Three-Dimensional Phase Resolved Functional Lung Magnetic Resonance Imaging

Filip Klime&#353;; Andreas Voskrebenzev; Frank Wacker; Jens Vogel-Claussen

doi:10.3791/66385

JoVE Journal > Medicine

医学

Three-Dimensional Phase Resolved Functional Lung Magnetic Resonance Imaging

Published: June 21, 2024

doi:

10.3791/66385

Filip Klimeš^1,2, Andreas Voskrebenzev^1,2, Frank Wacker^1,2, Jens Vogel-Claussen^1,2

¹Institute of Diagnostic and Interventional Radiology,Hannover Medical School, ²Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH),Member of the German Centre for Lung Research (DZL)

概要

Three-dimensional (3D) phase-resolved functional lung (PREFUL) is a functional magnetic resonance imaging (MRI) technique that allows for quantification of regional ventilation of the whole human lung volume, using tidal breathing and contrast-agent free acquisition for 8 min. Here, we present an MR protocol to collect and analyze 3D PREFUL imaging data.

Abstract

Pulmonary magnetic resonance imaging (MRI) offers a variety of radiation-free techniques tailored to assess regional lung ventilation or its surrogates. These techniques encompass direct measurements, exemplified by hyperpolarized gas MRI and fluorinated gas MRI, as well as indirect measurements facilitated by oxygen-enhanced MRI and proton-based Fourier decomposition (FD) MRI. In recent times, there has been substantial progress in the field of FD MRI, which involved improving spatial/temporal resolution, refining sequence design and postprocessing, and developing a comprehensive whole-lung approach.

The two-dimensional (2D) phase-resolved functional lung (PREFUL) MRI stands out as an FD-based approach developed for the comprehensive assessment of regional ventilation and perfusion dynamics, all within a single MR acquisition. Recently, a new advancement has been made with the development of 3D PREFUL to assess dynamic ventilation of the entire lung using 8 min exam with a self-gated sequence.

The 3D PREFUL acquisition involves employing a stack-of-stars spoiled-gradient-echo sequence with a golden angle increment. Following the compressed sensing image reconstruction of approximately 40 breathing phases, all the reconstructed respiratory-resolved images undergo registration onto a fixed breathing phase. Subsequently, the ventilation parameters are extracted from the registered images.

In a study cohort comprising healthy volunteers and patients with chronic obstructive pulmonary disease, the 3D PREFUL ventilation parameters demonstrated strong correlations with measurements obtained from pulmonary function tests. Additionally, the interscan repeatability of the 3D PREFUL technique was deemed to be acceptable, indicating its reliability for repeated assessments of the same individuals.

In summary, 3D PREFUL ventilation MRI provides a whole lung coverage and captures ventilation dynamics with enhanced spatial resolution compared to 2D PREFUL. 3D PREFUL technique offers a cost-effective alternative to hyperpolarized ¹²⁹Xe MRI, making it an attractive option for patient-friendly evaluation of pulmonary ventilation.

Introduction

According to the World Health Organization (WHO), chronic respiratory diseases are the third leading cause of death, placing a significant burden on healthcare¹. The diagnosis and monitoring of several respiratory diseases involve pulmonary functional tests, which lack spatial information and may not be feasible in young patients. Multiple other nuclear medicine modalities provide spatial measures of ventilation, such as positron emission tomography (PET)², single-photon emission computed tomography (SPECT)³^, or computed tomography⁴. A significant drawback of these techniques is the usage of ionizing radiation for imaging. Therefore, those measurements are not feasible in sensitive populations like children or for repeated measurements in clinical studies.

Magnetic resonance imaging methods gained interest in the last two decades because they offer radiation free measurement of pulmonary function. Above all, hyperpolarized gas MRI techniques⁵ have been used for the assessment of pulmonary ventilation in healthy controls and patients with pulmonary disease while achieving a superior signal-to-noise (SNR) ratio when compared to ¹⁹F⁶ or oxygen-enhanced MRI⁷. The common disadvantages of gas MRI techniques include the requirement for additional personnel, hardware costs, or the need for patient cooperation during the breathold measurement. To address these limitations, methods based on Fourier Decomposition (FD) MRI⁸ have been introduced for evaluating pulmonary ventilation and perfusion. As an alternative to FD MRI, a phase-resolved functional lung (PREFUL) MRI⁹ was developed, validated¹⁰^,¹¹^,¹², and tested in multiple studies, including multicentre studies¹³^,¹⁴. Nevertheless, the 2D acquisition results in long acquisition times for complete lung coverage and limited spatial resolution. An elegant solution is offered by self-gated 3D acquisitions, albeit at the expense of the perfusion information¹⁵^,¹⁶^,¹⁷. One of these techniques, 3D PREFUL MRI¹⁷, has been developed not only to assess static ventilation but also ventilation dynamics during an 8 min MR exam, providing superior image resolution when compared to 2D methods.

