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阻塞性睡眠呼吸暂停对糖尿病视网膜病变进展及全身并发症的影响。

Impact of Obstructive Sleep Apnea on Diabetic Retinopathy Progression and Systemic Complications.

作者信息

Rahimy Ehsan, Koo Euna B, Wai Karen M, Ludwig Cassie A, Kossler Andrea L, Mruthyunjaya Prithvi

机构信息

From the Department of Ophthalmology, Horngren Family Vitreoretinal Center, Byers Eye Institute, Stanford University School of Medicine (E.R., E.B.K., K.M.W., C.A.L., A.L.K., P.M.); Department of Ophthalmology, Palo Alto Medical Foundation (E.R.), Palo Alto, California, USA..

From the Department of Ophthalmology, Horngren Family Vitreoretinal Center, Byers Eye Institute, Stanford University School of Medicine (E.R., E.B.K., K.M.W., C.A.L., A.L.K., P.M.).

出版信息

Am J Ophthalmol. 2025 Feb;270:93-102. doi: 10.1016/j.ajo.2024.07.021. Epub 2024 Jul 31.

Abstract

PURPOSE

To evaluate the risk of diabetic retinopathy progression and systemic vascular events, including death, in patients with nonproliferative diabetic retinopathy (NPDR) with obstructive sleep apnea (OSA).

DESIGN

Retrospective cohort study.

METHODS

Electronic chart query using TriNetX, an electronic health records network comprising data from over 124 million patients. Patients with NPDR with and without OSA were identified. Patients were excluded if they had a history of proliferative disease (proliferative diabetic retinopathy), diabetic macular edema, or prior ocular intervention (intravitreal injection, laser, or pars plana vitrectomy). Propensity score matching was performed to control for baseline demographics and comorbidities. The rate of progression to vision-threatening complications, need for ocular intervention, and systemic events was measured at 1, 3, and 5 years.

RESULTS

A total of 11 931 patients in each group were analyzed after propensity score matching. There was an elevated risk of proliferative diabetic retinopathy in the OSA cohort at 1 (risk ratio [RR]: 1.34, P < .001), 3 (RR: 1.31, P < .001), and 5 years (RR: 1.28, P < .001). There was an elevated risk of diabetic macular edema in the OSA group at all time points: 1 (RR: 1.31, P < .001), 3 (RR: 1.19, P<.001), and 5 years (RR: 1.18, P < .001). With respect to ocular interventions, there was an increased risk of intravitreal injection in patients with OSA at 1 (RR: 1.59, P < .001), 3 (RR: 1.58, P < .001), and 5 years (RR: 1.54, P < .001), and similar trends were noted with laser photocoagulation, but not vitrectomy. Regarding systemic events, patients with NPDR with OSA had a greater risk of stroke (1 year RR: 1.80, P < .001; 3 years RR: 1.56, P < .001; and 5 years RR: 1.49, P < .001), myocardial infarction (1 year RR: 1.51, P < .001; 3 years RR: 1.46, P < .001; and 5 years RR: 1.43, P < .001), and death (1 year RR: 1.31, P < .001; 3 years RR: 1.19, P < .001; and 5 years RR: 1.15, P < .001).

CONCLUSIONS

There is an increased rate of diabetic retinopathy progression to vision-threatening complications, need for ocular intervention, and systemic complications, including death, for patients with OSA. We emphasize the need for improved screening measures of patients with NPDR and potential OSA.

摘要

目的

评估患有阻塞性睡眠呼吸暂停(OSA)的非增殖性糖尿病视网膜病变(NPDR)患者糖尿病视网膜病变进展及全身性血管事件(包括死亡)的风险。

设计

回顾性队列研究。

方法

使用TriNetX进行电子病历查询,TriNetX是一个电子健康记录网络,包含来自超过1.24亿患者的数据。识别出患有和未患有OSA的NPDR患者。如果患者有增殖性疾病(增殖性糖尿病视网膜病变)、糖尿病黄斑水肿或既往眼部干预(玻璃体腔内注射、激光或玻璃体切除术)病史,则将其排除。进行倾向得分匹配以控制基线人口统计学和合并症。在1年、3年和5年时测量进展为威胁视力并发症的发生率、眼部干预的需求以及全身性事件。

结果

倾向得分匹配后,每组共分析了11931例患者。OSA队列在1年(风险比[RR]:1.34,P <.001)、3年(RR:1.31,P <.001)和5年(RR:1.28,P <.001)时增殖性糖尿病视网膜病变的风险升高。OSA组在所有时间点糖尿病黄斑水肿的风险均升高:1年(RR:1.31,P <.001)、3年(RR:1.19,P<.001)和5年(RR:1.18,P <.001)。关于眼部干预,OSA患者在1年(RR:1.59,P <.001)、3年(RR:1.58,P <.001)和5年(RR:1.54,P <.001)时玻璃体腔内注射的风险增加,并在激光光凝方面观察到类似趋势,但玻璃体切除术未见此趋势。关于全身性事件,患有OSA的NPDR患者发生中风的风险更高(1年RR:1.80,P <.001;3年RR:1.56,P <.001;5年RR:1.49,P <.001)、心肌梗死(1年RR:1.51,P <.001;3年RR:1.46,P <.001;5年RR:1.43,P <.001)和死亡(1年RR:1.31,P <.001;3年RR:1.19,P <.001;5年RR:1.15,P <.001)。

结论

对于患有OSA的患者,糖尿病视网膜病变进展为威胁视力并发症、眼部干预需求以及全身性并发症(包括死亡)的发生率增加。我们强调需要改进对NPDR和潜在OSA患者的筛查措施。

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