Today: Dec 26, 2024
RU / EN
Last update: Oct 30, 2024
Correlation between Joint Ultrasound Data and Clinical, Laboratory and Instrumental Indices in Patients with Rheumatoid Arthritis

Correlation between Joint Ultrasound Data and Clinical, Laboratory and Instrumental Indices in Patients with Rheumatoid Arthritis

Komarova E.B.
Key words: rheumatoid arthritis; synovial membrane; rheumatoid arthritis activity; arthroscopy.
2017, volume 9, issue 1, page 92.

Full text

html pdf
2119
2071

The aim of the investigation was to assess the correlation between the main ultrasound indices of joints and clinical, laboratory and instrumental indices in patients with rheumatoid arthritis (RA).

Materials and Methods. A total of 114 patients with RA underwent complex clinical, laboratory and instrumental examination, including clinical assessment of the patients’ health, according to RA activity index DAS28. Concentrations of C-reactive protein, TNF-α, anti-cyclic citrullinated peptide antibodies (ACPA), angiogenesis marker VEGF and proliferation factor FGF were measured using ELISA technique. Ultrasound examination of knee joints was carried out using ESAOTE MyLAB40 device (The Netherlands), the knee joint arthroscopy was performed using an arthroscope (Karl Storz, Germany) with a diameter of 2.4 mm and an angle of 30°. The synovial membrane samples were fixed in 10% buffered formalin solution, stained with hematoxylin and eosin and studied using Axiostar microscope (Carl Zeiss, Germany).

Results. There were established statistically significant correlations between the deterioration of ultrasound indices of synovitis, synovial membrane vascularization and the increase in the markers of immune-inflammatory RA activity and VEGF marker in the blood, which indicated decline in clinical assessment of the patients’ health. The increase in ultrasound indices of synovial membrane thickness, pannus, osteochondral erosions closely correlated with the increase in RA duration, high blood levels of C-reactive protein, ACPA and FGF, which also spoke of deterioration of the clinical indices of the disease and radiographic progression of joint destruction.

Conclusion. The intensity of immune-inflammatory, proliferative and destructive processes and the synovial membrane angiogenesis can be assessed by ultrasound examination of joints in RA patients. The data obtained provide the possibility of recommending the application of the non-invasive technique of synovial membrane ultrasound for diagnosis and monitoring treatment efficacy in RA patients instead of expensive invasive techniques.

