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Indian Journal of Ophthalmology logoLink to Indian Journal of Ophthalmology
. 2023 Jan;71(1):241. doi: 10.4103/ijo.IJO_2248_22

Commentary: Erythropoietin as a treatment option for indirect optic neuropathy: A pilot study

Jawahar Lal Goyal 1,, Naorem Holmes 1
PMCID: PMC10155554  PMID: 36588243

In this pilot study, the advantages of adopting intravenous erythropoietin (EPO) as an option for the treatment of indirect optic neuropathy, especially in cases where steroids are contra-indicated, have been explored. Indirect optic neuropathy is common and usually responds to treatment with 40–60% of cases having visual recovery.[1] Electro-physiological tests such as visual evoked potential (VEP) and electro-retinography (ERG) are helpful tools not only for diagnosis but also for predicting prognosis. In addition to the use of EPO in traumatic optic neuropathy, it has also been tried in cases of optic neuritis, non-arteritic arterior ischemic optic neuropathy (NAION), and methanol optic neuropathy. In optic neuritis, Lagrèze et al.’s[2] study on 103 patients found no added beneficial effect as compared to I/V methylprednisolone. In NAION also, EPO was tried by Modarres et al.,[3] and they found beneficial effects in improving the best corrected visual acuity (BCVA) at 3 months follow-up, which was retained at 6 months follow-up. However, in a study by Nikkhah et al.,[4] they did not find any significant difference in the outcome of BCVA between the three groups, that is, I/V EPO, oral prednisolone, and placebo. However, Pakdel et al.[5] in a phase 2 clinical trial reported beneficial effects of I/V EPO in cases of methanol optic neuropathy.

The major therapeutic option currently in practice for the treatment of traumatic optic neuropathy is the use of corticosteroids. Apart from the various side effects that the use of intravenous corticosteroids entails, there are also various contra-indications to their use. EPO has been shown to have neuro-protective action, especially when given early. “Several studies have highlighted the neuro-protective function of EPO in extra-hematopoietic tissues, especially the retina. EPO could interact with its heterodimer receptor (EPOR/bcR) to exert its anti-apoptosis, anti-inflammatory, and anti-oxidative effects in preventing retinal ganglion cell death through different intracellular signalling pathways.”[6] It has thus been hypothesized that EPO may improve visual functions in indirect traumatic optic neuropathy by reducing apoptosis of retinal ganglion cells and by promoting neuro-regeneration in the damaged axons.[7]

The author has demonstrated the possibility of the use of EPO in indirect optic neuropathy in a small pilot study; however, further research as case control studies is essential to confirm the beneficial effects of EPO in indirect optic neuropathy.

References

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