Corneal aberrations and anterior segment parameters in preterm children with or without a history of retinopathy of prematurity

早产儿视网膜病变 医学 眼科 角膜 胎龄 怀孕 遗传学 生物
作者
Marzieh Najjaran,Hadi Ostadimoghaddam,Siamak Zarei‐Ghanavati,Alireza Eslampoor,Jorge L. Alió,Mohammed Ziaei
出处
期刊:Ophthalmic and Physiological Optics [Wiley]
标识
DOI:10.1111/opo.13493
摘要

Abstract Purpose This study aimed to compare corneal aberrations and anterior segment parameters in preterm children, aged 4–8 years, with or without a history of retinopathy of prematurity (ROP). Methods A comparative cohort study was conducted using corneal tomography to analyse anterior segment parameters in preterm children. Four groups of children were included ( n = 30 in each group): children with a history of ROP who were treated with intravitreal bevacizumab, children whose ROP regressed spontaneously and received no treatment, preterm children without ROP and age‐ and gender‐matched full‐term children. Results A total of 120 eyes from 120 children with a mean age of 6.63 ± 1.25 years were analysed. Mean anterior corneal curvature was significantly steeper in the treated ROP, spontaneously regressed ROP and preterm (no ROP) groups compared with full‐term children ( p < 0.001, p = 0.001 and p = 0.04, respectively). Similarly, posterior corneal curvature was steeper in these same groups compared with full‐term children ( p < 0.001, p < 0.001 and p = 0.007, respectively). Further, the treated and spontaneously regressed ROP groups exhibited narrower iridocorneal angles compared with full‐term children ( p = 0.02 and p = 0.002, respectively). Higher order aberrations of the anterior cornea and trefoil of the total cornea were elevated in the treated ROP group compared with preterm children (both p = 0.02). Posterior spherical aberration was significantly higher in the spontaneously regressed ROP group compared with full‐term controls ( p = 0.02). Conclusion Preterm children, regardless of their ROP status, demonstrated steeper anterior and posterior corneal curvatures than full‐term children. Children with a history of ROP also exhibited narrower iridocorneal angles and increased corneal aberrations.
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