Chaudhary Attiqa, Abbott Carla J, Wu Zhichao, Fang Wendy Y, Raj Palaniraj R, Naughton Matthew, Heriot Wilson J, Guymer Robyn H
Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
Department of Surgery (Ophthalmology), The University of Melbourne, Parkville, Victoria, Australia.
Clin Exp Ophthalmol. 2024 Dec;52(9):973-980. doi: 10.1111/ceo.14428. Epub 2024 Aug 1.
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).
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.
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).
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.
夜间缺氧很常见,诊断不足,且在与年龄相关性黄斑变性(AMD)风险相同的人群中也有发现。本研究的目的是确定夜间缺氧与AMD、其严重程度以及网状假性玻璃膜疣(RPD)的高危亚表型之间是否存在关联。
这项横断面研究纳入了年龄≥50岁的AMD患者或正常对照者,排除接受阻塞性睡眠呼吸暂停治疗的患者。所有参与者均在家中进行过夜(最多3晚)脉搏血氧饱和度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)的分类基于氧去饱和指数[ODI],轻度的ODI值为5-15,中度至重度>15。
共纳入225名参与者,其中76%患有AMD,其中42%同时存在RPD。在AMD参与者中,53%患有早期/中期AMD,30%患有地图状萎缩(GA),17%患有新生血管性AMD(nAMD)。总体而言,轻度或中度至重度OSA与患AMD或伴有RPD的AMD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(优势比=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AMD的几率差异无关(p≥0.277)。
通过ODI测量的夜间缺氧与nAMD之间存在关联。因此,夜间缺氧可能是nAMD一个未得到充分认识的重要可改变风险因素。