From the Hamilton Glaucoma Center, Shiley Eye Institute, Viterbi Family Department of Ophthalmology, University of California (R.C.C.D., S.M., E.E., J.L.D., H.H., J.A.P., A.K., T.N., R.N.W.), San Diego, La Jolla, California.
Department of Ophthalmology and Visual Science, Callahan Eye Hospital, University of Alabama-Birmingham (C.A.G.), Alabama and.
Am J Ophthalmol. 2021 Sep;229:8-17. doi: 10.1016/j.ajo.2021.04.010. Epub 2021 Apr 25.
To compare spectral-domain optical coherence tomography (SDOCT) measured circumpapillary retinal nerve fiber layer (cpRNFL) among 4 glaucomatous optic disc phenotypes in early glaucoma.
Clinical cohort study METHODS: In this study, 218 early glaucoma eyes that had at least 3 years of follow-up and a minimum of 4 SDOCT scans were recruited. The optic discs were classified into 4 types based on appearance: 76 generalized cup enlargement (GE), 53 focal ischemic (FI), 22 myopic glaucomatous (MY), and 67 senile sclerotic (SS). A linear mixed effects model was used to compare the rates of global and regional cpRNFL thinning among optic disc phenotypes.
After adjusting for confounders, the SS group (mean [95% CI]: -1.01 [-1.30, -0.73] µm/y) had the fastest mean rate of global cpRNFL thinning followed by FI (-0.77 [-0.97, -0.57] µm/y), MY (0.59 [-0.81, -0.36] µm/y), and GE (-0.58 [-0.75, -0.40] µm/y) at P < .001. The inferior temporal sector had the fastest rate of cpRNFL thinning among the regional measurements except for the MY group (-0.68 [-1.10, -0.26] µm/y, P = .002). In the multivariable analysis, GE (P = .002) and MY (P = .010) phenotypes were associated with significantly slower global rates of cpRNFL thinning compared with the SS phenotype.
Rates of cpRNFL thinning were different among the 4 glaucomatous optic disc phenotypes. Those patients with early glaucoma with SS phenotype have the fastest cpRNFL thinning. These patients may benefit from more frequent monitoring and the need to advance therapy if cpRNFL thinning is detected.
比较 4 种早期青光眼视盘形态的光谱域光学相干断层扫描(SDOCT)测量的周边视网膜神经纤维层(cpRNFL)。
临床队列研究。
本研究纳入了 218 只至少有 3 年随访且至少有 4 次 SDOCT 扫描的早期青光眼眼。根据视盘的外观将其分为 4 种类型:76 只视杯扩大(GE)、53 只局灶性缺血(FI)、22 只近视性青光眼(MY)和 67 只老年性硬化(SS)。采用线性混合效应模型比较视盘形态之间的全周和局部 cpRNFL 变薄率。
在调整混杂因素后,SS 组(平均[95%CI]:-1.01[-1.30,-0.73]µm/y)的全周 cpRNFL 变薄率最快,其次是 FI 组(-0.77[-0.97,-0.57]µm/y)、MY 组(0.59[-0.81,-0.36]µm/y)和 GE 组(-0.58[-0.75,-0.40]µm/y),P<.001。在局部测量中,除 MY 组外(-0.68[-1.10,-0.26]µm/y,P=0.002),下颞部的 cpRNFL 变薄率最快。在多变量分析中,与 SS 形态相比,GE(P=0.002)和 MY(P=0.010)形态与全周 cpRNFL 变薄率较慢显著相关。
4 种青光眼视盘形态的 cpRNFL 变薄率不同。SS 形态的早期青光眼患者的 cpRNFL 变薄最快。如果检测到 cpRNFL 变薄,这些患者可能需要更频繁的监测和更积极的治疗。