Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2013 May 1.
Published in final edited form as: J Magn Reson Imaging. 2012 Jan 26;35(5):1222–1226. doi: 10.1002/jmri.23571

Improved B1 Homogeneity of 3 Tesla Breast MRI Using Dual-Source Parallel Radiofrequency Excitation

Habib Rahbar 1, Savannah C Partridge 1, Wendy B DeMartini 1, Robert L Gutierrez 1, Sana Parsian 1, Constance D Lehman 1
PMCID: PMC3326217  NIHMSID: NIHMS342929  PMID: 22282269

Abstract

Purpose

To compare breast MRI B1 homogeneity at 3 Tesla with and without dual-source parallel radiofrequency (RF) excitation.

Materials and Methods

After institutional review board approval, we evaluated 14 consecutive breast MR examinations performed at 3 Tesla that included 3D B1 maps created separately with conventional single-source and dual-source parallel RF excitation techniques. We measured B1 values (expressed as % of intended B1) on each B1 map at nipple level in multiple bilateral locations: anterior, lateral, central, medial, and posterior. Mean whole breast and location specific B1 values were calculated and compared between right and left breasts using paired t-test.

Results

Mean whole breast B1 values differed significantly between right and left breasts with standard single-source RF excitation (difference L-R, Δ=9.2%; p<0.001) but not with dual-source parallel RF excitation (Δ=2.3%; p=0.085). Location specific B1 values differed significantly between right and left on single-source in the lateral (p=0.014), central (p=0.0001), medial (p=0.0013), and posterior (p<0.0001) locations. Conversely, mean B1 values differed significantly on dual-source parallel RF excitation for only the anterior (p=0.030) and lateral (p=0.0003) locations.

Conclusion

B1 homogeneity is improved with dual-source parallel RF excitation on 3T breast MRI when compared to standard single-source RF excitation technique.

Introduction

The use of magnetic resonance imaging (MRI) at 3 Tesla (T) has increased substantially in recent years. This increase in field strength over the more commonly used 1.5T scanners provides higher signal to noise (SNR), leading to potential benefits including greater spatial resolution and decreased scan times. Despite these advantages, MRI at 3T also creates significant technical challenges. Chief among these, particularly in breast imaging, is tissue signal variability or “shading” due to B1 transmit field inhomogeneity resulting from dielectric resonance effects.

First reported in breast MRI by Kuhl et al (1) and further quantitatively described by Azlan et al (2), these adverse B1 effects are due to the higher frequency B1 transmit fields that are used at greater field strengths. This results in non-uniform flip angles and measured signal, most pronounced from right-to-left for bilateral axial breast imaging (3),. The non-uniformity can lead to significant variations in T1 contrast that in turn cause significant spatial variations in signal intensity and contrast-enhancement or variations in fat saturation uniformity for non-adiabatic radiofrequency (RF) pulses. This resulting tissue contrast and signal enhancement inhomogeneity is particularly problematic in dynamic contrast-enhanced (DCE) breast MRI.

Proposed solutions to address the issue of tissue shading effects include techniques to maximize T1 contrast, including 3D imaging and increased flip angles (3,4). Recently, dual-source parallel excitation techniques have been developed to address the challenge of dielectric shading by increasing uniformity of the applied RF field. The use of independent transmit channels also allows for optimization of the local and whole-body specific energy absorption rate (SAR) using patient adaptive techniques, leading to reduced SAR deposition levels and decreased scan times (5). This technique has been shown to be useful in body and musculoskeletal imaging (5,6), but to date there are no published studies examining its effectiveness in reducing B1 inhomogeneities in breast MRI at 3T. We thus sought to evaluate MRI B1 homogeneity in breast imaging at 3T with and without dual-source parallel RF excitation.

Methods

Patient Population

The protocol for this study was approved by our institutional review board and was compliant with the Health Insurance Portability and Accountability Act. Our institutional review board waived informed consent. We included 15 consecutive patients who underwent a clinical breast MRI from February 18, 2010 to March 8, 2010. Several patient body composition factors were assessed. Patient height, weight, and body-mass-index were obtained from the medical records. Breast size was visually assessed for each patient by examining the B1 maps at the level of the nipple and categorized as small, medium, or large while also noting any asymmetry.

B1 Maps Acquisition

All MR examinations were performed on a Philips Achieva Tx 3T scanner using a dedicated 16-channel bilateral breast coil (Philips Healthcare, Best, the Netherlands). Patients were scanned axially in the prone position with feet first. After the standard clinical breast MRI sequences were obtained (including a T2-weighted fast spin echo sequence, T1-weighted non-fat suppressed sequence, and a T1-weighted fat-suppressed dynamic contrast-enhanced MRI sequence), B1 transmission field mapping was performed separately with conventional single-source RF excitation and dual-source parallel RF excitation (MultiTransmit, Philips Healthcare, Best, the Netherlands) techniques (7).

