Background: Uterine leiomyomata (also known as fibroids) are benign tumors of uterine smooth muscle that are characterized by overproduction of extracellular matrix. Fibroids are the leading indication for hysterectomy in the United States. The active metabolite of vitamin D has been shown to inhibit cell proliferation and extracellular matrix production in fibroid tissue culture and to reduce fibroid volume in the Eker rat. No previous study has examined whether vitamin D is related to fibroid status in women.
Methods: The National Institute of Environmental Health Sciences Uterine Fibroid Study enrolled randomly selected 35- to 49-year-old women who were members of an urban health plan during 1996–1999. Fibroid status was determined by ultrasound screening of premenopausal women (620 blacks, 416 whites). Vitamin D status was assessed in stored plasma by radioimmunoassay of 25-hydroxyvitamin D (25(OH)D) and questionnaire data on sun exposure. Associations were evaluated with logistic regression, controlling for potential confounders.
Results: Only 10% of blacks and 50% of whites had levels of 25(OH)D regarded as sufficient (>20 ng/ml). Women with sufficient vitamin D had an estimated 32% lower odds of fibroids compared with those with vitamin D insufficiency (adjusted odds ratio [aOR] = 0.68, 95% confidence interval [CI] = 0.48–0.96). The association was similar for blacks and whites. Self-reported sun exposure ≥1 hour per day (weather permitting) was also associated with reduced odds of fibroids (aOR = 06. [0.4–0.9]), with no evidence of heterogeneity by ethnicity.
Conclusions: The consistency of findings for questionnaire and biomarker data, the similar patterns seen in blacks and whites, and the biological plausibility provide evidence that sufficient vitamin D is associated with a reduced risk of uterine fibroids.
From the aEpidemiology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC; bDepartment of Radiology, George Washington University Medical Center, George Washington University, Washington, DC; cDepartment of Health Care Sciences, George Washington University Medical Center, George Washington University, Washington, DC; and dDepartment of Pediatrics, The Medical University of South Carolina, Charleston, SC.
Current affiliation: Joel M. Schectman, University of Virginia, Charlottesville, VA.
Supported by the intramural program at the National Institute of Environmental Health Sciences, NIH, with support from the Office of Research on Minority Health, National Institutes of Health, HHS.
Correspondence: Donna D. Baird, National Institute of Environmental Health Sciences, P.O. Box 12233, Research Triangle Park, NC 27709. E-mail: firstname.lastname@example.org.
Received July 31, 2012
Accepted December 30, 2012