MR Angiogram

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Continuing Education Activity

Magnetic resonance angiography (MRA) encompasses several imaging techniques based on magnetic resonance imaging (MRI) developed for studying the arterial and venous systems. The benefits of an MRA in comparison to traditional angiography is that it is noninvasive, it lacks ionizing radiation exposure, it has the potential for a non-contrast examination and it has the ability of high-resolution volumetric images. The MRA gadolinium contrast material is less likely to cause an allergic reaction than the iodine-based contrast materials used for computed tomography scanning. This activity illustrates the technical aspects of MR angiography, its use, and its role in specific diagnostic scenarios.


  • Identify the indications and contraindications of MR angiography.
  • Describe the physics of the different MR angiography techniques.
  • Outline the potential complications and clinical significance of MR angiography.
  • Review interprofessional team strategies for improving care coordination and the use of MR angiography to improve diagnostic outcomes.


Magnetic resonance angiography (MRA) encompasses several imaging techniques based on magnetic resonance imaging (MRI) developed for studying the arterial and venous systems. The benefits of an MRA in comparison to traditional angiography is that it is noninvasive, it lacks ionizing radiation exposure, it has the potential for a non-contrast examination, and it has the ability of high-resolution volumetric images. The MRA gadolinium contrast material is less likely to cause an allergic reaction than the iodine-based contrast materials used for computed tomography scanning. In this review, the different techniques for MRA are discussed, and the indications for different pathologies are disclosed.


An MRA is used to evaluate the following abnormalities:


MRA has the same contraindications as for the MRI exam without contrast medium. MRA does not use radiation, and to date, side effects from the magnetic fields and radio-waves have not been reported. Gadolinium-based contrast agents can cross the placenta; therefore, it should not be administered during pregnancy, particularly during the first trimester.[25] It has been shown that patients with gadolinium exposure can present gadolinium deposition in the brain, especially in the dentate nuclei and globus pallidus, but no clinical consequences specific to neurological toxicity have been demonstrated.[26]

Non-contrast Study

Absolute contraindication: A cardiac implantable electronic device, mechanical metallic heart valves, metallic foreign bodies, implantable neurostimulation system, cochlear implants/ear implant, non-removable drug infusion pumps, catheters with metallic components, cerebral artery aneurysm clips which are non-MRI compatible, tissue expanders with magnetic infusion ports.

Relative contraindications: Coronary and peripheral artery stents, programmable shunts, airway stents, intrauterine devices, ocular prosthesis, stapes implants, surgical clips, or wire sutures, penile prosthesis, recent joint replacement or prosthesis, inferior vena cava filter, physical limitations, and non-removable piercings.

Contrast Medium

Absolute contraindications: Patients who had a previous allergic or anaphylactic reaction to gadolinium, or patients who have a glomerular filtration rate below 30 mL/min/1.73 m^2.[27]

Relative contraindications: A history of renal disease and dialysis. Patients with impaired renal function are at risk of nephrogenic systemic fibrosis (NSF), which was previously called nephrogenic fibrosing dermopathy. Pregnancy is also a relative contraindication.[28]

Technique or Treatment

MRA is a term that groups various imaging techniques based on different physical principles and is employed for diverse diagnostic purposes. MRA techniques can be categorized into "non-contrast" and "contrast-enhanced" techniques.[29][30]

Non-contrast MRA

Non-contrast media techniques can be further divided into two groups according to the blood signal characteristics:

  • Black–blood sequences (or dark-blood), in which the intravascular signal is lower than that of the surrounding stationary tissues.[31]
  • Bright–blood sequences (or white-blood), where the intravascular signal is higher than that of the surrounding stationary tissues.[32]

Black–blood sequences: Black-blood sequences are not used in the routine evaluation of the peripheral vasculature, but they are essential in specific clinical scenarios, such as vasculitis, cardiac imaging, and susceptibility venography. The rapidly flowing blood has a naturally low signal because of phase-dispersion and time-of-flight signal losses. This is evident in the vascular "flow voids" artifact commonly found on routine MRI that represents a raw form of dark-blood MRA. To evaluate the vessel wall in vasculitis, the combination of black-blood sequences pre-contrast and post-contrast T1 weighted are the gold standard.

This effect is extremely accentuated in black-blood sequences by the application of specific procedures:

  • Short Repetition Time (TR): The blood signal is saturated because of its long T1.
  • Medium Echo Time (TE): At 20 to 30 seconds TE, the protons in movement inside the blood vessel are dephased.
  • Inversion Recovery (IR): The inversion time is set to reduce the signal intensity of the incoming blood.
  • Spatial Saturation: A series of techniques used to produce the signal saturation of the blood outside the volume under examination.
  • Gradient Dephasing: Increasing the movement-induced dephasement of the blood protons inside the vessels.
  • 90° to 180° Wash-out: On spin-echo sequences, the signal of the protons of the blood leaving the voxel under analysis in the time included between the application of the 90° and 180° radio-frequency (RF) pulse and at 180° is lost.

