Table 1.
MRI Technique | Basic Principle | Outcome Variable |
---|---|---|
Blood oxygenation level–dependent MRI | Tissue oxygenation is estimated by using the paramagnetic properties of deoxyHb that shortens transverse relaxation time constant T2* | R2* (1/T2*, sec−1): high R2* corresponds to high local deoxyHb levels and presumes low tissue oxygenation in kidneys and vice versa |
R2* is also influenced by magnetic field inhomogeneities (because of air in bowels), hemoglobin levels, hydration status, and salt intake | ||
Arterial spin labeling | Subtraction technique that uses magnetically labeled water protons to measure cortical (and medullary) perfusion | Tissue blood flow of kidneys, expressed in ml/min per 100 ml |
No gold standard against which to validate. Technically challenging, motion and breathing artifacts | ||
Diffusion-weighted imaging | The ADC of water is detected and provides information on tissue microstructure | ADC (mm2/s): in general, lower ADC indicates greater kidney fibrosis |
ADC also depends of renal blood flow and tubular flow | ||
Phase-contrast MRI | Moving protons of blood in the renal artery induce a phase-shift that corresponds to its velocity | Renal blood flow (per artery) in ml/s |
Sensitive to background noise and aliasing; technically difficult in case of tortuous renal arteries | ||
T1 mapping | In T1 mapping, a whole-kidney map of all quantified T1 relaxation times is obtained. Alterations of T1 are nonspecific, but may indicate interstitial edema or inflammation | Msec |
T1 values are influenced by many other factors such as body temperature, perfusion, and fibrosis of the kidney tissue |
MRI, magnetic resonance imaging; deoxyHb, deoxygenated hemoglobin; R2*, inverse transverse relaxation time T2*; ADC, apparent diffusion coefficient.