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鉴定 为年龄相关性黄斑变性和息肉样脉络膜血管病变的易感性基因。

Identification of as a susceptibility gene for neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.

机构信息

Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong, China.

Current affiliation: Department of Ophthalmology, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.

出版信息

Br J Ophthalmol. 2021 Jul;105(7):1035-1040. doi: 10.1136/bjophthalmol-2019-315746. Epub 2020 Mar 9.

Abstract

PURPOSE

The endothelial and cell-specific angiopoietin-Tie pathway plays an important regulatory role in angiogenesis. In this study, we investigated the associations of the () gene with neovascular age-related macular degeneration (nAMD) and polypoidal choroidal vasculopathy (PCV), using haplotype-tagging single-nucleotide polymorphisms (SNPs) analysis.

METHODS

This study involved totally 2343 subjects, including a Hong Kong Chinese cohort (214 nAMD patients, 236 PCV patients and 433 control subjects), a Shantou Chinese cohort (189 nAMD patients, 187 PCV patients and 531 control subjects) and an Osaka Japanese cohort (192 nAMD patients, 204 PCV patients and 157 control subjects). Thirty haplotype-tagging SNPs in were genotyped in the Hong Kong cohort using TaqMan technology. Two SNPs (rs625767 and rs2273717) showing association in the Hong Kong cohort were genotyped in the Shantou and Osaka cohorts. The SNP-disease association of individual and pooled cohorts were analysed.

RESULTS

Two SNPs (rs625767 and rs2273717) showed suggestive association with both nAMD and PCV in the Hong Kong cohort. In the meta-analysis involving all the three cohorts, rs625767 showed significant associations with nAMD (p=0.01; OR=0.82, 95% CI 0.70 to 0.96; I=0%), PCV (p=0.02; OR=0.83, 95% CI 0.71 to 0.97; I=27%) and pooled nAMD and PCV (p=0.002; OR=0.82, 95% CI 0.72 to 0.93; I=0%), with low inter-cohort heterogeneities.

CONCLUSION

This study revealed as a novel susceptibility gene for nAMD and PCV in Japanese and Chinese. Further studies in other populations are warranted to confirm its role.

摘要

目的

内皮细胞和细胞特异性血管生成素- Tie 通路在血管生成中发挥重要的调节作用。本研究采用单体型标签单核苷酸多态性(SNP)分析,探讨了()基因与新生血管性年龄相关性黄斑变性(nAMD)和息肉状脉络膜血管病变(PCV)的相关性。

方法

本研究共纳入 2343 名受试者,包括香港中文队列(214 名 nAMD 患者、236 名 PCV 患者和 433 名对照组)、汕头中文队列(189 名 nAMD 患者、187 名 PCV 患者和 531 名对照组)和大阪日本队列(192 名 nAMD 患者、204 名 PCV 患者和 157 名对照组)。采用 TaqMan 技术对香港队列中的 30 个单体型标签 SNP 进行基因分型。在香港队列中发现与疾病相关的两个 SNP(rs625767 和 rs2273717)在汕头和大阪队列中进行基因分型。分析了个体和汇总队列中 SNP 与疾病的相关性。

结果

两个 SNP(rs625767 和 rs2273717)在香港队列中与 nAMD 和 PCV 均有相关性。在涉及所有三个队列的荟萃分析中,rs625767 与 nAMD(p=0.01;OR=0.82,95%CI 0.70 至 0.96;I=0%)、PCV(p=0.02;OR=0.83,95%CI 0.71 至 0.97;I=27%)和 nAMD 和 PCV 的汇总分析(p=0.002;OR=0.82,95%CI 0.72 至 0.93;I=0%)均有显著相关性,且组间异质性较低。

结论

本研究揭示了()是日本和中国人群中 nAMD 和 PCV 的一个新的易感基因。需要在其他人群中进一步研究以确认其作用。

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