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Association of GRM7 Variants with Different Phenotype Patterns of Age-Related Hearing Impairment in an Elderly Male Han Chinese Population

机译:GRM7变体与老年汉族人口中与年龄相关的听力障碍的不同表型的关联

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摘要

Several single nucleotide polymorphisms (SNPs) of the Glutamate metabotrophic receptor 7 gene (GRM7) have recently been identified by the genome-wide association study (GWAS) as potentially playing a role in susceptibility to age-related hearing impairment (ARHI), however this has not been validated in the Han Chinese population. The aim of this study was to determine if these SNPs are also associated with ARHI in an elderly male Han Chinese population. In this case-control candidate genes association study, a total of 982 men with ARHI and 324 normal-hearing controls subjects were studied. Using K-means cluster analysis, four audiogram shape subtypes of ARHI were identified in the case group: ‘‘flat shape (FL)’’, ‘‘sloping shape (SL)’’, ‘‘2-4 kHz abrupt loss (AL) shape’’ and ‘‘8 kHz dip (8D) shape’’. Results suggested that the SNP rs11928865 (A>T) of GRM7 was significantly associated with ARHI after adjusting for non-genetic factors (p= 0.000472, OR= 1.599, 95%CI= 1.229~2.081). Furthermore, frequency of TT genotype (rs11928865) were significant higher in the SL subgroup and AL subgroup with compared to controls group (p= 9.41E-05, OR= 1.945, 95%CI= 1.393~2.715; p= 0.000109, OR= 1.915, 95%CI= 1.378~2.661 adjusted, respectively) after Bonferroni correction. However, there wasn’t significant difference in the frequency of the TT genotype between cases in the FL subgroup or the 8D subgroup with when compared with controls. Results of the current study suggest that, in an elderly male Han Chinese population, GRM7 SNP rs11928865 (TT) occurs more frequently in ARHI patients with SL and AL phenotype patterns.
机译:最近,全基因组关联研究(GWAS)已识别出谷氨酸代谢营养型受体7基因(GRM7)的几个单核苷酸多态性(SNPs)可能在与年龄相关的听力障碍(ARHI)的易感性中起作用。尚未在汉族人群中得到验证。这项研究的目的是确定这些SNP是否也与老年汉族汉族人群中的ARHI相关。在这项病例对照候选基因关联研究中,总共研究了982名ARHI男性和324名正常听力的对照受试者。使用K均值聚类分析,在病例组中确定了ARHI的四种听力图形状亚型:``平坦形状(FL)'',``倾斜形状(SL)'',``2-4 kHz突然损失(AL )形状和``8 kHz倾斜(8D)形状''。结果表明,调整非遗传因素后,GRM7的SNP rs11928865(A> T)与ARHI显着相关(p = 0.000472,OR = 1.599,95%CI = 1.229〜2.081)。此外,与对照组相比,SL亚组和AL亚组的TT基因型频率(rs11928865)显着更高(p = 9.41E-05,OR = 1.945,95%CI = 1.393〜2.715; p = 0.000109,OR = Bonferroni校正后分别调整为1.915、95%CI = 1.378〜2.661。但是,与对照组相比,FL亚组或8D亚组的TT基因型频率没有明显差异。目前的研究结果表明,在老年汉族男性汉族人群中,具有SL和AL表型的ARHI患者中GRM7 SNP rs11928865(TT)的发生率更高。

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