Vitamin D Receptor Polymorphisms Relate to Risk of Adenomatous Polyps in a Sex-Specific Manner

被引:15
作者
Beckett, Emma Louise [1 ,2 ]
Le Gras, Kathleen [1 ]
Martin, Charlotte [1 ]
Boyd, Lyndell [1 ]
Ng, Xiaowei [1 ]
Duesing, Konsta [2 ]
Yates, Zoe [3 ]
Veysey, Martin [4 ]
Lucock, Mark [1 ]
机构
[1] Univ Newcastle, Sch Environm & Life Sci, Brush Rd,POB 127, Ourimbah, NSW 2258, Australia
[2] CSIRO, Food & Nutr Flagship, N Ryde, NSW 2113, Australia
[3] Univ Newcastle, Sch Biomed Sci & Pharm, Ourimbah, NSW 2258, Australia
[4] Cent Coast Local Hlth Dist, Teaching & Res Unit, POB 361, Gosford 2250, Australia
来源
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL | 2016年 / 68卷 / 02期
关键词
GENE POLYMORPHISMS; COLORECTAL-CANCER; HEPATOCELLULAR-CARCINOMA; HAPLOTYPE RECONSTRUCTION; DIETARY CALCIUM; COLON; ASSOCIATION; VDR; METABOLITES; GENOTYPES;
D O I
10.1080/01635581.2016.1142584
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
VitaminD receptor(VDR) genepolymorphisms may influence risk for adenomatous polyps (AP), a benign precursor to colon cancer, via modulation of vitamin D sensitive pathways, including cell proliferation and differentiation. However, results have been mixed and any association remains contentious. Failure to clinically exclude the presence of (AP in control cohorts may contribute to the lack of consensus. Therefore, we assessed the role of the FokI, BsmI, ApaI, and TaqI VDR polymorphisms in modifying risk for AP, adjusting for a range of dietary and lifestyle variables. Blood was collected from colonoscopy patients (n = 258) and VDR polymorphisms assessed by restriction fragment length polymorphism. Dietary habits were estimated from food frequency questionnaires. Odds ratios for AP were calculated by genotype, stratified by sex, and adjusted for age, lifestyle, and dietary factors. FokI was associated with modified risk for AP in males, whereas the BsmI/ApaI/TaqI haplotype was associated with modified risk in females. No interaction was found between VDR variants and vitamin D intake. This study offers novel insight into the potential for VDR genetics to contribute to risk for AP and is the first to demonstrate a sex-specific relationship between these polymorphisms and risk for AP.
引用
收藏
页码:193 / 200
页数:8
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