Following the original publication describing the method¹⁷, the technique's repeatability has been assessed and compared to clinically the well-established spirometric measurements¹⁸^, and more recently, an accelerated image registration framework has been introduced while improving the repeatability of ventilation parameters and preserving the image quality of ventilation maps¹⁹. This patient-friendly and easily scalable technique, capable of quantitatively mapping regional ventilation in the human lung, has the potential to significantly contribute to early detection, diagnosis of respiratory disease, or follow-up monitoring of therapy effects²⁰. These treatment changes in regional lung function, such as improved ventilation volume, have the potential to become biomarkers for assessing the impact of therapies and could be a useful tool in multicenter clinical studies.

The article aims to provide a comprehensive and visual explanation of the 3D PREFUL technology, with the goal of fostering a wider translation of this technique.

Protocol

This study received approval from the ethics committee of Hannover Medical School, ensuring that it adhered to rigorous ethical standards throughout the research process. The investigation strictly followed the guidelines outlined in the Declaration of Helsinki, emphasizing the ethical conduct of medical research. Additionally, informed consent was diligently obtained from all study participants (or their parents or legal guardians) before their participation in the MRI examination.

NOTE: The inclusion/exclusion criteria for studies involving 3D PREFUL MRI vary and depend on the study design. Typically, inclusion criteria for healthy volunteers in a 3D PREFUL MRI examination involve individuals who (a) are free from any significant medical conditions that could affect the study outcomes, (b) are not taking any medications that may interfere with the MRI results, (c) have no claustrophobia, anxiety, metallic implants or devices, (d) meet specific age and gender criteria relevant to the study objectives, (e) have no smoking history, (f) have normal findings of spirometry (FEV₁/FVC > 0.7 and both FEV₁ and FVC > 80% of predictive value). Exclusion criteria for all study participants undergoing a 3D PREFUL MRI examination may include: (a) pregnancy, (b) have any condition that may compromise the safety or validity of the 3D PREFUL MRI examination, (c) intolerance to gadolinium-based contrast agents when dynamic contrast-enhanced MRI in included in a study protocol.

1. Pre-MRI interview

Have a medical doctor gather important information regarding the subject's medical history.
Explain the potential contraindications, risks, and the MRI procedure.
Obtain written, informed consent from the subject.
NOTE: If no pulmonary function test results are available, request the subject to undergo a pulmonary function test prior to the MRI examination and verify that the obtained results meet the inclusion criteria.

2. Preparation of the radiographer for the MR exam

Register the subject in the MR console and choose the MR protocol of the study with 3D PREFUL acquisition.
Verify that the subject, his or her pockets, and clothing are free from metal-containing pieces.
Place the sheets on the scanner table so that a sterile environment is guaranteed.
Enter the MR room with the subject.

3. Preparing the subject for the MR exam

Have the subject lie on the MRI table in a supine position (however, a prone position is possible).
Make sure that the torso coil provides adequate coverage of the thorax, placing the top element of the torso coil near the subject's chin.
Provide the subject with headphones (alternatively earplugs or both) to protect hearing from loud MRI-induced noise.
Provide the subject with a safety button (or an alternate safety mechanism) so that it can be easily accessed and squeezed.
Place a pad under the subject's head and legs to enhance comfort during the MR exam.
Place the subject into the MR scanner, using the laser light navigation to make sure that the imaged area occupies the isocentre of the bore.

