T2 mapping magnetic resonance imaging of cartilage in hemophilia.

Res Pract Thromb Haemost

Department of Diagnostic Imaging, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Published: August 2023

Background: In hemophilia, recurrent hemarthrosis may lead to irreversible arthropathy. T2 mapping MRI may reflect cartilage changes at an earlier reversible stage of arthropathy as opposed to structural MRI.

Objectives: To evaluate interval changes of T2 mapping compared with the International Prophylaxis Study Group (IPSG) structural MRI scores of ankle cartilage in boys with hemophilia receiving prophylaxis.

Methods: Eight boys with hemophilia A (median age, 13; range, 9-17 years), 7 age- and sex-matched healthy boys (controls, median age, 15; range, 7-16 years). A multiecho spin-echo T2-weighted MRI sequence at 3.0T was used to obtain T2 maps of cartilage of boys with hemophilia and controls. Structural joint status was evaluated using the IPSG MRI score.

Results: T2 relaxation times of ankle cartilage increased significantly over time in both persons with hemophilia and controls ( .002 and .00009, respectively). Changes in T2 relaxation time strongly correlated with changes in IPSG cartilage scores ( = 0.93 to  = 0.78 [ = .0007 to .023]), but not with changes in age ( .304 to .840). Responsiveness of T2 relaxation times were higher than that of IPSG cartilage scores, with standardized response means >1.4 for T2 mapping in all regions-of-interest compared with 0.84 for IPSG cartilage scores. Baseline T2 relaxation time strongly correlated with timepoint 2 IPSG cartilage score ( = 0.93 to  = 0.82 [ = .001 to .012]) and T2 relaxation time ( = 0.98 to  = .88 [ = .00003 to .004]) changes in most regions-of-interest.

Conclusion: T2 mapping shows sensitivity to biochemical changes in cartilage prior to detectable damage using conventional MRI, offering potential for early detection of bleed-related cartilage damage in boys with hemophilia.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520564PMC
http://dx.doi.org/10.1016/j.rpth.2023.102182DOI Listing

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