with a decrease in DAS28 in long term follow-up in ERA (p=0.002). Levels of circulating miR-223 in treatment naïve ERA correlated with C reactive protein (p=0.008), DAS28 (p=0.031) and change in DAS28 after 3 months (p=0.003) and 12 months (p=0.011) of follow-up. However, neither miR-16 nor miR-223 could distinguish ERA from HC. CONCLUSIONS: Differential expression of circulating miR-146a, miR-155 and miR-16 in the sera of ERA patients may characterise an early stage of the disease. We suggest miR-223 as a marker of disease activity and miR-16 and miR-223 as possible predictors for disease outcome in ERA.
Centre of Experimental Rheumatology University Hospital Zurich Zurich Switzerland
Royal Orthopaedic Hospital Birmingham NHS Foundation Trust Birmingham UK
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Is there a potential of circulating miRNAs as biomarkers in rheumatic diseases?