Intravoxel Incoherent Motion Magnetic Resonance Imaging in Skeletal Muscle: Review and Future Directions

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Abstract
Throughout the body, muscle structure and function can be interrogated using a variety of noninvasive magnetic resonance imaging (MRI) methods. Recently, intravoxel incoherent motion (IVIM) MRI has gained momentum as a method to evaluate components of blood flow and tissue diffusion simultaneously. Much of the prior research has focused on highly vascularized organs, including the brain, kidney, and liver. Unique aspects of skeletal muscle, including the relatively low perfusion at rest and large dynamic range of perfusion between resting and maximal hyperemic states, may influence the acquisition, postprocessing, and interpretation of IVIM data. Here, we introduce several of those unique features of skeletal muscle; review existing studies of IVIM in skeletal muscle at rest, in response to exercise, and in disease states; and consider possible confounds that should be addressed for muscle‐specific evaluations. Most studies used segmented nonlinear least squares fitting with a b‐value threshold of 200 sec/mm2 to obtain IVIM parameters of perfusion fraction (f), pseudo‐diffusion coefficient (D*), and diffusion coefficient (D). In healthy individuals, across all muscles, the average ± standard deviation of D was 1.46 ± 0.30 × 10−3 mm2/sec, D* was 29.7 ± 38.1 × 10−3 mm2/sec, and f was 11.1 ± 6.7%. Comparisons of reported IVIM parameters in muscles of the back, thigh, and leg of healthy individuals showed no significant difference between anatomic locations. Throughout the body, exercise elicited a positive change of all IVIM parameters. Future directions including advanced postprocessing models and potential sequence modifications are discussed.Level of Evidence: 2Technical Efficacy: Stage 2
Funding Information
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (R03HD094598)
  • National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR070830)
  • National Institute of Biomedical Imaging and Bioengineering (R21EB009535)
  • National Institute of Diabetes and Digestive and Kidney Diseases (U24DK076169, U24DK115255)
  • NIH Office of the Director (S10OD021702)

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