As previously described (6), the dual-source parallel RF excitation technique employed in our study distributes RF power to the ports of the system body coil using two independent RF transmit channels under full software control. The resulting applied B1 field is effectively a linear combination of the B1 fields generated by each source. Using patient-adaptive RF shimming, the power, amplitude, phase and waveform of the two RF sources are automatically adjusted for optimal uniformity in each patient’s unique anatomy. In practice, the process involves first acquiring a short B1 calibration scan on a per-patient basis to map the B1 field produced in the subject by each of the independent RF sources and determine the expected RF energy deposition in the patient. For breast imaging, parallel RF excitation can be used during particular acquisitions (by selecting it in the protocol) to improve B1 homogeneity, without requiring changes to other sequence parameters.

For our study, B1 maps were calculated using both standard single-source and parallel dual-source RF excitation. In each case, optimal B0 homogeneity was first achieved using a patient-adaptive image-based B0 shimming technique (SmartExam Breast, Philips Healthcare, Best, The Netherlands). Next, B1 transmission field maps were created using a previously described actual flip-angle imaging (AFI) approach (2,7), which enables accurate and rapid 3D in vivo measurement of the B1 field. This method employs a 3D gradient echo pulse sequence incorporating two identical RF pulses but with different TRs, and imaging parameters were defined based on previous recommendations (2,7): TR1/TR2 = 30/150 msec, TE = 2.2 msec, flip angle = 60°, matrix size = 128 × 128, FOV = 40 × 40 cm, slice thickness = 12 mm, and number of slices = 7. The same imaging parameters were used for standard single-source and dual-source RF excitation acquisitions. A B1 calibration scan was run prior to the dual-source RF excitation acquisition, as described above.

Image Measurements

B1 maps were calculated by measuring the actual flip angles generated in the subject relative to the intended flip angle, expressed as a percentage, using the relationship:

αcos1rn1nr (1)

where α is the actual flip angle, r is the signal ratio S1/S2 with S1 and S2 the signals measured after the corresponding TRs (TR1=30msec, TR2=150msec), n = TR2/TR1. Profile plots were defined on B1 maps to quantify right to left variation across the field of view using ImageJ (National Institute of Health, Bethesda, MD). B1 values were measured by defining five circular regions of interest (ROIs) of equal area (1.2 cm2) in each breast on each B1 map at the level of the nipple. ROIs were drawn for each subject in the following bilateral locations: anterior, lateral, central, medial, and posterior (figure 1). Mean whole breast B1 values were also calculated for each subject by averaging the five ROI values for each breast.

Figure 1.

Figure 1

Figure 1

Example of regions of interest (ROIs) drawn at the level of the nipple on the B1 maps acquired with standard single-source RF excitation (A) and with dual-source parallel RF excitation (B).

Statistical Analysis

Intra-patient differences between right and left whole breast and location-specific B1 values for both dual-source parallel RF and single-source RF excitation techniques were evaluated using paired t-test. All computations were performed using JMP version 9.0.2 (SAS Institute Inc, Cary, NC).

Results

We scanned 15 patients with both single-source and dual-source parallel RF excitation techniques. A single patient who had undergone left mastectomy with silicone breast implant reconstruction was excluded (n=1) due to inability to draw ROIs of left breast tissue. Thus, the final cohort included 14 patients. Indications for the clinical breast MRI in the study patients were high risk screening (n=7), evaluation of extent of disease in patients with known breast cancer (n=6), and short-interval 6 month follow-up for a prior MRI finding in a high risk screening patient (n=1). The mean patient age was 55 years.

The patient cohort exhibited varied body compositions, with a relatively even distribution of breast sizes (small n=5 patients, medium n=6 patients, large n=3 patients). Only one patient demonstrated visually perceptible breast size asymmetry (right breast was larger than the left). Mean patient height was 164.6 ± 6.8 cm, mean patient weight was 69.9 ± 9.2 kg, and mean patient body-mass-index was 25.4 ± 2.8 cm/kg.

