Comparison of inversion recovery gradient echo with inversion recovery fast spin echo techniques for magnetic resonance imaging detection of navicular bone marrow lesions in horses

Julien Olive Diagnostic Imaging Department, Faculty of Veterinary Medicine, University of Montreal, St-Hyacinthe, QC J2S 7C6, Canada.
Teleradiology Service, Capinghem, 59160, France.

Search for other papers by Julien Olive in
Current site
Google Scholar
PubMed
Close
 DMV, MSc
,
Thibault Vila Clinique Vétérinaire Equine de Chantilly, 20bis Rue Victor Hugo, 60500 Chantilly, France.

Search for other papers by Thibault Vila in
Current site
Google Scholar
PubMed
Close
 DMV
, and
Nicolas Serraud Imavet, 3910 Route de Launac, 31330 Grenade-sur-Garonne, France.

Search for other papers by Nicolas Serraud in
Current site
Google Scholar
PubMed
Close
 DMV

Abstract

Objective—To compare navicular bone marrow lesion (BML) conspicuity in the feet of horses as determined via 2 fat-suppressed MRI techniques, including standard short tau inversion recovery (STIR) and inversion recovery gradient echo (IRGE).

Sample—Feet (n = 150) of horses with lameness referable to the distal portion of the digit.

Procedures—STIR and IRGE sequences were obtained prospectively in all feet with a standing low-field equine MRI system. Presence of a BML was ascertained by identification of a characteristic combination of marrow alterations in T1-weighted, T2*-weighted, T2-weighted, and STIR images. Signal-to-noise and contrast-to-noise ratios were calculated on STIR and IRGE sequences in 56 feet with a navicular BML.

Results—Signal-to-noise and contrast-to-noise ratios of both sequences correlated linearly (r = 0.87 and r = 0.92, respectively) but were significantly higher for STIR images (mean ± SD, 22.6 ± 12.7 and 12.4 ± 11.4, respectively), compared with IRGE images (13.7 ± 8.0 and 5.9 ± 7.2, respectively).

Conclusions and Clinical Relevance—Results suggested that the IRGE sequence revealed BMLs significantly less conspicuously, compared with the standard STIR sequence. The 2 techniques cannot be used interchangeably, and IRGE is therefore not recommended as the sole fat-suppressed sequence for routine equine standing MRI protocols.

Abstract

Objective—To compare navicular bone marrow lesion (BML) conspicuity in the feet of horses as determined via 2 fat-suppressed MRI techniques, including standard short tau inversion recovery (STIR) and inversion recovery gradient echo (IRGE).

Sample—Feet (n = 150) of horses with lameness referable to the distal portion of the digit.

Procedures—STIR and IRGE sequences were obtained prospectively in all feet with a standing low-field equine MRI system. Presence of a BML was ascertained by identification of a characteristic combination of marrow alterations in T1-weighted, T2*-weighted, T2-weighted, and STIR images. Signal-to-noise and contrast-to-noise ratios were calculated on STIR and IRGE sequences in 56 feet with a navicular BML.

Results—Signal-to-noise and contrast-to-noise ratios of both sequences correlated linearly (r = 0.87 and r = 0.92, respectively) but were significantly higher for STIR images (mean ± SD, 22.6 ± 12.7 and 12.4 ± 11.4, respectively), compared with IRGE images (13.7 ± 8.0 and 5.9 ± 7.2, respectively).

Conclusions and Clinical Relevance—Results suggested that the IRGE sequence revealed BMLs significantly less conspicuously, compared with the standard STIR sequence. The 2 techniques cannot be used interchangeably, and IRGE is therefore not recommended as the sole fat-suppressed sequence for routine equine standing MRI protocols.

Contributor Notes

The authors thank Dr. Guy Beauchamp for statistical analyses and Dr. Steve Roberts for providing manufacturer details about sequence conception.

Address correspondence to Dr. Olive (julien_olive_veto@hotmail.com).
  • 1. McRobbie DW, Moore EA, Graves MJ, et al. MRI from picture to proton. 2nd ed. Cambridge, England: Cambridge University Press, 2007.

  • 2. Zanetti M, Bruder E, Romero J, et al. Bone marrow edema pattern in osteoarthritic knees: correlation between MR imaging and histologic findings. Radiology 2000; 215: 835840.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 3. Conaghan PG, Felson D, Gold G, et al. MRI and non-cartilaginous structures in knee osteoarthritis. Osteoarthritis Cartilage 2006; 14:A87A94.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 4. d'Anjou MA, Troncy E, Moreau M, et al. Temporal assessment of bone marrow lesions on magnetic resonance imaging in a canine model of knee osteoarthritis: impact of sequence selection. Osteoarthritis Cartilage 2008; 16: 13071311.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 5. Roemer FW, Frobell R, Hunter DJ, et al. MRI-detected subchondral bone marrow signal alterations of the knee joint: terminology, imaging appearance, relevance and radiological differential diagnosis. Osteoarthritis Cartilage 2009; 17: 11151131.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 6. Sampson SN, Schneider RK, Gavin PR, et al. Magnetic resonance imaging findings in horses with recent onset navicular syndrome but without radiographic abnormalities. Vet Radiol Ultrasound 2009; 50: 339346.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 7. Dyson SJ, Murray R, Schramme MC. Lameness associated with foot pain: results of magnetic resonance imaging in 199 horses and response to treatment. Equine Vet J 2005; 37: 113121.

