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1 From the Departments of Radiology, Division of Pediatric Radiology (L.F.D., J.R.M., H.P.M., J.S., D.P.F., P.B., H.C.C., C.E.R.) and Pediatrics, Division of Pulmonary Medicine (J.M.M.), Duke University Medical Center, Durham, NC. From the 1998 RSNA scientific assembly. Received September 17, 1998; revision requested November 10; revision received November 19; accepted March 29, 1999. Address reprint requests to L.F.D., Department of Radiology, Children's Hospital Medical Center and the University of Cincinnati, 3333 Burnet Ave, Cincinnati, OH 45229-3039.
| Abstract |
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Index terms: Fibrosis, cystic, 60.252 Helium, 60.12147 Lung, MR, 60.12143 Magnetic resonance (MR), contrast enhancement, 60.12143 Magnetic resonance (MR), nuclei other than H, 60.12147
| Introduction |
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Thin-section CT and chest radiography are performed to evaluate morphologic changes of CF to determine the severity of disease. Findings in multiple studies in patients with CF suggest thin-section CT is superior to chest radiography for the evaluation of lung disease, such as bronchiectasis, peribronchial thickening, mucus plugging, and emphysema (14). Thin-section CT is also more sensitive for early lung changes. However, there has been concern that the morphologic changes seen at thin-section CT and chest radiography may not reflect early functional pulmonary disease, which has been depicted at SPECT perfusion or ventilation imaging. Functional imaging may offer a more sensitive way with which to detect early changes of CF in patients with minimal disease (1,6,8). Morphologically normal lung can at times demonstrate marked functional abnormalities at ventilation and perfusion imaging (1,8). This is of particular importance in the evaluation of progression in young patients with minimal disease and no or minimal findings at thin-section CT. Since many protocols that evaluate new therapies involve young children with minimal or no lung disease, the detection of early lung changes in CF is critical. Functional and morphologic evaluation can be performed with a combination of both thin-section CT and SPECT, but the cost and radiation dose associated with both examinations is prohibitive, especially when these examinations are performed serially.
The optimal single imaging modality with which to grade progression of the pulmonary changes seen in patients with CF would provide both morphologic and functional information and, because of the sequential nature of following up of progression of disease, would not use radiation. Use of combined hyperpolarized helium 3enhanced and conventional proton magnetic resonance (MR) imaging may meet these criteria. By imaging with a hyperpolarized ventilation contrast agent, such as 3He, high signal intensity (SI) can be generated within the pulmonary air spaces. In patients with CF, 3He MR imaging may provide both functional information related to airway occlusion and absent ventilation, as has been previously demonstrated with SPECT (1), and anatomic information by means of conventional proton-based, fast spin-echo (SE) imaging. The purpose of this study was to evaluate the preliminary findings with combined 3He and proton MR imaging in four patients with CF.
| Materials and Methods |
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Initially, with the 3He torso coil in place, conventional proton-based MR images were obtained throughout the chest with use of the body coil. Fast SE intermediate- and T2-weighted images were obtained in the coronal plane (repetition time msec/echo time msec = 3,000/80, 6-mm section thickness, 2-mm gap, 128 x 256 matrix, 32-cm field of view, one signal acquired, respiratory gating). After acquisition of the proton images and without moving the patient or the 3He torso coil, hyperpolarized 3He images were obtained with use of the 3He torso coil.
3He gas was hyperpolarized by means of a process that involves a collision exchange between rubidium and helium gases mixed together, heated to 180°C, and subjected to high-intensity laser illumination for several hours (9). When the container is cooled to room temperature, the rubidium is absorbed on the surface of the production container with residual concentrations of less than one in 100,000,000,000 atoms per cubic centimeter. The helium gas was polarized by using a prototypic unit (Magnetic Imaging Technologies, Durham, NC). Unit calibration tests demonstrated 9%11% polarization of the helium after the process. After the 3He was polarized and cooled, it was placed in a delivery apparatusa plastic bag with an attached tube containing a simple plastic stopcock on-off valve. The bag had a maximum capacity of 1 L. The bag was filled to between 0.7 and 0.9 L. Subjects were instructed to inhale the gas and hold their breath.