Whole Breast B1 Values and Comparisons

B1 measures are reported in Table 1. Mean whole breast B1 values per patient ranged from 72 – 108% (median, 90%) for single-source RF excitation technique and 90 – 116% (median, 102%) for dual-source parallel RF excitation technique. Mean right whole breast B1 values differed significantly from mean left whole breast B1 values with single-source RF excitation (mean difference L-R, Δ=9.2%; p<0.001) but not with dual-source parallel RF excitation (mean difference L-R, Δ=2.3%; p=0.085) (figure 2). An example comparing the variations in B1 values between the right and left breast with conventional single-source and dual-source parallel RF excitation techniques in a single patient is provided in figure 3.

Table 1.

Mean region-specific B1 values (% of intended B1) for single-source RF excitation and dual-source parallel RF excitation techniques.

ROI
Location
Single-Source RF Excitation Dual-Source Parallel RF
Excitation
Right
(%)
Left
(%)
Difference
(%)
P value Right
(%)
Left
(%)
Difference
(%)
P
value
Anterior 97.99±8.50 94.15±7.15 −3.83±7.92 0.094 103.99±8.31 108.76±8.64 4.77±7.32 0.030*
Lateral 96.12±8.37 87.84±6.14 −8.28±10.86 0.014* 99.86±5.41 107.39±6.73 7.52±5.67 0.0003*
Central 96.3±7.19 85.34±7.36 −10.95±7.93 0.0001* 102.82±8.60 102.06±8.94 −0.76±6.51 0.668
Medial 96.13±7.62 87.01±7.52 −9.11±8.36 0.0013* 105.24±9.89 104.96±8.33 −0.29±8.12 0.897
Posterior 92.36±8.07 78.37±6.70 −13.99±9.02 <0.0001* 97.45±7.56 98.16±8.66 0.71±7.50 0.727
Whole Breast 95.78±6.74 86.55±6.22 −9.23±6.93 0.0002* 101.87±7.14 104.27±7.42 2.39±4.81 0.085

Abbreviations:

ROI=region of interest

Statistical analysis: two tailed, paired student t test

*

Statistically significant

Figure 2.

Figure 2

Box plots demonstrating the mean B1 signal (% of intended B1) and standard deviations between the right and left breasts for all patients in the study. Whole breast B1 signal significantly differed between right and left breast with single-source RF excitation. However, there was no statistically difference in whole breast B1 signal with dual-source parallel RF excitation.

Figure 3.

Figure 3

Figure 3

B1 homogeneity between the right and left breasts in the same patient obtained with conventional single-source RF excitation (A) and dual-source parallel RF excitation (B) techniques. Note that both visually and quantitatively, there is a significant decrease in B1 signal intensity in the left breast with single-source RF excitation whereas a more homogeneous B1 signal is obtained across the breasts with dual-source parallel RF excitation technique.

Regional B1 Values and Comparisons

Intra-patient regional B1 values significantly differed between right and left on single-source RF excitation in the lateral (p=0.014), central (p=0.0001), medial (p=0.0013), and posterior (p<0.0001) locations, with posterior regions demonstrating the greatest B1 inhomogeneities (Δ=−14%). Conversely, mean B1 values differed significantly on dual-source parallel RF excitation for only the anterior (p=0.030) and lateral (p=0.0003) locations, Table 1.

Discussion

Single-source RF transmission attempts to generate a circularly polarized RF field by utilizing a single RF source that is split between two ports 90° apart. This design, termed quadrature drive or mode, was adequate at 1.5T and lower magnetic (B0) field strengths. However, at 3T field strength, standing wave effects are more problematic, particularly in larger patients, resulting in non-uniform RF excitation across the field of view. Recently, several studies have demonstrated that the use of multiple channels with parallel RF excitation can substantially improve image homogeneity in both body and musculoskeletal imaging applications (5,6,810). However, there are currently no published studies that specifically examine the use of this novel technique for the breast imaging application, where B1 inhomogeneities are particularly problematic due to off-center positioning of patients’ breasts in the whole-body RF coil (2).

The system utilized in our study enables the use of both single-source RF excitation and dual-source excitation within the body coil, allowing for our intra-examination comparisons. We demonstrated that there is improvement in B1 homogeneity with dual-source parallel RF excitation techniques on 3D breast MRI when compared to the conventional single-source technique. For whole breast averaged B1 measures, there were significant right-to-left differences on single-source RF excitation maps, but not on dual-source RF excitation maps. When evaluating location specific B1 values, we noted that improvements in B1 homogeneity were greatest in the central, medial, and posterior aspects of the breasts.

However, we did note that there was significant right-to-left B1 inhomogeneity on dual-source RF excitation B1 maps at the anterior location that was not significant on the single-source maps. The reason for this is unclear but could demonstrate that the dual-source method is only able to correct low-order spatial variations in B1. Higher channel parallel RF excitation techniques may further improve B1 homogeneity for breast imaging. Additional investigation into this phenomenon is warranted.

