What Is Cardiac MRI and How Does It Work?

Introduction

Cardiac MRI provides detailed images of the heart without radiation or invasive catheters. Unlike echocardiography, which uses sound waves through the chest wall, or CT angiography, which relies on x-rays, cardiac MRI uses powerful magnetic fields and radio waves to create high-resolution images of heart muscle, valves, and blood flow. The technology reveals information no other test can provide, particularly about the composition of heart tissue itself.

For patients with heart disease, this matters because the distinction between different causes of heart dysfunction can fundamentally change treatment. A heart weakened by blocked arteries requires different management than one damaged by inflammation or infiltrated by abnormal proteins. Cardiac MRI can make these distinctions with remarkable precision. This article explains the technology, the key techniques involved, and what to expect if your cardiologist recommends the test.

Understanding cardiac MRI fundamentals provides the foundation for evaluating whether this test might be useful for your care. Subsequent articles in this series address how cardiac MRI compares to alternative tests, what specific findings mean, and how to navigate insurance and access.

What is cardiac MRI and how does it create images of the heart?

Cardiac MRI uses a powerful magnet, typically 1.5 or 3 Tesla, to align hydrogen atoms in body tissues. Radiofrequency pulses then disturb this alignment, and sensors detect the signals emitted as atoms return to their baseline state. Different tissues produce different signals based on their water and fat content, enabling computers to construct detailed cross-sectional images without ionizing radiation.

The heart presents unique imaging challenges because it moves constantly. Cardiac MRI addresses this through electrocardiogram gating, synchronizing image acquisition to the cardiac cycle. Images are acquired over multiple heartbeats and reconstructed into movies showing the heart in motion. This allows precise measurement of heart function, including ejection fraction and wall motion abnormalities (Poon et al., 2002).

Modern cardiac MRI protocols combine multiple sequences in a single examination. Cine imaging captures heart motion. Flow imaging quantifies blood movement through valves and vessels. Tissue characterization sequences reveal abnormalities in the heart muscle itself. This comprehensive approach has led some to describe cardiac MRI as a “one-stop-shop” for cardiac evaluation (Poon et al., 2002).

What structures and functions of the heart can cardiac MRI evaluate that other tests cannot?

Cardiac MRI excels at visualizing the heart muscle itself. While echocardiography shows wall motion and CT angiography depicts coronary anatomy, cardiac MRI reveals what is happening inside the myocardium. It can distinguish between healthy muscle, scar tissue, inflammation, fat infiltration, and edema. This tissue characterization capability is unmatched by other noninvasive imaging modalities (Kolentinis et al., 2020).

The right ventricle is notoriously difficult to image with echocardiography due to its position and complex geometry. Cardiac MRI provides accurate right ventricular volumes and function, making it the reference standard for conditions affecting this chamber. Congenital heart disease assessment similarly benefits from the ability to image in any plane without acoustic window limitations.

Cardiac MRI also quantifies blood flow with precision that echocardiography cannot match. Regurgitant volumes through leaky valves, shunt quantification in congenital defects, and flow through bypass grafts can all be measured directly. This comprehensive functional assessment adds value beyond what anatomical imaging alone provides (Wu and Kwong, 2008).

What is the difference between anatomical imaging and functional imaging in cardiac MRI?

Anatomical imaging provides still pictures of cardiac structures at a single point in time. It shows the size and shape of chambers, the thickness of walls, and the presence of structural abnormalities like tumors or thrombi. Dark blood sequences suppress blood signal to highlight chamber walls and vessels, while bright blood sequences make flowing blood appear white.

Functional imaging captures the heart in motion. Cine MRI acquires images throughout the cardiac cycle, creating movies that show contraction and relaxation patterns. From these movies, software calculates ejection fraction, stroke volume, and cardiac output with high reproducibility. Regional wall motion abnormalities indicating prior infarction or ischemia become visible.

The distinction matters clinically because structural abnormalities do not always correlate with functional impairment. A heart may appear anatomically normal but contract poorly due to microvascular disease. Conversely, structural abnormalities may not impair function. Cardiac MRI provides both pieces of information in a single examination, enabling comprehensive assessment that guides treatment decisions (Sawlani and Collins, 2016).

