Laser-Assisted In Situ Keratomileusis Surgery on a Patient with Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease or Neuromyelitis Optica Spectrum Disorder

Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and neuromyelitis optica spectrum disorder (NMOSD) are rare central demyelinating diseases that may affect refractive surgery outcomes. Optic neuritis and brainstem syndromes affecting cranial nerves are particularly relevant to corneal refractive surgery (CRS), such as laser-assisted in situ keratomileusis (LASIK), photorefractive keratectomy, or small incision lenticule extraction. There is currently no existing literature concerning the outcomes of CRS in patients with MOGAD or NMOSD. This article reports the clinical outcome of a MOGAD patient who underwent LASIK.


Introduction
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and neuromyelitis optica spectrum disorder (NMOSD) are autoantibody-mediated diseases of the central nervous system.For decades, they were considered severe forms of multiple sclerosis (MS), but researchers recently delineated specific antibodies (Ab) that target myelin oligodendrocyte glycoprotein (MOG) or aquaporin-4 (AQP4) in the spinal cord, optic nerve, dorsal medulla, thalamus/hypothalamus, and brainstem [1,2].While MOGAD often meets the clinical criteria for NMOSD, defined as longitudinally extensive transverse myelitis, optic neuritis (ON), area postrema syndrome, and diencephalic, cerebral, or symptomatic brainstem syndromes [1,2], MOGAD requires MOG-Ab seropositivity for diagnosis [2].Studies examining laser-assisted in situ keratomileusis (LASIK) and photorefractive keratectomy (PRK) in patients with a history of MS-associated optic neuritis suggest that the procedure is safe [3].However, little is reported about the safety and efficacy of refractive surgery in MOGAD or NMOSD patients.This article presents a case of successful LASIK surgery in a patient with MOGAD.

Case Report
A 28-year-old female with MOGAD presented for corneal refractive surgery (CRS) consultation.She was diagnosed with MOG-Ab seropositivity three years prior and was well controlled on rituximab 1 g infusion every 6 months.She was asymptomatic apart from ocular dryness that was well controlled with artificial tears.On examination, nystagmus was noted with rightward gaze worse than leftward gaze.Marcus Gunn testing showed no relative afferent pupillary defect.Slit lamp and dilated fundus examinations were unremarkable, and the visual fields were full to confrontation OU.Assessments of contrast sensitivity, corneal sensation, and color vision were within normal limits.testing without anesthesia over 5 minutes was 27 mm OD and 30 mm OS.Best-corrected distance visual acuity was 20/20 OU, and manifest refraction was -4.00 OD and −4:75 − 0:25 × 178 OS.After discussing the risks and benefits of this elective procedure and consultation with the patient's neuroophthalmologist and neurologist, femtosecond-assisted LASIK was performed without complications.Her postoperative course was uneventful, without relapse of MOGAD symptoms, alterations in contrast sensitivity or corneal surface dryness, or postoperative infectious keratitis.Her last uncorrected distance visual acuity was 20/20 OU at 6 months postoperatively, and the patient continues to follow-up with her neurologist and eye care provider.
A thorough history is critical as these diseases differ significantly in epidemiology, characteristic manifestations, and prognosis (Table 1).It is important to review cranial magnetic resonance imaging and optic nerve optical coherence tomography to determine the extent of baseline optic nerve damage and to preoperatively evaluate corneal sensation, color plates, automated visual field, and corneal dryness (Table 2).
Minor ocular trauma has been shown to trigger the onset of NMOSD and ON [4]; consequently, LASIK and PRK may carry this risk.Each attack of ON risks persistent (or permanent) loss of contrast sensitivity, color vision, and visual fields [3].Therefore, we suggest that practitioners evaluate the baseline level of contrast sensitivity in MOGAD and NMOSD patients and utilize wavefront-guided technology [5] or customized topography laser treatments [6] that have been shown to minimize reductions in contrast sensitivity in the general population.While AQP4-Abs commonly involve relapsing disease with progressive vision loss [1,2], adult patients with MOGAD generally present with relapsing ON with better visual recovery or monophasic disease altogether [1,2].Thus, CRS may be relatively safer and have prolonged visual benefits for MOGAD patients.
Beyond optic nerve involvement, MOGAD and NMOSD patients may have cranial nerve deficits, neuropathic pain, and oculomotor dysfunction [1,2].The presumed disruption of the corneal nerve plexus during LASIK and PRK may exacerbate ocular surface dryness and impede corneal wound healing [7] in these patients, who carry an elevated risk of cranial nerve deficits that could affect ocular surface homeostasis.Considering that over 83% of NMOSD and MOGAD patients suffer from neuropathic pain [2], the risk of postoperative corneal neuropathic pain may increase.Thus, we recommend a thorough investigation of ocular surface integrity and cranial nerve deficits preoperatively (Table 2).Regarding nystagmus, we suggest utilizing advanced ocular tracking platforms shown to be effective for existing excimer lasers [8].
Table 2: Suggested questions and testing for patients with neuromyelitis optica spectrum disorder and myelin oligodendrocyte glycoprotein antibody-associated disease to include in a thorough ophthalmologic evaluation.

