Vitamin D receptor polymorphisms and breast cancer risk in a large population-based case-control study of Caucasian and African-American women
2007

Vitamin D Receptor Polymorphisms and Breast Cancer Risk

Sample size: 3066 publication 10 minutes Evidence: moderate

Author Information

Author(s): Trabert Britton, Malone Kathleen E, Daling Janet R, Doody David R, Bernstein Leslie, Ursin Giske, Marchbanks Polly A, Strom Brian L, Humphrey Mariela C, Ostrander Elaine A

Primary Institution: Fred Hutchinson Cancer Research Center

Hypothesis

Are polymorphisms in the vitamin D receptor gene associated with breast cancer risk in Caucasian and African-American women?

Conclusion

The study found an increased risk for breast cancer in postmenopausal Caucasian women with the BsmI bb genotype, but no significant associations were observed in African-American women.

Supporting Evidence

  • The study included a large sample size of 3,066 women.
  • Significant associations were found for the BsmI genotype in postmenopausal Caucasian women.
  • No significant associations were observed for the Poly(A) genotype.
  • The study controlled for various known breast cancer risk factors.

Takeaway

This study looked at how certain gene changes might affect the risk of getting breast cancer, especially in older white women.

Methodology

The study used a population-based case-control design, examining the association between VDR gene polymorphisms and breast cancer risk among women aged 35 to 64.

Potential Biases

Potential biases may arise from the over-sampling of women with a family history of breast cancer.

Limitations

The study was limited by the fact that only two positions of the VDR gene were examined, and the sample size for certain genotypes was small.

Participant Demographics

Participants included Caucasian and African-American women aged 35 to 64, with a total of 1,631 cases and 1,435 controls.

Statistical Information

P-Value

0.03

Confidence Interval

1.04 to 2.27

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/bcr1833

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