Variants in Vitamin D-related Genes and Prostate Cancer Risk in Black Men

Author:

Layne Tracy M.ORCID,Rothstein Joseph H.,Song Xiaoyu,Andersen Shaneda Warren,Benn Emma K.T.,Sieh Weiva,Klein Robert J.

Abstract

ABSTRACTBACKGROUNDThe relationship between vitamin D and prostate cancer has primarily been characterized among White men. However, Black men have higher prostate cancer incidence and mortality rates, chronically low circulating vitamin D levels, and ancestry-specific genetic variants in vitamin D-related genes. Here, we examine six critical genes in the vitamin D pathway and prostate cancer risk in Black men.METHODSWe assessed a total of 69 candidate variants in six genes (GC, CYP27A1, CYP27B1, CYP24A1, VDR, andRXRA) including functional variants previously associated with prostate cancer and circulating 25(OHD) in White men. Associations with prostate cancer risk were examined using genome-wide association study data for approximately 10,000 prostate cancer cases and 10,000 controls among Black men and over 85,000 cases and 91,000 controls among White men. A statistical significance threshold of 0.000724 was used to account for the 69 variants tested.RESULTSNone of the variants examined were significantly associated with prostate cancer risk among Black men after multiple comparison adjustment. Four variants tested P<0.05 in Black men, including two inRXRA(rs41400444 OR=1.09, 95% CI: 1.01-1.17,P= 0.024 and rs10881574 OR = 0.93, 0.87-1.00,P= 0.046) and two inVDR(rs2853563 OR = 1.07, 1.01-1.13,P= 0.017 and rs1156882 OR = 1.06, 1.00-1.12,P= 0.045). Two variants inVDRwere also positively associated with risk in White men (rs11568820 OR = 1.04, 1.02-1.06,P= 0.00024 and rs4516035 OR = 1.03, 1.01-1.04,P= 0.00055).CONCLUSIONWe observed suggestive non-significant associations between genetic variants inRXRAandVDRand prostate cancer risk in Black men. Future research exploring the relationship of vitamin D with cancer risk in Black men will need larger sample sizes to identify ancestry-specific variants relevant to risk in this population.

Publisher

Cold Spring Harbor Laboratory

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