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What does “late gadolinium enhancement” mean and why is it clinically important?

Late gadolinium enhancement refers to the pattern of contrast retention in abnormal myocardium 10-20 minutes after intravenous gadolinium administration. Normal heart muscle rapidly washes out gadolinium contrast. Scarred or fibrotic tissue retains the contrast agent longer due to expanded extracellular space and impaired cellular function. This retained contrast appears bright on specially timed MRI sequences.

The landmark Kim et al. study in the New England Journal of Medicine demonstrated that the transmural extent of late gadolinium enhancement predicts whether dysfunctional heart segments will recover function after revascularization (Kim et al., 2000). Segments with less than 25% transmural scar thickness typically improve after bypass surgery or stenting. Those with more extensive scar do not. This viability assessment fundamentally changed how cardiologists approach revascularization decisions (Al-Sabeq et al., 2019).

The pattern of enhancement also distinguishes different causes of heart disease. Ischemic injury from coronary disease produces subendocardial or transmural enhancement in coronary distributions. Myocarditis creates patchy mid-wall or epicardial enhancement (Singh et al., 2024). Cardiac amyloidosis shows diffuse subendocardial enhancement. These patterns provide diagnostic information that often eliminates the need for cardiac biopsy.

What is T1 mapping and T2 mapping, and what do they reveal about heart tissue?

T1 and T2 mapping are quantitative techniques that assign numerical values to each pixel in the image based on tissue relaxation properties. Unlike conventional images that show relative signal differences, mapping produces absolute measurements that can be compared to reference ranges. This objectivity reduces interpreter variability and enables detection of subtle, diffuse abnormalities.

Native T1 mapping, performed without contrast, detects fibrosis, edema, and infiltrative diseases. Elevated native T1 values occur in conditions that expand the extracellular space, including cardiac amyloidosis and Anderson-Fabry disease. Post-contrast T1 mapping enables calculation of extracellular volume fraction, a marker of diffuse fibrosis that correlates with outcomes in multiple cardiac conditions.

T2 mapping detects myocardial edema, making it valuable for diagnosing acute inflammatory conditions. In myocarditis, elevated T2 values indicate active inflammation, while T1 elevation suggests fibrosis. The ability to distinguish acute from chronic processes helps guide treatment intensity and timing (Rafiee et al., 2024). Updated Lake Louise criteria for myocarditis diagnosis incorporate these mapping techniques.

How long does a cardiac MRI take and what does the patient experience during the scan?

A comprehensive cardiac MRI examination typically requires 45-60 minutes of scanner time, though protocols vary based on clinical indication. Simpler studies focusing on ventricular function alone may take 30 minutes. Complex evaluations including stress perfusion, detailed valve assessment, and tissue characterization extend to 75-90 minutes. Add time for preparation, positioning, and IV placement.

Patients lie on their back in a tube-shaped scanner with a coil placed over the chest. The scanner produces loud knocking and banging sounds during image acquisition, so ear protection is provided. Patients must remain still during each sequence, typically 10-20 seconds, though free-breathing sequences exist for those who cannot hold their breath reliably.

Claustrophobia affects approximately 5-10% of patients and represents a significant barrier for some. Open MRI systems exist but generally produce lower image quality for cardiac applications. Mild sedation helps many claustrophobic patients complete the examination. Coaching and psychological support also improve success rates for anxious patients (Rafiee et al., 2024).

Why do some cardiac MRI protocols require breath-holding, and what happens if a patient cannot hold their breath?

Respiratory motion blurs cardiac MRI images just as camera shake blurs photographs. Traditional cardiac MRI protocols address this through breath-holding, asking patients to suspend respiration for 10-15 seconds while each image sequence is acquired. Most adults can accomplish this with coaching, though heart failure patients may struggle due to dyspnea.

When breath-holding is impossible, alternative techniques exist. Navigator-gated imaging uses a small excitation beam to track diaphragm position, acquiring data only during the same phase of the respiratory cycle. This free-breathing approach extends scan time substantially but produces diagnostic images in cooperative patients. Real-time imaging sacrifices some resolution for robustness against motion (Klemenz et al., 2024).

