Abstract
Myopia is a common refractive error, characterized by an excessive increase in axial length relative to the refractive power of the eye. Despite much research, the mechanisms underlying the development of myopia are unknown. A large body of work on animal models (such as chicks, guinea pigs, and monkeys) has been instrumental to our understanding of visually guided ocular growth, and potential mechanisms leading to myopia. These studies have shown that experimentally degrading the quality of the image formed on the retina by introducing translucent diffusers (i.e., form-deprivation), or altering the focal point of the image with respect to the retinal plane by imposing plus or minus lenses to the eyes (i.e., lens induced defocus) results in abnormal eye growth and development of reflective errors. Ocular changes in response to form-deprivation and lens induced defocus are primarily associated with changes in axial length (mainly due to changes in vitreous chamber depth) and choroidal thickness. These experimentally induced ocular changes quickly revert to normal upon removal of the imposed optical treatment. Physiological changes in retinal cells and neurotransmitters (such as dopamine), presence of ocular aberrations, altered accommodative response to visual stimuli, and even subtle variations in natural circadian rhythms of axial length may all influence ocular growth, and hence susceptibility to myopia. In fact, several optical interventions alter ocular aberrations, peripheral refraction, and the accommodative response of the eye in an attempt to arrest myopia development. Epidemiological studies have also linked excessive near work, better socioeconomic status, and urbanization to myopia, although the exact cause for these associations remain elusive. Based on decades of work on the effects of ambient lighting on refractive development in laboratory animals, recent clinical studies have revealed protective effects of greater outdoor exposures on development and progression of myopia in children. Experimental models continue to provide valuable information on the cellular and biochemical mechanisms of myopia.
| Original language | English |
|---|---|
| Title of host publication | Updates on Myopia |
| Subtitle of host publication | A Clinical Perspective |
| Editors | Marcus Ang, Tien Y. Wong |
| Place of Publication | Singapore |
| Publisher | Springer |
| Chapter | 4 |
| Pages | 65-94 |
| Number of pages | 30 |
| ISBN (Electronic) | 9789811384912 |
| ISBN (Print) | 9789811384905 |
| DOIs | |
| Publication status | Published - 10 Oct 2019 |
Bibliographical note
Open Access. This chapter is licensed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made.Keywords
- Open access
- Clinical concepts of myopia
- Complications of myopia
- Myopia in children and adults
- Imaging in myopia
- Pathological myopia
- Dopamine
- Defocus
- Emmetropization
- Myopia
- Choroid
- Form-deprivation
- Light
- Axial length
- Accommodation