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Nocturnal hypoxia and age-related macular degeneration.
Chaudhary, Attiqa; Abbott, Carla J; Wu, Zhichao; Fang, Wendy Y; Raj, Palaniraj R; Naughton, Matthew; Heriot, Wilson J; Guymer, Robyn H.
  • Chaudhary A; Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
  • Abbott CJ; Department of Surgery (Ophthalmology), The University of Melbourne, Parkville, Victoria, Australia.
  • Wu Z; Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
  • Fang WY; Department of Surgery (Ophthalmology), The University of Melbourne, Parkville, Victoria, Australia.
  • Raj PR; Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
  • Naughton M; Department of Surgery (Ophthalmology), The University of Melbourne, Parkville, Victoria, Australia.
  • Heriot WJ; Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
  • Guymer RH; Department of Surgery (Ophthalmology), The University of Melbourne, Parkville, Victoria, Australia.
Clin Exp Ophthalmol ; 2024 Aug 01.
Article en En | MEDLINE | ID: mdl-39089690
ABSTRACT

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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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article