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评估闭角型青光眼早期患者的原发性闭角型青光眼易感性基因座。

Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci in Patients with Early Stages of Angle-Closure Disease.

机构信息

Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Republic of Singapore; Duke-National University of Singapore Medical School, Singapore, Republic of Singapore.

Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Republic of Singapore; Duke-National University of Singapore Medical School, Singapore, Republic of Singapore; Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Republic of Singapore.

出版信息

Ophthalmology. 2018 May;125(5):664-670. doi: 10.1016/j.ophtha.2017.11.016. Epub 2018 Jan 6.

Abstract

PURPOSE

To investigate whether newly identified genetic loci for primary angle-closure glaucoma (PACG) are associated with early stage angle-closure disease defined as primary angle closure suspect (PACS).

DESIGN

Case-control study.

PARTICIPANTS

A total of 1397 PACS patients and 943 controls of Chinese ethnicity from Singapore and 604 PACS patients and 287 controls of Indian ethnicity.

METHODS

The 8 PACG single nucleotide polymorphisms (SNPs; rs11024102 at PLEKHA7, rs3753841 at COL11A1, rs1015213 located between PCMTD1 and ST18 son chromosome 8q, rs3816415 at EPDR1, rs1258267 at CHAT, rs736893 at GLIS3, rs7494379 at FERMT2, and rs3739821 mapping in between DPM2 and FAM102A) were genotyped by Taqman assays. The association between SNP genotypes and PACS status was measured using logistic regression. A P value of 0.006 was set to account for the testing of 8 genetic loci using a Bonferroni correction. A meta-analysis was conducted to calculate the overall P value and accompanying per-allele odds ratios for each SNP analyzed.

MAIN OUTCOME MEASURES

Association of PACG loci with PACS status.

RESULTS

The PACS patients were significantly older in both cohorts (Chinese, P < 0.001; Indian, P = 0.002), and there were also more women (P < 0.001, both Chinese and Indian cohorts). In the Chinese cohort, significant evidence of association was noted at 3 SNPs: rs1015213 [A] in PCMTD1-ST18 (odds ratio [OR], 2.36; 95% confidence interval [CI], 1.36-4.11; P = 0.002), rs3816415 [A] in EPDR1 (OR, 1.49; 95% CI, 1.19-1.85; P < 0.001), and rs3739821 [G] in DPM2-FAM102A (OR, 1.40; 95% CI, 1.18-1.65; P < 0.001). Only PCMTD1-ST-18 was replicated modestly in the Indian population (P = 0.056). Meta-analysis showed significant evidence of association for PCMTD1-ST-18 (OR, 1.55; 95% CI, 1.18-2.04; P = 0.002) and DPM2-FAM102A (OR, 1.27; 95% CI, 1.12-1.45; P = 0.0002).

CONCLUSIONS

In this study, 2 of 8 PACG-associated loci were associated significantly with PACS status, the earliest stage in the angle-closure glaucoma disease course. The association of these PACG loci with PACS status suggests that these loci may confer susceptibility to a narrow angle configuration.

摘要

目的

研究新鉴定的原发性闭角型青光眼 (PACG) 遗传位点是否与定义为原发性闭角型青光眼疑似病例 (PACS) 的早期闭角型疾病有关。

设计

病例对照研究。

参与者

来自新加坡的共 1397 名 PACS 患者和 943 名对照以及来自印度的共 604 名 PACS 患者和 287 名对照。

方法

对 8 个 PACG 单核苷酸多态性(SNP;PLEKHA7 上的 rs11024102、COL11A1 上的 rs3753841、位于 8q 染色体上的 PCMTD1 和 ST18 之间的 rs1015213、EPDR1 上的 rs3816415、CHAT 上的 rs1258267、GLIS3 上的 rs736893、FERMT2 上的 rs7494379 和位于 DPM2 和 FAM102A 之间的 rs3739821)进行基因分型,使用逻辑回归测量 SNP 基因型与 PACS 状态之间的关联。为了校正 8 个遗传位点的测试,设置了 P 值为 0.006。进行了荟萃分析,以计算分析的每个 SNP 的总体 P 值和伴随的每个等位基因的优势比。

主要观察指标

PACG 基因座与 PACS 状态的关联。

结果

在两个队列中,PACS 患者的年龄明显较大(中国,P < 0.001;印度,P = 0.002),并且女性也更多(P < 0.001,中国和印度队列)。在中国队列中,3 个 SNP 显示出显著的关联证据:PCMTD1-ST18 上的 rs1015213[A](优势比[OR],2.36;95%置信区间[CI],1.36-4.11;P = 0.002)、EPDR1 上的 rs3816415[A](OR,1.49;95%CI,1.19-1.85;P < 0.001)和 DPM2-FAM102A 上的 rs3739821[G](OR,1.40;95%CI,1.18-1.65;P < 0.001)。在印度人群中,仅 PCMTD1-ST-18 得到适度复制(P = 0.056)。荟萃分析显示 PCMTD1-ST-18(OR,1.55;95%CI,1.18-2.04;P = 0.002)和 DPM2-FAM102A(OR,1.27;95%CI,1.12-1.45;P = 0.0002)存在显著关联的证据。

结论

在这项研究中,8 个与 PACG 相关的基因座中有 2 个与 PACS 状态显著相关,PACS 是闭角型青光眼疾病过程中的最早阶段。这些 PACG 基因座与 PACS 状态的关联表明,这些基因座可能赋予了窄角构型的易感性。

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