Immediately after the patients inhaled the 3He gas, gradient-echo images were obtained in the coronal plane (9.5/3.0 with 8° flip angle, single breath hold, 6-mm section thickness, 2-mm gap, 128 x 256 matrix, 32-cm field of view, one signal acquired). 3He gas inhalation and MR imaging were repeated in each subject to evaluate reproducibility.
During the examination, the patient's respiratory rate, pulse rate, and blood oxygenation levels were monitored. The patient's ability to cooperate with the examination was noted as were any changes in these vital signs during the study.
For comparison, the conventional proton fast SE and 3He images were printed with identical anatomic levels side by side. This aided interpretation of absent ventilation on the 3He images by defining the expected extent of the lung. Grading systems were constructed to help interpret both the 3He images and the conventional proton images. Each lung was divided into six zones that were independently graded. Three lung regions were based on superior to inferior thirds: upper, middle, and lower. Each region was then divided into an anterior and posterior zone, which yielded a total of six zones per lung.
Each lung zone was given a functional score based on the degree of ventilation as seen on the 3He MR images. Scores were based on the percentage of lung ventilated (percentage ventilation = area enhanced/total area of zone). Scores ranged from 0 (normal) to 4 (less than 25% of lung zone ventilated) (Table 1). The potential scores per patient (12 lung zones) ranged from 0 to 48. The 3He MR studies of two healthy male volunteers, who had no history or symptoms of pulmonary disease, showed diffuse homogeneous SI throughout the lungs (Fig 1). These studies were used as a normal reference. Imaging in the healthy volunteers was also approved by our institutional review board.
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In each patient, scores were compared with findings at chest radiography and pulmonary function testing (Table 3). Chest radiographs were scored for the severity of disease on the basis of the scoring system described by Brasfield et al (4,5). The potential Brasfield scores ranged from 0 (normal) to 25 (severe disease) (4,5). Findings at MR imaging were also compared with those at pulmonary function testing in each subject. Parameters evaluated included the forced vital capacity (FVC) and forced expiratory volume in 1 second (FEV1). The percentage of predicted values was calculated for each pulmonary function parameter by means of the Knudson equations (10).
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| Results |
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In all subjects, areas of absent lung ventilation were depicted on the hyperpolarized 3He MR images. These areas of absent ventilation ranged from wedge- shaped peripheral defects to entire lung zones (Figs 2, 3). The 3He lung zone scores ranged from normal ventilation (score, 0) to completely absent ventilation (score, 4). Total 3He ventilation scores ranged from 18 (38% of maximum score) to 31 (65% of maximum score) (Table 3). In all subjects, the lack of ventilation was most severe in the upper posterior lung zones, and ventilation was most normal in the lower lung zones. The mean 3He score for the upper posterior lung zone in the four subjects was 3.9. The mean score for the lower lung zones was 1.2. Concerning reproducibility, the individual lung zone scores were identical in all subjects for the two 3He data sets obtained at each examination.
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In a comparison of the percentage of maximum score for the functional 3He image and morphologic conventional image scores for individual lung zones, 3He ventilation scores indicated more severe disease than did the morphologic scores in 29 (60%) of the 48 lung zones evaluated (Fig 2). The severity of disease indicated by the 3He image scores was equal to that indicated by the morphologic conventional image scores in 19 (40%) lung zones (Fig 3). In no zones was the morphologic score higher than the 3He ventilation score. In many of the lung zones, the degree of absent ventilation was severe despite minimal morphologic changes (Fig 2). In addition, the percentage of maximum total 3He scores was greater than that of the morphologic scores in all cases (Table 3).