Do you have any history of eye pain?
Have you ever been diagnosed with optic neuritis?How many recurrences of optic neuritis, if any?
When was the last episode?Has anything triggered an episode (e.g., severe allergic reaction, surgery, trauma, etc.)?
Are you currently on steroids or any long-term immunosuppressive agents?Do you have any history of dry eyes or recurrent corneal erosions?Do you have any history of eye infections (especially bacterial or viral corneal infection)?
Have you ever had an episode of facial palsy, double vision, or nystagmus?Do you have any lasting visual deficits?Do you have neuropathic pain?Testing Imaging Review MRI brain/orbits with contrast to determine the extent of optic nerve involvement.Chiasmal involvement, longitudinally extensive optic nerve enhancement, and/or bilateral optic nerve involvement point to ON of NMOSD or MOGAD versus MS-associated ON. 1,2  Review OCT optic nerve to determine the extent of optic nerve damage.
Markedly reduced peripapillary nerve fiber layer thickness is commonly seen following ON of NMOSD and MOGAD.

Other
Determine the seropositivity with a cell-based assay to detect AQP4-IgG or MOG-IgG in serum.Titers do not reliably predict remission. 2 Spontaneous nystagmus testing Comprehensive neurologic exam to determine the extent of neurologic deficits (especially cranial nerves 2, 3, 5, 7) Case Reports in Ophthalmological Medicine Treatment for MOGAD and NMOSD typically involves intensive steroid use and chronic immunomodulating apy for relapsing disease [1,2].Realizing that high-dose steroid use can transiently increase intraocular pressure and cause refractive instability [9], we recommend waiting for an extended period after acute therapy to allow for accurate evaluation of stable refractive error preoperatively.Due to the high relapse rate, especially with AQP4-Ab-positive NMOSD, these patients may be on long-term immunosuppressive agents [1,2] that can increase the risk of viral and bacterial keratitis [10].Although maintenance therapy reduces the number of relapses and improves overall prognosis, progressive deterioration may still occur [2].
In conclusion, significant visual impairment is a common finding in this population, and patients may seek refractive surgery to improve unaided visual acuity and decrease dependence on glasses and contact lenses.For those with strong visual recovery, as seen in our MOGAD patient, LASIK may be a successful option.We recommend a thorough preoperative workup assessing ocular surface integrity and visual function, along with a neurology consult.Candidates for CRS must be fully informed and understand that MOGAD and NMOSD carry the risk of ON with impaired vision and contrast sensitivity, cranial nerve deficits, and certain postoperative complications seen in immunocompromised patients.As minimal ocular trauma could potentially induce ON attacks, we advise extreme caution when considering CRS in patients with active or relapsing disease, especially those with AQP4-Abs.These recommendations are based on the most common clinical findings of MOGAD and NMOSD; however, given the wide spectrum of possible presentations, every patient should be individually evaluated by their ophthalmologist and care team.

Table 1 :
Neuromyelitis optica spectrum disorder, further broken down into AQP4-seropositive and seronegative NMOSD, and myelin oligodendrocyte glycoprotein antibody-associated disease epidemiology, characteristic manifestations, and prognosis with risk factors for more severe disease.