Abstract
Purpose:
This study aimed to examine the relationship between axial length (AL) and anterior segment biometry in Chinese children and adolescents with high axial myopia.
Methods:
A cross-sectional study was conducted involving 366,278 Chinese students aged 7 to 18 years from January 2020 to December 2022. The SUOER μ-Meter optical biometric was used for measuring ocular biometric parameters. A multivariate linear regression model was used to examine the correlation with AL.
Results:
Among the participants, 28,877 exhibited high axial myopia (AL ≥ 26 mm). The average keratometry (K) and lens thickness (LT) in the high axial myopia group were significantly lower than those in both the non-myopia and normal myopia groups (all p < 0.001). Central corneal thickness (CCT) and anterior chamber depth (ACD) were significantly greater in the high axial myopia group compared to both non-myopia and normal myopia groups (all p < 0.001). Multivariate linear regression analysis demonstrated that K (β = −0.265), CCT (β = 0.001), ACD (β = 1.609), and LT (β = −0.607) were all correlated with AL (all p < 0.001). After adjusting for gender and age, when AL was <27 mm, AL was negatively correlated with LT; similarly, when AL exceeded 27 mm, there was no linear correlation between AL and LT (p > 0.05).
Conclusion:
In Chinese children and adolescents, a high AL (i.e., ≥26 mm) was associated with significantly lower K, thicker CCT, and deeper ACD, and thinner LT compared with subjects having AL < 26 mm. When AL was <27 mm, LT thinning may contribute to myopia compensation; however, when AL exceeds 27 mm, this compensatory effect of crystalline lens thickness appears to diminish.
1 Introduction
The increase in near-work activities and reduced outdoor time, coupled with genetic factors, has contributed to the early onset and high incidence of myopia among young people (1–3). Particularly in East and Southeast Asia, the incidence of myopia among young individuals reaches 80–90%, with rates among school-age children as high as 60% (measured under cycloplegic refraction), far exceeding the rates in Europe (40%) and North America (42%) (2, 4). Progression of myopia can result in serious complications and is a leading cause of irreversible visual impairment and blindness worldwide. It is further associated with increased healthcare expenditures, reduced productivity, and diminished quality of life (5, 6). It is currently established that myopia, especially high myopia, is significantly associated with severe complications, including retinal detachment, retinal neovascularization, early cataracts, and glaucoma (7).
During normal eye development, the emmetropization process coordinates the growth of axial length (AL) with the optical power of the cornea and lens to achieve optimal focus (8). This process involves complex interactions between anterior segment structures and ocular elongation. Disruption of this coordination leads to excessive AL elongation, resulting in myopia (9, 10).
Studies have shown distinct AL growth patterns in myopic children, with accelerated AL growth in the year preceding myopia onset, followed by relatively slower and stable growth thereafter (11, 12). Rapid AL growth markedly increased the risk of axial myopia development, which is currently predominant in children and adolescents (13). This pattern is further supported by a large multicenter study involving 14,127 children and adolescents aged 4–18 years in China, which showed rapid AL growth between ages 4 and 9, slowing after age 9, and stabilizing around age 15 (14). Thus, in myopic children, if progression is not controlled, AL can continue to grow abnormally during this period, leading to high myopia (14).
Previous studies (15, 16) have consistently reported inverse correlations between AL and anterior segment parameters in both emmetropic and myopic populations. Longer AL was associated with flatter corneal curvature, decreased corneal thickness, and reduced endothelial cell density. However, one study (17) reported that this negative correlation between AL and corneal curvature disappeared when AL exceeded 28 mm. Furthermore, there remains no consensus on the relationship between AL and anterior segment parameters such as central corneal thickness (CCT) and lens thickness (LT), specifically in children and adolescents with high axial myopia. Thus, the main aim of this study was to understand the growth characteristics of AL and anterior segment biometry in children and adolescents with high axial myopia and to analyze their correlations.
2 Study population and methods
2.1 Study area and study population
The investigation was conducted in Chengdu City, China. According to the data published in the Seventh National Population Census of China (refer to Chengdu City’s Seventh National Population Census Report), as of 1 November 2020, the permanent population of Chengdu was 20.93 million. This study used a stratified cluster sampling method based on districts (counties) to select all primary and secondary schools from 8 administrative districts within 23 districts (counties) in Chengdu for investigation. Ultimately, 368,083 students from 916 schools (506 primary schools, 274 middle schools, and 136 high schools) in Chengdu were included. Following inclusion criteria and excluding individuals with incomplete information or those unwilling to undergo ophthalmic examinations, a final cross-sectional study of 366,278 students aged 7 to 18 years was established. The study commenced in January 2020 and concluded in December 2022.
2.2 Inclusion and exclusion criteria
Inclusion criteria included: (1) students enrolled in schools within Chengdu City (primary, middle, and high schools) and (2) an age range of 7 to 18 years.
Exclusion criteria included: (1) patients with various forms of glaucoma, corneal disorders, lens disorders, retinal disorders, and optic nerve diseases; (2) patients with amblyopia, strabismus, or severe visual function impairments; (3) patients with evident congenital or metabolic systemic diseases, such as trisomy 21 syndrome (Down syndrome, DS), type 1 diabetes, and similar conditions; (4) individuals with poor compliance, psychiatric disorders, or cognitive impairments; and (5) those who have worn corneal reshaping lenses or similar devices within the past 3 months.
2.3 Study design
This study was a large-scale cross-sectional survey based on school myopia screening, with children and adolescents as research subjects. Students in Chengdu undergo two eye examinations annually as part of routine myopia screening. In order to better implement myopia screening on the Chengdu campus, a dedicated myopia screening working group was established. During the peak months (March to April and September to October), up to 12 groups were divided, each group consisted of 1 ophthalmologist or PhD student with a medical license and 6 nurses. Each team was equipped with three light-box E-word standard logarithmic visual acuity charts (GB 11533), one Topcon Fully-Automated Kerato-Refractometer, and three SUOERμ-Meter optical biometric instruments. Each group screened an average of approximately 200 students per day. The project was officially initiated in January 2020. With the assistance of the Chengdu Education Bureau and Health Bureau, the Ineye Hospital of Chengdu University of Traditional Chinese Medicine (TCM) collected basic student information in advance, including school type, school name, grade, class, name, gender, and age. An eye health record was established through an eye health record system, encompassing all student information and a unique identification code. This identification code was utilized for transmitting examination results. All participants underwent ophthalmic examinations, including unaided visual acuity assessment, non-cycloplegic autorefraction, and ocular biometric parameters assessment.
