Udaondo Mirete Patricia, Muñoz-Morata Carmen, Albarrán-Diego César, España-Gregori Enrique
Department of Ophthalmology, Hospital Universitario y Politécnico La Fe, 46026 Valencia, Spain.
Aiken Clinic, 46004 Valencia, Spain.
J Clin Med. 2023 Jan 1;12(1):348. doi: 10.3390/jcm12010348.
This study aimed to analyze the variation in subfoveal choroidal thickness (SFCT) and its relationship with the variation in central macular thickness (CME) in response to intravitreal therapy with an antiangiogenic (anti-VEGF) drug or corticosteroid in type 2 diabetic patients with diabetic macular edema (DME).
This retrospective study included 70 eyes of 35 patients: 26 eyes received 4-5 intravitreal injections of aflibercept, 26 eyes were treated with a single intravitreal implant injection of dexamethasone, and 18 eyes without DME did not receive intravitreal therapy. SPECTRALIS® optical coherence tomography (OCT) (Heidelberg Engineering, Heidelberg, Germany) was used to measure the SFCT and CME before and at the end of the follow-up period.
The mean reductions in CME were 18.8 +/- 14.7% (aflibercept) and 29.7 +/- 16.9% (dexamethasone). The mean reductions in SFCT were 13.8 +/- 13.1% (aflibercept) and 19.5 +/- 9.6% (dexamethasone). The lowering effects of both parameters were significantly greater in the group treated with the dexamethasone implant ( = 0.022 and = 0.046 for CMT and SFCT, respectively). Both therapies significantly decreased both CME and SFCT, independent of factors such as age, sex, previous intravitreal therapy, antidiabetic treatment, and the time of diabetes progression. There were no changes in the mean values of CME and SFCT in the untreated eyes.
SFCT significantly decreased in response to intravitreal therapy with anti-VEGF or corticosteroids, irrespective of age, sex, previous intravitreal therapy, antidiabetic treatment, and the time of diabetes progression. There was a correlation between the changes in CME and SFCT after intravitreal therapy with aflibercept or dexamethasone implantation. SFCT was not a good predictor of the CME response but could be used to monitor the response to treatment. Local intravitreal therapy only affected the treated eye.
本研究旨在分析2型糖尿病性黄斑水肿(DME)患者接受抗血管生成(抗VEGF)药物或皮质类固醇玻璃体内注射治疗后,黄斑中心凹下脉络膜厚度(SFCT)的变化及其与中心黄斑厚度(CME)变化的关系。
本回顾性研究纳入35例患者的70只眼:26只眼接受4 - 5次阿柏西普玻璃体内注射,26只眼接受地塞米松玻璃体内植入剂单次注射治疗,18只无DME的眼未接受玻璃体内治疗。使用SPECTRALIS®光学相干断层扫描(OCT)(德国海德堡海德堡工程公司)在随访期开始前及结束时测量SFCT和CME。
CME的平均降低幅度分别为18.8±14.7%(阿柏西普)和29.7±16.9%(地塞米松)。SFCT的平均降低幅度分别为13.8±13.1%(阿柏西普)和19.5±9.6%(地塞米松)。地塞米松植入剂治疗组这两个参数的降低效果均显著更大(CMT和SFCT分别为P = 0.022和P = 0.046)。两种治疗均显著降低了CME和SFCT,且不受年龄、性别、既往玻璃体内治疗、抗糖尿病治疗及糖尿病病程等因素影响。未治疗眼的CME和SFCT平均值无变化。
无论年龄、性别、既往玻璃体内治疗、抗糖尿病治疗及糖尿病病程如何,抗VEGF或皮质类固醇玻璃体内注射治疗均可使SFCT显著降低。阿柏西普或地塞米松植入剂玻璃体内注射治疗后,CME和SFCT的变化之间存在相关性。SFCT并非CME反应的良好预测指标,但可用于监测治疗反应。局部玻璃体内治疗仅影响治疗眼。