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. 2023 Aug;37(4):328-339.
doi: 10.3341/kjo.2022.0166. Epub 2023 Aug 5.

Neuroprotective Strategies for Nonarteritic Anterior Ischemic Optic Neuropathy: A Systematic Review

Affiliations

Neuroprotective Strategies for Nonarteritic Anterior Ischemic Optic Neuropathy: A Systematic Review

Brigitta Marcia Budihardja et al. Korean J Ophthalmol. 2023 Aug.

Abstract

Purpose: Nonarteritic anterior ischemic optic neuropathy (NAION) is the second most common form of optic neuropathy. Most patients show no improvement over time. Until now, there is still no definitive therapy for NAION. The available literatures on the possible treatment of NAION are quite diverse and controversial. Neuroprotection strategies have been suggested as one of the potential treatments for NAION. This review aims to critically evaluate the literature on neuroprotective strategy for NAION.

Methods: This report was written in accordance with PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) guidelines. We performed a systematic literature search in Pubmed, Science Direct, Proquest, and Cochrane databases. Only neuroprotective agents that directly work in protecting neurons were included. The outcome of interest in this review is retinal ganglion cell density and apoptosis for animal studies and retinal nerve fiber layer thickness for human studies.

Results: The systematic search identified 591 studies of which 24 met the eligibility criteria, including 21 animal studies and three human studies. Only a few of the studies evaluated the same treatments, showing how diverse neuroprotector treatments are currently being evaluated as NAION treatment. From 21 animal studies, 14 studies showed significantly higher retinal ganglion cell density (1.49- to 2.81-fold) with neuroprotective treatment compared to control group. Two of three human studies in this review had also found a beneficial effect of preserving retinal nerve fiber layer thickness in NAION patients.

Conclusions: This review suggests the potential of neuroprotection as a viable option in the quest for an effective treatment strategy for NAION. Further studies, particularly clinical studies, are necessary to establish its efficacy in NAION patients.

Keywords: Ischemic optic neuropathy; Neuroprotection; Retinal ganglion cells.

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Conflict of interest statement

Conflicts of Interest: None.

Figures

Fig. 1
Fig. 1
PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) flowchart illustrating the process of article selection. The article selection process commenced with a comprehensive database search and hand-searching, followed by a screening procedure based on predetermined eligibility criteria. After careful screening and assessment of eligibility, a total of 24 studies were included in this review.
Fig. 2
Fig. 2
Risk-of-bias assessment for all animal studies using SYRCLE [16]. While none of the studies exhibited a high risk of bias, several studies presented an “unclear” risk of bias due to lack of detailed description in the methods section. D = domain.
Fig. 3
Fig. 3
Neuroprotective strategies for nonarteritic anterior ischemic optic neuropathy (NAION). Numerous neuroprotective strategies have been proposed as potential treatments for NAION. These strategies exert their effects through various mechanisms, such as antiapoptosis, stabilization of the blood-optic nerve barrier, anti-inflammation, and neurotrophic mechanisms. Some strategies demonstrate neuroprotective effects through multiple mechanisms. However, further research is necessary to explore the efficacy and underlying mechanisms of these strategies. G-CSF = granulocyte colony-stimulating factor; ω-3 PUFA = omega-3 polyunsaturated fatty acids; MSC = mesenchymal stem cell; PGJ2 = 15-deoxy-Δ12,14-prostaglandin J2.

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References

    1. Miller NR, Arnold AC. Current concepts in the diagnosis, pathogenesis and management of nonarteritic anterior ischaemic optic neuropathy. Eye (Lond) 2015;29:65–79. - PMC - PubMed
    1. Arnold AC, Hepler RS. Fluorescein angiography in acute nonarteritic anterior ischemic optic neuropathy. Am J Ophthalmol. 1994;117:222–30. - PubMed
    1. Hattenhauer MG, Leavitt JA, Hodge DO, et al. Incidence of nonarteritic anterior ischemic optic neuropathy. Am J Ophthalmol. 1997;123:103–7. - PubMed
    1. Lee JY, Park KA, Oh SY. Prevalence and incidence of non-arteritic anterior ischaemic optic neuropathy in South Korea: a nationwide population-based study. Br J Ophthalmol. 2018;102:936–41. - PubMed
    1. Xu L, Wang Y, Jonas JB. Incidence of nonarteritic anterior ischemic optic neuropathy in adult Chinese: the Beijing Eye Study. Eur J Ophthalmol. 2007;17:459–60. - PubMed

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