4. MRI exam

Localizer
1. Perform a localizer sequence (with similar parameters as listed in Table 1A) to obtain low-resolution anatomical images in three planes (with large field-of-view) that will be used to plan the 3D PREFUL exam.
3D PREFUL imaging
1. Set the acquisition parameters according to Table 1B for imaging acquisition.
2. Set the number of radial projections accordingly so that the acquisition takes approximately 8 min.
3. Tell the subject to breathe normally (tidal-free breathing) for the whole acquisition.
4. Check that the whole thorax is included in the field of view and start the acquisition.
After the imaging is complete, remove the subject from the scanner.

5. Raw data transfer

Ordinarily, the acquired raw data is not saved on the MR vendor platform. Save the raw 3D PREFUL kspace data using the vendor-specific steps on the MR console.

6. Data analysis and postprocessing

Start evaluating the acquired data using the image reconstruction script (Table of Materials) on the designated workstation, e.g., in MATLAB, by setting the path to the raw data.
NOTE: The designated workstation should already have the following packages installed:
(a) The Berkeley Advanced Reconstruction Toolbox (BART)
(b) Advanced Normalization Tools (ANTs)
Image reconstruction
1. Estimate the MR system-dependent gradient delays using the calibration projections with the estdelay function implemented in Berkeley advanced reconstruction toolbox (BART)²¹^,²².
2. Apply a shift to each projection according to the calculated gradient delay.
3. Apply Hanning filtering (using the hann function in MATLAB) to the gradient-delay corrected data using a periodic window in the x-y plane and the z-direction.
4. Low-resolution image reconstruction for respiratory binning
  1. Select one-eight/one-fourth of the k-space data centered around the middle index of the readout/partition dimension.
    NOTE: Depending on the subject's size, this step results in a matrix size of 32 x 32 x (12-20).
  2. Reshape the matrices of k-space data and corresponding trajectories to include additional time dimension, with each time point comprising 14 radial projections.
    NOTE: Each subsequent time point includes 13 radial projections from the previous time point plus one new successive radial projection.
  3. Utilize the parallel imaging and compressed sensing (pics) command implemented in BART for image reconstruction.
    NOTE: Apply L2 norm (λ = 0.1) and total variation (λ = 0.0001) regularization in the spatial domain and total variation (λ = 0.01) regularization in the time domain.
5. Extraction of the respiratory gating signal
  1. Segment the lung parenchyma in each reconstructed low-resolution 3D image using Otsu's thresholding²³, and calculate the lung parenchyma volume for each time point.
  2. Apply a low-pass filter with a cutoff frequency of 0.7 Hz to the extracted volume time series and calculate the breathing frequency.
  3. Exclude extreme outliers from the time series (time points above the 95^th percentile and below the 10^th percentile).
    NOTE: Arranging the time series by their amplitude and phase allows to reconstruct a single respiratory cycle.
6. Perform fast Fourier transform (FFT, fft function in MATLAB) on the hanning-filtered data along the slice direction to enable slice-by-slice image reconstruction.
7. Reshape the k-space data matrix based on the extracted time series so that each respiratory bin contains a minimum of 100 spokes.
8. Utilize 20% of projections from adjacent bins to enhance the SNR²⁴^,²⁵ of each respiratory bin.
9. Reshape the k-space trajectories matrix to match the size of the k-space data.
10. Execute the pics command for image reconstruction for each slice.
  NOTE: Apply L2 norm (λ = 0.1) and total variation (λ = 0.0001) regularization in the spatial domain and total variation (λ = 0.01) regularization in the time domain.
11. Save the variables, including the reconstructed images of one complete respiratory cycle, breathing frequency, and acquisition times, in a .mat file.
Image registration
1. Invert the signal intensities of the reconstructed images.
2. Register the images to a selected respiratory state, such as inspiration, using non-rigid registration.
  NOTE: To improve the registration accuracy, a group-oriented approach²⁶ may be employed. The registration process can be executed on either CPU or GPU using tools such as Advanced Normalization Tools (ANTs)²⁷ or the Forsberg registration package²⁸.
Lung parenchyma segmentation
1. Segment the lung parenchyma of the end-inspiratory 3D image using a convolutional neuronal network with, e.g., nnUnet architecture²⁹.
2. Exclude lung vessels using a vessel recognition algorithm, such as the one described by Wernz et al.³⁰.
  NOTE: The lung vessel recognition step is not mandatory if you do not have access to such an algorithm. In some cases, manual resegmentation may be necessary.
Filtering
1. Apply Nadaraya-Watson kernel regression (with σ = 0.3) to the registered and reinverted images to interpolate 16 phases onto a uniformly spaced time grid.
2. Eliminate signal variations unrelated to respiration by applying a low-pass filter at 0.7 Hz to the interpolated data in the time domain.
3. Denoise the low-pass filtered images using image-guided filtering³¹, with the temporally averaged registered image serving as the guiding image. Set the following parameters: Window Size = [5, 5, 5], lambda = 0.001.
Ventilation analysis
1. Calculate the regional ventilation (RVent) maps in milliliter/milliliter (mL/mL) for each respiratory phase N using the following formula³²:
  [1]
  NOTE: S_Insp represents the target image for image registration, corresponding to the end-inspiratory level. S_Exp refers to the end-expiratory image, while S_N represents the N-th respiratory state.
2. Calculate the ventilation defect (VD_RVent) map of the RVent map of 8^th phase, which represents the maximal ventilation.
  NOTE: To calculate VD, voxels below the threshold of the 90^th percentile value, multiplied by a factor of 0.4, are considered defects³³.
3. Calculate the flow-volume-loop correlation metric (FVL-CM) map.
  1. Calculate the flow as the first derivative of RVent.
    NOTE: The volume is directly measured by RVent.
  2. Establish a reference FVL for each slice, computed from a healthy region defined by RVent values between 75^th and 95^th percentile.
  3. Determine the similarity between each lung parenchyma voxel's FVL and the reference FVL using cross-correlation with zero-lag.
4. Compute VD_FVL-CM map, where voxels with FVL-CM values below 0.9 are identified as voxels with ventilation defect³⁴.
5. Compute ventilation time-to-peak (VTTP) maps in percentage (%) of respiratory cycle.
  NOTE: Theoretically, the interpolated respiratory cycle starts/ends at peak expiration and is symmetrical about the peak inspiration at 50% of the ventilation cycle for a healthy voxel. For voxels undergoing advanced/delayed ventilation dynamics, the VTTP map will display a value below/above 50%.
6. Compute the deviation of VTTP value (VTTP_Dev) from the peak inspiration at 50% as follows:
  [2]
  NOTE: For a healthy region, the VTTP_Dev should be close to 0%.
7. 統計
  1. Describe statistically the parameters RVent, FVL-CM, VTTP, and VTTP_Dev for all slices, providing median, mean, standard deviation values, and interquartile ranges.
  2. Calculate the ventilation defect percentage values derived from the generated VD maps.
  3. Export all calculated parameters to a spreadsheet file (refer to the example provided in Table 3).

