Alam Taseen, Das Nikhil, Maatouk Christopher, Zhao Alison, Singh Rishi P, Talcott Katherine E
Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, OH, USA.
Eye (Lond). 2025 Sep 12. doi: 10.1038/s41433-025-03968-y.
This study assesses the predictiveness of retinal thickness variability on long-term visual acuity (VA) outcomes in patients with diabetic macular oedema (DMO) undergoing anti-VEGF therapy.
Retrospective chart review at a single institution.
184 and 138 patients underwent initial treatment for DMO and continued to follow-up at 3 and 5 years, respectively.
Baseline demographics, past medical, and clinical data were collected through electronic medical record query. Central subfield thickness (CST), choroidal volume (CV), and cube average thickness (CAT) variability over the first year of treatment were calculated using standard deviation, amplitude, and area under the curve. CST, CV, CAT, and best corrected visual acuity (BCVA) were noted at the initial treatment date and 3 and 5 years. CST variability quartiles were compared on baseline, final, and change in BCVA alongside final and change in CST. Multiple linear regression was used to evaluate factors associated with final BCVA at 3 and 5 years while adjusting for confounders.
There is no significant association between larger fluctuations in macular thickness and change in BCVA at 3 and 5 years. Individuals in the highest CST variability quartile had the lowest final BCVA but also the lowest baseline BCVA and no difference in BCVA change. Linear regression revealed that CST variability was not predictive of final BCVA. Baseline BCVA and total number of anti-VEGF injections were predictive of BCVA at 3 years and 5 years respectively.
Macular thickness variability did not predict long-term visual outcomes at 3 and 5 years.
本研究评估糖尿病性黄斑水肿(DMO)患者接受抗血管内皮生长因子(VEGF)治疗时,视网膜厚度变异性对长期视力(VA)结果的预测能力。
在单一机构进行回顾性病历审查。
184例和138例患者分别接受了DMO的初始治疗,并在3年和5年持续进行随访。
通过电子病历查询收集基线人口统计学、既往病史和临床数据。使用标准差、振幅和曲线下面积计算治疗第一年的中心子区域厚度(CST)、脉络膜体积(CV)和立方体平均厚度(CAT)变异性。在初始治疗日期以及3年和5年时记录CST、CV、CAT和最佳矫正视力(BCVA)。比较CST变异性四分位数在基线、最终和BCVA变化方面的情况,以及最终和CST变化情况。使用多元线性回归评估在调整混杂因素后与3年和5年最终BCVA相关的因素。
黄斑厚度较大波动与3年和5年时BCVA变化之间无显著关联。CST变异性最高四分位数的个体最终BCVA最低,但基线BCVA也最低,且BCVA变化无差异。线性回归显示CST变异性不能预测最终BCVA。基线BCVA和抗VEGF注射总数分别可预测3年和5年时的BCVA。
黄斑厚度变异性不能预测3年和5年时的长期视力结果。