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Obesity and Metabolic Dysfunction Correlate with Background Parenchymal Enhancement in Premenopausal Women

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Abstract

Objective: This study tested the hypothesis that obesity and metabolic abnormalities correlate with background parenchymal enhancement (BPE), the volume and intensity of enhancing fibroglandular breast tissue on dynamic contrast-enhanced magnetic resonance imaging.

Methods: Participants included 59 premenopausal women at high risk of breast cancer. Obesity was defined as BMI ≥ 30 kg/m . Metabolic parameters included dual-energy x-ray absorptiometry-quantified body composition, plasma biomarkers of insulin resistance, adipokines, inflammation, lipids, and urinary sex hormones. BPE was assessed using computerized algorithms on dynamic contrast-enhanced magnetic resonance imaging.

Results: BMI was positively correlated with BPE (r = 0.69; p < 0.001); participants with obesity had higher BPE than those without obesity (404.9 ± 189.6 vs. 261.8 ± 143.8 cm ; Δ: 143.1 cm [95% CI: 49.5-236.7]; p = 0.003). Total body fat mass (r = 0.68; p < 0.001), body fat percentage (r = 0.64; p < 0.001), visceral adipose tissue area (r = 0.65; p < 0.001), subcutaneous adipose tissue area (r = 0.60; p < 0.001), insulin (r = 0.59; p < 0.001), glucose (r = 0.35; p = 0.011), homeostatic model of insulin resistance (r = 0.62; p < 0.001), and leptin (r = 0.60; p < 0.001) were positively correlated with BPE. Adiponectin (r = -0.44; p < 0.001) was negatively correlated with BPE. Plasma biomarkers of inflammation and lipids and urinary sex hormones were not correlated with BPE.

Conclusions: In premenopausal women at high risk of breast cancer, increased BPE is associated with obesity, insulin resistance, leptin, and adiponectin.

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References
1.
Arasu V, Miglioretti D, Sprague B, Alsheik N, Buist D, Henderson L . Population-Based Assessment of the Association Between Magnetic Resonance Imaging Background Parenchymal Enhancement and Future Primary Breast Cancer Risk. J Clin Oncol. 2019; 37(12):954-963. PMC: 6494266. DOI: 10.1200/JCO.18.00378. View

2.
Wei D, Jahani N, Cohen E, Weinstein S, Hsieh M, Pantalone L . Fully automatic quantification of fibroglandular tissue and background parenchymal enhancement with accurate implementation for axial and sagittal breast MRI protocols. Med Phys. 2020; 48(1):238-252. PMC: 7902433. DOI: 10.1002/mp.14581. View

3.
King V, Gu Y, Kaplan J, Brooks J, Pike M, Morris E . Impact of menopausal status on background parenchymal enhancement and fibroglandular tissue on breast MRI. Eur Radiol. 2012; 22(12):2641-7. DOI: 10.1007/s00330-012-2553-8. View

4.
Shepherd J, Ng B, Sommer M, Heymsfield S . Body composition by DXA. Bone. 2017; 104:101-105. PMC: 5659281. DOI: 10.1016/j.bone.2017.06.010. View

5.
Ehret C, Zhou S, Tchou J, Schmitz K, Sturgeon K . Dose-dependent effects of aerobic exercise on clinically relevant biomarkers among healthy women at high genetic risk for breast cancer: A secondary analysis of a randomized controlled study. Cancer Rep (Hoboken). 2021; 5(5):e1497. PMC: 9124506. DOI: 10.1002/cnr2.1497. View