2.4 Inspection methods
Non-cycloplegic visual acuity and refraction assessments were performed. Uncorrected visual acuity (UCVA) was measured for each eye using a standard logarithmic visual acuity chart at 5 meters under standard illumination and recorded in logMAR notation. Subsequently, autorefraction was conducted. Before the examination, screening personnel scanned the unique identification code of the student to initiate the process. Examination results were automatically uploaded to the eye health record system. The examination used the Topcon Fully-Automated Kerato-Refractometer (KR-1, Japan Topcon Healthcare Trading Co., Ltd.). The height of the KR-1 was set based on the height of the surveyed children and adolescents. Each eye was measured at least three times. If one measurement differed from the other two measurements by more than the maximum allowable error (spherical equivalent within the range of 0.50 to 0.75D), the measurement was repeated. The average of three reliable measurements was used for the final statistical analysis.
Measurement of ocular biometric parameters was performed using the SUOERμ-Meter optical biometric instrument (SW-9000, Tianjin Suoerwei Electronic Technology Co., Ltd.). To ensure data accuracy, the instrument was calibrated daily prior to data collection. The SUOERμ-Meter optical biometric instrument was used to measure the optic axis. The fast measurement speed and non-contact are intended for patient comfort. Capturing eight different measurements in less than 5 s, which are corneal thickness, anterior chamber depth, lens thickness, axial length, corneal curvature, axial angle, white-to-white distance measurement (corneal diameter), and pupil diameter. The average of three reliable measurements was used for the final statistical analysis. High axial myopia was defined as an AL ≥ 26 mm (17), super-high axial myopia was defined as an AL ≥ 28 mm. The following analyses were conducted using right eye statistics. Following the method outlined by Jin et al. (17), the AL was segmented into 1 mm intervals for analysis (Figure 1). This segmented approach aids in elucidating the finer relationship between AL development and anterior segment biometry, enhancing the precision of this study. It enables researchers to specifically investigate the complex relationship between AL and anterior segment biometry.
Figure 1

Anterior segment biometry among different AL groups. (a) Trends in the K among different AL groups; (b) Trends in the CCT among different AL groups; (c) Trends in the ACD among different AL groups; and (d) Trends in the LT among different AL groups (the points represent the mean, and error bars represent the standard deviation).
2.5 Statistical methods
All statistical analyses were performed using SPSS software (version 26.0, Chicago, IL, USA). Continuous variables that follow a normal distribution were expressed as mean ± standard deviation, while those that do not follow a normal distribution were described as median (25th percentile, 75th percentile). Comparisons of continuous variables were performed using independent samples t-test and one-way analysis of variance (ANOVA) for normally distributed variables, and Mann–Whitney U-test or Kruskal–Wallis test for non-normally distributed variables.
Pearson’s correlation analysis was used to assess correlations. The relationship between AL and anterior segment biometry was investigated using multiple linear regression models, adjusted for age and gender, as well as segmented multiple linear regression models. The significance level was set at α = 0.05. Given the high correlation (r = 0.96) between the AL of the left and right eyes, the analysis in this study focused primarily on the right eye.
2.6 Medical ethics
This study received approval from the Ethics Committee of Ineye Hospital of Chengdu University of TCM (2019yh-007). All research methods adhered to the principles outlined in the “Declaration of Helsinki.” Before conducting the study, the objectives and methods were presented to the principals, teachers, and parents of the participating schools to obtain informed consent.
3 Results
3.1 Study population
After a 3-year student eye health study conducted in Chengdu, China (January 2020–December 2022), data from 366,278 enrolled students were collected. This information included school type, school name, grade, class, name, gender, and age, along with refractive errors and various ocular biometric parameters. The data were obtained from 916 schools (506 primary schools, 274 middle schools, and 136 high schools), covering a population of children and adolescents aged 7–18 years. Among this group, 52.06% (190,674) were male, and 47.94% (175,604) were female.
3.2 Diopter and ocular biometric parameters
Significant age- and gender-related differences were observed across all measured parameters (SE, K, AL, CCT, ACD, LT, and UCVA; all p < 0.001). Female students exhibited significantly longer AL and deeper ACD compared to male students, whereas male students demonstrated steeper corneal curvature (K) and lens thickness (LT). Participants were classified into three refractive status groups: non-myopia (35.09%, n = 128,549), normal myopia with AL < 26 mm (57.02%, n = 208,852), and high axial myopia (7.89%, n = 28,877). All ocular parameters differed significantly among the three refractive status groups (all p < 0.001). The high axial myopia group exhibited the most pronounced characteristics with the longest AL, deepest ACD, thinnest LT, and poorest UCVA among all groups (Table 1).
