4.6 Article

Changes in Body Mass Index, Leptin, and Leptin Receptor Polymorphisms and Breast Cancer Risk

Journal

DNA AND CELL BIOLOGY
Volume 37, Issue 3, Pages 182-188

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/dna.2017.4047

Keywords

breast cancer; body mass index; leptin polymorphisms; leptin receptor polymorphisms; case-control study

Funding

  1. National Natural Science Foundation of China [81302500]
  2. People-benefit Project of Chengdu Science and Technology Bureau [2015-HM01-00049-SF]

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Obesity is a strong risk factor for breast cancer. The polymorphisms of leptin (LEP) and leptin receptor (LEPR) may be associated with breast cancer by regulator of adipose tissue mass and tumor cell growth. A total of 794 cases and 805 matched controls were sequentially enrolled. Time-of-flight mass spectrometry was used to determine the LEPrs7799039, LEPRrs1137100, and LEPRrs1137101 genotypes for each participant. Associations between polymorphisms of these genes, change in body mass index (BMI), and breast cancer risk were assessed by unconditional multivariable logistic regression models. The unconditional logistic regression model showed that persistent overweight (BMI 24kg/m(2)) over the preceding 10 years was associated with increased breast cancer risk in premenopausal women (odds ratio [OR]=1.67, 95% confidence interval [CI]: 1.19-2.35). No associations between LEPrs7799039, LEPRrs1137100, or LEPRrs1137101 polymorphisms alone and breast cancer risk were found. Persistent overweight over the preceding 10 years and carrying the LEPrs7799039 AA genotype together increased breast cancer risk in premenopausal women (ORadj=2.00, 95% CI: 1.26-3.16). Persistent overweight over the preceding 10 years and carrying the LEPRrs1137100 GG genotype increased breast cancer risk in premenopausal women (ORadj=1.68, 95% CI: 1.06-2.68). In premenopausal women, persistent overweight (BMI 24kg/m(2)) over the preceding 10 years increases breast cancer risk. Persistent overweight along with LEPrs7799039 AA or LEPRrs1137100 GG genotypes synergistically increase risk of breast cancer among premenopausal women.

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