An inverse correlation between cancer mortality rates and regional solar UV-B radiation exposure, a major source of vitamin D (vit D), has been found for cancers of the breast, colon, rectum, ovary, prostate, stomach, and numerous other cancers. Dietary and serum studies also demonstrate that vit D is a risk factor in colonic adenomas and for numerous cancers. The anticancer effect of vit D is strongly supported by in vitro and animal studies. However, no randomized clinical trials have used a vit D intervention sufficient to raise serum 25OHD to optimum levels and have targeted a cancer outcome. We reported a double-blind, placebo-controlled, randomized trial of calcium (Ca) and vit D supplementation in a population-based sample of postmenopausal women. A secondary objective of that study was to determine the efficacy of Ca alone and of Ca plus vit D3 in reducing risk of cancer of all types. We found that vit D3 significantly reduced the risk of all-types cancer by 60%. These findings need to be confirmed with a clinical trial designed with incidence of cancer as the primary outcome. In this application we propose to test whether increasing serum 25OHD to optimal levels, while maintaining adequate Ca intake, reduces the incidence of cancer in a population-based sample of postmenopausal women 60+ years of age.
The Specific Aims are to: 1. Sample randomly the population of healthy independently-living postmenopausal women 60 years and older from 9 rural counties;2. Enroll 2300 women into an intervention study, assign them randomly to 1 of 2 treatment groups: 1) vit D3 (2000 IU/d) and Ca (1200 mg/d), or 2) vit D3 placebo and Ca placebo, and to follow each subject for 4 years;3. Collect and store white blood cells from every subject to test for genetic markers should the intervention be found effective;4. Determine the effect of supplementation with vit D3 on incidence of all types of cancer combined;5. Determine in a nested-case control study the association of serum 25OHD collected at baseline and the end of year 1 with risk of cancer over 4 years;6. Determine the effect of supplementation with calcium and vit D3 on incidence of specific cancers: breast, lung, colon and myeloma, leukemia, lymphoma. 7. Determine the effect of supplementation on incidence of other disorders, specifically hypertension, cardiovascular disease, osteoarthritis, colonic adenomas and diabetes, upper respiratory infections and falls. At each 6-mo visit, we will assess: medical and social history;adverse events;cancer diagnoses;and adherence to supplement/placebo. Annually, we will obtain height and weight and analyze serum 25OHD. At baseline and end of 4 yrs, we will assess dietary intake and physical activity. The proposed study addresses the goal of NCI's Strategic Plan to """"""""eliminate the suffering and death due to cancer by 2015."""""""" It specifically addresses Strategic Objective 2, to """"""""accelerate progress in cancer prevention."""""""" Positive findings from our nutritional intervention study will result in an inexpensive, safe method of preventing cancer.

Public Health Relevance

Project Narrative The purpose of this project is to determine whether, in a rigorous clinical trial, vitamin D3 and calcium supplementation decreases risk of all types of cancer. Positive findings will provide support for health policy changes to promote optimal vitamin D levels in the population.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA129488-05
Application #
8391272
Study Section
Chemo/Dietary Prevention Study Section (CDP)
Program Officer
Riscuta, Gabriela
Project Start
2009-01-01
Project End
2014-11-30
Budget Start
2012-12-12
Budget End
2014-11-30
Support Year
5
Fiscal Year
2013
Total Cost
$663,406
Indirect Cost
$197,032
Name
Creighton University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
053309332
City
Omaha
State
NE
Country
United States
Zip Code
68178
Zhang, Mingzhi; Zhao, Lan-Juan; Zhou, Yu et al. (2017) SNP rs11185644 of RXRA gene is identified for dose-response variability to vitamin D3 supplementation: a randomized clinical trial. Sci Rep 7:40593
Zhou, Yu; Zhao, Lan-Juan; Xu, Xiaojing et al. (2014) DNA methylation levels of CYP2R1 and CYP24A1 predict vitamin D response variation. J Steroid Biochem Mol Biol 144 Pt A:207-14
Zhou, Qiu-Hong; Zhao, Lan-Juan; Wang, Ping et al. (2014) Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women. PLoS One 9:e112358
Zhao, Lan-Juan; Zhou, Yu; Bu, Fengxiao et al. (2012) Factors predicting vitamin D response variation in non-Hispanic white postmenopausal women. J Clin Endocrinol Metab 97:2699-705
Bu, Feng-Xiao; Armas, Laura; Lappe, Joan et al. (2010) Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects. Hum Genet 128:549-56