Table 1
| Participant characteristics | N | SE(D) | K(D) | AL(mm) | CCT(um) | ACD(mm) | LT(mm) | UCVA(LogMAR) | |
|---|---|---|---|---|---|---|---|---|---|
| Age | 7 | 41,809 | −0.12 ± 1.01 | 43.26 ± 1.59 | 23.03 ± 0.74 | 541.09 ± 32.09 | 2.91 ± 0.27 | 3.69 ± 0.25 | 0.06 ± 0.16 |
| 8 | 36,454 | −0.46 ± 1.22 | 43.27 ± 1.60 | 23.37 ± 0.82 | 542.88 ± 32.23 | 3.01 ± 0.28 | 3.60 ± 0.25 | 0.12 ± 0.24 | |
| 9 | 37,352 | −0.83 ± 1.40 | 43.24 ± 1.58 | 23.68 ± 0.89 | 544.07 ± 32.47 | 3.08 ± 0.27 | 3.54 ± 0.23 | 0.19 ± 0.30 | |
| 10 | 34,594 | −1.20 ± 1.58 | 43.21 ± 1.60 | 23.94 ± 0.95 | 544.46 ± 32.63 | 3.13 ± 0.27 | 3.50 ± 0.22 | 0.27 ± 0.34 | |
| 11 | 33,259 | −1.57 ± 1.73 | 43.21 ± 1.60 | 24.16 ± 1.01 | 545.19 ± 32.85 | 3.16 ± 0.27 | 3.48 ± 0.22 | 0.33 ± 0.36 | |
| 12 | 34,860 | −1.94 ± 1.89 | 43.19 ± 1.61 | 24.38 ± 1.06 | 545.89 ± 33.17 | 3.18 ± 0.27 | 3.48 ± 0.21 | 0.40 ± 0.38 | |
| 13 | 32,499 | −2.39 ± 2.02 | 43.15 ± 1.61 | 24.59 ± 1.10 | 546.04 ± 33.42 | 3.21 ± 0.27 | 3.48 ± 0.21 | 0.48 ± 0.39 | |
| 14 | 30,998 | −2.77 ± 2.14 | 43.17 ± 1.61 | 24.76 ± 1.15 | 545.96 ± 33.22 | 3.21 ± 0.27 | 3.48 ± 0.21 | 0.55 ± 0.39 | |
| 15 | 30,782 | −2.97 ± 2.20 | 43.12 ± 1.62 | 24.86 ± 1.19 | 545.21 ± 33.82 | 3.21 ± 0.27 | 3.50 ± 0.21 | 0.59 ± 0.40 | |
| 16 | 24,528 | −3.07 ± 2.28 | 43.03 ± 1.75 | 24.90 ± 1.23 | 544.20 ± 34.69 | 3.20 ± 0.27 | 3.52 ± 0.21 | 0.61 ± 0.40 | |
| 17 | 21,027 | −3.30 ± 2.38 | 43.03 ± 1.78 | 25.01 ± 1.25 | 543.66 ± 35.36 | 3.20 ± 0.28 | 3.53 ± 0.22 | 0.63 ± 0.40 | |
| 18 | 8,116 | −3.42 ± 2.44 | 43.17 ± 1.78 | 25.02 ± 1.29 | 543.11 ± 36.05 | 3.18 ± 0.28 | 3.55 ± 0.22 | 0.62 ± 0.40 | |
| All | 366,278 | −1.75 ± 2.10 | 43.18 ± 1.63 | 24.17 ± 1.22 | 544.32 ± 33.22 | 3.13 ± 0.29 | 3.53 ± 0.23 | 0.36 ± 0.39 | |
| p-value | – | <0.001 | <0.001 | <0.001 | <0.001 | <0.001 | <0.001 | <0.001 | |
| Gender | Male | 190,674 | −1.68 ± 2.11 | 42.85 ± 1.59 | 24.41 ± 1.21 | 546.00 ± 33.26 | 3.18 ± 0.29 | 3.51 ± 0.23 | 0.34 ± 0.39 |
| Female | 175,604 | −1.83 ± 2.09 | 43.55 ± 1.59 | 23.91 ± 1.17 | 542.50 ± 33.09 | 3.07 ± 0.28 | 3.55 ± 0.24 | 0.39 ± 0.40 | |
| p-value | – | <0.001 | <0.001 | <0.001 | <0.001 | <0.001 | <0.001 | <0.001 | |
| Refractive status | NMa | 128,549 | 0.20 ± 0.58 | 43.11 ± 1.60 | 23.28 ± 0.77 | 544.22 ± 33.10 | 2.98 ± 0.27 | 3.62 ± 0.24 | 0.04 ± 0.14 |
| Mb | 208,852 | −2.46 ± 1.53 | 43.37 ± 1.59 | 24.38 ± 0.90 | 544.06 ± 33.11 | 3.18 ± 0.26 | 3.50 ± 0.22 | 0.49 ± 0.37 | |
| HAMc | 28,877 | −5.32 ± 2.07 | 42.13 ± 1.62 | 26.64 ± 0.58 | 546.60 ± 34.44 | 3.38 ± 0.24 | 3.41 ± 0.19 | 0.84 ± 0.28 | |
| p-value | – | <0.001 | <0.001 | <0.001 | <0.001 | <0.001 | <0.001 | <0.001 | |
Distribution of the anterior segment biometry and axial length at different ages and genders.
ᵃ NM, non-myopia group (SE ≥ − 0.05); b M, myopia group (SE <−0.05 and AL <26 mm); c HAM, high axial myopia group (AL ≥ 26 mm); SE, spherical equivalent; AL, axial length; K, average keratometry; CCT, central corneal thickness; ACD, anterior chamber depth; LT, lens thickness; UCVA, uncorrected visual acuity.
3.3 Comparison of anterior segment parameters across refractive status groups
Cross-sectional analysis comparing the three refractive status groups revealed significant differences in anterior segment parameters, independent of age and gender effects. The high axial myopia group exhibited significantly higher K values, thicker CCT, deeper ACD, and lower LT compared to both the non-myopia and normal myopia groups (all p < 0.001). The normal myopia group demonstrated intermediate values for these parameters, showing significant differences from the non-myopia group (all p < 0.05) but less pronounced changes than the high axial myopia group (Table 2; Figure 2).
Table 2
| Participant characteristics | K(D) | CCT(um) | ACD(mm) | LT(mm) | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| NM | M | HAM | NM | M | HAM | NM | M | HAM | NM | M | HAM | ||
| Age | 7 | 43.23 ± 1.59 | 43.38 ± 1.58* | 42.46 ± 1.80† | 541.32 ± 32.13 | 540.39 ± 31.98* | 540.44 ± 30.85 | 2.90 ± 0.27 | 2.97 ± 0.29* | 3.20 ± 0.28† | 3.70 ± 0.24 | 3.66 ± 0.27* | 3.51 ± 0.20† |
| 8 | 43.20 ± 1.58 | 43.39 ± 1.61* | 41.97 ± 1.88† | 543.14 ± 32.22 | 542.47 ± 32.26 | 540.40 ± 29.48 | 2.96 ± 0.26 | 3.09 ± 0.28* | 3.28 ± 0.28† | 3.63 ± 0.24 | 3.55 ± 0.24* | 3.42 ± 0.20† | |
| 9 | 43.14 ± 1.57 | 43.37 ± 1.57* | 41.50 ± 1.53† | 544.68 ± 32.55 | 543.36 ± 32.33* | 548.30 ± 34.39† | 3.00 ± 0.26 | 3.15 ± 0.26* | 3.35 ± 0.22† | 3.59 ± 0.23 | 3.49 ± 0.23* | 3.35 ± 0.17† | |
