Li Ang, Rieveschl Nathaniel B, Conti Felipe F, Silva Fabiana Q, Sears Jonathan E, Srivastava Sunil, Ehlers Justis P, Schachat Andrew P, Babiuch Amy S, Kaiser Peter K, Martin Daniel F, Singh Rishi P
Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.
Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.
Ophthalmol Retina. 2018 Jun;2(6):550-557. doi: 10.1016/j.oret.2017.10.010. Epub 2017 Dec 19.
Although intravitreal anti-vascular endothelial growth factor (VEGF) injection has become the mainstay treatment for neovascular age-related macular degeneration (nAMD), emerging studies suggest that anti-VEGF may be correlated with the development of macular atrophy (MA) in chronic therapy. The purpose of the current study is to determine the prevalence and progression of MA in nAMD treated with chronic anti-VEGF in a routine clinical practice.
Retrospective cohort.
Patients with nAMD who were previously treatment-naïve and treated with anti-VEGF at the Cole Eye Institute for at least 4 years.
This is chart review on anti-VEGF treated patients with nAMD with baseline and yearly follow-up spectral domain-OCT for at least 4 years. Retinal pigment epithelium subillumination analysis was used to automate identification of atrophy. Segmentation errors were manually corrected by 4 expert raters using a standardized grading protocol to quantify MA size. Patient baseline characteristics and treatment course were analyzed to identify predictive factors for the development of MA.
MA growth rate and prevalence in cohorts with and without baseline atrophy.
A total of 79 eyes from 66 patients (79.8±7.4 years, 63% were female) with nAMD and 4 years of follow-up with anti-VEGF injections were identified. The mean baseline visual acuity was 0.48±0.25 logarithm of the minimum angle of resolution (20/60 Snellen equivalent), and the mean final visual acuity was 0.48±0.49 logarithm of the minimum angle of resolution (20/44 Snellen equivalent, P = 0.23). The average number of injections was 19.8±9.8. MA was observed in 12.7% of eyes at baseline with an average annual growth rate of 0.7±0.5 mm. In eyes without baseline MA, atrophy developed in 53.6% eyes by year 4 with a growth rate of 0.2±0.4 mm per year. Multiple linear regression analysis revealed that the progression of MA was positively correlated with age (R = 0.02, P = 0.009).
More than half of patients with nAMD treated with anti-VEGF injections for 4 years developed new MA. Atrophy progression was most strongly correlated with age, which suggests that baseline disease characteristics may be more predictive of MA progression than cumulative anti-VEGF treatment.
尽管玻璃体内注射抗血管内皮生长因子(VEGF)已成为新生血管性年龄相关性黄斑变性(nAMD)的主要治疗方法,但越来越多的研究表明,在长期治疗中,抗VEGF可能与黄斑萎缩(MA)的发生有关。本研究的目的是确定在常规临床实践中,接受长期抗VEGF治疗的nAMD患者中MA的患病率和进展情况。
回顾性队列研究。
既往未接受过治疗、在科尔眼科研究所接受抗VEGF治疗至少4年的nAMD患者。
这是一项对接受抗VEGF治疗的nAMD患者的病历回顾研究,患者接受基线及每年一次的光谱域光学相干断层扫描(SD-OCT)检查,随访至少4年。采用视网膜色素上皮层下照明分析自动识别萎缩区域。4位专家评分者使用标准化分级方案对分割误差进行人工校正,以量化MA的大小。分析患者的基线特征和治疗过程,以确定MA发生的预测因素。
有或无基线萎缩的队列中MA的增长率和患病率。
共纳入66例nAMD患者的79只眼(年龄79.8±7.4岁,63%为女性),这些患者接受抗VEGF注射治疗并随访4年。平均基线视力为最小分辨角对数(logMAR)0.48±0.25(相当于Snellen视力表20/60),平均最终视力为logMAR 0.48±0.49(相当于Snellen视力表20/44,P = 0.23)。平均注射次数为19.8±9.8次。基线时12.7%的眼观察到MA,平均年增长率为0.7±0.5 mm。在无基线MA的眼中,到第4年时萎缩发生在53.6%的眼中,年增长率为0.2±0.4 mm。多元线性回归分析显示,MA的进展与年龄呈正相关(R = 0.02,P = 0.009)。
接受抗VEGF注射治疗4年的nAMD患者中,超过一半出现了新的MA。萎缩进展与年龄的相关性最强,这表明基线疾病特征可能比累积抗VEGF治疗更能预测MA的进展。