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患有婴儿型与迟发性调节性内斜视的远视儿童眼部生物测量成分及屈光不正的纵向发展

Longitudinal development of ocular biometric components and refractive error in hyperopic children with infantile versus late-onset accommodative esotropia.

作者信息

Wang Jingyun, Jost Reed M, Koritala Brooke A, Birch Eileen E

机构信息

State University of New York College of Optometry, New York, New York, USA.

Retina Foundation of the Southwest, Dallas, Texas, USA.

出版信息

Ophthalmic Physiol Opt. 2025 May;45(3):810-819. doi: 10.1111/opo.13468. Epub 2025 Feb 17.

DOI:10.1111/opo.13468
PMID:39960102
Abstract

PURPOSE

To examine the developmental patterns of refractive error and optical components in hyperopic children with infantile (onset ≤12 months of age) accommodative or late-onset (18-48 months of age) accommodative esotropia.

METHODS

This prospective longitudinal study included children with infantile (n = 34) or late-onset (n = 63) accommodative esotropia. Axial length (AL), anterior chamber depth (ACD), lens thickness (LT) and keratometry (K1, K2) were obtained with a Lenstar LS 900. Lenstar measures were recorded <6 months after cycloplegic spherical equivalent refraction (SER) was derived. An initial examination was conducted at 5.8 ± 1.5 years of age, with a follow-up duration of 4.8 ± 0.8 years. A linear mixed-effects model was used to estimate the rate of individual development for each ocular component and SER, and to compare the two groups.

RESULTS

All biometric components changed with age. The rates of change with age for SER and AL were significantly different between the infantile and late-onset groups (SER: -0.18 vs. -0.12D/year, p < 0.001; AL: 0.16 vs. 0.14 mm/year, p < 0.01). The rate of change with age of the AL/CR ratio was significantly different between the infantile and late-onset groups (0.019 vs. 0.016, p < 0.001). No significant differences in the rates of change in ACD, LT, K1 or K2 were identified.

CONCLUSIONS

Major ocular biometric components in children continue to mature in both infantile and late-onset accommodative esotropia. Annual change in axial length is smaller in late-onset accommodative esotropia than for infantile accommodative esotropia, consistent with less change in the SER with age.

摘要

目的

研究患有婴儿期(发病年龄≤12个月)调节性或迟发性(18 - 48个月)调节性内斜视的远视儿童屈光不正和眼屈光成分的发育模式。

方法

这项前瞻性纵向研究纳入了患有婴儿期(n = 34)或迟发性(n = 63)调节性内斜视的儿童。使用Lenstar LS 900测量眼轴长度(AL)、前房深度(ACD)、晶状体厚度(LT)和角膜曲率(K1、K2)。在获得睫状肌麻痹等效球镜度(SER)后<6个月记录Lenstar测量值。初始检查在5.8±1.5岁时进行,随访时间为4.8±0.8年。采用线性混合效应模型估计每个眼成分和SER的个体发育率,并比较两组。

结果

所有生物测量成分均随年龄变化。婴儿期组和迟发性组之间SER和AL的年龄变化率有显著差异(SER:-0.18 vs. -0.12D/年,p < 0.001;AL:0.16 vs. 0.14mm/年,p < 0.01)。婴儿期组和迟发性组之间AL/CR比值的年龄变化率有显著差异(0.019 vs. 0.016,p < 0.001)。未发现ACD、LT、K1或K2的变化率有显著差异。

结论

患有婴儿期和迟发性调节性内斜视的儿童主要眼生物测量成分持续成熟。迟发性调节性内斜视的眼轴长度年变化小于婴儿期调节性内斜视,这与SER随年龄变化较小一致。

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Curr Eye Res. 2024 Jul;49(7):768-775. doi: 10.1080/02713683.2024.2336162. Epub 2024 Apr 14.
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Diagnostics (Basel). 2021 Aug 26;11(9):1547. doi: 10.3390/diagnostics11091547.
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Axial length targets for myopia control.近视控制的眼轴长度目标。
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