Nocturnal hypoxia and age-related macular degeneration

被引:0
|
作者
Chaudhary, Attiqa [1 ,2 ]
Abbott, Carla J. [1 ,2 ]
Wu, Zhichao [1 ,2 ]
Fang, Wendy Y. [1 ,2 ,3 ]
Raj, Palaniraj R. [1 ,4 ]
Naughton, Matthew [5 ,6 ]
Heriot, Wilson J. [1 ,2 ,7 ]
Guymer, Robyn H. [1 ,2 ]
机构
[1] Royal Victorian Eye & Ear Hosp, Ctr Eye Res Australia, Level 7,32 Gisborne St, East Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Dept Surg Ophthalmol, Parkville, Vic, Australia
[3] Monash Univ, Sch Publ Hlth & Prevent Med, Dept Epidemiol & Prevent Med, Clayton, Vic, Australia
[4] Univ Sydney, Save Sight Inst, Discipline Clin Ophthalmol & Eye Hlth, Sydney, NSW, Australia
[5] Alfred Hosp, Dept Resp & Sleep Med, Melbourne, Vic, Australia
[6] Monash Univ, Fac Med Nursing & Hlth Sci, Melbourne, Vic, Australia
[7] Retinol Inst, Glen Iris, Vic, Australia
来源
基金
英国医学研究理事会;
关键词
age-related macular degeneration; nocturnal hypoxia; oxygen desaturation index; pulse oximetry; sleep-disordered breathing; OBSTRUCTIVE SLEEP-APNEA; OXYGEN DESATURATION INDEX; PULSE OXIMETRY; BEVACIZUMAB;
D O I
10.1111/ceo.14428
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
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.
引用
收藏
页码:973 / 980
页数:8
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