April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Obstructive Sleep Apnea is an Independent Risk Factor for Non-Arteritic Ischemic Optic Neuropathy
Author Affiliations & Notes
  • D. T. Nguyen
    Doheny Eye Institute USC Keck School of Medicine, Los Angeles, California
    VMR Institute, Huntington Beach, California
  • Y. Emoto
    Department of Neuro-Ophthalmology, Inouye Eye Hospital, Tokyo, Japan
  • H. Emoto
    Department of Ophthalmology, Tokyo Medical and Dental University, Tokyo, Japan
  • J. Sebag
    Doheny Eye Institute USC Keck School of Medicine, Los Angeles, California
    VMR Institute, Huntington Beach, California
  • M. Y. Wang
    Doheny Eye Institute USC Keck School of Medicine, Los Angeles, California
    VMR Institute, Huntington Beach, California
  • D. Levendowski
    Advanced Brain Monitoring, Inc, Carlsbad, California
  • D. Scarfeo
    Advanced Brain Monitoring, Inc, Carlsbad, California
  • P. Westbrook
    Advanced Brain Monitoring, Inc, Carlsbad, California
  • A. A. Sadun
    Doheny Eye Institute USC Keck School of Medicine, Los Angeles, California
  • Footnotes
    Commercial Relationships  D.T. Nguyen, None; Y. Emoto, None; H. Emoto, None; J. Sebag, None; M.Y. Wang, None; D. Levendowski, Advanced Brain Monitoring, Inc, I; D. Scarfeo, Advanced Brain Monitoring, Inc, E; P. Westbrook, Advanced Brain Monitoring, Inc, I; A.A. Sadun, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 1454. doi:
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      D. T. Nguyen, Y. Emoto, H. Emoto, J. Sebag, M. Y. Wang, D. Levendowski, D. Scarfeo, P. Westbrook, A. A. Sadun; Obstructive Sleep Apnea is an Independent Risk Factor for Non-Arteritic Ischemic Optic Neuropathy. Invest. Ophthalmol. Vis. Sci. 2010;51(13):1454.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To determine whether obstructive sleep apnea (OSA) is a risk factor for non-arteritic ischemic optic neuropathy (NAION) by measuring objective parameters of OSA in NAION subjects and non-NAION controls, taking into account confounding risk factors.

Methods: : Thirty-two subjects were recruited from the VMR Institute and the Doheny Eye Institute neuro-ophthalmology clinic. There were 24 NAION patients (16 males, 8 females, mean age = 60.3 years) and 8 controls (2 males, 6 females, mean age 51.9 years). Using the Apnea Risk Evaluation System Unicorder (ARES, Advanced Brain Monitoring, Inc, Carlsbad, CA) subjects acquired 2-3 nights of sleep study data at home. An apnea-hypopnea index (AHI) with 4% desaturation (AHI-4% = the average number of obstructive breathing events associated with 4% oxygen desaturation per hour) and an AHI with 1% desaturation (AHI-1%) was calculated for each patient using the formula: AHI = Number of Abnormal Breathing Events / [Total Recording Time - (Actigraphically Awake Time + Invalid Signal Time)]. AHI-4% scores of 5-14 were defined as mild OSA, and AHI-4% scores ≥ 15 were defined as moderate OSA.

Results: : Using AHI-4%, 14/24 (59%) NAION patients had mild to moderate OSA. Of the non-NAION controls, only 1/8 (13%) had mild to moderate OSA. Using AHI-1%, 14/24 (58%) NAION patients had AHI ≥ 15, as compared to 0/8 (0%) non-NAION controls with an AHI ≥ 15. The average AHI-4% (± SEM) for NAION patients was 5-fold higher (8.8 ± 1.8) than for non-NAION controls (1.8 ± 0.75; P = 0.0065). Similarly, the average AHI-1% for NAION patients (18.9 ± 2.3) was greater than for controls (7.6 ± 1.7; P=0.006). Subgroup analysis of subjects without diabetes or hypertension [NAION (n=12) & non-NAION (n=5)] found an AHI-4% (± SEM) for NAION patients of 8.2 (± 2.7), which was significantly greater than non-NAION controls (AHI-4% =1.6 ± 1.1; P=0.026).

Conclusions: : There is an increased prevalence of OSA in NAION. Even after accounting for the confounders of diabetes and hypertension by subgroup analysis, there was an independent association of OSA with NAION.

Keywords: clinical (human) or epidemiologic studies: risk factor assessment • neuro-ophthalmology: optic nerve 
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