By Loujain Alqahtani, Optometry doctor
and student of the Expert Certificate in Clinical Optometry
Myopia is an emerging pandemic with prevalence reaching an alarmingly high level globally. The accelerated evolution of lifestyles over recent decades with more time dedicated to near work, combined with a marked reduction of outdoor activities likely explains this epidemic (He et al., 2015; Ip et al., 2008; Nickels et al., 2019). Myopia has been predicted to affect nearly 50% of the world’s population by 2050 (Holden et al., 2016). Due to the significant economic health burden and serious sight-threatening complications associated with myopia such as myopic macular degeneration, retinal detachment, glaucoma, and cataract, controlling myopia progression is obligatory nowadays more than ever to increase the quality of life and ocular health and reduce the social impact and burden (Holden et al., 2013). However, this article will focus on optical intervention in controlling myopia progression.
During the normal process of emmetropisation, the eye expands in all directions and is associated with mechanical stretching and thinning of the crystalline lens, which reduces the lens power. A decoupling between this process of axial elongation and flattening of the corneal and lens curvature causes escalated axial growth and arrest of lens thinning by disruption of the equatorial expansion, leading to myopia (Mutti, 2010). The Collaborative Longitudinal Evaluation of Ethnicity and Refractive Error (CLEERE) Study, an observational study of ocular development and myopia onset, found that children who became myopic showed significantly more axial elongation that accelerated (up to 3 times faster) one year before the onset of myopia, making axial growth a major determinant of the refractive status of the eye (Mutti et al., 2007).
Myopic eyes usually have greater accommodative lag during near viewing, producing more peripheral retinal hyperopic defocus (a blur caused by having the image focused behind the retina) than emmetropic eyes, which has been theorized to encourage more axial elongation (Seidemann et al., 2002). Peripheral hyperopic defocus was first indicated as a potential mechanism for myopia progression in the 1970s (Hoogerheide et al., 1971). Since that time, several animal and human clinical studies have strongly suggested that peripheral retinal defocus might mediate eye growth even under a clear foveal image (Smith et al., 2009). Based on these findings, the discovery of the retinal ability to detect the sign of defocus was key in developing optical interventions to control myopia progression. It is still unknown how the optical signals are activated or inhibited in the choroid, retina, and sclera, and how the signals control structural changes that cause increased axial length (AL).
Progression of more than 0.5D over a year with adequate refractive correction.
(Saxena et al., 2022)
Myopia control should start as soon as possible. Experiments have demonstrated that reducing accommodation lag and/or central and peripheral hyperopic defocus can be used to alter eye growth in a highly regulated manner involving both direction and magnitude. (Figure2) Until recently, numerous hypotheses have been proposed to explain the myopia control effect of optical interventions, including:
– Reduction and correction of accommodative lag (Aller et al., 2016).
– Alteration of the peripheral retinal image to decrease hyperopic defocus (Sankaridurg et al., 2011).
– Obligation of extended myopic defocus in the retina (Lam et al., 2013).
– Optimization of the quality of retinal image for the points in front of the retina and degrading quality of retinal image for the points behind the retina (Cooper et al., 2018).
Figure 2. The design of the Defocus Incorporated Multiple Segments (DIMS) spectacle lens. (Lam et al., 2019).
Soft multifocal contact lenses have been explored in several RCTs so far, which demonstrated a reduction in myopia progression of on average 36.4% and a decrease in axial elongation by 37.9% (Cheng et al., 2016; Sankaridurg et al., 2019; Walline et al., 2013)
MiSight® 1 day (CooperVision) is a daily disposable soft CL that has been recently approved by the US Food and Drug Administration (FDA) to control the progression of myopia in children. The lens has a large central correction zone of 3.36 mm surrounded by concentric zones of alternating distance and near powers which together produce two focal planes. The correction zone corrects the refractive error, while the treatment zones produce 2.00D of simultaneous myopic defocus during both distance and near viewing. A 3-year multicentric RCT reported a 59% reduction in mean cycloplegic SE and a 52% reduction in AL elongation with the MiSight lens compared with soft SVL. These lenses are currently indicated in myopes aged 8–12 years with −0.75D to − 4D of myopia (Chamberlain et al., 2019).
This article covers a variety of interventions aimed at slowing myopia progression. No one strategy appears to reliably achieve this outcome in all individuals, and their role in high myopia is still unclear. The possibility of a rebound phenomenon after discontinuation of such a myopia treatment remains unknown. Ongoing research may lead to a better understanding of the persistence of treatment effects over time, as well as the exploration of more novel approaches to myopia control.
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