Our results confirm quantitatively the B1 inhomogeneity challenges that have been previously described (1,2). Prior authors have reported that tissue signal variability due to reduced B1 occurred most prominently in the right breast while we observed this phenomenon affecting the left breast. This difference is readily explained by patient positioning; the 16-channel coil used for our study enables us to scan patients oriented feet first rather than head first (as was utilized by Azlan et al and Kuhl et al).

Our study has several limitations. We evaluated a small number of patients (n=14), and future larger studies would be useful to confirm our results. However, our results agree with those of previous reports for body MR applications demonstrating improved B1 homogeneity with dual-source parallel RF excitation (6). Additionally, we sought only to evaluate quantitative differences in B1 homogeneity; we did not qualitatively assess the appearance of corresponding T1-weighted and T2-weighted images or the effect of B1 inhomogeneity on clinical interpretation. Finally, as our study was performed on a single 3T Philips MR scanner, our results of improved B1 homogeneity using dual-source parallel excitation may be vendor specific.

In conclusion, our study confirms that dual-source parallel excitation can significantly improve B1 homogeneity over conventional single-source excitation techniques in breast MRI at 3T. This technique has the potential to substantially reduce a major challenge of breast MRI at higher field strength and improve tissue contrast and lesion conspicuity.

Acknowledgements

The authors would like to acknowledge our talented MRI technologists, [BLINDED], for their dedicated technical assistance.

Funding Support: NIH Grant RO1CA151326

References

  • 1.Kuhl CK, Kooijman H, Gieseke J, Schild HH. Effect of B1 inhomogeneity on breast MR imaging at 3.0 T. Radiology. 2007;244(3):929–930. doi: 10.1148/radiol.2443070266. [DOI] [PubMed] [Google Scholar]
  • 2.Azlan CA, Di Giovanni P, Ahearn TS, Semple SI, Gilbert FJ, Redpath TW. B1 transmission-field inhomogeneity and enhancement ratio errors in dynamic contrast-enhanced MRI (DCE-MRI) of the breast at 3T. J Magn Reson Imaging. 2010;31(1):234–239. doi: 10.1002/jmri.22018. [DOI] [PubMed] [Google Scholar]
  • 3.Rakow-Penner R, Hargreaves BA, Glover GH, Daniel B. Breast MRI at 3T. Applied Radiology. 2009;38(3):6–13. [Google Scholar]
  • 4.Partridge SC, Rahbar H, Lehman CD. Breast MR imaging. In: Kamel IR, Merkle EM, editors. Body MR Imaging at 3 Tesla. Cambridge University Press; 2011. pp. 26–33. [Google Scholar]
  • 5.Nelles M, Konig RS, Gieseke J, et al. Dual-source parallel RF transmission for clinical MR imaging of the spine at 3.0 T: intraindividual comparison with conventional single-source transmission. Radiology. 2010;257(3):743–753. doi: 10.1148/radiol.10092146. [DOI] [PubMed] [Google Scholar]
  • 6.Willinek WA, Gieseke J, Kukuk GM, et al. Dual-source parallel radiofrequency excitation body MR imaging compared with standard MR imaging at 3.0 T: initial clinical experience. Radiology. 2010;256(3):966–975. doi: 10.1148/radiol.10092127. [DOI] [PubMed] [Google Scholar]
  • 7.Yarnykh VL. Actual flip-angle imaging in the pulsed steady state: a method for rapid three-dimensional mapping of the transmitted radiofrequency field. Magn Reson Med. 2007;57(1):192–200. doi: 10.1002/mrm.21120. [DOI] [PubMed] [Google Scholar]
  • 8.Katscher U, Bornert P. Parallel RF transmission in MRI. NMR Biomed. 2006;19(3):393–400. doi: 10.1002/nbm.1049. [DOI] [PubMed] [Google Scholar]
  • 9.Ullmann P, Junge S, Wick M, Seifert F, Ruhm W, Hennig J. Experimental analysis of parallel excitation using dedicated coil setups and simultaneous RF transmission on multiple channels. Magn Reson Med. 2005;54(4):994–1001. doi: 10.1002/mrm.20646. [DOI] [PubMed] [Google Scholar]
  • 10.Vernickel P, Roschmann P, Findeklee C, et al. Eight-channel transmit/receive body MRI coil at 3T. Magn Reson Med. 2007;58(2):381–389. doi: 10.1002/mrm.21294. [DOI] [PubMed] [Google Scholar]

RESOURCES