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First Pregnancy Characteristics, Postmenopausal Breast Density, and Salivary Sex Hormone Levels in a Population at High Risk for Breast Cancer

Supporting Files


Details

  • Alternative Title:
    BBA Clin
  • Personal Author:
  • Description:
    Background

    It remains unknown if later life breast cancer risk as determined by reproductive history is mediated by postmenopausal breast density and/or sex steroid levels.

    Methods

    Increased breast density is a strong surrogate for future breast cancer risk. A cross-sectional study with a longitudinal follow up for breast health outcomes evaluated women without breast cancer (n = 1,023; 682 = parous), drawn from a high risk postmenopausal population, with questionnaire reported reproductive histories. The questionnaire was linked to prospective screening mammogram breast density measurements, and saliva biospecimens that were used to assess sex steroid hormone levels.

    Results

    Expected age and postmenopause related declines in salivary estradiol (E), progesterone (P), dehydroepiandrosterone (DHEA) and testosterone (T) levels were observed. This was most pronounced for DHEA and T, which were also the only postmenopausal hormone levels significantly associated with any reproductive characteristics: parity and breast feeding for DHEA, age-at-first birth for T. Postmenopausal breast density was borderline significantly lower with parity and higher body mass index (BMI). After multivariate analysis, T was the only hormone level to retain any association (negative, p<0.05) with breast density.

    Conclusions and General Significance

    While reproductive characteristics, in particular parity, generally demonstrated independent associations with postmenopausal breast density and E, P and DHEA levels, T levels showed concordant inverse associations with age-at-first birth and breast density. These findings suggest that reproductive effects and later life salivary sex steroid hormone levels may have independent effects on later life breast density and cancer risk.

  • Subjects:
  • Source:
    BBA Clin. 3:189-195.
  • Pubmed ID:
    26317068
  • Pubmed Central ID:
    PMC4547694
  • Document Type:
  • Funding:
  • Volume:
    3
  • Collection(s):
  • Main Document Checksum:
    urn:sha256:64877d153583eacd288ca8fbcb061c7a58fdc5b4974760fc3b3e046635b6ac30
  • Download URL:
  • File Type:
    Filetype[PDF - 367.79 KB ]
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