与患有青光眼的非洲裔个体的可见颅底角膜孔相关的特征:原发性开角型非洲裔青光眼遗传学(POAAGG)研究

Vision Pub Date : 2024-04-18 DOI:10.3390/vision8020024
Jalin A. Jordan, Ebenezer Daniel, Yineng Chen, Rebecca J. Salowe, Yan Zhu, E. Miller-Ellis, Victoria M. Addis, P. Sankar, Di Zhu, Eli J. Smith, Roy Lee, Gui-Shuang Ying, Joan M. O’Brien
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引用次数: 0

摘要

关于原发性开角型青光眼(POAG)的发生率以及非洲血统的人眼中可见的颅底角膜板层孔(LCPs)的数据很少;这些特征对疾病负担的潜在影响仍然未知。我们在原发性开角型非裔美国人青光眼遗传学(POAAGG)研究中招募了患有 POAG 的受试者。通过回归模型,我们评估了 LCP 的存在与各种表型特征之间的关联。在对 1187 只青光眼眼球进行的多变量分析中发现,杯盘比 (CDR) ≥0.9 的眼球(调整风险比 (aRR) 1.11,95%CI:1.04-1.19,p = 0.005)、圆柱形眼球(aRR 1.22,95%CI:1.11-1.33)和豆瓣形眼球(aRR 1.24,95%CI:1.13-1.36)与锥形杯相比(p < 0.0001),中等杯深(aRR 1.24,95%CI:1.06-1.46)和深杯(aRR 1.27,95%CI:1.07-1.50)与浅杯相比(p = 0.01),以及视网膜中央血管鼻化(aRR 1.33,95%CI:1.23-1.44),p < 0.0001)。通过 SNP 分析(aRR 0.96,95%CI:0.93-0.99,q0 每增加 0.1,p = 0.005)确定,患有 LCP 的眼睛更有可能具有较高程度的非洲血统(q0)。我们的大型非洲血统 POAG 病例队列显示,LCPs 可能是识别严重疾病的一个重要风险因素,可能需要医生进行更密切的监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Features Associated with Visible Lamina Cribrosa Pores in Individuals of African Ancestry with Glaucoma: Primary Open-Angle African Ancestry Glaucoma Genetics (POAAGG) Study
There are scarce data regarding the rate of the occurrence of primary open-angle glaucoma (POAG) and visible lamina cribrosa pores (LCPs) in the eyes of individuals with African ancestry; the potential impact of these features on disease burden remains unknown. We recruited subjects with POAG to the Primary Open-Angle African American Glaucoma Genetics (POAAGG) study. Through regression models, we evaluated the association between the presence of LCPs and various phenotypic features. In a multivariable analysis of 1187 glaucomatous eyes, LCPs were found to be more likely to be present in eyes with cup-to-disc ratios (CDR) of ≥0.9 (adjusted risk ratio (aRR) 1.11, 95%CI: 1.04–1.19, p = 0.005), eyes with cylindrical-shaped (aRR 1.22, 95%CI: 1.11–1.33) and bean pot (aRR 1.24, 95%CI: 1.13–1.36) cups versus conical cups (p < 0.0001), moderate cup depth (aRR 1.24, 95%CI: 1.06–1.46) and deep cups (aRR 1.27, 95%CI: 1.07–1.50) compared to shallow cups (p = 0.01), and the nasalization of central retinal vessels (aRR 1.33, 95%CI: 1.23–1.44), p < 0.0001). Eyes with LCPs were more likely to have a higher degree of African ancestry (q0), determined by means of SNP analysis (aRR 0.96, 95%CI: 0.93–0.99, p = 0.005 for per 0.1 increase in q0). Our large cohort of POAG cases of people with African ancestry showed that LCPs may be an important risk factor in identifying severe disease, potentially warranting closer monitoring by physicians.
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