Delayed macular development in preterm infants with spontaneously regressed retinopathy of prematurity.

IF 1.7 4区 医学 Q3 OPHTHALMOLOGY
Xiaojing Cai, Xiaohong Zhou, Tiancheng Wu, Yian Li, Weiming Yang, Chenhao Yang
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Abstract

Purpose: To evaluate the macular development in preterm infants with spontaneously regressed retinopathy of prematurity (ROP) utilizing handheld spectral domain optical coherence tomography (SD-OCT) during the early postnatal period.

Design: A cross-sectional observational study.

Methods: Using handheld SD-OCT, OCT images were acquired in non-sedated infants ages about 37 weeks(w) post-menstrual-age (PMA = gestational age in weeks + chronological age). Central foveal thickness (CFT), mean parafoveal thickness (PT, mean of the temporal and nasal-lateral retinal thickness 1000 μm from the foveal center), the thickness of inner retina layers (IRL) and outer retina layers (ORL) of the foveal center and parafoveal, the depth of the macular fovea (FD), and the angle of the macular fovea (FA) were measured and analyzed.

Results: In contrast to the infants without ROP (group 1), OCT images of the infants with spontaneously regressed ROP (group 2) were more immature. The FD of Group 2 was shallower than Group 1 (P < 0.05); CFT and the foveal center IRL (FIRL) of Group 2 were thicker than Group 1 (P < 0.05); conversely, PT and the mean parafoveal IRL (PIRL) of Group 2 were thinner than Group 1 (P < 0.05); FA of Group 2 was bigger than Group 1 (P < 0.05); however, there was no significant difference in the foveal center ORL (FORL) and the mean parafoveal ORL (PORL) between Groups 1 and 2 (P > 0.05). Furthermore, in preterm infants, ROP was moderately correlated with FD, CFT, PT, FIRL, and PIRL (P < 0.05).

Conclusions: The spontaneously regressed ROP resulted in immature macular development in the early postnatal period. The inner retinal layers mainly contribute to this but not the outer retinal layers, indicating that the macular fovea's inner and outer retina layers developed asynchronously. ROP is an influential factor in macular development and maturation. This may be associated with the higher probability of visual impairment in children with a history of spontaneous regression of ROP at a prior time.

自发性退行性早产儿视网膜病变的延迟黄斑发育。
目的:应用手持式光谱域光学相干断层扫描(SD-OCT)评价早产儿自发性退行性早产儿视网膜病变(ROP)的黄斑发育情况。设计:横断面观察性研究。方法:采用手持式SD-OCT,对经后37周(PMA =周胎龄+实足年龄)未服用镇静剂的婴儿进行OCT图像采集。测量并分析中央中央凹厚度(CFT)、平均中央凹旁厚度(PT)、距中央凹中心1000 μm的颞部和鼻侧视网膜厚度(PT)、中央凹中心和中央凹旁视网膜内层厚度(IRL)和视网膜外层厚度(ORL)、黄斑中央凹深度(FD)和黄斑中央凹角度(FA)。结果:与没有ROP的婴儿(1组)相比,自发消退ROP的婴儿(2组)的OCT图像更不成熟。2组的FD较1组浅(p0.05)。此外,在早产儿中,ROP与FD、CFT、PT、FIRL和PIRL有中等相关性(P)。结论:自发消退的ROP导致出生后早期黄斑发育不成熟。这主要是视网膜内层的作用,而不是视网膜外层的作用,说明黄斑中央凹的视网膜内、外层是不同步发育的。ROP是影响黄斑发育成熟的重要因素。这可能与先前有ROP自发消退史的儿童出现视力障碍的可能性较高有关。
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来源期刊
BMC Ophthalmology
BMC Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
5.00%
发文量
441
审稿时长
6-12 weeks
期刊介绍: BMC Ophthalmology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of eye disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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