TY - JOUR
T1 - Choroidal thickness predicts progression of myopic maculopathy in high myopes: a 2-year longitudinal study
AU - Li, Zhixi
AU - Liu, Ran
AU - Wang, Decai
AU - Zhang, Jian
AU - Xiao, Ou
AU - Guo, Xinxing
AU - Jong, Monica
AU - Sankaridurg, Padmaja
AU - Ohno-Matsui, Kyoko
AU - He, Mingguang
N1 - Funding Information:
Funding This work was supported by the National Key R&D Program of China (2018YFC0116500), Fundamental Research Funds of the State Key Laboratory of Ophthalmology, National Natural Science Foundation of China (81420108008), Science and Technology Planning Project of Guangdong Province in China (2013B20400003) and a grant from the Brien Holden Vision Institute, Australia. The sponsor or funding organisation had no role in the design or conduct of this research.
Publisher Copyright:
© 2021 BMJ Publishing Group. All rights reserved.
PY - 2021/12/1
Y1 - 2021/12/1
N2 - Aim To prospectively determine the impact of choroidal thickness (CT) on the myopic maculopathy progression.
Methods This is a prospective, longitudinal, observational study. In total, 434 participants aged 7–70 years with bilateral high myopia (≤-6 D spherical error, range, −6 to −27.0 D) completed follow-up visits for 2 years. The baseline CT centred on the fovea was measured using a swept-source optical coherence tomography (OCT). Myopic maculopathy progression was determined by fundus photography. Logistic model was used to examine the impact of CT at baseline on the myopic maculopathy progression. Likelihood ratio test was adopted for model comparison.
Results The mean baseline age, spherical equivalence and subfoveal CT (SFCT) of the participants were 23.2±12.5 years, −10.50±3.18 D and 153.20±72.76 μm, respectively. Over 2-year’s follow-up, 74 of 434 eyes (17.1%) had myopic maculopathy progression. Baseline SFCT was thinner in eyes with myopic maculopathy progression than those without (67.26±37.67 μm vs 170.95±65.45 μm; mean difference, 99.31 μm; 95% CI 83.61 to 115.01 μm; p<0.001). The same patterns of differences were observed in 7–18 years, 19–39 years and 40–70 years. In multivariate logistic regression model, SFCT was a significant risk factor (adjusted OR=0.97, p<0.005) when age, gender, axial length and baseline myopic maculopathy category were adjusted for. The addition of SFCT significantly improved the predictive discrimination of myopic maculopathy progression in comparison with that included established risk factors alone (area under the receiver operating characteristic curve, 0.899 vs 0.942, p<0.001).
Conclusion CT is an independent predictor for myopic maculopathy progression.
AB - Aim To prospectively determine the impact of choroidal thickness (CT) on the myopic maculopathy progression.
Methods This is a prospective, longitudinal, observational study. In total, 434 participants aged 7–70 years with bilateral high myopia (≤-6 D spherical error, range, −6 to −27.0 D) completed follow-up visits for 2 years. The baseline CT centred on the fovea was measured using a swept-source optical coherence tomography (OCT). Myopic maculopathy progression was determined by fundus photography. Logistic model was used to examine the impact of CT at baseline on the myopic maculopathy progression. Likelihood ratio test was adopted for model comparison.
Results The mean baseline age, spherical equivalence and subfoveal CT (SFCT) of the participants were 23.2±12.5 years, −10.50±3.18 D and 153.20±72.76 μm, respectively. Over 2-year’s follow-up, 74 of 434 eyes (17.1%) had myopic maculopathy progression. Baseline SFCT was thinner in eyes with myopic maculopathy progression than those without (67.26±37.67 μm vs 170.95±65.45 μm; mean difference, 99.31 μm; 95% CI 83.61 to 115.01 μm; p<0.001). The same patterns of differences were observed in 7–18 years, 19–39 years and 40–70 years. In multivariate logistic regression model, SFCT was a significant risk factor (adjusted OR=0.97, p<0.005) when age, gender, axial length and baseline myopic maculopathy category were adjusted for. The addition of SFCT significantly improved the predictive discrimination of myopic maculopathy progression in comparison with that included established risk factors alone (area under the receiver operating characteristic curve, 0.899 vs 0.942, p<0.001).
Conclusion CT is an independent predictor for myopic maculopathy progression.
KW - Choroid
KW - Epidemiology
KW - Retina
UR - http://www.scopus.com/inward/record.url?scp=85091764465&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/45563b40-bed7-3c49-940a-31e1436921a4/
U2 - 10.1136/bjophthalmol-2020-316866
DO - 10.1136/bjophthalmol-2020-316866
M3 - Article
C2 - 32972914
SN - 0007-1161
VL - 105
SP - 1744
EP - 1750
JO - British Journal of Ophthalmology
JF - British Journal of Ophthalmology
IS - 12
ER -