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Gut microbiome, body weight, and mammographic breast density in healthy postmenopausal women.
Yaghjyan, Lusine; Mai, Volker; Wang, Xuefeng; Ukhanova, Maria; Tagliamonte, Maximiliano; Martinez, Yessica C; Rich, Shannan N; Egan, Kathleen M.
Affiliation
  • Yaghjyan L; Department of Epidemiology, College of Public Health and Health Professions and College of Medicine, University of Florida, Gainesville, FL, USA.
  • Mai V; Department of Epidemiology, College of Public Health and Health Professions and College of Medicine, University of Florida, Gainesville, FL, USA.
  • Wang X; Emerging Pathogens Institute, University of Florida, Gainesville, FL, USA.
  • Ukhanova M; H. Lee Moffitt Cancer Center, Tampa, FL, USA.
  • Tagliamonte M; Emerging Pathogens Institute, University of Florida, Gainesville, FL, USA.
  • Martinez YC; Emerging Pathogens Institute, University of Florida, Gainesville, FL, USA.
  • Rich SN; H. Lee Moffitt Cancer Center, Tampa, FL, USA.
  • Egan KM; Department of Epidemiology, College of Public Health and Health Professions and College of Medicine, University of Florida, Gainesville, FL, USA.
Cancer Causes Control ; 32(7): 681-692, 2021 Jul.
Article in En | MEDLINE | ID: mdl-33772705
ABSTRACT

PURPOSE:

We examined gut microbiome (GM) profiles in relation to mammographic breast density (BD) and body mass index (BMI) in healthy postmenopausal women.

METHODS:

Eligible women were postmenopausal, had a BMI ≤ 35 kg/m2, and had not recently taken oral/IV antibiotics. All women provided a fecal sample and information on breast cancer risk factors. Mammographic BD was classified with the American College of Radiology's BI-RADS BD classification system. Bacterial DNA was isolated from fecal samples and the V1-V2 hypervariable regions of 16S rRNA were sequenced on the Illumina MiSeq platform. We examined associations of GM with indices of within-sample (alpha) diversity and the ratio of the two main phyla (Firmicutes and Bacteroidetes; F/B ratio) with BD and BMI.

RESULTS:

Among 69 women with BD data, 39 had low BD (BI-RADS I/II) and 30 had high BD (BI-RADS III/IV). BMI was inversely associated with BD (mean BMI = 23.8 and 28.0 in women with high and low BD, respectively, p = 1.07 × 10-5). Similar levels of GM diversity were found across weight groups according to Shannon (p = 0.83); Inverse Simpson (p = 0.97); and Chao1 (p = 0.31) indices. F/B ratio and microbiota diversity were suggestively greater in women with high vs. low BD (p = 0.35, 0.14, 0.15, and 0.17 for F/B ratio, Shannon, Inverse Simpson and Chao1, respectively).

CONCLUSION:

Suggestive differences observed in women with high and low BD with respect to GM alpha diversity and prevalence of specific GM taxa need to be confirmed in larger studies.
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Full text: 1 Database: MEDLINE Main subject: Body Weight / Microbiota / Gastrointestinal Microbiome Type of study: Risk_factors_studies Limits: Aged / Female / Humans / Middle aged Language: En Journal: Cancer Causes Control Journal subject: EPIDEMIOLOGIA / NEOPLASIAS Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Body Weight / Microbiota / Gastrointestinal Microbiome Type of study: Risk_factors_studies Limits: Aged / Female / Humans / Middle aged Language: En Journal: Cancer Causes Control Journal subject: EPIDEMIOLOGIA / NEOPLASIAS Year: 2021 Type: Article Affiliation country: United States