Representative Results

The simplest 3D PREFUL imaging protocol includes two sequences. One anatomical localizer + one free breathing measurement using golden-angle 3D stack-of-stars acquisition. The stack-of-stars trajectory is shown in Figure 1. This trajectory combines radial sampling (in-plane) with linear cartesian sampling (in z-direction). Initially, samples in the k_z partition direction are acquired, followed by the rotation of the golden angle to sample the k_x-k_y plane. The golden angle acquisition scheme promotes self-gating with uniform coverage of k-space, facilitating image reconstruction with heavily undersampled data.The whole exam does not exceed 10 minutes. Further details of the 3D PREFUL acquisition are placed in the Table of Materials.

Figure 1: Golden ratio rotated stack of stars trajectory. Note radial sampling applied along in-plane dimension (kx-ky) and Cartesian sampling applied along slice direction (kz). This scheme results in cylindrical coverage of the acquired k-space. In this example, three partitions, including 32 radial projections per partition, are depicted. Please click here to view a larger version of this figure.

A list of typical MRI parameters used for 3D PREFUL imaging on 1.5 T scanner is presented in Table 1B. For the 3T scanner, the sequence parameters listed in Table 2 are proposed.

After the data acquisition and data transfer are completed, the image reconstruction part starts. This step is done by a MATLAB code that belongs to the intellectual property (IP) of a company (BioVisioneers GmbH) and cannot be shared openly. The script is fully automated once the path to the raw data is provided. A schematic overview of the reconstruction procedure is depicted in Figure 2.