| 10 | 43.08 ± 1.56 | 43.35 ± 1.59* | 41.67 ± 1.64† | 545.25 ± 32.71 | 543.97 ± 32.51* | 543.44 ± 34.54 | 3.03 ± 0.26 | 3.19 ± 0.25* | 3.39 ± 0.24† | 3.56 ± 0.23 | 3.46 ± 0.21* | 3.35 ± 0.19† | |
| 11 | 43.07 ± 1.58 | 43.36 ± 1.56* | 41.85 ± 1.60† | 545.79 ± 33.23 | 544.90 ± 32.62* | 545.13 ± 33.55 | 3.04 ± 0.27 | 3.20 ± 0.25* | 3.40 ± 0.23† | 3.56 ± 0.23 | 3.46 ± 0.21* | 3.35 ± 0.18† | |
| 12 | 42.99 ± 1.56 | 43.38 ± 1.58* | 42.01 ± 1.55† | 547.05 ± 33.07 | 545.34 ± 33.19* | 546.97 ± 33.17# | 3.05 ± 0.26 | 3.22 ± 0.25* | 3.39 ± 0.24† | 3.56 ± 0.23 | 3.45 ± 0.20* | 3.37 ± 0.18† | |
| 13 | 42.94 ± 1.57 | 43.38 ± 1.54* | 42.04 ± 1.56† | 546.87 ± 33.71 | 545.57 ± 33.27* | 547.68 ± 33.77# | 3.05 ± 0.27 | 3.22 ± 0.25* | 3.40 ± 0.23† | 3.57 ± 0.22 | 3.47 ± 0.21* | 3.38 ± 0.18† | |
| 14 | 42.97 ± 1.57 | 43.41 ± 1.55* | 42.18 ± 1.53† | 547.13 ± 33.51 | 545.28 ± 32.96* | 548.14 ± 34.11# | 3.03 ± 0.28 | 3.22 ± 0.25* | 3.39 ± 0.23† | 3.59 ± 0.23 | 3.48 ± 0.20* | 3.39 ± 0.18† | |
| 15 | 42.91 ± 1.60 | 43.39 ± 1.55* | 42.20 ± 1.57† | 546.86 ± 34.87 | 544.45 ± 33.51* | 546.90 ± 34.06# | 3.02 ± 0.28 | 3.20 ± 0.25* | 3.38 ± 0.24† | 3.62 ± 0.23 | 3.50 ± 0.21* | 3.41 ± 0.18† | |
| 16 | 42.86 ± 1.82 | 43.30 ± 1.68* | 42.19 ± 1.68† | 546.35 ± 37.13 | 543.38 ± 34.08* | 545.46 ± 34.77# | 3.01 ± 0.27 | 3.20 ± 0.25* | 3.37 ± 0.24† | 3.63 ± 0.23 | 3.52 ± 0.21* | 3.43 ± 0.19† | |
| 17 | 42.77 ± 1.83 | 43.36 ± 1.68* | 42.19 ± 1.71† | 545.96 ± 39.05 | 542.36 ± 34.35* | 546.26 ± 35.87# | 2.99 ± 0.28 | 3.19 ± 0.25* | 3.36 ± 0.24† | 3.65 ± 0.23 | 3.54 ± 0.21* | 3.45 ± 0.19† | |
| 18 | 42.83 ± 1.84 | 43.51 ± 1.70* | 42.36 ± 1.69† | 542.16 ± 42.29 | 542.36 ± 34.94 | 545.77 ± 35.50† | 2.98 ± 0.30 | 3.17 ± 0.26* | 3.34 ± 0.24† | 3.67 ± 0.23 | 3.55 ± 0.21* | 3.47 ± 0.20† | |
| Gender | Male | 42.79 ± 1.56 | 43.06 ± 1.56* | 42.01 ± 1.58† | 545.86 ± 33.00 | 545.79 ± 33.28 | 547.48 ± 33.98† | 3.04 ± 0.27 | 3.23 ± 0.26* | 3.41 ± 0.23† | 3.60 ± 0.24 | 3.48 ± 0.22* | 3.40 ± 0.19† |
| Female | 43.49 ± 1.56 | 43.66 ± 1.56* | 42.43 ± 1.67† | 542.23 ± 33.12 | 542.50 ± 32.88 | 544.42 ± 35.47† | 2.91 ± 0.27 | 3.13 ± 0.26* | 3.31 ± 0.23† | 3.65 ± 0.24 | 3.51 ± 0.22* | 3.43 ± 0.19† | |
Comparison of ocular biometric parameters among different refractive status groups by age and gender.
NM, non-myopia group (SE ≥ − 0.05); M, myopia group (SE < −0.05, and AL <26 mm); HAM: high axial myopia group (AL ≥ 26 mm).
* means p < 0.05 vs. NM group; † means p < 0.05 vs. both non-myopia and normal myopia groups.
K, average keratometry; CCT, central corneal thickness; ACD, anterior chamber depth; LT, lens thickness.
Figure 2

Anterior segment biometry among different age groups. (a) Trends in the K among different age groups; (b) Trends in the CCT among different age groups; (c) Trends in the ACD among different age groups; and (d) Trends in the LT among different age groups. (The points represent the mean, and error bars represent the standard deviation).
3.4 Correlation between anterior segment biometry and AL
Pearson’s correlation analysis revealed significant associations between AL and all anterior segment parameters (all p < 0.001). AL exhibited moderate negative correlations with both K and LT, a strong positive correlation with ACD, and a weak but significant positive correlation with CCT.
Inter-parameter correlations among anterior segment biometric parameters were also examined. ACD and LT demonstrated a moderate negative correlation (p < 0.001). K showed a weak negative correlation with both CCT and LT (both p < 0.001), while demonstrating a negligible correlation with ACD (p = 0.006). Weak but significant correlations were observed between CCT and both ACD and LT (both p < 0.001) (Table 3).
Table 3
| Variable | r | 95% CI | p-value |
|---|---|---|---|
| AL vs. K | −0.3746 | [−0.3774, −0.3718] | <0.001 |
| AL vs. CCT | 0.0507 | [0.0475, 0.054] | <0.001 |
| AL vs. ACD | 0.5671 | [0.5649, 0.5693] | <0.001 |
| AL vs. LT | −0.3968 | [−0.3996, −0.3941] | <0.001 |
| K vs. CCT | −0.1184 | [−0.1216, −0.1152] | <0.001 |
| K vs. ACD | 0.0045 | [0.0013, 0.0078] | 0.005912 |
| K vs. LT | −0.0494 | [−0.0527, −0.0462] | <0.001 |
| CCT vs. ACD | −0.0735 | [−0.0767, −0.0703] | <0.001 |
| CCT vs. LT | 0.0254 | [0.0221, 0.0286] | <0.001 |
| ACD vs. LT | −0.5963 | [−0.5984, −0.5942] | <0.001 |
Pearson’s correlation coefficients among ocular parameters.
AL, axial length; K, average keratometry; CCT, central corneal thickness; ACD, anterior chamber depth; LT, lens thickness.