Bright–blood sequences: These sequences are optimal for the study of the vascular lumen, but they have less accuracy in the evaluation of the vessel wall in comparison to dark-blood techniques.[33][34] This kind of sequence is characterized by very low TR and amplifies the transverse magnetization of the protons of the moving blood by the use of additional gradients, resulting in sequence with a high intravascular signal and fast acquisition.

Time of Flight (TOF) Technique

The TOF technique is based on the "inflow effect." When protons are subjected to RF pulses applied at very short repetition times (RT), the signal derived from them will be zero, because of the constant saturation of their longitudinal magnetization. The blood protons entering the acquisition volume aren't subjected to this saturation, and therefore they release a high signal, determining vascular enhancement related to the "inflow effect." Stair-step artifact in which the image shows a pixelated appearance to obliquely oriented vessels is caused because the slices in 2D are relatively thick (1mm to 3 mm) compared to the in-plane spatial resolution of 0.5 mm to 1.0 mm. They can be minimized by overlapping slices, however, with an important increase in scan time.

This technique represents the first diagnostic choice for the study of intracranial circulation and the second choice for the epi-aortic vessels when a study with a contrast medium cannot be performed. It allows the study of vessels at high flow speed, such as arteries, and it ignores much of the signal coming from the veins. Images are susceptible to motion artifacts and to protons dephasing related to very slow flow velocity as observed in severe stenosis or tortuosity in vessels, with the risk of an overestimation of the degree of stenosis. TOF can be performed with 2D and 3D acquisitions. 2D acquisitions are particularly sensible to proton dephasing artifacts with the very slow flows at the level of vascular stenosis. In peripheral MR angiography, flow is oriented craniocaudally, and two-dimensional (2D) TOF has is an accurate method to diagnose peripheral vascular disease and cervical carotid disease.[32] The introduction of the 3D acquisitions resulted in a noticeable increase in diagnostic accuracy.

Phase-Contrast (PC) Technique

The physical basis of the PC technique is the application of a couple of bipolar gradients that sequentially phase/dephase the proton spins into the acquisition volume. The signal intensity of the pixels is directly related to the values of the speed protons of the blood moving in the volume of interest, with the complete saturation of the static tissue signal. 

By selecting the correct speed encoding parameters (VElocity ENCoding, VENC), it is possible to obtain selective imaging of the arterial vessels (VENC factor > 40 cm/sec) and of the veins (VENC factor < 20 cm/sec). It can create a venogram with an accurate study of the low-speed flowing vessels. Its use is limited by the extremely long acquisition times.[32] The use of PC is restricted to the study of the intracranial circulation (particularly the venous system), while in other anatomic regions, the application is limited.

Several newer non-contrast techniques/sequences are frequently used:

Hybrid of Opposite-contrast (HOP-MRA)

The HOP-MRA method is an extension of 3D TOF. The HOP-MRA pulse sequence uses flow-compensated echo acquisition, similar to conventional 3D TOF. Because it is fundamentally a 3D TOF, it detects fast-flowing blood better than slow-flowing blood. Dark-blood image better depicts slow-flowing spins. Bright-blood and dark-blood images are combined to yield a final angiogram and are able to depict vessels with both fast- and slow-flowing blood.[33] Fine cerebral vessels like those in moyamoya disease are clearly visualized.

Quiescent Interval Single-shot (QISS)

QISS is an inflow-based MRA which relies on a presaturation RF pulse. Following the presaturation, "quiescent interval" (QI), fresh inflowing blood enters the saturated slice.[33] A common application is for run-off studies in peripheral arteries.

Electrocardiographically (cardiac) ECG-gated 3D Partial-Fourier Fast Spin-echo FSE

This MRA technique relies on an ECG-gated 3D partial Fourier FSE sequence, which is triggered for systolic and diastolic acquisitions.[33] This relies on the loss of signal, or flow void, as a result of fast arterial flow during systole. In contrast, during diastole, the slow flow in arteries causes them to have high signal intensity on T2-weighted images. Because of its relatively slow flow, venous blood is bright during both systole and diastole. Bright-blood MR angiography is then achieved by subtracting systolic from diastolic images. It is used for aorta, pulmonary, and peripheral imaging.