  1. Hitchon C.A., El-Gabalawy H.S. The synovium in rheumatoid arthritis. Open Rheumatol J 2011; 5: 107–114, https://doi.org/10.2174/1874312901105010107.
  2. Dhaouadi T., Sfar I., Abelmoula L., Jendoubi-Ayed S., Aouadi H., Ben Abdellah T., Ayed K., Zouari R., Gorgi Y. Role of immune system, apoptosis and angiogenesis in pathogenesis of rheumatoid arthritis and joint destruction, a systematic review. Tunis Med 2007; 85(12): 991–998.
  3. Malemud C.J. Growth hormone, VEGF and FGF: involvement in rheumatoid arthritis. Clin Chim Acta 2007; 375(1–2): 10–19, https://doi.org/10.1016/j.cca.2006.06.033.
  4. Lyalina V.V., Shekhter A.B. Artroskopiya i morfologiya sinovitov [Arthroscopy and morphology of synovitis]. Moscow: Nauka; 2007; 108 p.
  5. Af Klint E., Catrina A.I., Matt P., Neregråd P., Lampa J., Ulfgren A.K., Klareskog L., Lindblad S. Evaluation of arthroscopy and macroscopic scoring. Arthritis Res Ther 2009; 11(3): R81, https://doi.org/10.1186/ar2714.
  6. Ten Cate D.F., Luime J.J., Swen N., Gerards A.H., De Jager M.H., Basoski N.M., Hazes J.M., Haagsma C.J., Jacobs J.W. Role of ultrasonography in diagnosing early rheumatoid arthritis and remission of rheumatoid arthritis — a systematic review of the literature. Arthritis Res Ther 2013; 15(1): R4, https://doi.org/10.1186/ar4132.
  7. Fukae J., Tanimura K., Atsumi T., Koike T. Sonographic synovial vascularity of synovitis in rheumatoid arthritis. Rheumatology (Oxford) 2014; 53(4): 586–591, https://doi.org/10.1093/rheumatology/ket311.
  8. Korobkova A.S., Agafonov A.V., Tuev A.V., Vasilets L.M., Khlynova O.V., Zhelobov V.G., Grigoriadi N.E. Possibilities of ultrasonography in assessment local inflammation in rheumatoid arthritis. Modern Problems of Science and Education 2013; 6. URL: http://www.science-education.ru/ru/article/view?id=11383.
  9. Kurzantseva O.M., Murashkovskiy A.L., Trofimov A.F., Fedorov V.I. Ultrasound differential diagnosis of deforming osteoarthrosis and rheumatoid arthritis in knee joint lesion. SonoAce International 2005; 13: 78–81. URL: http://www.medison.ru/si/art198.htm .
  10. Ozgocmen S., Ozdemir H., Kiris A., Bozgeyik Z., Ardicoglu O. Clinical evaluation and power Doppler sonography in rheumatoid arthritis: evidence for ongoing synovial inflammation in clinical remission. South Med J 2008; 101(3): 240–245, https://doi.org/10.1097/SMJ.0b013e318164e16a.
  11. Hama M., Uehara T., Takase K., Ihata A., Ueda A., Takeno M., Shizukuishi K., Tateishi U., Ishigatsubo Y. Power Doppler ultrasonography is useful for assessing disease activity and predicting joint destruction in rheumatoid arthritis patients receiving tocilizumab — preliminary data. Rheumatol Int 2012; 32(5): 1327–1333, https://doi.org/10.1007/s00296-011-1802-5.
  12. Zufferey P., Möller B., Brulhart L., Tamborrini G., Scherer A., Finckh A., Ziswiler H.R. Persistence of ultrasound synovitis in patients with rheumatoid arthritis fulfilling the DAS28 and/or the new ACR/EULAR RA remission definitions: results of an observational cohort study. Joint Bone Spine 2014; 81(5): 426–432, https://doi.org/10.1016/j.jbspin.2014.04.014.
  13. Ramírez J., Ruíz-Esquide V., Pomés I., Celis R., Cuervo A., Hernández M.V., Pomés J., Pablos J.L., Sanmartí R., Cañete J.D. Patients with rheumatoid arthritis in clinical remission and ultrasound-defined active synovitis exhibit higher disease activity and increased serum levels of angiogenic biomarkers. Arthritis Res Ther 2014; 16(1): R5, https://doi.org/10.1186/ar4431.
  14. Dougados M., Devauchelle-Pensec V., Ferlet J.F., Jousse-Joulin S., D’Agostino M.A., Backhaus M., Bentin J., Chalès G., Chary-Valckenaere I., Conaghan P., Wakefield R.J., Etchepare F., Gaudin P., Grassi W., van der Heijde D., Mariette X., Naredo E., Szkudlarek M. The ability of synovitis to predict structural damage in rheumatoid arthritis: a comparative study between clinical examination and ultrasound. Ann Rheum Dis 2013; 72(5): 665–671, https://doi.org/10.1136/annrheumdis-2012-201469.
  15. Rönnelid J., Wick M.C., Lampa J., Lindblad S., Nordmark B., Klareskog L., van Vollenhoven R.F. Longitudinal analysis of citrullinated protein/peptide antibodies (anti-CP) during 5 year follow up in early rheumatoid arthritis: anti-CP status predicts worse disease activity and greater radiological progression. Ann Rheum Dis 2005; 64(12): 1744–1749.
  16. Valesini G., Alessandri C. Anticitrullinated protein/peptide antibodies and rheumatoid factors: two distinct autoantibody systems. Arthritis Res Ther 2009; 11(5): 125, https://doi.org/10.1186/ar2786.
Komarova E.B. Correlation between Joint Ultrasound Data and Clinical, Laboratory and Instrumental Indices in Patients with Rheumatoid Arthritis. Sovremennye tehnologii v medicine 2017; 9(1): 92, https://doi.org/10.17691/stm2017.9.1.11


Journal in Databases

pubmed_logo.jpg

web_of_science.jpg

scopus.jpg

crossref.jpg

ebsco.jpg

embase.jpg

ulrich.jpg

cyberleninka.jpg

e-library.jpg

lan.jpg

ajd.jpg

SCImago Journal & Country Rank