Jones Patrice, Lucock Mark, Chaplin George, Jablonski Nina G, Veysey Martin, Scarlett Christopher, Beckett Emma
School of Environmental & Life Sciences, University of Newcastle, 10 Chittaway Rd, Ourimbah, NSW, 2258, Australia.
Hunter Medical Research Institute, New Lambton Heights, NSW, Australia.
Genes Nutr. 2020 Mar 13;15(1):5. doi: 10.1186/s12263-020-00663-3.
The frequency of vitamin D-associated gene variants appear to reflect changes in long-term ultraviolet B radiation (UVB) environment, indicating interactions exist between the primary determinant of vitamin D status, UVB exposure and genetic disposition. Such interactions could have health implications, where UVB could modulate the impact of vitamin D genetic variants identified as disease risk factors. However, the current understanding of how vitamin D variants differ between populations from disparate UVB environments is limited, with previous work examining a small pool of variants and restricted populations only.
Genotypic data for 46 variants within multiple vitamin D-related loci (DHCR7/NADSYN1, GC, CYP2R1, CYP11A1, CYP27A1, CYP24A1, VDR, RXRα and RXRγ) was collated from 60 sample sets (2633 subjects) with European, East Asian and Sub-Saharan African origin via the NCBI 1000 Genomes Browser and ALFRED (Allele Frequency Database), with the aim to examine for patterns in the distribution of vitamin D-associated variants across these geographic areas.
The frequency of all examined genetic variants differed between populations of European, East Asian and Sub-Saharan African ancestry. Changes in the distribution of variants in CYP2R1, CYP11A1, CYP24A1, RXRα and RXRγ genes between these populations are novel findings which have not been previously reported. The distribution of several variants reflected changes in the UVB environment of the population's ancestry. However, multiple variants displayed population-specific patterns in frequency that appears not to relate to UVB changes.
The reported population differences in vitamin D-related variants provides insight into the extent by which activity of the vitamin D system can differ between cohorts due to genetic variance, with potential consequences for future dietary recommendations and disease outcomes.
维生素D相关基因变异的频率似乎反映了长期紫外线B辐射(UVB)环境的变化,这表明维生素D状态的主要决定因素、UVB暴露和遗传倾向之间存在相互作用。这种相互作用可能对健康产生影响,UVB可能会调节被确定为疾病风险因素的维生素D基因变异的影响。然而,目前对于来自不同UVB环境的人群中维生素D变异如何不同的理解有限,之前的研究仅考察了一小部分变异和有限的人群。
通过NCBI 1000基因组浏览器和ALFRED(等位基因频率数据库),整理了来自欧洲、东亚和撒哈拉以南非洲的60个样本集(2633名受试者)中多个维生素D相关基因座(DHCR7/NADSYN1、GC、CYP2R1、CYP11A1、CYP27A1、CYP24A1、VDR、RXRα和RXRγ)内46个变异的基因型数据,旨在研究这些地理区域中维生素D相关变异的分布模式。
所有检测的基因变异在欧洲、东亚和撒哈拉以南非洲血统的人群中频率不同。CYP2R1、CYP11A1、CYP24A1、RXRα和RXRγ基因变异在这些人群中的分布变化是此前未报道的新发现。几个变异的分布反映了人群祖先UVB环境的变化。然而,多个变异在频率上呈现出特定人群的模式,似乎与UVB变化无关。
所报道的维生素D相关变异的人群差异揭示了由于基因变异,维生素D系统活性在不同队列之间可能存在的差异程度,这可能对未来的饮食建议和疾病结局产生潜在影响。