Keck School of Medicine at the University of Southern California.
Department of Ophthalmology, Roski Eye Institute.
J Glaucoma. 2023 Apr 1;32(4):257-264. doi: 10.1097/IJG.0000000000002154. Epub 2023 Feb 22.
The risk of primary angle closure disease (PACD) rises rapidly with greater hyperopia while remaining relatively low for all degrees of myopia. Refractive error (RE) is useful for angle closure risk stratification in the absence of biometric data.
To assess the role of RE and anterior chamber depth (ACD) as risk factors in PACD.
Chinese American Eye Study participants received complete eye examinations including refraction, gonioscopy, amplitude-scan biometry, and anterior segment ocular coherence tomography imaging. PACD included primary angle closure suspect (≥3 quadrants of angle closure on gonioscopy) and primary angle closure/primary angle closure glaucoma (peripheral anterior synechiae or intraocular pressure >21 mm Hg). Logistic regression models were developed to assess associations between PACD and RE and/or ACD adjusted for sex and age. Locally weighted scatterplot smoothing curves were plotted to assess continuous relationships between variables.
Three thousand nine hundred seventy eyes (3403 open angle and 567 PACD) were included. The risk of PACD increased with greater hyperopia [odds ratio (OR) = 1.41 per diopter (D); P < 0.001] and shallower ACD (OR = 1.75 per 0.1 mm; P < 0.001). Hyperopia (≥ + 0.5 D; OR = 5.03) and emmetropia (-0.5 D to +0.5 D; OR = 2.78) conferred a significantly higher risk of PACD compared with myopia (≤0.5 D). ACD (standardized regression coefficient = -0.54) was a 2.5-fold stronger predictor of PACD risk compared with RE (standardized regression coefficient = 0.22) when both variables were included in one multivariable model. The sensitivity and specificity of a 2.6 mm ACD cutoff for PACD were 77.5% and 83.2% and of a +2.0 D RE cutoff were 22.3% and 89.1%.
The risk of PACD rises rapidly with greater hyperopia while remaining relatively low for all degrees of myopia. Although RE is a weaker predictor of PACD than ACD, it remains a useful metric to identify patients who would benefit from gonioscopy in the absence of biometric data.
原发性闭角型青光眼(PACG)的风险随着远视度数的增加而迅速上升,而对于所有近视度数,其风险仍然相对较低。在没有生物测量数据的情况下,屈光不正(RE)可用于进行房角关闭风险分层。
评估 RE 和前房深度(ACD)作为 PACG 危险因素的作用。
中美眼科学者研究参与者接受了完整的眼部检查,包括验光、房角镜检查、振幅扫描生物测量和眼前节光学相干断层扫描成像。PACG 包括原发性房角关闭可疑(房角镜检查≥3 个象限房角关闭)和原发性房角关闭/原发性房角关闭性青光眼(周边前粘连或眼压>21mmHg)。建立了 logistic 回归模型,以评估 PACG 与 RE 和/或 ACD 之间的关联,这些关联在性别和年龄方面进行了调整。绘制局部加权散点图平滑曲线,以评估变量之间的连续关系。
共纳入 3977 只眼(3403 只开角眼和 567 只 PACG)。PACG 的风险随着远视度数的增加而增加[每增加 1 屈光度(D)的优势比(OR)为 1.41(P<0.001)]和 ACD 变浅[OR = 0.1mm(P<0.001)]。远视(≥+0.5D;OR=5.03)和正视(-0.5D 至+0.5D;OR=2.78)与近视(≤0.5D)相比,PACG 的风险显著更高。当两个变量都包含在一个多变量模型中时,ACD(标准化回归系数=-0.54)对 PACG 风险的预测能力是 RE(标准化回归系数=0.22)的 2.5 倍。2.6mm ACD 截点对 PACG 的敏感性和特异性分别为 77.5%和 83.2%,+2.0D RE 截点的敏感性和特异性分别为 22.3%和 89.1%。
PACG 的风险随着远视度数的增加而迅速上升,而对于所有近视度数,其风险仍然相对较低。尽管 RE 对 PACG 的预测能力弱于 ACD,但它仍然是一种有用的指标,可以在没有生物测量数据的情况下识别出需要进行房角镜检查的患者。