Background Studies on intravoxel incoherent motion (IVIM) imaging are carried out with different acquisition protocols. Purpose To investigate the dependence of IVIM parameters on the B0 field strength when using a bi‐ or triexponential model. Study Type Prospective. Study Population 20 healthy volunteers (age: 19–28 years). Field Strength/Sequence Volunteers were examined at two field strengths (1.5 and 3T). Diffusion‐weighted images of the abdomen were acquired at 24 b‐values ranging from 0.2 to 500 s/mm2. Assessment ROIs were manually drawn in the liver. Data were fitted with a bi‐ and a triexponential IVIM model. The resulting parameters were compared between both field strengths. Statistical Tests One‐way analysis of variance (ANOVA) and Kruskal–Wallis test were used to test the obtained IVIM parameters for a significant field strength dependency. Results At b‐values below 6 s/mm2, the triexponential model provided better agreement with the data than the biexponential model. The average tissue diffusivity was D = 1.22/1.00 μm2/msec at 1.5/3T. The average pseudodiffusion coefficients for the biexponential model were D* = 308/260 μm2/msec at 1.5/3T; and for the triexponential model D1* = 81.3/65.9 μm2/msec, D2* = 2453/2333 μm2/msec at 1.5/3T. The average perfusion fractions for the biexponential model were f = 0.286/0.303 at 1.5/3T; and for the triexponential model f1 = 0.161/0.174 and f2 = 0.152/0.159 at 1.5/3T. A significant B0 dependence was only found for the biexponential pseudodiffusion coefficient (ANOVA/KW P = 0.037/0.0453) and tissue diffusivity (ANOVA/KW: P < 0.001). Data Conclusion Our experimental results suggest that triexponential pseudodiffusion coefficients and perfusion fractions obtained at different field strengths could be compared across different studies using different B0. However, it is recommended to take the field strength into account when comparing tissue diffusivities or using the biexponential IVIM model. Considering published values for oxygenation‐dependent transversal relaxation times of blood, it is unlikely that the two blood compartments of the triexponential model represent venous and arterial blood. Level of Evidence: 1 Technical Efficacy Stage: 2 J. Magn. Reson. Imaging 2019;50:1883–1892.
The aim of this prospective cohort study was to evaluate the effect of compression garments under resting conditions and after the induction of delayed-onset muscle soreness (DOMS) by MR perfusion imaging using intravoxel incoherent motion (IVIM). Magnetic resonance imaging of both lower legs of 16 volunteers was performed before and after standardized eccentric exercises that induced DOMS. A compression garment (21-22 mmHg) was worn during and for 6 h after exercise on one randomly selected leg. IVIM MR imaging, represented as total muscle perfusion D*f, perfusion fraction f and tissue diffusivity D, were compared between baseline and directly, 30 min, 6 h and 48 h after exhausting exercise with and without compression. Creatine kinase levels and T2-weighted images were acquired at baseline and after 48 h. DOMS was induced in the medial head of the gastrocnemius muscle (MGM) in all volunteers. Compression garments did not show any significant effect on IVIM perfusion parameters at any time point in the MGM or the tibialis anterior muscle (p > 0.05). Microvascular perfusion in the MGM increased significantly in both the compressed and noncompressed leg between baseline measurements and those taken directly after and 30 min after the exercise: the relative median f increased by 31.5% and 24.7% in the compressed and noncompressed leg, respectively, directly after the exercise compared with the baseline value. No significant change in tissue perfusion occurred 48 h after the induction of DOMS compared with baseline. It was concluded that compression garments (21-22 mmHg) do not alter microvascular muscle perfusion at rest, nor do they have any significant Abbreviations used: C, compressed; CK, creatine kinase; DOMS, delayed-onset muscle soreness; EIMD, exercise-induced muscle damage; IFCC, International Federation of Clinical Chemistry and Laboratory Medicine; IVIM, intravoxel incoherent motion; MGM, medial head of the gastrocnemius muscle; NC, noncompressed; NEX, number of excitations; ROI, region of interest; SPAIR, spectral attenuated inversion recovery; TA, tibialis anterior muscle; TE, echo time; TIRM, turbo inversion recovery magnitude; TR, repetition time.
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