In the four patients, there was general correlation between the total MR imaging scores, the Brasfield chest radiograph scores, and the pulmonary function test results (Table 3). The small number of subjects precluded statistical analysis. The FVC was 3.03 L (88% of predicted value) for subject 1, 1.74 L (51% of predicted value) for subject 2, 3.18 L (75% of predicted value) for subject 3, and 2.60 L (58% of predicted value) for subject 4. The FEV1 was 1.96 L (62% of predicted value) for subject 1, 0.89 L (29% of predicted value) for subject 2, 1.55 L (39% of predicted value) for subject 3, and 1.28 L (30% of predicted value) for subject 4.
| Discussion |
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In this study, high-quality images of the lung were generated in all subjects, even in the presence of moderate to severe pulmonary disease from CF. Because of the short time of acquisition for the 3He images, all of the subjects were able to cooperate with the length of breath holding required. We did not test the ability of young children to cooperate with this examination. The time of breath holding for 3He MR imaging is approximately 10 seconds. For CT examinations, we have had success with breath holding for longer times in children as young as 4 years and routinely in children older than 6 years. Therefore, we would not anticipate difficulty with cooperation for 3He MR imaging except with very young children. For very young children, it may be possible to achieve 3He MR imaging by using a "stop ventilation" technique (12). None of our patients demonstrated any signs of respiratory compromise related to the administration of the 3He gas. Therefore, no technical or safety issues seem to prohibit the evaluation of patients with CF by means of 3He MR imaging. In addition, in this small series, results of 3He MR imaging were reproducible, with identical imaging findings in two separate data acquisitions.
In all subjects, abnormalities of both ventilation and morphology were readily detected. In the majority of individual lung zones and for all total 3He scores, the 3He functional MR image scores demonstrated more severe findings than did the scores for changes on conventional morphologic MR images. In many lung zones, severe ventilation abnormalities were seen despite minimal morphologic abnormalities. Morphologic changes at chest radiography and thin-section CT have been used as the basis for following up patients with CF for progression of disease (15). However, a study (1) comparing functional information obtained at pulmonary perfusion SPECT with morphologic changes seen at thin-section CT suggested that functional changes may be present prior to the occurrence of morphologic changes. Our preliminary results and the results of the previous study (1) suggest that functional abnormalities may be more sensitive to pulmonary changes of CF than are morphologic changes. Because many treatment protocols involve young children with minimal or no apparent lung disease, the ability to detect early changes in CF is critical for a modality to be used in following up progression of disease.
The standard of reference for evaluation of morphologic changes in CF is thin-section CT (13). To our knowledge, conventional hydrogen proton MR imaging has not been previously described as a method with which to evaluate morphologic changes in patients with CF. This is most likely related to the previously limited use of MR imaging in pulmonary imaging. However, with both the increasing speed at which fast SE images can be generated and improved techniques of respiratory gating, our preliminary results show promising potential for MR imaging to be accurate in this capacity. However, the unknown accuracy of MR imaging for depicting morphologic pulmonary changes is a limitation of our study. Further studies are needed that compare findings with combined 3He and proton MR imaging to those with thin-section CT.
Because both functional and morphologic information concerning the pulmonary status of patients with CF can be generated on hyperpolarized 3He MR imaging studies in a safe, reproducible, and technically feasible manner and because radiation is not used, 3He MR imaging may be an ideal way of serially evaluating patients with CF for progression of disease. We believe our preliminary results warrant further investigation, including application of this technology in the cases of younger patients with CF and minimal lung disease.
| Acknowledgments |
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| Footnotes |
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Author contributions: Guarantors of integrity of entire study, L.F.D., J.R.M.; study concepts, L.F.D., J.R.M., H.P.M., D.P.F., J.M.M.; study design, L.F.D., J.R.M., H.P.M.; literature research, all authors; clinical studies, all authors; data acquisition, all authors; data analysis, L.F.D., H.P.M., D.P.F.; manuscript preparation, L.F.D.; manuscript editing and review, all authors.
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