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Original Articles

Metabolic Syndrome and Mammographic Density in Premenopausal Chilean Women

, , &
Pages 254-260 | Received 11 May 2016, Accepted 04 Nov 2016, Published online: 03 Jan 2017
 

ABSTRACT

Background: Metabolic syndrome (MetS) has been previously associated with an increased risk of breast cancer in postmenopausal women. Mammographic density (MD) is a marker of breast cancer risk. There is little evidence of an association between MetS and MD in premenopausal women. Methods: Through a cross-sectional study, we evaluated 364 premenopausal Chilean women in which we measured anthropometric, blood pressure, and metabolic markers. MetS and its components were defined according to the National Cholesterol Education Program Adult Treatment Plan III criteria. We estimated MD by absolute dense volume (ADV, cm3), nondense volume (NDV, cm3), and percentage of dense volume (PDV, %). The relationship between MetS and MD was assessed by linear regression models. Results: After adjusting for sociodemographic and gyneco-obstetrics variables, nonsignificant association was found between MetS and ADV (log β = 0.10; 95%CI: −0.01, 0.21). However, abdominal obesity, high triglycerides, and number of components of MetS were directly related to higher ADV (P < 0.05). Conclusion: Our results showed no association between MetS and ADV; nevertheless, abdominal obesity and triglycerides were related to higher ADV. If MD could be modifiable through nutritional factors, it would open new perspectives for the prevention of breast cancer through obesity prevention strategies at population level.

Abbreviations

MetS=

Metabolic syndrome

ADV=

Absolute dense volume

NDV=

Nondense volume

PDV=

Percentage of dense volume

ADA=

Absolute dense area

PDA=

Percentage of dense area

Acknowledgments

The authors' responsibilities were as follows: MLG and AM: designed the study; MLG and HM: planned analyses; HM and AM: conducted the analyses; AM and MLG wrote the original draft of the article; and AP, HM, and MLG: helped in editing the drafts.

Funding

This study was financially supported by grant Fondecyt #11100238, Fondecyt # 1120326, Fondecyt # 1130277 and the World Cancer Research Fund 2010/245. Ana Pereira Scalabrino is funded by the Ellison Medical Foundation Grant.

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