3.5 Multiple linear regression analysis with AL
The multiple linear regression model was constructed to estimate the AL based on age, gender, and anterior segment biometry, yielding an R-squared value of 0.601 (F = 91948.012, p < 0.001). After adjusting for gender and age, K, CCT, ACD, and LT were significantly associated with AL (for K, β = −0.265 [95%CI −0.267 to −0.264]; for CCT, β = 0.001 [95%CI 0.001 to 0.001]; for ACD, β = 1.609 [95%CI 1.598 to 1.620]; for LT, β = −0.607 [95%CI −0.620 to −0.594]; all p-values<0.001). However, after adjusting for gender and age, LT was significantly negatively associated with AL only when AL was <26 mm (β = −1.379 [95%CI −1.390 to −1.367], p < 0.001) and when AL was between 26 and 27 mm (β = −0.027 [95%CI −0.047 to −0.008], p < 0.01). There was no significant association between LT and AL when AL was between 27 and 28 mm (β = 0.025 [95%CI −0.013 to 0.064], p = 0.195), and when AL was ≥28 mm (β = 0.043 [95%CI −0.111 to 0.198], p = 0.581). After adjusting for gender and age, CCT was significantly negatively associated with AL only when AL was <26 mm (β = 0.002 [95%CI 0.001to 0.002], p < 0.001). There was no significant association between CCT and AL when AL was between 26 and 27 mm (β = −3.787E-5 [95%CI 0.000 to 0.000], p = 0.497), when between 27 and 28 mm (β = 1.134E-5 [95%CI 0.000 to 0.000], p = 0.914), and when AL was ≥28 mm (β = 0.000 [95%CI −0.001 to 0.000], p = 0.405) (Table 4).
Table 4
| Parameters | β | 95% CI | p-value |
|---|---|---|---|
| Age | 0.142 | 0.141 to 0.143 | <0.001 |
| Gender | 0.105 | 0.100 to 0.110 | <0.001 |
| K | −0.265 | −0.267 to −0.264 | <0.001 |
| CCT | 0.001 | 0.001 to 0.001 | <0.001 |
| ACD | 1.609 | 1.598 to 1.620 | <0.001 |
| LT | −0.607 | −0.620 to −0.594 | <0.001 |
Multiple linear regression analysis with AL.
Age per year older; gender: male vs female; AL: axial length, per 1 mm longer; K, average keratometry, per 1D increase; CCT, central corneal thickness: per 1 μm increase; ACD, anterior chamber depth; per 1 mm longer; LT, lens per 1 mm longer.
4 Discussion
In this study, the anterior segment biometry was investigated in Chinese children and adolescents across three refractive status groups: non-myopia, normal myopia (AL < 26 mm), and high axial myopia (AL ≥ 26 mm). We analyzed the associations between AL and anterior segment biometry in children of similar for age and gender. The results indicated that the average K and LT in the high axial myopia group were significantly lower than those in both the non-myopia and normal myopia groups (all p < 0.001), whereas CCT and ACD were significantly greater in the high axial myopia group compared to the other two groups (all p < 0.001). Progressive trends were observed across the three groups, with normal myopia showing intermediate characteristics. As AL increased, CCT and ACD exhibited a growth trend, while K exhibited a decreasing trend. When AL was less than 27 mm, LT showed a thinning trend as AL increased. Similarly, when AL exceeded 27 mm, LT exhibited a gradual thickening trend with increasing AL. An AL of 27 mm served as the truncation point for the distribution of LT. Beyond an AL of 27 mm, there was no linear correlation between AL and LT, suggesting that the crystalline lens may gradually disappear as a compensatory mechanism for myopia.
This study revealed a negative correlation between AL and LT (r = −0.4, p < 0.001). As AL increases, LT exhibits a U-shaped curve trend. After AL surpasses 27 mm, LT gradually becomes thinner and then slowly thickens. Additionally, it was observed that there was no significant linear correlation between AL and LT. Previous research has also been conducted on 459 high myopic students aged 4 to 19 years, indicating that within a certain range of AL growth, changes in LP could potentially compensate for the effects of AL growth on myopia. However, this compensatory effect of the crystalline lens disappears when AL exceeds 27 mm (18). Related studies found that a sudden loss of compensatory changes in the crystalline lens characterizes the onset of myopia. Subsequently, the compensatory role of the crystalline lens weakened during the progression of myopia (19–21). Research also suggested that the rate of AL growth may be compensated for by an increased rate of LP loss, which continued until the year prior to the onset of myopia (22). For children and adolescents, the refractive state was primarily determined by the dynamic balance between AL and LP. Thinning of the lens thickness or reaching a certain physiological limit in LP loss can lead to a sudden decrease in LT or LP loss rate, accompanied by rapid AL growth, resulting in myopia (19, 23). Following the onset of myopia, as AL increases to a critical point, the compensatory ability of the lens may be diminished due to mechanisms such as abnormal thickening and elongation of the ciliary muscle, causing equatorial growth restrictions (24, 25).
This study also discovered that with increasing age, the LT becomes thinner until age 11, after which it gradually thickens. Moreover, the LT changes in individuals with high axial myopia were more pronounced than in both the non-myopia and normal myopia groups, consistent with findings from other studies on ocular growth (26). We speculated that apart from naturally thinning in children and adolescents with age (23), the thinning of the crystalline lens may play a role in compensating for myopia progression in axial elongation. However, the compensatory ability of the crystalline lens for myopia-related AL growth was limited. In the future, there should be a stronger emphasis on longitudinal cohort studies focusing on ocular biometry, especially in cases of myopia and high myopia, including observations of the ciliary muscle, to confirm the causal relationship between AL and LT.
The AL was the sum of corneal thickness, ACD, LT, and vitreous chamber depth. ACD was the distance from the inner surface of the cornea to the anterior surface of the lens, and studies have shown that changes in ACD were inversely proportional to lens thickness (26). Research indicated that ACD in young individuals increases with changes in refractive error, gradually deepening from the hyperopic to the high myopic group (27). Data also showed that eyes with longer AL (and more myopia) have deeper ACD and thinner LT, with myopic patients exhibiting a deeper ACD likely due to geometric scaling during AL growth (28). These findings were consistent with the results of our analysis. AL was positively correlated with ACD (r = 0.57, p < 0.001), ACD was negatively correlated with LT (r = −0.596, p < 0.001), and as AL increases, ACD gradually deepens, but the deepening trend of ACD became more gradual after AL exceeded 27 mm. The relationship between ACD and AL was influenced by ocular structure and physiological factors. When AL surpasses a certain threshold, LT no longer continues to thin and may even undergo compensatory thickening to maintain optical balance. This compensatory change in LT may help slow the rate of the ACD increase.