Figure 2: Schematic overview of the 3D Phase Resolved Functional Lung (PREFUL) MRI method. At first, the data is acquired using an 8-minute-long free-breathing MR acquisition with a stack-of-stars trajectory. After the data is transferred from MR scanner to a computing unit, low-resolution 3D images with a temporal resolution of approximately 100 ms are reconstructed. The lung parenchyma of each image is segmented, and the lung volume is computed. The lung volume information is further used as a gating signal. Based on the amplitude and phase of the gating signal, the radial projections are sorted into respiratory bins that cover one respiratory cycle. The binning part is followed by the dynamic reconstruction of full-resolution images, which are subsequently registered to the end-inspiratory level. After several postprocessing steps, the regional ventilation (RVent) cycle is calculated, and the image analysis part, including parameter extraction, is performed. The RVent cycle is assessed by calculating the flow-volume loop (FVL) for each voxel. The FVL-CM ventilation maps are extracted through an assessment of each voxel FVL against healthy reference FVL, with similarity being evaluated using cross-correlation metric. For both RVent and FVL-CM, the global total ventilation defect percentage (VDP) values quantified. Furthermore, the dynamics of the RVent cycle is analyzed through time-to-peak analysis, resulting in a ventilation time-to-peak (VTTP) parameter map. Additionally, the deviation of the expected peak ventilation at 50% of the RVent cycle is quantified in the VTTP_Dev map. Please click here to view a larger version of this figure.

After the image reconstruction procedure, all images are spatially aligned to a single fixed state. The registration itself is performed on CPU using Advanced Normalization Tools (ANTs²⁷) or Forsberg registration package²⁸. While the ANTs package remains a gold standard for image registration tasks in MRI and CT imaging, the Forsberg registration facilitates a 10-fold faster registration procedure up to 9 minutes with comparable results¹⁹. The registration package might be chosen depending on the user priorities and available computing units. After the registration is done, the registered morphological images are again reinverted so that the lung appears dark in the grayscale image.

In Figure 3, the next step of the pipeline, which involves lung parenchyma segmentation, is depicted. First, the lung parenchyma is segmented from the end-inspiratory image using a convolutional neuronal network with nnUnet architecture²⁹. The lung parenchyma segmentation is followed by a vessel recognition³⁰, which is excluded from the final segmentation mask.

Figure 3: Exemplary results of deep learning-based segmentation for a 32-year-old male subject. The top row displays morphological images of eight representative coronal slices. In the second and third rows, one can observe the corresponding lung parenchyma mask and the final mask with the exclusion of vessels, respectively. Please click here to view a larger version of this figure.

An example of incorrect lung parenchyma segmentation is depicted in Figure 4. It is essential to visually inspect the deep-learning-based segmentations, and if deemed unsatisfactory, manual corrections should be considered to enhance the accuracy of the final lung parenchyma mask.

Figure 4: Exemplary results of incorrect deep learning-based segmentation for a 57-year-old male subject. The top row displays morphological images of eight representative coronal slices. In the second and third rows, one can observe the corresponding lung parenchyma mask and the final mask with the exclusion of vessels, respectively. As evident, several fibrotic regions are erroneously recognized as vessels or non-pulmonary structures. These inaccuracies have been corrected manually, as demonstrated in the fourth row. Please click here to view a larger version of this figure.

After several filtering steps outlined in the protocol, ventilation surrogates are calculated. 3D PREFUL MRI generates quantitative maps for static regional ventilation (RVent), dynamic flow-volume correlation metrics (FVL-CM), and two parameters based on ventilation time-to-peak (VTTP) analysis, as illustrated in Figure 5. This figure presents eight coronal slices of a 32-year-old healthy male. Note the expected homogenous distribution of all ventilation parameters.

Figure 5: 3D PREFUL MRI of a healthy volunteer (32-year-old male). Representative morphological (top row) and 3D PREFUL MRI ventilation parameters (second to fifth row) maps for a healthy volunteer (32-year-old male). The static regional ventilation is represented by regional ventilation (RVent), while the ventilation dynamics is assessed using the flow-volume loop correlation metric (FVL-CM), ventilation time-to-peak (VTTP), and deviation of VTTP (VTTP_Dev) represent ventilation parameters assessing the ventilation dynamics. As expected, homogenous ventilation values are observed for all ventilation parameter maps. Please click here to view a larger version of this figure.