    • Search Google Scholar
    • Export Citation
  • 8. Olive J, Mair TS, Charles B. Use of standing low-field magnetic resonance imaging to diagnose middle phalanx bone marrow lesions in horses. Equine Vet Educ 2009; 21: 116123.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 9. Holowinski M, Judy C, Saveraid T, et al. Resolution of lesions on STIR images is associated with improved lameness status in horses. Vet Radiol Ultrasound 2010; 51: 479484.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 10. Jenner F, Kirker-Head C. Core decompression of the equine navicular bone: an in vivo study in healthy horses. Vet Surg 2011; 40: 151162.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 11. Bonel H, Helmberger T, Geiss HC, et al. Comparison of sequences for depicting bone marrow alterations in osteomyelitis applied in a low field strength magnetic resonance imaging system. MAGMA 1998; 7: 18.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 12. Bonel H, Helmberger T, Sittek H, et al. A comparison of pulse sequences in the detection of post-traumatic bone marrow abnormalities at low field strength MRI. Skeletal Radiol 1997; 26: 538543.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 13. Piola V, Posch B, Radke H, et al. Magnetic resonance imaging features of canine incomplete humeral condyle ossification. Vet Radiol Ultrasound 2012; 53: 560565.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 14. Murray RC, Werpy N. Image interpretation and artefacts. In: Murray RC, ed. Equine MRI. Ames, Iowa: Wiley-Blackwell, 2011;101113.

  • 15. Olive J, d'Anjou MA, Alexander K, et al. Correlation of signal attenuation–based quantitative magnetic resonance imaging with quantitative computed tomographic measurements of subchondral bone mineral density in metacarpophalangeal joints of horses. Am J Vet Res 2010; 71: 412420.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 16. Adrian AM, Koene M, Roberts S, et al. The influence of temperature and age on the T1 relaxation time of the equine distal limb. Vet Radiol Ultrasound 2012; 53: 296303.

    • Search Google Scholar
    • Export Citation
  • 17. Wohlgemuth WA, Roemer FW, Bohndorf K. Short tau inversion recovery and three-point Dixon water-fat separation sequences in acute traumatic bone fractures at open 0.35 Tesla MRI. Skeletal Radiol 2002; 31: 343348.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 18. Arndt WF III, Truax AL, Barnett FM, et al. MR diagnosis of bone contusions of the knee: comparison of coronal T2-weighted fast spin-echo with fat saturation and fast spin-echo STIR images with conventional STIR images. AJR Am J Roentgenol 1996; 166: 119124.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 19. Mirowitz SA, Apicella P, Reinus WR, et al. MR imaging of bone marrow lesions: relative conspicuousness on T1-weighted, fat-suppressed T2-weighted, and STIR images. AJR Am J Roentgenol 1994; 162: 215221.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 20. Pui MH, Goh PS, Choo HF, et al. Magnetic resonance imaging of musculoskeletal lesions: comparison of three fat-saturation pulse sequences. Australas Radiol 1997; 41: 99102.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 21. Pui MH, Chang SK. Comparison of inversion recovery fast spin-echo (FSE) with T2-weighted fat-saturated FSE and T1-weighted MR imaging in bone marrow lesion detection. Skeletal Radiol 1996; 25: 149152.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 22. Hilfiker P, Zanetti M, Debatin JF, et al. Fast spin-echo inversion-recovery imaging versus fast T2-weighted spin-echo imaging in bone marrow abnormalities. Invest Radiol 1995; 30: 110114.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 23. Yoshioka H, Stevens K, Hargreaves BA, et al. Magnetic resonance imaging of articular cartilage of the knee: comparison between fat-suppressed three-dimensional SPGR imaging, fat-suppressed FSE imaging, and fat suppressed three-dimensional DEFT imaging, and correlation with arthroscopy. J Magn Reson Imaging 2004; 20: 857864.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 24. Roemer FW, Hunter DJ, Guermazi A. MRI-based semiquantitative assessment of subchondral bone marrow lesions in osteoarthritis research. Osteoarthritis Cartilage 2009; 17: 414415.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 25. Zampa V, Carafoli D, Grassi L, et al. Usefulness of opposed-phase gradient-echo technique in the diagnosis of occult lesions of the knee and comparison with traditional T1-weight sequences (in-phase) [in Italian]. Radiol Med 2000; 99: 3135.

    • Search Google Scholar
    • Export Citation
  • 26. Vande Berg BC, Malghem J, Lecouvet FE, et al. Classification and detection of bone marrow lesions with magnetic resonance imaging. Skeletal Radiol 1998; 27: 529545.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 27. Murray RC, Blunden TS, Schramme MC, et al. How does magnetic resonance imaging represent histologic findings in the equine digit? Vet Radiol Ultrasound 2006; 47: 1731.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 28. Dyson S, Blunden T, Murray R. Comparison between magnetic resonance imaging and histological findings in the navicular bone of horses with foot pain. Equine Vet J 2012; 44: 692698.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 29. Dyson S, Murray R. Use of concurrent scintigraphic and magnetic resonance imaging evaluation to improve understanding of the pathogenesis of injury of the podotrochlear apparatus. Equine Vet J 2007; 39: 365369.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 30. Dyson SJ, Murray RC, Schramme MC, et al. Magnetic resonance imaging in 18 horses with palmar foot pain, in Proceedings. 48th Am Assoc Equine Pract Annu Conv 2002;145154.

    • Search Google Scholar
    • Export Citation

Advertisement