Earlier studies (15, 29, 30) have explored the negative correlation between corneal curvature and AL in the progression of myopia within an AL range of <28 mm. This suggested that the cornea compensates for AL growth through changes in its curvature, serving as a physiological adaptation for achieving optimal focusing. Similarly, in this study, it was observed that among different AL groups, high axial myopic children with longer AL have flatter corneas. Furthermore, it was noted that as AL continues to increase, the trend of corneal curvature changes slows down with increasing AL.
Wang et al. (31) have also found that as AL increases, corneal curvature becomes flatter to compensate for longer AL. However, this corneal compensation phenomenon disappeared when AL is >28 mm, as confirmed by Jin G (17). Similarly, in a long-term clinical cohort study involving myopic children and adolescents aged 7–18 over 14 years, a strong correlation was observed between corneal curvature and AL during the early stages of myopia progression (32). However, as myopia progression slowed and eventually stabilized, this correlation gradually diminished.
Additionally, in this study, it was observed that corneal curvature was significantly higher in females than in males of the same age, while AL was significantly shorter in females compared to males of the same age. This observation aligned with the results of a large-scale retrospective study conducted in Italy and was attributed to physiological differences between genders (33).
This study indicated that in the population of children and adolescents aged 7–18 years, CCT generally exhibited a slow thickening trend with increasing AL. However, when AL exceeded 26 mm, there was no linear correlation between AL and CCT (p > 0.05). This may be because corneal hysteresis was negatively correlated with axial elongation in children (34), and corneal hysteresis was statistically associated with CCT (35). A previous study involving 450 myopic individuals aged 21–66 years found that CCT was unrelated to AL, age, gender, or refractive error (36). In a study conducted in Hong Kong with 151 participants aged 10–60 years, CCT was observed to thin with increasing age, particularly in the age group of 10–25 years, where the decline in CCT was most significant (37). Other research has shown that CCT in the myopic group aged 18–55 years (527.7 ± 35.0 μm) was thinner compared to the emmetropic group (538.6 ± 32.1 μm) (38). Furthermore, a study involving participants with an average age of 22.2 ± 4.2 years revealed that CCT was thinner in cases of high myopia (16).
CCT may be correlated with body mass index (BMI) (39). Conversely, thinning of CCT in high myopia may be due to the rapid progression of myopia, resulting in rapid AL growth, scleral thinning, and potential thinning of the corneal stroma (40). Additionally, Zhou P (41) found that CCT was negatively correlated with the rate of myopia progression (spherical equivalent, SE) and AL growth rate. Children with thinner CCT tend to have faster myopia progression and AL growth rates. Current research has generated controversy regarding the relationship between CCT and AL at different age stages. The main point of contention revolved around the physiological thickening of CCT during the rapid growth and development period in children and adolescents, as opposed to the pathological thinning of CCT due to continuous axial elongation. In light of these findings, CCT may be considered a potential risk factor for myopia, or it may be a consequence of myopia development. Further research is required to validate these findings, which could contribute to the development of more effective strategies for myopia prevention and treatment.
This study demonstrated significant gender-related differences in anterior segment biometry, with males exhibiting longer AL, deeper ACD, and flatter corneas, whereas females showed thicker crystalline lenses (all p < 0.001). These findings were consistent across pediatric (42, 43) and adult cohorts (15, 33), suggesting early establishment and persistence of gender dimorphism in ocular development. Such coordinated gender-specific patterns suggest compensatory mechanisms for maintaining optical balance during emmetropization (42, 43). These differences have important implications for refractive development prediction and personalized myopia management.
This study included a student population in Chengdu, aged 7–18 years, totaling 366,278 individuals. This extensive sample size improved the credibility and reliability of the study results, making them more representative and generalizable. Additionally, the study conducted comprehensive measurements of ocular biometric parameters in 366,278 children and adolescents, including AL, K, LT, ACD, and CCT, among others. This study provided a comprehensive dataset on ocular structure and ocular biometric parameters, thereby enriching the field of research. However, several limitations should be noted in this study. The cross-sectional design includes inference of causal relationships for associations observed in different age groups, especially regarding the relationship between LT and AL. To address these limitations, our research team plans to strengthen longitudinal cohort studies in future research, allowing for a more precise and scientific analysis of myopia-related data.
In summary, findings from this large-scale study of Chinese children and adolescents aged 7–18 years indicated that, in high axial myopic patients, the average K and LT were significantly lower than both the non-myopia and normal myopia groups, while CCT and ACD were significantly greater than the other two groups. Within an AL range of 27 mm, changes in crystalline lens shape provide optical compensation for myopia. However, in cases of extremely high myopia (AL > 27 mm), this effect was not detected. Furthermore, beyond an AL of 26 mm, there was no linear correlation observed between AL and CCT. As AL increases, pathological thinning of CCT gradually surpasses physiological thickening. In the high myopic population studied, there was limited evidence of regulatory changes in the LT and CCT associated with AL growth. These findings highlight the importance of focusing on AL growth characteristics and anterior segment biometry in children and adolescents with high myopia. Such an approach will enable a more accurate use of ocular biometric parameters for assessing and predicting high myopia, thereby aiding in the early detection and prevention of potential complications.
Statements
Data availability statement
The datasets presented in this article are not readily available because the datasets used and/or analysed during the current study available from the corresponding author on reasonable request. Requests to access the datasets should be directed to Junguo Duan, zeverett636@hotmail.com.
Ethics statement
The studies involving humans were approved by Ethics Committee of Ineye Hospital of Chengdu University of traditional Chinese medicine (2019yh-007). The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants’ legal guardians/next of kin. Written informed consent was obtained from the individual(s), and minor(s)’ legal guardian/next of kin, for the publication of any potentially identifiable images or data included in this article.
Author contributions
ZZ: Methodology, Data curation, Writing – review & editing, Investigation, Validation, Supervision, Conceptualization, Writing – original draft, Software, Visualization. JM: Funding acquisition, Supervision, Software, Writing – review & editing, Formal analysis, Writing – original draft, Methodology, Data curation, Investigation, Conceptualization. YY: Writing – original draft. YD: Writing – review & editing, Supervision, Conceptualization, Validation, Funding acquisition, Project administration, Writing – original draft, Data curation. JD: Writing – review & editing, Validation, Supervision, Data curation, Project administration, Conceptualization, Writing – original draft, Funding acquisition.