To simplify the ventilation maps, ventilation defect (VD) maps are derived for RVent and FVL-CM, which enable faster interpretation of the results. The exemplary VD maps are presented in Figure 6. For both VD_RVent and VD_FVL-CM, the VDP values were found to be 3.6% and 3.0%, respectively, falling within the healthy normal range. Ideally, and depending on the age of the healthy volunteers, the VDP value should not exceed 10%. The above-mentioned parameters (RVent, FVL-CM, and their VD maps) were validated in several studies¹¹^,¹²^,³⁵^,³⁶ and are sensitive in the detection of disease as well as in the detection of therapy-induced effects²⁰^,³⁴^,³⁷^,³⁸^,³⁹.

Figure 6: Representative RVent and FVL-CM maps, including their ventilation defect maps. The RVent (top row) and FVL-CM (second row) maps, including their ventilation defect maps (third and fourth row) derived by 3D PREFUL MRI for a healthy volunteer (32-year-old male), are depicted. In VD maps, healthy regions are green, and ventilation-deficit areas are marked in red. Please click here to view a larger version of this figure.

Several pulmonary MRI studies have been reported at both 1.5 T and 3 T magnetic field strengths. While there is the theoretical advantage of 3T due to increased signal-to-noise ratio (SNR), this advantage may be outweighed by more pronounced magnetic susceptibility effects at 3T. The exact influence of magnetic field strengths on the image quality of 3D PREFUL ventilation maps is currently unknown. Here, we present feasibility results (Figure 7) obtained for a healthy volunteer (35-year-old male) using a 3 T MR scanner. Note the more heterogeneous appearance of ventilation parameters at 3 T when compared to 1.5T (Figure 5).

Figure 7: 3D PREFUL MRI of a healthy volunteer (35-year-old male). Representative morphological (top row) and 3D PREFUL MRI ventilation parameters (second to fifth row) maps for a healthy volunteer (35-year-old male) at 3T. The static regional ventilation is represented by regional ventilation (RVent), while the ventilation dynamics is assessed using the flow-volume loop correlation metric (FVL-CM), ventilation time-to-peak (VTTP), and deviation of VTTP (VTTP_Dev) represent ventilation parameters assessing the ventilation dynamics. Please click here to view a larger version of this figure.

Comparison/validation of 3D PREFUL derived with more direct measurements is currently not published. There are several studies reporting a positive correlation between VDP values and spatial overlap of ventilation defects between 2D PREFUL technique and ¹²⁹Xe¹¹^,¹²^,¹⁴ and ¹⁹F MRI³⁵. A recent comparison between 3D PREFUL-derived ventilation and direct ventilation measurements using ¹⁹F MRI in patients with chronic obstructive pulmonary disease (COPD), asthma, and healthy volunteers revealed a moderate to strong correlation at a global level⁴⁰. Presented is an example comparison (Figure 8) for a patient diagnosed with chronic obstructive lung disease (54-year-old female, FEV₁ = 42% predicted value), which was examined using 3D PREFUL and ¹⁹F wash-in MRI.

Figure 8: 3D PREFUL MRI of a 54-year-old female COPD patient. Morphological images (top row), ventilation parameters, and respective ventilation defect maps of a 54-year-old female COPD patient (FEV₁ = 42 % pred., FVC = 102% pred.) obtained via 3D PREFUL MRI (2nd and 3rd row) and ¹⁹F MRI (4th and 5th row) are presented, along with a comparison of ventilation defect maps from both methods (last row). Overall, across all slices, the Sørensen-Dice coefficient was 25.5% in defective areas and 80.6% in healthy regions, resulting in a total spatial overlap of 69.2%. Notably, there's a visual correlation between matched ventilation areas in healthy and defective regions (depicted in dark green). Please click here to view a larger version of this figure.

3D PREFUL MRI can be used to measure regional responses to therapy²⁰. As an example, Figure 9 shows a comparison of three slices from the lung of a cystic fibrosis subject (43-year-old female) at baseline (on the left,FEV₁ = 94% predicted value) and after CFTR-modulator therapy (on the right, FEV₁ = 112% predicted value). Because both measurements are spatially matched, 3D PREFUL enables regional treatment response analysis, as illustrated at the bottom of Figure 9. Please note the increased values of the flow-volume-loop correlation metric as well as the reduction in ventilation defects after therapy.

