Quantitative MRI assessment of joint effusion using T2-relaxometry at 3 Tesla: a feasibility and reproducibility study
- PMID: 38512365
- PMCID: PMC11410847
- DOI: 10.1007/s00256-024-04652-0
Quantitative MRI assessment of joint effusion using T2-relaxometry at 3 Tesla: a feasibility and reproducibility study
Abstract
Objective: T2-relaxometry could differentiate between physiological and haemorrhagic joint effusion (≥ 5% blood) in vitro. Are quantitative T2-relaxation time measurements of synovial fluid feasible and reproducible in vivo in clinically bleed-free joints of men with haemophilia?
Materials and methods: In this cross-sectional study, we measured T2-relaxation times of synovial fluid in clinically bleed-free ankles, knees or elbows of men with severe haemophilia A using a T2-mapping sequence (duration ≤ 7 min) at 3 Tesla MRI. Manual and circular regions of interest (ROI) were drawn in the synovial fluid of each joint by two independent observers to measure T2-relaxation times. Measurement feasibility was expressed as the success rate of the measurements by both observers. The interobserver and intraobserver reproducibility of the measurements were evaluated by the intraclass correlation coefficient of absolute agreement (ICC) and the limits of agreement (LoA) from Bland Altman analysis.
Results: We evaluated 39 clinically bleed-free joints (11 ankles, 12 knees, 16 elbows) of 39 men (median age, 24 years; range 17-33) with severe haemophilia A. The success rate of the T2-measurements was ≥ 90%. Interobserver reliability was good to excellent (manual ROI: ICC = 0.92, 95% CI 0.76-0.97; circular ROI: ICC = 0.82, 95% CI 0.66-0.91) and interobserver agreement was adequate (manual ROI: LoA = 71 ms; circular ROI: LoA = 146 ms). Intraobserver reliability was good to excellent (manual ROI: ICC = 0.78, 95% CI - 0.06-0.94; circular RO: ICC = 0.99, 95% CI 0.98-0.99) and intraobserver agreement was good (manual ROI: LoA = 63 ms; circular ROI: LoA = 41 ms).
Conclusion: T2-relaxometry of synovial fluid in haemophilia patients is feasible with good interobserver and intraobserver reproducibility.
Keywords: Haemarthrosis; Haemophilia; Magnetic resonance imaging; Reproducibility of results; Synovial fluid.
© 2024. The Author(s).
Conflict of interest statement
This study was funded by an independent clinical research grant from NovoNordisk (Access to Insight 2018) received by W. Foppen which was paid to the institution. M.A. Timmer, and L.F.D. van Vulpen have also received research grants from NovoNordisk. K. Fischer has performed consultancy for NovoNordisk and has received speaker’s fees and research support from NovoNordisk. The other authors declare no financial relationship with NovoNordisk.
In addition, F.H.P. van Leeuwen, B. Lena, E.D.P. van Bergen, J.J. van Klei and C. Bos declare no conflicts of interest. M.A. Timmer has received research grants from SOBI, which were paid to the institution. L.F.D. van Vulpen has received research grants from CSL Behring and Grifols; and has performed consultancy for Sobi, CSL Behring, and Octapharma; all fees paid to the institution. K. Fischer has received speaker’s fees from Bayer, Baxter/Shire, Sobi/Biogen, CSL Behring; has performed consultancy for Bayer, Biogen, CSL Behring, Freeline, Roche and Sobi; and has received research support from Bayer, Baxter/Shire, Pfizer and Biogen; all fees were paid to the institution. P.A. de Jong declares a research collaboration with Vifor Pharma. W. Foppen has received a research grant from Pfizer, which was paid to the institution, and consultancy fees from Pfizer. The Department of Radiology & Nuclear Medicine of the UMC Utrecht has received research support from Philips Healthcare.
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References
-
- Berntorp E, Fischer K, Hart DP, Mancuso ME, Stephensen D, Shapiro AD, et al. Haemophilia. Nat Rev Dis Prim. 2021;7:45. - PubMed
-
- van Galen KPM, Mauser-Bunschoten EP, Leebeek FWG. Hemophilic arthropathy in patients with von Willebrand disease. Blood Rev. 2012;26:261–6. - PubMed
-
- Pulles AE, Mastbergen SC, Schutgens REG, Lafeber FPJG, van Vulpen LFD. Pathophysiology of hemophilic arthropathy and potential targets for therapy. Pharmacol Res. 2017;115:192–9. - PubMed
-
- Jansen NWD, Roosendaal G, Lafeber FPJG. Understanding haemophilic arthropathy: an exploration of current open issues. Br J Haematol. 2008;143:632–40. - PubMed
-
- Roosendaal G, Lafeber FP. Pathogenesis of haemophilic arthropathy. Haemophilia. 2006;12:117–21. - PubMed
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