夜间缺氧与老年黄斑变性

IF 4.9 2区 医学 Q1 OPHTHALMOLOGY Clinical and Experimental Ophthalmology Pub Date : 2024-08-01 DOI:10.1111/ceo.14428
Attiqa Chaudhary, Carla J Abbott, Zhichao Wu, Wendy Y Fang, Palaniraj R Raj, Matthew Naughton, Wilson J Heriot, Robyn H Guymer
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引用次数: 0

摘要

背景:夜间缺氧是一种常见病,但诊断率低,而且与老年性黄斑变性(AMD)的高危人群相同。本研究旨在确定夜间缺氧与老年性黄斑变性、其严重程度以及网状假性黄斑变性(RPD)高风险亚型之间的关系:这项横断面研究包括年龄≥50 岁的老年性视网膜病变患者或正常对照组,不包括正在接受阻塞性睡眠呼吸暂停治疗的患者。所有参与者都在家中进行了一夜(最多 3 晚)脉搏血氧仪记录和多模态成像,以对 AMD 进行分类。阻塞性睡眠呼吸暂停(OSA)的分类是根据氧饱和度指数[ODI]确定的,轻度为5-15,中重度>15:共纳入 225 名参与者,其中 76% 患有 AMD,42% 同时患有 RPD。在AMD患者中,53%为早期/中期AMD,30%为地理性萎缩(GA),17%为新生血管性AMD(nAMD)。总体而言,轻度或中重度 OSA 与 AMD 或 AMD 伴有 RPD 的几率增加无关(p ≥ 0.180)。然而,与对照组相比,中度至重度 OSA 与患 nAMD 的几率增加有关(几率比 = 6.35;95% 置信区间 = 1.18 至 34.28;p = 0.032),但与早期/中期 AMD 或 GA 无关(p ≥ 0.130)。轻度 OSA 与任何严重程度的老年性视网膜病变的几率差异无关(p ≥ 0.277):结论:通过 ODI 测定的夜间缺氧与 nAMD 之间存在关联。因此,夜间缺氧可能是导致 nAMD 的一个未被充分重视的重要可调节风险因素。
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Nocturnal hypoxia and age-related macular degeneration.

Background: Nocturnal hypoxia is common, under-diagnosed and is found in the same demographic at risk of age-related macular degeneration (AMD). The objective of this study was to determine any association between nocturnal hypoxia and AMD, its severity, and the high-risk sub-phenotype of reticular pseudodrusen (RPD).

Methods: This cross-sectional study included participants aged ≥50 years with AMD, or normal controls, exclusive of those on treatment for obstructive sleep apnoea. All participants had at home, overnight (up to 3 nights) pulse oximetry recordings and multimodal imaging to classify AMD. Classification of Obstructive Sleep Apnea (OSA) was determined based on oxygen desaturation index [ODI] with mild having values of 5-15 and moderate-to-severe >15.

Results: A total of 225 participants were included with 76% having AMD, of which 42% had coexistent RPD. Of the AMD participants, 53% had early/intermediate AMD, 30% had geographic atrophy (GA) and 17% had neovascular AMD (nAMD). Overall, mild or moderate-to-severe OSAwas not associated with an increased odds of having AMD nor AMD with RPD (p ≥ 0.180). However, moderate-to-severe OSA was associated with increased odds of having nAMD (odds ratio = 6.35; 95% confidence interval = 1.18 to 34.28; p = 0.032), but not early/intermediate AMD or GA, compared to controls (p ≥ 0.130). Mild OSA was not associated with differences in odds of having AMD of any severity (p ≥ 0.277).

Conclusions: There was an association between nocturnal hypoxia as measured by the ODI and nAMD. Hence, nocturnal hypoxia may be an under-appreciated important modifiable risk factor for nAMD.

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来源期刊
CiteScore
7.60
自引率
12.50%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Clinical & Experimental Ophthalmology is the official journal of The Royal Australian and New Zealand College of Ophthalmologists. The journal publishes peer-reviewed original research and reviews dealing with all aspects of clinical practice and research which are international in scope and application. CEO recognises the importance of collaborative research and welcomes papers that have a direct influence on ophthalmic practice but are not unique to ophthalmology.
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