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Erschienen in: Autoimmunity Highlights 1-2/2015

Open Access 01.08.2015 | Original Article

Decreased serum cell-free DNA levels in rheumatoid arthritis

verfasst von: Marina Dunaeva, Bastiaan C. Buddingh’, René E. M. Toes, Jolanda J. Luime, Erik Lubberts, Ger J. M. Pruijn

Erschienen in: Autoimmunity Highlights | Ausgabe 1-2/2015

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Abstract

Purpose

Recent studies have demonstrated that serum/plasma DNA and RNA molecules in addition to proteins can serve as biomarkers. Elevated levels of these nucleic acids have been found not only in acute, but also in chronic conditions, including autoimmune diseases. The aim of this study was to assess cell-free DNA (cfDNA) levels in sera of rheumatoid arthritis (RA) patients compared to controls.

Methods

cfDNA was extracted from sera of patients with early and established RA, relapsing-remitting multiple sclerosis patients (RRMS) and healthy subjects, and its concentration was determined by quantitative PCR using two amplicons, Alu115 and β-actin205, corresponding to Alu repetitive elements and the β-actin single-copy gene, respectively. Serum DNase activity was measured by a single radial enzyme diffusion method.

Results

Reduced levels of cfDNA were observed in patients with established RA in comparison with healthy controls, early RA patients and RRMS patients. There were no significant differences in cfDNA concentration between healthy controls, early RA and RRMS patients. Total DNase activity appeared to be similar in the sera of all tested groups.

Conclusions

Our results demonstrate that cfDNA levels are strongly reduced in the sera of established RA patients, which is not caused by changes in DNase activity. Measurement of cfDNA can distinguish established RA patients from early RA patients. Thus, cfDNA may serve as a biomarker in RA.
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Metadaten
Titel
Decreased serum cell-free DNA levels in rheumatoid arthritis
verfasst von
Marina Dunaeva
Bastiaan C. Buddingh’
René E. M. Toes
Jolanda J. Luime
Erik Lubberts
Ger J. M. Pruijn
Publikationsdatum
01.08.2015
Verlag
Springer International Publishing
Erschienen in
Autoimmunity Highlights / Ausgabe 1-2/2015
Print ISSN: 2038-0305
Elektronische ISSN: 2038-3274
DOI
https://doi.org/10.1007/s13317-015-0066-6

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