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Obesity and metabolic dysfunction correlate with background parenchymal enhancement in premenopausal women.
Brown, Justin C; Ligibel, Jennifer A; Crane, Tracy E; Kontos, Despina; Yang, Shengping; Conant, Emily F; Mack, Julie A; Ahima, Rexford S; Schmitz, Kathryn H.
Afiliação
  • Brown JC; Pennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
  • Ligibel JA; LSU Health Sciences Center New Orleans School of Medicine, New Orleans, Louisiana, USA.
  • Crane TE; Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, Louisiana, USA.
  • Kontos D; Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • Yang S; Miller School of Medicine, University of Miami, Miami, Florida, USA.
  • Conant EF; University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Mack JA; Pennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
  • Ahima RS; University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Schmitz KH; Penn State College of Medicine, Hershey, Pennsylvania, USA.
Obesity (Silver Spring) ; 31(2): 479-486, 2023 02.
Article em En | MEDLINE | ID: mdl-36628617
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/m2 . 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 cm2 ; Δ: 143.1 cm2 [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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Resistência à Insulina Limite: Female / Humans Idioma: En Revista: Obesity (Silver Spring) Assunto da revista: CIENCIAS DA NUTRICAO / FISIOLOGIA / METABOLISMO Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Resistência à Insulina Limite: Female / Humans Idioma: En Revista: Obesity (Silver Spring) Assunto da revista: CIENCIAS DA NUTRICAO / FISIOLOGIA / METABOLISMO Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos