Yu Jun, Zhang Yuzhou, Kam Ka Wai, Ho Mary, Young Alvin L, Pang Chi Pui, Tham Clement C, Yam Jason C, Chen Li Jia
Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong.
Department of Ophthalmology and Visual Sciences, Prince of Wales Hospital, Hong Kong.
Invest Ophthalmol Vis Sci. 2025 Feb 3;66(2):48. doi: 10.1167/iovs.66.2.48.
To investigate the associations of lung function with glaucoma and related traits, explore the interactions between glaucoma genetic risk and lung function, and assess the causal relationships using Mendelian randomization (MR).
This cross-sectional study involved 85,369 participants with lung function measurements at baseline from the UK Biobank. Associations between lung function parameters and glaucoma and related traits were tested by multivariable logistic and linear regression. Two-sample MR analyses were conducted using summary statistics from large genetic datasets.
Forced vital capacity (FVC), forced expiratory volume in 1 second (FEV1), and FEV1/FVC ratio were inversely associated with glaucoma, with the lowest quartiles conferring odds ratios (ORs) of 1.51 (95% confidence interval [CI], 1.31-1.74; P = 7.6 × 10-8), 1.58 (95% CI, 1.37-1.81; P = 4.7 × 10-10) and 1.20 (95% CI, 1.08-1.34; P = 0.002), respectively, compared with the highest quartiles (P trends < 0.001 observed for each). Similar associations were found for impaired lung function (FEV1 <80% Global Lung Initiative predicted FEV1: OR, 1.22, 95% CI, 1.11-1.33; P = 1.2 × 10-5; FEV1/FVC <0.7: OR, 1.13, 95% CI, 1.03-1.24; P = 0.01). Lower lung function was associated with lower intraocular pressure (IOP), thinner macular retinal nerve fiber layer thickness, and thinner ganglion cell-inner plexiform layer thickness. No interactions were observed between glaucoma genetic risk and lung function. MR analyses did not suggest causal relationships.
Lower FVC, FEV1, FEV1/FVC, and impaired lung function are potential biomarkers for glaucoma risk. These findings may facilitate clinical strategies for glaucoma management, particularly for individuals with impaired lung function.
研究肺功能与青光眼及相关特征之间的关联,探讨青光眼遗传风险与肺功能之间的相互作用,并使用孟德尔随机化(MR)评估因果关系。
这项横断面研究纳入了英国生物银行中85369名在基线时进行了肺功能测量的参与者。通过多变量逻辑回归和线性回归测试肺功能参数与青光眼及相关特征之间的关联。使用大型遗传数据集的汇总统计数据进行两样本MR分析。
用力肺活量(FVC)、第1秒用力呼气量(FEV1)和FEV1/FVC比值与青光眼呈负相关,与最高四分位数相比,最低四分位数的比值比(OR)分别为1.51(95%置信区间[CI],1.31 - 1.74;P = 7.6×10⁻⁸)、1.58(95%CI,1.37 - 1.81;P = 4.7×10⁻¹⁰)和1.20(95%CI,1.08 - 1.34;P = 0.002)(各观察到的P趋势<0.001)。肺功能受损(FEV1<全球肺倡议预测FEV1的80%:OR,1.22,95%CI,1.11 - 1.33;P = 1.2×10⁻⁵;FEV1/FVC<0.7:OR,1.13,95%CI,1.03 - 1.24;P = 0.01)也发现了类似的关联。较低的肺功能与较低的眼压、较薄的黄斑视网膜神经纤维层厚度和较薄的神经节细胞 - 内丛状层厚度相关。未观察到青光眼遗传风险与肺功能之间的相互作用。MR分析未提示因果关系。
较低的FVC、FEV1、FEV1/FVC和肺功能受损是青光眼风险的潜在生物标志物。这些发现可能有助于青光眼管理的临床策略,特别是对于肺功能受损的个体。