Balanced Steady-state Free Precession (SSFP)

Balanced SSFP without arterial spin labeling (ASL) can be performed with ECG gating for thoracic aortic MRA and with both ECG gating and navigator-gated free-breathing for whole-heart coronary artery MRA.[32] In this technique, the image contrast is determined by T2/T1 ratios, which produce bright-blood imaging without reliance on inflow. ASL can be utilized and relied on the spin tagging upstream of the arteries of interest by using an inversion pulse to generate image contrast. It is used for pulmonary, carotid, renal, and distal peripheral MRA.[32][33]

Four-Dimensional PC-MRA (4D Flow)

This technique generates time-resolved 3D PC flow maps acquired with cine mode ECG gating and allows the evaluation of regional aortic flow characteristics.[33]

Flow-sensitive Dephasing (FSD)

In this technique, the flow-induced phase generated by the bipolar gradients is not used for flow-encoding, but rather flow-dephasing.[33]

Contrast-enhanced (CE) MRA

CE MRA is based on the vascular enhancement of T1 sequences thanks to the paramagnetic contrast agent gadolinium. The contrast medium represents the main difference between CE MRA and the other MRA techniques based on flow physical properties. For this reason, this technique is very low influenced by dephasing artifacts that are seen in the other MRA techniques.[29][35]

The MRI sequences used in CE MRA are very rapid gradient echo, which is sensitive to the T1 shortening due to gadolinium. For this reason, this technique is very dependent on the correct timing of the arrival of the bolus of contrast agent in the vessels. The plane of acquisition should be as close as possible to the plane of the vessel studied. For this reason, the coronal plane is usually preferred, while in TOF, the acquisition plane is usually orthogonal to the vessel of interest.

Two CE-MRA techniques are used:

  1. Elliptical-centric: The acquisition begins as the contrast agent enters the artery of interest with the use of an automatic bolus detection software or by determining the time it takes the gadolinium to reach the artery of interest.
  2. Multiphase Techniques: When the bolus is injected, multiple acquisitions are made to cover different phases (early arterial phase, late arterial phase, hepatic or late portal phase, nephrogenic phase, delayed phase).[36] One of the limitations of multiphase imaging is the loss of the spatial resolution to get a high temporal resolution. To increase the spatial resolution of the multiphase exam, the central region of the k-space rich in the MRI signal is acquired more often than the outer parts of k-space. This technique is defined as "time-resolved imaging of contrast kinetics" (TRICKS). In TRICKS, the 3D k-space is divided into subvolumes located at different distances from a central core subvolume. This central region of k-space is oversampled while the outer areas have a lower sampling rate. In this way, TRICKS can consistently capture the arterial phase free of the venous component.[37]


MRA has similar complications as with MRI exams. A meta-analysis of 716,978 contrast-enhanced MRI exams from 9 studies revealed an overall rate of allergic-like reactions of 9.2 per 10,000 administrations, and a rate of severe allergic-like reactions was 0.52 per 10,000 administrations.[38]

A recent study reviewed the MRI-related adverse event reports received by the Food and Drug Administration during a 10-year period.[39] A total of 1,548 adverse events were recorded, which were divided into eight different categories.

  • Thermal: Skin reddening, blisters, warming, or heating sensation;
  • Acoustic: Hearing loss and/or tinnitus;
  • Image Quality: Lost exams, inadequate images, or images attributed to the incorrect patient;
  • Projectile: Objects were pulled into or attracted to the main static magnetic field;  
  • Mechanical: Falls, crush injuries, broken bones, cuts, or musculoskeletal injuries;  
  • Peripheral Nerve Stimulation: Nerve or muscle stimulation or patients experiencing tingling, twitching, or involuntary movements;    
  • Miscellaneous: Adverse event that can not be classified in any of the other categories;  
  • Unclear: Insufficient information was available to make conclusions regarding the connection to the MRI exam.

Clinical Significance

MRA offers a noninvasive alternative to conventional angiography in patients with suspected or confirmed vascular pathologies. For this reason, MRA is an imaging method that has long become an essential part of the common clinical routine.

Enhancing Healthcare Team Outcomes

An MRA scan takes less time than traditional catheter angiography and requires no recovery period. MRA is less costly than catheter angiography. Collaboration with shared indication and decision making and communication are key elements for a good outcome. The MRA is usually recommended by a specialist treating a specific disorder. It is important to orient the patient about the procedure as some patients are afraid of the machine or have physical limitations. Some patients are unable to lie flat or stay in the position for a long period of time.

It is very important for the referring physician to clearly annotate the indications for the study, so the neuroradiologist and MRA technician performs the preferred technique to yield the best diagnostic outcomes. 

(Click Image to Enlarge)
Axial and coronal post-contrast black blood images of the brain.
Axial and coronal post-contrast black blood images of the brain.
Contributed by Alessandro De Leucio, MD

(Click Image to Enlarge)
Coronal and axial "phase contrast" 3D reconstruction of cerebral venous system.
Coronal and axial "phase contrast" 3D reconstruction of cerebral venous system.
Contributed by Alessandro De Leucio, MD

(Click Image to Enlarge)
Contrast enhanced T1 images. Sagittal and coronal slices.
Contrast enhanced T1 images. Sagittal and coronal slices.
Contributed by Alessandro De Leucio, MD

(Click Image to Enlarge)
Coronal and axial "time of flight" (TOF) 3D reconstruction of the Willis polygon.
Coronal and axial "time of flight" (TOF) 3D reconstruction of the Willis polygon.
Contributed by Alessandro De Leucio, MD
Article Details

Article Author

Alessandro De Leucio

Article Editor:

Orlando De Jesus


2/12/2023 5:13:46 AM



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