Figure 9: 3D PREFUL measurements of a 43-year-old female cystic fibrosis (CF) patient. Exemplary ventilation marker maps of baseline (left) and post-treatment (right) 3D PREFUL measurements of a 43-year-old female CF patient. VDP_FVL-CM decreased from 18.0% (baseline) to 3.6% (post-treatment). FEV₁ % pred. baseline: 94%, FEV₁ % pred. post-treatment: 112%. LCI baseline: 10.48, LCI post-treatment: 9.39. The corresponding treatment response maps are depicted at the bottom. Please note the green areas indicating the resolved ventilation after the therapy. Please click here to view a larger version of this figure.

Table 1: List of typical MRI parameters used for localizer and 3D PREFUL acquisition on a 1.5T scanner. (A) Localizer and (B) 3D PREFUL acquisition. Please click here to download this Table.

Table 2: Proposed MRI parameters for 3D PREFUL acquisition on a 3T scanner. Please click here to download this Table.

Table 3: Exemplary statistical report of 3D PREFUL Parameters for a healthy volunteer (35-year-old male) Please click here to download this Table.

Discussion

One of the most critical pitfalls is the acquisition itself. Care must be taken to ensure that the MR sequence parameters are set properly. Importantly, echo time, repetition time, number of slices, matrix size, and pixel bandwidth are the crucial parameters. Deviations from the recommended settings may result in insufficient temporal resolution or prolonged acquisitions. Also, data transfer is important to ensure that the data are completely delivered to the selected computer or server for evaluation. The data evaluation proceeds entirely automatically once the path to the acquired data is set. Postprocessing commences with image reconstruction, where retrospective binning plays a crucial role. Verifying the binning signal is recommended to ensure a clear depiction of the breathing pattern.After inspecting the binning signal, no additional steps are necessary, as the algorithm itself handles poor breathing patterns by excluding outliers (data points above the 95^th percentile and below the 10^th percentile). After image reconstruction, the process of image registration occurs. This step should be verified as follows: the registered images should be free from breathing and cardiac motion. Specifically, the positions of the diaphragm and heart should be 'frozen'. The next step involves deep-learning-based segmentation of lung parenchyma and vessels. This segmentation process is highly time-consuming for the entire 3D lung volume; hence, the use of AI-based tools is beneficial. However, in certain situations, such as the occurrence of peripheral consolidations, these algorithms may not yield accurate results. Consequently, the segmentation mask should be thoroughly checked and manually corrected if necessary. All of these steps are critical for evaluating the ventilation parameters and may result in inaccurate calculations.

Since the original publication¹⁷, several developments have been made in the 3D PREFUL technique. The sorting algorithm of the acquired radial projections has been fully automated and improved so that the whole lung is segmented using Otsu's thresholding method and used as a navigator signal for binning data into respiratory phases. Further, the manual lung parenchyma and vessel segmentation have been replaced by fully automatic deep-learning-based algorithms to reduce time-consuming procedures. Additionally, the processing time of the image registration part might be reduced up to 10 minutes if the Forsberg registration toolbox is implemented¹⁹. Along with previous developments, the implemented code enables to coregister images of two-time points (follow-up measurements) and evaluate the voxelwise progression of the disease or therapy-induced ventilation changes²⁰. The current version of the Matlab script does not require any user interaction and could be implemented in a pipeline for the automated processing of data with specific flags in the future.

The main disadvantage of 3D PREFUL is that no local blood flow measurement is feasible since the inflow effect cannot be captured when using a nonselective hard RF pulse for excitation. Secondly, currently, the whole postprocessing (including data transfer, image reconstruction, image registration, and ventilation analysis) requires 2 hours for each subject. Thirdly, currently, only a preliminary comparison of 3D PREFUL-derived ventilation parameters to more validated techniques was demonstrated⁴⁰. Fourthly, the evaluation of acquired data is performed on a high-performance computer; therefore, the results are not directly available to the physician at the console. Fifthly, feasibility studies of 3D PREFUL on different field strengths and various scanner vendors are lacking.