Funding
The author(s) declared that financial support was received for this work and/or its publication. This study was funded by the Sichuan Provincial Science and Technology Plan “Unveiling and Leading” Project (2023YFS0506), the National Natural Science Foundation of China (62175022), the Chengdu University of Traditional Chinese Medicine “Xinglin Scholars “Discipline Talent Research Enhancement Plan (ZDZX2022004), and the Sichuan Natural Science Foundation (2022NSFSC0803). Construction of Myopia Prevention and Control System for Children and Adolescents in County Areas and Real-world Clinical Research (Grant No. 2024ZYD0293). This grant provided partial data support in the later research stage and contributed to the publication fees
Acknowledgments
The authors thank the Eye School of Chengdu University of TCM, the Ineye Hospital of Chengdu University of TCM, the Key Laboratory of Sichuan Province Ophthalmopathy Prevention & Cure, Visual Function Protection with TCM Laboratory, Retinal Image Technology and Chronic Vascular Disease Prevention& Control, and Collaborative Innovation Center for its technical support.
Conflict of interest
The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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The author(s) declared that Generative AI was not used in the creation of this manuscript.
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References
1.
Rudnicka AR Kapetanakis VV Wathern AK Logan NS Gilmartin B Whincup PH et al . Global variations and time trends in the prevalence of childhood myopia, a systematic review and quantitative meta-analysis: implications for aetiology and early prevention. Br J Ophthalmol. (2016) 100:882–90. doi: 10.1136/bjophthalmol-2015-307724,
2.
Grzybowski A Kanclerz P Tsubota K Lanca C Saw SM . A review on the epidemiology of myopia in school children worldwide. BMC Ophthalmol. (2020) 20:27. doi: 10.1186/s12886-019-1220-0,
3.
He M Xiang F Zeng Y Mai J Chen Q Zhang J et al . Effect of time spent outdoors at school on the development of myopia among children in China: a randomized clinical trial. JAMA. (2015) 314:1142–8. doi: 10.1001/jama.2015.10803,
4.
Ezegwui IR Oguego NC Okoye OI Maduka-Okafor FC Udeh N Aghaji AE et al . Prevalence of refractive errors and visual impairment in school children in Enugu south-East Nigeria. Niger J Clin Pract. (2021) 24:380–6. doi: 10.4103/njcp.njcp_521_19,
5.
Ikuno Y . Overview of the complications of high myopia. Retina. (2017) 37:2347–51. doi: 10.1097/IAE.0000000000001489,
6.
Wong TY Ferreira A Hughes R Carter G Mitchell P . Epidemiology and disease burden of pathologic myopia and myopic choroidal neovascularization: an evidence-based systematic review. Am J Ophthalmol. (2014) 157:9–25.e12. doi: 10.1016/j.ajo.2013.08.010,
7.
Bremond-Gignac D . Myopia in children. Med Sci. (2020) 36:763–8. doi: 10.1051/medsci/2020131,
8.
Iribarren R . Crystalline lens and refractive development. Prog Retin Eye Res. (2015) 47:86–106. doi: 10.1016/j.preteyeres.2015.02.002,
9.
Chen Y Ding X Xiong R Zhang J Song F Zhao Z et al . Physiological growth of ocular axial length among Chinese children and teenagers: a 6-year cohort study. PLoS One. (2025) 20:e0317756. doi: 10.1371/journal.pone.0317756,
10.
Chen S Guo Y Han X Yu X Chen Q Wang D et al . Axial growth driven by physical development and myopia among children: a two year cohort study. J Clin Med. (2022) 11:3642. doi: 10.3390/jcm11133642,
11.
Mutti DO Hayes JR Mitchell GL Jones LA Moeschberger ML Cotter SA et al . Refractive error, axial length, and relative peripheral refractive error before and after the onset of myopia. Invest Ophthalmol Vis Sci. (2007) 48:2510–9. doi: 10.1167/iovs.06-0562,
12.
Xiang F He M Morgan IG . Annual changes in refractive errors and ocular components before and after the onset of myopia in Chinese children. Ophthalmology. (2012) 119:1478–84. doi: 10.1016/j.ophtha.2012.01.017,
13.
Flitcroft DI He M Jonas JB Jong M Naidoo K Ohno-Matsui K et al . IMI - defining and classifying myopia: a proposed set of standards for clinical and epidemiologic studies. Invest Ophthalmol Vis Sci. (2019) 60:M20–m30. doi: 10.1167/iovs.18-25957,
14.
He X Sankaridurg P Naduvilath T Wang J Xiong S Weng R et al . Normative data and percentile curves for axial length and axial length/corneal curvature in Chinese children and adolescents aged 4-18 years. Br J Ophthalmol. (2023) 107:167–75. doi: 10.1136/bjophthalmol-2021-319431,
15.
Benzir M Afroze A Zahan A Naznin RA Khanam A Sumi SA et al . A study linking axial length, corneal curvature, and eye Axis with demographic characteristics in the Emmetropic eyes of Bangladeshi people. Cureus. (2022) 14:e29925. doi: 10.7759/cureus.29925,
16.
Chang SW Tsai IL Hu FR Lin LL Shih YF . The cornea in young myopic adults. Br J Ophthalmol. (2001) 85:916–20. doi: 10.1136/bjo.85.8.916,
17.
Jin G Liu Z Wang L Zhu Y Luo L Liu Y . Corneal biometric features and their association with axial length in high myopia. Am J Ophthalmol. (2022) 238:45–51. doi: 10.1016/j.ajo.2021.11.031,
18.
Cheng T Deng J Xiong S Yu S Zhang B Wang J et al . Crystalline Lens power and associated factors in highly myopic children and adolescents aged 4 to 19 years. Am J Ophthalmol. (2021) 223:169–77. doi: 10.1016/j.ajo.2020.07.007,
19.
Mutti DO Mitchell GL Sinnott LT Jones-Jordan LA Moeschberger ML Cotter SA et al . Corneal and crystalline lens dimensions before and after myopia onset. Optom Vis Sci. (2012) 89:251–62. doi: 10.1097/OPX.0b013e3182418213,
20.
Iribarren R Morgan IG Chan YH Lin X Saw SM . Changes in lens power in Singapore Chinese children during refractive development. Invest Ophthalmol Vis Sci. (2012) 53:5124–30. doi: 10.1167/iovs.12-9637,
21.
Iribarren R Midelfart A Kinge B . Lens power loss in early adulthood. Acta Ophthalmol. (2015) 93:e233–4. doi: 10.1111/aos.12552,
22.
