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Progression and Longitudinal Biometric Changes in Highly Myopic Eyes

PURPOSE: To examine 2-year progression rate and associated biometric changes in highly myopic eyes. METHODS: This is a longitudinal, observational cohort study that included 657 participants aged 7 to 70 years with bilateral high myopia (≤−6.00 diopters [D]) and followed for 2 years. All participant...

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Autores principales: Lee, Jonathan Tak Loong, Guo, Xinxing, Li, Zhixi, Jong, Monica, Sankaridurg, Padmaja, He, Mingguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401968/
https://www.ncbi.nlm.nih.gov/pubmed/32334434
http://dx.doi.org/10.1167/iovs.61.4.34
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author Lee, Jonathan Tak Loong
Guo, Xinxing
Li, Zhixi
Jong, Monica
Sankaridurg, Padmaja
He, Mingguang
author_facet Lee, Jonathan Tak Loong
Guo, Xinxing
Li, Zhixi
Jong, Monica
Sankaridurg, Padmaja
He, Mingguang
author_sort Lee, Jonathan Tak Loong
collection PubMed
description PURPOSE: To examine 2-year progression rate and associated biometric changes in highly myopic eyes. METHODS: This is a longitudinal, observational cohort study that included 657 participants aged 7 to 70 years with bilateral high myopia (≤−6.00 diopters [D]) and followed for 2 years. All participants underwent ocular biometry and cycloplegic refraction examinations. Main outcome measures were changes in spherical equivalent refraction (SE) and ocular biometry in the right eyes. RESULTS: Mean age of participants was 21.6 ± 12.2 years. At baseline, mean SE was −9.82 ± 3.28 D and ocular biometric measurements were 27.40 ± 1.56 mm for axial length, 3.16 ± 0.27 mm for anterior chamber depth, 3.60 ± 0.35 mm for lens thickness, and 20.09 ± 1.50 mm for vitreous chamber depth. After 2 years of follow-up, there was a trend toward more myopia and greater axial elongation in all age groups. Younger participants (≤20 years) had significantly (P < 0.001) greater rates of myopic shift and axial elongation compared with older participants (>20 years). However, highly myopic adults aged 40 to 70 years continued to demonstrate refractive progression, particularly if they had extremely high myopia (≤−10.00 D). In the multiple regression analysis, each additional diopter of myopia at baseline was associated with a 11% higher risk of a >1.00-D/y myopic shift (odds ratio, 1.11; 95% confidence interval, 1.04–1.18; P = 0.002). CONCLUSIONS: Longitudinal data from this large Chinese cohort suggest that highly myopic eyes continue to progress in SE throughout life, with the greatest rates of progression observed in younger participants. Axial elongation rates appeared to stabilize after 20 years of age and were predominantly due to an increase in the vitreous chamber depth. Other risk factors for a myopic shift included a higher degree of myopic refraction at baseline.
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spelling pubmed-74019682020-08-18 Progression and Longitudinal Biometric Changes in Highly Myopic Eyes Lee, Jonathan Tak Loong Guo, Xinxing Li, Zhixi Jong, Monica Sankaridurg, Padmaja He, Mingguang Invest Ophthalmol Vis Sci Clinical and Epidemiologic Research PURPOSE: To examine 2-year progression rate and associated biometric changes in highly myopic eyes. METHODS: This is a longitudinal, observational cohort study that included 657 participants aged 7 to 70 years with bilateral high myopia (≤−6.00 diopters [D]) and followed for 2 years. All participants underwent ocular biometry and cycloplegic refraction examinations. Main outcome measures were changes in spherical equivalent refraction (SE) and ocular biometry in the right eyes. RESULTS: Mean age of participants was 21.6 ± 12.2 years. At baseline, mean SE was −9.82 ± 3.28 D and ocular biometric measurements were 27.40 ± 1.56 mm for axial length, 3.16 ± 0.27 mm for anterior chamber depth, 3.60 ± 0.35 mm for lens thickness, and 20.09 ± 1.50 mm for vitreous chamber depth. After 2 years of follow-up, there was a trend toward more myopia and greater axial elongation in all age groups. Younger participants (≤20 years) had significantly (P < 0.001) greater rates of myopic shift and axial elongation compared with older participants (>20 years). However, highly myopic adults aged 40 to 70 years continued to demonstrate refractive progression, particularly if they had extremely high myopia (≤−10.00 D). In the multiple regression analysis, each additional diopter of myopia at baseline was associated with a 11% higher risk of a >1.00-D/y myopic shift (odds ratio, 1.11; 95% confidence interval, 1.04–1.18; P = 0.002). CONCLUSIONS: Longitudinal data from this large Chinese cohort suggest that highly myopic eyes continue to progress in SE throughout life, with the greatest rates of progression observed in younger participants. Axial elongation rates appeared to stabilize after 20 years of age and were predominantly due to an increase in the vitreous chamber depth. Other risk factors for a myopic shift included a higher degree of myopic refraction at baseline. The Association for Research in Vision and Ophthalmology 2020-04-25 /pmc/articles/PMC7401968/ /pubmed/32334434 http://dx.doi.org/10.1167/iovs.61.4.34 Text en Copyright 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Clinical and Epidemiologic Research
Lee, Jonathan Tak Loong
Guo, Xinxing
Li, Zhixi
Jong, Monica
Sankaridurg, Padmaja
He, Mingguang
Progression and Longitudinal Biometric Changes in Highly Myopic Eyes
title Progression and Longitudinal Biometric Changes in Highly Myopic Eyes
title_full Progression and Longitudinal Biometric Changes in Highly Myopic Eyes
title_fullStr Progression and Longitudinal Biometric Changes in Highly Myopic Eyes
title_full_unstemmed Progression and Longitudinal Biometric Changes in Highly Myopic Eyes
title_short Progression and Longitudinal Biometric Changes in Highly Myopic Eyes
title_sort progression and longitudinal biometric changes in highly myopic eyes
topic Clinical and Epidemiologic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401968/
https://www.ncbi.nlm.nih.gov/pubmed/32334434
http://dx.doi.org/10.1167/iovs.61.4.34
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