Mehran Baboli1, Pippa Storey2, Terlika Pandit Sood2, Justin Fogarty2, Melanie Moccaldi2, Alana Lewin2, Linda Moy2, and Sungheon Gene Kim1
1Radiology, Weill Cornell Medicine, New York, NY, United States, 2Radiology, NYU Langone Health, New York, NY, United States
Synopsis
We
assessed the distribution of saturated fatty acid (SFA) in the adipose tissue around
malignant tumors and the whole breast of patients with benign and malignant
lesions. Bilateral gradient echo spectroscopic imaging sequence was acquired
simultaneously. A voxel-wise analysis in the frequency domain was then applied
to measure the SFA in each breast's adipose tissues and peri-tumoral region. Our
results showed that the SFA was significantly higher around the malignant tumor
than on the contralateral side, while no significant changes were observed with
benign lesions. The results indicate that the SFA may be closely associated
with the malignancy of lesions.
Introduction
The
breast is composed mainly of fibroglandular and adipose tissue (1). While breast cancer typically originates from the epithelial
cells in breast glandular tissue (2,3), it seems that the tumor initiates and progresses at the boundary
with adipose or other surrounding tissues (3). Studies have also discovered cross-talk between breast tumor
cells and neighboring adipocytes (3,4). These
findings suggest that adipocytes play an active part in the development
of breast cancer. In addition to the overall amount of body fat, fatty
acid composition (FAC) may also be important in cancer development. The purpose
of the study is to compare the saturated fatty acid in the mammary adipose
tissues around malignant and benign lesions with those in the ipsi- and contralateral
breasts.Methods
Nine women with a malignant
and/or benign (age: 63 ± 7 years) lesion in one breast were recruited for this IRB-approved study. Bilateral scans were
acquired using the 3D gradient-echo spectroscopic imaging (GSI) sequence with
dual slab excitation (5). on a whole-body 3T MRI scanner (TIM Trio; Siemens,
Erlangen, Germany) with a dedicated 16-element bilateral breast coil (In vivo,
Orlando, FL). The imaging parameters were: 2.8mm × 2.8mm × 2.8mm, GRAPPA
acceleration factor = 8, inter-echo spacing = 1.44ms, receiver bandwidth = 1410
Hz/pixel, flip angle =10° and TR = 213ms. The total scan time was
5:27 minutes. A clinical fat-saturated T1-weighted scan was also acquired, and
the ROIs were drawn in the clinical image by a fellowship-trained breast
imaging radiologist with four years of experience. The ROIs were then mapped on the GSI images for
further analysis. Fatty acid composition analysis was performed to measure the
saturated fatty acid (SFA) in the adipose tissue for both ipsi- and
contralateral breast as well as small ROI around the tumor. Results
Figure
1 shows an example of ROI drawn on clinical and GSI images. An example of SFA
maps in both breasts and around the tumor in patients with malignant and benign
lesions are shown in Figure 2. Figure 3 shows the boxplot comparison of SFA
between the whole contra and ipsilateral breast and the peri-lesion ROI for
benign and malignant lesions. Although the SFA is higher in the ipsilateral
breast than the contralateral breast in patients with the malignant lesion,
their difference is not significant (p=0.71). In contrast, a
significantly higher (p=0.007) SFA was observed in the adipose tissue
around the tumor compared to those in the ipsi and contralateral breasts. No
significant changes were observed for benign lesions.Discussion and Conclusion
The higher
SFA measurement around the tumor observed in this study agreed with previous mammary
adipose tissue studies (6). The voxel-wise spectral analysis used in this study
can effectively account for spatial variation in B0 and T2*
differences among lipid peaks. The results of this proof-of-concept study
demonstrate the importance of the spatial distribution of fatty acid
composition with respect to the lesion location. We plan to extend to a larger
cohort of women with malignant and benign lesions to assess the FAC's
diagnostic utility further.Acknowledgements
This
work was supported by grants R01CA160620, R01CA219964, and UG3CA228699 from the
National Institutes of Health.References
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