Tyurin Anton, Shapovalova Daria, Gantseva Halida, Pavlov Valentin, Khusainova Rita
Internal Medicine Department, Bashkir State Medical University, 450008 Ufa, Russia.
Laboratory of Human Molecular Genetics, Institute of Biochemistry and Genetics, 450000 Ufa, Russia.
Diagnostics (Basel). 2021 Jul 6;11(7):1222. doi: 10.3390/diagnostics11071222.
Over the past decades, numerous studies on the genetic markers of osteoarthritis (OA) have been conducted. MiRNA targets sites are a promising new area of research. In this study, we analyzed the polymorphic variants in 3' UTR regions of , , , , , , , , , and genes to examine the association between miRNA target site alteration and the incidence of OA in women from the Volga-Ural region of Russia using competitive allele-specific PCR. The T allele of the rs9659030 was associated with generalized OA (OR = 2.0), whereas the C allele of the rs229069 was associated with total OA (OR = 1.43). The T allele of the rs13317 was associated with the total OA (OR = 1.67). After Benjamini-Hochberg correction, only rs13317 remained statistically significant. According to ethnic heterogeneity, associations between the T allele (rs1061237) with OA in women of Russian descent (OR = 1.77), the G allele (rs6854081) in women of Tatar descent (OR = 4.78), the C allele (rs229069) and the T allele (rs73611720) in women of mixed descent and other ethnic groups (OR = 2.25 and OR = 3.02, respectively) were identified. All associations remained statistically significant after Benjamini-Hochberg correction. Together, this study identified miRNA target sites as a genetic marker for the development of OA in various ethnic groups.
在过去几十年里,已经开展了大量关于骨关节炎(OA)基因标记的研究。微小RNA(miRNA)靶位点是一个很有前景的新研究领域。在本研究中,我们分析了、、、、、、、、和基因3'非翻译区(UTR)的多态性变体,采用竞争性等位基因特异性PCR检测俄罗斯伏尔加 - 乌拉尔地区女性中miRNA靶位点改变与OA发病率之间的关联。rs9659030的T等位基因与全身性OA相关(比值比[OR]=2.0),而rs229069的C等位基因与总OA相关(OR = 1.43)。rs13317的T等位基因与总OA相关(OR = 1.67)。经过Benjamini - Hochberg校正后,只有rs13317仍具有统计学意义。根据种族异质性,确定了俄罗斯血统女性中T等位基因(rs1061237)与OA的关联(OR = 1.77),鞑靼血统女性中G等位基因(rs6854081)与OA的关联(OR = 4.78),以及混血和其他种族女性中C等位基因(rs229069)和T等位基因(rs73611720)与OA的关联(分别为OR = 2.25和OR = 3.02)。经过Benjamini - Hochberg校正后,所有关联仍具有统计学意义。总之,本研究确定miRNA靶位点是不同种族中OA发生发展的一种基因标记。