Alshaikhsalama Ahmed M, Alsoudi Amer F, Wai Karen M, Koo Euna, Mruthyunjaya Prithvi, Rahimy Ehsan
Department of Ophthalmology, UT Southwestern Medical Center, Dallas, Texas.
Department of Ophthalmology, Baylor College of Medicine, Houston, Texas.
Ophthalmol Retina. 2025 Jun;9(6):537-545. doi: 10.1016/j.oret.2024.12.004. Epub 2024 Dec 9.
To evaluate the risk of age-related macular degeneration (AMD) development and progression in individuals with diagnosed obstructive sleep apnea (OSA).
Retrospective cohort study.
Before propensity score matching (PSM), 60 652 and 1 173 723 individuals with OSA or not, respectively, were included in the study. After PSM and applying inclusion/exclusion criteria, 58 700 individuals in each cohort were subsequently analyzed.
Data were collected using TriNetX, a deidentified electronic health records research network. Individuals with an International Classification of Diseases, 10th Revision, code for OSA confirmed with polysomnography and an additional code for continuous positive airway pressure use were compared with individuals without diagnosed OSA (control cohort) for the development of main outcome measures at 5 years. Secondary analyses were included to assess nonadvanced AMD progression in individuals with and without diagnosed OSA at 5 years.
The main outcome measures were the incidence of AMD, macular hemorrhage, legal blindness, and requiring anti-VEGF intervention at 5 years. Individuals with nonadvanced AMD with and without an OSA diagnosis were separately analyzed for progression to late AMD and the development of macular hemorrhage, legal blindness, and requiring anti-VEGF therapy at 5 years.
At 5 years, individuals with diagnosed OSA had a significantly elevated risk of nonexudative AMD (hazard ratio [HR], 2.64; 95% confidence interval [CI], 2.37-2.96; P < 0.001), exudative AMD (HR, 2.48; 95% CI, 1.99-3.11; P = 0.002), and requiring anti-VEGF therapy (HR, 2.85; 95% CI, 2.26-3.59; P < 0.001) compared with the control cohort. In the secondary analysis, individuals with nonadvanced AMD with diagnosed OSA were associated with an elevated risk of geographic atrophy (HR, 7.00; 95% CI, 4.47-11.0; P = 0.03), exudative AMD (HR, 2.87; 95% CI, 2.37-3.48; P = 0.03), and requiring anti-VEGF injections (HR, 4.72; 95% CI, 3.59-6.22; P = 0.02) compared with those with nonadvanced AMD without diagnosed OSA.
In a large, heterogeneous database, an elevated risk of developing AMD and progression to later stages of the disease was observed among individuals with diagnosed OSA.
FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
评估已确诊阻塞性睡眠呼吸暂停(OSA)的个体发生年龄相关性黄斑变性(AMD)及其进展的风险。
回顾性队列研究。
在倾向得分匹配(PSM)之前,分别有60652例和1173723例患有或未患有OSA的个体纳入本研究。经过PSM并应用纳入/排除标准后,随后对每个队列中的58700例个体进行分析。
使用TriNetX(一个去识别化电子健康记录研究网络)收集数据。将经多导睡眠图确诊为OSA且有持续气道正压通气使用附加代码的国际疾病分类第10版编码个体与未确诊OSA的个体(对照队列)进行比较,以观察5年时主要结局指标的发生情况。纳入二次分析以评估5年时已确诊和未确诊OSA个体的非晚期AMD进展情况。
主要结局指标为5年时AMD、黄斑出血、法定盲以及需要抗VEGF干预的发生率。对已确诊和未确诊OSA的非晚期AMD个体分别分析其进展为晚期AMD以及5年时黄斑出血、法定盲和需要抗VEGF治疗的情况。
5年时,与对照队列相比,已确诊OSA的个体发生非渗出性AMD(风险比[HR],2.64;95%置信区间[CI],2.37 - 2.96;P < 0.001)、渗出性AMD(HR,2.48;95% CI,1.99 - 3.11;P = 0.002)以及需要抗VEGF治疗(HR,2.85;95% CI,2.26 - 3.59;P < 0.001)的风险显著升高。在二次分析中,与未确诊OSA的非晚期AMD个体相比,已确诊OSA的非晚期AMD个体发生地图样萎缩(HR,7.00;95% CI,4.47 - 11.0;P = 0.03)、渗出性AMD(HR,2.87;95% CI,2.37 - 3.48;P = 0.03)以及需要抗VEGF注射(HR,4.72;95% CI,3.59 - 6.22;P = 0.02)的风险升高。
在一个大型异质性数据库中,观察到已确诊OSA的个体发生AMD及疾病进展至晚期的风险升高。
在本文末尾的脚注和披露中可能会发现专有或商业披露信息。