Suppr超能文献

糙面头样蛋白 2 基因(GRHL2)单核苷酸多态性与汉族人群年龄相关性听力损失无关。

The grainyhead-like 2 gene (GRHL2) single nucleotide polymorphism is not associated with age-related hearing impairment in Han Chinese.

机构信息

Department of Otolaryngology, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

Laryngoscope. 2011 Jun;121(6):1303-7. doi: 10.1002/lary.21771. Epub 2011 May 6.

Abstract

OBJECTIVES/HYPOTHESIS: The grainyhead-like 2 gene (GRHL2) was found to be associated with age-related hearing impairment (ARHI) in Europeans. We tested whether the same association exists in the Han Chinese population.

STUDY DESIGN

Individual cohort study.

METHODS

Among a total of 1,175 Han Chinese volunteers, 310 were classified into the case group (the 26% with poorest hearing), and 308 were placed into the control group (the 26% with best hearing) according to the Zhigh scores converted from the original frequency-specific hearing thresholds. The GRHL2 single nucleotide polymorphism locus (rs10955255: A/G) in intron 1 (coordinate: 102605581) shown in the HapMap was genotyped with correlation to the audiologic phenotypes.

RESULTS

The genotype distributions of GRHL2 (AA/AG/GG) were not significantly different between the control and the case groups (P = .349). Compared to genotype AA, the odds ratios of the GRHL2 genotypes AG and GG for ARHI were not significantly different after adjustment for other environmental risk factors by logistic regression analyses; 0.78 ± 0.139, 95% confidence interval (CI) = 0.55-1.10, P = .160 for AG; 0.85 ± 0.283, 95% CI = 0.44-1.63, P = .625 for GG. In each audiogram pattern, AA was most common, but the adjusted odds ratios of the genotypes AG and GG for ARHI still were not significantly different.

CONCLUSIONS

Our results showed no positive association between GRHL2 polymorphisms and ARHI in Han Chinese individuals. Population differences might be a key factor leading to nonreplication of the association.

摘要

目的/假设:颗粒体基因 2 (GRHL2)与欧洲人的年龄相关性听力损失(ARHI)有关。我们测试了相同的关联是否存在于汉族人群中。

研究设计

个体队列研究。

方法

在总共 1175 名汉族志愿者中,根据原始频率特异性听力阈值转换的 Z 值,将 310 名志愿者分为病例组(听力最差的 26%),308 名志愿者分为对照组(听力最好的 26%)。根据 HapMap 显示的内含子 1 (坐标:102605581)中的 GRHL2 单核苷酸多态性位点(rs10955255:A/G),与听力表型相关联进行基因分型。

结果

GRHL2(AA/AG/GG)的基因型分布在对照组和病例组之间没有显著差异(P=.349)。与 AA 基因型相比,GRHL2 基因型 AG 和 GG 的 ARHI 比值比在通过逻辑回归分析调整其他环境风险因素后没有显著差异;0.78±0.139,95%置信区间(CI)=0.55-1.10,P=.160 为 AG;0.85±0.283,95%CI=0.44-1.63,P=.625 为 GG。在每个听力图模式中,AA 最为常见,但基因型 AG 和 GG 的调整比值比仍无统计学差异。

结论

我们的结果表明,汉族人群中 GRHL2 多态性与 ARHI 之间没有正相关。人群差异可能是导致关联无法复制的关键因素。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验