ESTIMATION OF THE FREQUENCY OF GENETIC VARIANTS ASSOCIATED WITH VITAMIN D LEVELS AND OSTEOPOROSIS IN THE POPULATION OF UKRAINE

Khrystyna Shchubelka, Walter W Wolfsberger, O. Oleksyk, Taras K. Oleksyk
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Abstract

Circulating vitamin D levels and the risk of osteoporosis have significant inheritance. Single nucleotide polymorphisms (SNPs) in the GC, DHCR7/NADSYN1, CYP2R1, CYP24A1, and SEC23A genes have shown significant association with these conditions in previous genome-wide association studies (GWAS). Objective: to study the frequency of alleles associated with circulating levels of vitamin D and osteoporosis in the cohort of Ukrainians, as well as to compare the frequencies of these variants with individuals of Western and Northern European origin. Materials and Methods. This paper presents the results of the study of the frequencies of genomic variants associated with vitamin D levels and osteoporosis in a cohort of 97 Ukrainians based on genome data obtained by whole genome sequencing (WGS), as well as comparing their frequencies with the combined European population (CEU) of the "1000 genomes" project (persons of Western and Northern European ancestry). Files with the primary publicly available genomic data of Ukrainians were annotated using ANNOVAR and SNPEff software using the reference database of the human genome version hg38. Comparison of allele frequencies between populations was performed using Fisher's exact test using the number of alleles in the two studied populations and the construction of conjugated 2x2 tables. Results. It was found that of the 22 single nucleotide polymorphisms included in the analysis, 10, namely rs2282679; rs4855; rs10033936; rs3755967; rs17467825; rs12639968; rs1155563; rs17216707; rs10745742; rs180119, significantly differ in the Ukrainian cohort comparatively to CEU. Using correlation analysis, we also found that the genotypes of SNPs rs3755967, rs17467825, rs2282679 and rs4855 in Ukrainians are completely correlated with each other (r = 1), which means that they are in a state of complete linkage in Ukrainians of the given cohorts. Conclusion. Such findings may be the evidence of evolutionary and adaptation processes in the regulation of vitamin D levels and bone mineral density in the population of Ukraine and requires further studies of phenotype-genotype relationship.
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乌克兰人群中维生素D水平和骨质疏松症相关基因变异频率的估计
循环中的维生素D水平和骨质疏松症的风险具有显著的遗传性。GC、DHCR7/NADSYN1、CYP2R1、CYP24A1和SEC23A基因中的单核苷酸多态性(SNPs)在以前的全基因组关联研究(GWAS)中显示出与这些疾病的显著关联。目的:研究乌克兰人群中与维生素D循环水平和骨质疏松症相关的等位基因的频率,并将这些变异的频率与西欧和北欧血统的个体进行比较。材料和方法。本文根据全基因组测序(WGS)获得的基因组数据,对97名乌克兰人中与维生素D水平和骨质疏松症相关的基因组变异频率进行了研究,并将其频率与“1000个基因组”项目的欧洲综合人群(CEU)(西欧和北欧血统的人)进行了比较。使用人类基因组版本hg38的参考数据库,使用ANNOVAR和SNPEff软件对具有乌克兰人主要公开基因组数据的文件进行注释。群体间等位基因频率的比较使用Fisher精确检验,使用两个研究群体中的等位基因数量和共轭2x2表的构建。后果研究发现,在纳入分析的22个单核苷酸多态性中,有10个,即rs2282679;rs4855;rs10033936;rs3755967;rs17467825;rs12639968;rs1155563;rs17216707;rs10745742;rs180119在乌克兰队列中与CEU相比有显著差异。通过相关性分析,我们还发现乌克兰人的SNPs rs3755967、rs17467825、rs2282679和rs4855的基因型彼此完全相关(r=1),这意味着它们在给定队列的乌克兰人中处于完全连锁状态。结论这些发现可能是乌克兰人群维生素D水平和骨密度调节的进化和适应过程的证据,需要进一步研究表型-基因型关系。
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Problemi Endokrinnoi Patologii
Problemi Endokrinnoi Patologii Medicine-Endocrinology, Diabetes and Metabolism
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42
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