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Standardization of High Myopia Optic Nerve Head.1
Standardization of High Myopia Optic Nerve Head.1
yopia is a major worldwide public health issue, particularly in the Asia-Pacific region.1–3 The prevalence
M of myopia has exponentially increased in the past decades and is now recognized by the World Health
Organization as a leading cause of visual impairment.4 High myopia is of grave concern because it is associated
with sight-threatening ocular comorbidities like myopic maculopathy, glaucoma, and retinal detachment.
High myopia is generally defined as a refractive error of ≤ −6 D (spherical equivalent) in the context of axial
length ≥ 26.5 mm.5,6 Holden et al5 estimated that 163 million people (2.7% of the world population) had high
myopia in the year 2000 and was predicted to rise to 938 million (9.8% of the world population) by 2050. The
development of myopia involves the progressive and excessive axial elongation of the globe. Pathologic myopia
may occur in highly myopic eyes with characteristic degenerative changes in the posterior segment, which can
result in irreversible vision loss. The cardinal features of pathologic myopia include posterior staphyloma7 and
myopic maculopathy. To date, literature provides detailed definitions of the characteristic macular lesions in
myopic maculopathy based on the findings of fundus examination and optical coherence tomography (OCT).8,9
Currently, pathologic alterations of the optic nerve and optic neuropathy related to high myopia are recognized
yet ill-elaborated in myopia research. Earlier studies have reported a 28.5% of prevalence of glaucomatous optic
neuropathy (GON) in high myopia. Indeed, high myopia eyes were 5.9 times more likely to develop GON than
emmetropic eyes.10 Nevertheless, structural abnormalities in the optic nerve head (ONH) with corresponding
perimetric defects have also been demonstrated in pathologic myopia with myopic maculopathy.11 Therefore, it
would be of interest to clinicians to understand the underlying structural abnormalities of the optic nerve in high
myopia and to differentiate the optic neuropathy that arises due to high myopia from glaucoma.
In this issue of the Asia-Pacific Journal of Ophthalmology, Jiang et al11 conducted a cross-sectional study by
secondary analysis of data from a longitudinal cohort which included 1389 eyes of 857 highly myopic patients
without pathologic myopic maculopathy to determine the prevalence and characteristics of ONH structural
abnormalities on OCT and their relationship with visual field (VF) defects.
The authors reviewed swept-source OCT scans and classified 12 distinct ONH abnormalities based on 3 cate-
gories: optic disc morphology, papillary/peripapillary tissue defects, and papillary/peripapillary schisis. Their inves-
tigation revealed over 90% of eyes showed at least 1 ONH abnormality, and nearly 35% had 3 or more, with up to
27.3% demonstrating correspondence in the locations of VF defects were present. The most prevalent VF defect in
nonpathologic high myopia was the enlargement of a blind spot on perimetry. This is the first study to demonstrate
the presence of ONH structural abnormalities with a functional relationship to VF defects in nonpathologic high
current study has further demonstrated the structural-functional impairment caused by uncorrected refractive errors in 2004. Bull World
nonpathologic high myopia. This provides crucial evidence to 5. Holden BA, Fricke TR, Wilson DA, et al. Global prevalence of myopia
aid clinicians in establishing a diagnosis of HMON, which has and high myopia and temporal trends from 2000 through 2050.
been challenging to discern from GON and myopic maculop- Ophthalmology. 2016;123:1036–1042.
athy when VF defects arise in a highly myopic eye. Some in- 6. Lin F, Chen S, Song Y, et al. Classification of visual field abnormalities in
teresting findings emerge from this detailed phenotypic highly myopic eyes without pathologic change. Ophthalmology. 2022;129:
characterization. First, certain ONH abnormalities such as 803–812.
peripapillary hyperreflective ovoid mass-like structures 7. Ohno-Matsui K, Jonas JB. Posterior staphyloma in pathologic myopia.
(PHOMS), visible retrobulbar subarachnoid space, and prel- Prog Retin Eye Res. 2019;70:99–109.
aminar schisis were more prevalent than previously recognized. 8. Ruiz-Medrano J, Montero JA, Flores-Moreno I, et al. Myopic
Second, some ONH abnormalities coexisted frequently. Eyes maculopathy: current status and proposal for a new classification and
with shallow optic cups often had PHOMS, while those with grading system (ATN). Prog Retin Eye Res. 2019;69:80–115.
optic disc drusen commonly showed PHOMS. Those with per-
9. Ohno-Matsui K, Kawasaki R, Jonas JB, et al. International photographic
ipapillary retinoschisis often also had prelaminar schisis. Third,
classification and grading system for myopic maculopathy. Am J
ONH abnormalities corresponded to different VF defect pat-
Ophthalmol. 2015;159:877–883.
terns. Glaucoma-like defects occurred more often with deep
optic cups and pits, while high myopia defects correlated with 10. Pan CW, Cheung CY, Aung T, et al. Differential associations of myopia
tissue defects and schisis. It would be of immense relevance to with major age-related eye diseases: the Singapore Indian Eye Study.
and growing myopia population, among which GON and 11. Jiang J, Song Y, Kong K, et al. Optic nerve head abnormalities in non-
HMON are likely to become prevalent sight-threatening eye pathologic high myopia and the relationship with visual field. Asia Pac J
diseases. Ophthalmol (Phila). 2023;12:460–467.
In conclusion, there are rising interests in myopia 12. Xie S, Kamoi K, Igarashi-Yokoi T, et al. Structural abnormalities in
because of the growing myopic population and its related the papillary and peripapillary areas and corresponding visual field
ocular comorbidities. Zhang and colleagues have success- defects in eyes with pathologic myopia. Invest Ophthalmol Vis Sci.
fully demonstrated that characteristic ONH abnormalities 2022;63:13.
with corresponding VF defects were present in non- 13. Lanca C, Sun CH, Chong R, et al. Visual field defects and myopic
pathologic high myopia due to HMON. These results argue macular degeneration in Singapore adults with high myopia. Br J
for the inclusion of ONH evaluations in classifications and Ophthalmol. 2022;106:1423–1428.
monitoring of high myopia. The novel and fundamental
14. Ting DSW, Pasquale LR, Peng L, et al. Artificial intelligence and deep
knowledge of HMON and the classification of its structural
learning in ophthalmology. Br J Ophthalmol. 2019;103:167–175.
and functional abnormalities would propel and support fu-
ture clinical and epidemiologic research in this field. With 15. Clark P, Oermann EK, Chen D, et al. Federated AI, current state, and
the rapid advancement of artificial intelligence,14–16 the future potential. Asia Pac J Ophthalmol (Phila). 2023;12:310–314.
standardization in classification would be a crucial first step 16. Yang D, Ran AR, Nguyen TX, et al. Deep learning in optical coherence
in diagnosing and monitoring HMON in the era of digital tomography angiography: current progress, challenges, and future
medicine. directions. Diagnostics (Basel). 2023;13:326.