Modern accelerated imaging techniques using parallel imaging and compressed sensing have shortened breath-hold requirements. Deep learning-based reconstruction further reduces acquisition time while maintaining image quality (Klemenz et al., 2024). These advances expand cardiac MRI accessibility to patients previously unable to complete examinations due to respiratory limitations.

What is the difference between stress cardiac MRI and resting cardiac MRI?

Resting cardiac MRI evaluates heart structure and function in the baseline state. It detects established abnormalities like prior infarction scar, structural heart disease, and cardiomyopathies. However, resting imaging may miss significant coronary artery disease because blood flow to the heart muscle appears normal when oxygen demand is low.

Stress cardiac MRI adds pharmacological vasodilation, typically with adenosine or regadenoson, to unmask coronary flow limitations. During stress, normal coronary arteries dilate and increase blood flow three to four-fold. Diseased vessels cannot respond appropriately, creating perfusion deficits visible on first-pass contrast imaging. This stress perfusion approach detects ischemia with sensitivity and specificity exceeding 90% (de Mello et al., 2012).

The combination of stress perfusion and late gadolinium enhancement provides complementary information. Stress imaging shows areas at risk from coronary disease. Late enhancement shows areas already damaged. Together they inform decisions about whether revascularization versus medical therapy best serves the patient (Catania et al., 2025).

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What preparation is required before a cardiac MRI?

Preparation requirements depend on the specific protocol planned. For basic structural and functional assessment, patients typically fast for 4 hours before the examination to reduce motion artifact from bowel activity. Caffeine should be avoided for 24 hours before stress perfusion studies because it blocks adenosine receptors and can cause false-negative results.

Patients complete detailed safety screening questionnaires to identify MRI contraindications. Implanted devices, metallic foreign bodies, and certain medical conditions require evaluation before proceeding. Device cards for pacemakers or other implants should be brought to the appointment. Some older devices absolutely contraindicate MRI, while newer MR-conditional devices can be scanned under specific conditions.

Contrast-enhanced studies require assessment of kidney function, as gadolinium contrast agents are renally excreted. Most centers require recent creatinine or eGFR measurement, with additional precautions for patients with significant renal impairment. Patients should inform the technologist of prior allergic reactions to contrast agents, though gadolinium reactions are far less common than iodinated CT contrast reactions.

What is gadolinium contrast and when is it used versus when is a non-contrast study sufficient?

Gadolinium-based contrast agents are paramagnetic compounds that alter tissue T1 relaxation times, making tissues containing gadolinium appear bright on T1-weighted images. They distribute into the extracellular space and wash out of normal tissue within minutes. Abnormal tissues with expanded extracellular space or impaired perfusion retain gadolinium longer.

Contrast administration is essential for late gadolinium enhancement imaging, which requires the differential washout between normal and abnormal tissue to create image contrast. Stress perfusion imaging also requires gadolinium to visualize first-pass blood flow through the myocardium. Most comprehensive cardiac MRI examinations include contrast for these critical tissue characterization sequences.

Non-contrast cardiac MRI suffices for some indications. Ventricular function assessment, valve morphology evaluation, and native T1/T2 mapping can all be performed without gadolinium. For patients with significant renal impairment or gadolinium concerns, non-contrast protocols provide substantial diagnostic information (Campbell-Washburn et al., 2024). However, the inability to perform late enhancement imaging represents a significant limitation in many clinical scenarios.

Conclusion

Cardiac MRI provides unparalleled insight into heart structure, function, and tissue composition without ionizing radiation. The technology combines anatomical imaging, functional assessment, and tissue characterization in a single examination. Late gadolinium enhancement reveals scar patterns that distinguish between different causes of heart disease and predict recovery after treatment. Parametric mapping techniques add objectivity to these assessments.

The examination requires patient cooperation for breath-holding and tolerance of the scanner environment, though technical advances continue to reduce these barriers. Gadolinium contrast remains essential for most comprehensive protocols but can be omitted when specific contraindications exist. Understanding these fundamentals positions patients to discuss the potential role of cardiac MRI in their care with their cardiologists.

The next article examines how cardiac MRI compares to echocardiography, CT, and nuclear imaging, helping patients understand when each test adds value. Subsequent articles address interpreting results, clinical indications, and navigating access and insurance.