3D Phase Resolved Functional Lung (PREFUL) MRI allows quantitative mapping of regional ventilation dynamics of the whole human lung during free breathing¹⁷. There are several cost-effective alternatives to 3D PREFUL, such as spirometry or multiple breath washout techniques; however, both lack spatial information and require breathing maneuvers, and they are therefore not feasible for young children or neonates. Alternative imaging methods expose patients to ionizing radiation, such as nuclear medicine methods CT, or are not widely available (hyperpolarized ¹²⁹Xe or ¹⁹F gas imaging using MRI). 3D PREFUL provides an assessment of ventilation dynamics, can be performed using a standard clinical scanner, and does not require contrast agents, making it attractive to be translated to a clinical research setting. The fact that 3D PREFUL does not require the use of radiation or contrast agents and offers a patient-friendly, free-breathing acquisition makes it well-suited for repeat or longitudinal studies that quantitatively evaluate regional responses to therapy. Secondly, the 3D PREFUL assessment of lung ventilation may be especially valuable in young children, where radiation exposure should be avoided.

The capability of 3D PREFUL to generate functional ventilation images of the human lung holds the potential for early diagnosis. Specifically, the ability to produce repeatable and quantitative regional ventilation maps allows for longitudinal studies, e.g., disease progression or monitoring of therapy effects. Moreover, the regional information on ventilation dynamics can provide greater sensitivity to early changes related to lung disease that are not detectable by pulmonary function tests.

開示

The authors have nothing to disclose.

Acknowledgements

This work was funded by the German Center for Lung Research (DZL). The authors profited from a number of beneficial discussions with colleagues, in particular with Marcel Gutberlet, Agilo Kern, Lea Behrendt, Arnd Obert, Julian Glandorf, Till Kaireit, Tawfik Moher Alsady, Gesa Pöhler, Maximilian Zubke, Robin Müller, Marius Wernz, Cristian Crisosto, Milan Speth, Julienne Scheller, and Sonja Lüdiger. The authors acknowledge Robert Grimm (Siemens Healthineers) for writing the MR imaging sequence, and further, the authors would also like to thank Frank Schröder and Sven Thiele from the Department of Radiology (Hannover Medical School) for outstanding technical assistance in performing the MRI examinations.

Materials

ANTs	Open source medical image analysis research community		Image registration toolbox
BART	Open source imaging	https://www.opensourceimaging.org/project/berkeley-advanced-reconstruction-toolbox-bart/	Image reconstruction toolbox
Body coil	Siemens / Philips / GE	https://www.siemens-healthineers.com/en-us/magnetic-resonance-imaging/options-and-upgrades/coils	At least 6-channel body coil; Philips [https://www.usa.philips.com/healthcare/solutions/magnetic-resonance/coils-overview ]
Forsberg	Image registration toolbox	https://github.com/fordanic/image-registration	Image registration toolbox
Image reconstruction code	BioVisioneers GmbH	www.biovisioneers.com	Software for the MR reconstruction and analysis
Matlab	Mathworks		Software
MRI	Siemens / Philips / GE	https://www.siemens-healthineers.com/magnetic-resonance-imaging	Philips [https://www.philips.co.in/healthcare/solutions/magnetic-resonance], GE [https://www.gehealthcare.com/products/magnetic-resonance-imaging]; 1.5 T / 3 T
Sequence	Siemens / Philips / GE		MRI sequence, 3D gradient echo sequence with stack-of-stars trajectory and golden angle increment; 1. Siemens Grasp-Vibe Sequence – https://t.ly/P31kM , 2. Philips Multi Vane XD Sequence https://t.ly/wMWZZ , 3. GE Lava-Star, Disco-Star – https://t.ly/vimm2

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Three-Dimensional MRI Phase Resolved Functional Lung Imaging Pulmonary MRI Hyperpolarized Gas MRI Fluorinated Gas MRI Oxygen-enhanced MRI Proton-based Fourier Decomposition FD MRI 2D PREFUL MRI 3D PREFUL Ventilation Dynamics Spatial Resolution Compressed Sensing Image Reconstruction Chronic Obstructive Pulmonary Disease Pulmonary Function Tests

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Klimeš, F., Voskrebenzev, A., Wacker, F., Vogel-Claussen, J. Three-Dimensional Phase Resolved Functional Lung Magnetic Resonance Imaging. J. Vis. Exp. (208), e66385, doi:10.3791/66385 (2024).

Three-Dimensional Phase Resolved Functional Lung Magnetic Resonance Imaging