Rozema J Dankert S Iribarren R Lanca C Saw SM . Axial growth and Lens power loss at myopia onset in Singaporean children. Invest Ophthalmol Vis Sci. (2019) 60:3091–9. doi: 10.1167/iovs.18-26247,
23.
Xiong S Zhang B Hong Y He X Zhu J Zou H et al . The associations of Lens power with age and axial length in healthy Chinese children and adolescents aged 6 to 18 years. Invest Ophthalmol Vis Sci. (2017) 58:5849–55. doi: 10.1167/iovs.17-22639,
24.
Bailey MD Sinnott LT Mutti DO . Ciliary body thickness and refractive error in children. Invest Ophthalmol Vis Sci. (2008) 49:4353–60. doi: 10.1167/iovs.08-2008,
25.
Sheppard AL Davies LN . In vivo analysis of ciliary muscle morphologic changes with accommodation and axial ametropia. Invest Ophthalmol Vis Sci. (2010) 51:6882–9. doi: 10.1167/iovs.10-5787,
26.
Shih YF Chiang TH Lin LL . Lens thickness changes among schoolchildren in Taiwan. Invest Ophthalmol Vis Sci. (2009) 50:2637–44. doi: 10.1167/iovs.08-3090,
27.
Xu G Wu G Du Z Zhu S Guo Y Yu H et al . Distribution of white-to-white corneal diameter and anterior chamber depth in Chinese myopic patients. Front Med. (2021) 8:732719. doi: 10.3389/fmed.2021.732719,
28.
Muralidharan G Martínez-Enríquez E Birkenfeld J Velasco-Ocana M Pérez-Merino P Marcos S . Morphological changes of human crystalline lens in myopia. Biomed Opt Express. (2019) 10:6084–95. doi: 10.1364/BOE.10.006084,
29.
González Blanco F Sanz Ferńandez JC Muńoz Sanz MA . Axial length, corneal radius, and age of myopia onset. Optom Vis Sci. (2008) 85:89–96. doi: 10.1097/OPX.0b013e3181622602,
30.
Hoffmann PC Hütz WW . Analysis of biometry and prevalence data for corneal astigmatism in 23,239 eyes. J Cataract Refract Surg. (2010) 36:1479–85. doi: 10.1016/j.jcrs.2010.02.025,
31.
Wang XJ Bao YZ . Correlation between axial length and corneal curvature and spherical aberration. Zhonghua Yan Ke Za Zhi. (2017) 53:255–9. doi: 10.3760/cma.j.issn.0412-4081.2017.04.006,
32.
Scheiman M Gwiazda J Zhang Q Deng L Fern K Manny RE et al . Longitudinal changes in corneal curvature and its relationship to axial length in the correction of myopia evaluation trial (COMET) cohort. J Opt. (2016) 9:13–21. doi: 10.1016/j.optom.2015.10.003,
33.
De Bernardo M Zeppa L Zeppa L Cornetta P Vitiello L Rosa N . Biometric parameters and corneal astigmatism: differences between male and female eyes. Clin Ophthalmol. (2020) 14:571–80. doi: 10.2147/OPTH.S219912,
34.
Wan K Cheung SW Wolffsohn JS Orr JB Cho P . Role of corneal biomechanical properties in predicting of speed of myopic progression in children wearing orthokeratology lenses or single-vision spectacles. BMJ Open Ophthalmol. (2018) 3:e000204. doi: 10.1136/bmjophth-2018-000204,
35.
Rosa N Lanza M De Bernardo M Signoriello G Chiodini P . Relationship between corneal hysteresis and corneal resistance factor with other ocular parameters. Semin Ophthalmol. (2015) 30:335–9. doi: 10.3109/08820538.2013.874479,
36.
Price FW Jr Koller DL Price MO . Central corneal pachymetry in patients undergoing laser in situ keratomileusis. Ophthalmology. (1999) 106:2216–20. doi: 10.1016/S0161-6420(99)90508-0,
37.
Cho P Lam C . Factors affecting the central corneal thickness of Hong Kong-Chinese. Curr Eye Res. (1999) 18:368–74. doi: 10.1076/ceyr.18.5.368.5347,
38.
Pedersen L Hjortdal J Ehlers N . Central corneal thickness in high myopia. Acta Ophthalmol Scand. (2005) 83:539–42. doi: 10.1111/j.1600-0420.2005.00498.x,
39.
Su DH Wong TY Foster PJ Tay WT Saw SM Aung T . Central corneal thickness and its associations with ocular and systemic factors: the Singapore Malay eye study. Am J Ophthalmol. (2009) 147:709–716.e701. doi: 10.1016/j.ajo.2008.10.013
40.
Phillips JR McBrien NA . Form deprivation myopia: elastic properties of sclera. Ophthalmic Physiol Opt. (1995) 15:357–62. doi: 10.1046/j.1475-1313.1995.9500062i.x,
41.
Zhou P Wang DD Fan L Yang L Zhao MW . Thin central corneal thickness may be a risk factor for myopia progression in children. J Ophthalmol. (2023) 2023:3815863. doi: 10.1155/2023/3815863,
42.
Ganesh S Lusobya RC Uduman MS Rajan R Rajendran N Sanjeev K et al . Ocular biometric parameters in south-Indian children with myopia - a hospital-based retrospective descriptive analysis. Indian J Ophthalmol. (2025) 73:292–6. doi: 10.4103/IJO.IJO_546_24,
43.
Lu T Song J Wu Q Jiang W Tian Q Zhang X et al . Refractive lens power and lens thickness in children (6-16 years old). Sci Rep. (2021) 11:19284. doi: 10.1038/s41598-021-98817-9,
Summary
Keywords
anterior segment biometry, axial length, children, crystalline lens, high axial myopia
Citation
Zhang Z, Mu J, Yang Y, Dai Y and Duan J (2026) The relationship between axial length and anterior segment biometry in high axial myopic Chinese students aged 7 to 18 years. Front. Med. 12:1671451. doi: 10.3389/fmed.2025.1671451
Received
30 July 2025
Revised
14 December 2025
Accepted
23 December 2025
Published
13 January 2026
Volume
12 - 2025
Edited by
Vasudevan Lakshminarayanan, University of Waterloo, Canada
Reviewed by
Maria Letizia Salvetat, SOC di Oculistica - Azienda Sanitaria Friuli Occidentale (ASFO), Italy
Enzo Maria D'Ambrosio, Centro Oftalmico D'Ambosio, Italy
Updates
Copyright
© 2026 Zhang, Mu, Yang, Dai and Duan.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yun Dai, daiyunqq@163.com; Junguo Duan, duanjg@cdutcm.edu.cn
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.