Elucidating perifoveal vascular development in infants

阐明婴儿中心凹周围血管发育

基本信息

批准号：
10696178
负责人：
Xi Chen
金额：
$ 39.89万
依托单位：
DUKE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2022
资助国家：
美国
起止时间：
2022-09-30 至 2027-08-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10696178
关键词：
3-Dimensional Adult Age Anastomosis - action Angiography Animal Model Biomedical Engineering Blindness Blood Vessels Blood capillaries Child Childhood Complex Cone Data Development Devices Disease Early Diagnosis Elderly Etiology Exhibits Functional disorder Fundus Gestational Age Goals Human Image Imaging Techniques Impairment Individual Infant Infant Development Knowledge Location Methods Neurologic Ophthalmologist Optical Coherence Tomography Pathology Pattern Photoreceptors Pigmentation physiologic function Pregnancy Premature Birth Premature Infant Prevalence Process Recording of previous events Research Retina Retinopathy of Prematurity Sampling Source Speed System Three-dimensional analysis Translations Vascular Diseases Vascularization Vision Visual Visual Acuity Visual impairment Visualization Work density disability disorder of macula of retina fovea centralis imaging system improved in vivo insight longitudinal analysis macular edema multidisciplinary premature

项目摘要

PROJECT SUMMARY One out of every ten infants is born preterm. Preterm birth can cause retinopathy of prematurity (ROP), a leading cause of childhood blindness. Even in the absence of ROP or neurological disability, children born preterm exhibit subtle impairments in visual acuity and visual function, though the etiology of this suboptimal vision in preterm infants remains unclear. The fovea, an indentation in the central retina, is the most critical region determining visual acuity. The fovea is surrounded by anastomosis of three layers of capillaries, forming the foveal avascular zone. It is well-established that children and adults with history of prematurity have a small or absent foveal avascular zone, retained foveal inner retinal layers, and decreased photoreceptor function, and that these abnormalities are more severe in individuals with history of treated ROP. The development of human perifoveal vasculature, however, is difficult to study due to the absence of fovea in most easily accessible animal models and the rarity of human histopathological samples during late gestation. Our multidisciplinary team with complementary expertise will work together to use advanced bedside handheld optical coherence tomography (OCT) angiography imaging to fill the gap in our knowledge of perifoveal vascular development in infants. We propose to elucidate the human perifoveal vascular development through the following specific aims: 1) optimize bedside handheld infant OCT angiography to visualize perifoveal vascular development; 2) determine if perifoveal vascular development is delayed in preterm infants compared to term infants, further delayed in ROP, and associates with poor outer retinal maturation; and 3) determine the association of macular edema and decreased perifoveal deep vascular complex formation and outer retinal maturation in preterm infants. This research will expand our knowledge of human foveal development and inform the pathophysiology of diseases of macular and retinal vascular development.

项目概要每十个婴儿中就有一个是早产的。早产可导致早产儿视网膜病变 (ROP) 儿童失明的主要原因。即使没有 ROP 或神经功能障碍，出生的孩子早产儿在视力和视觉功能方面表现出轻微的损害，尽管这种次优的病因早产儿的视力仍不清楚。中央凹是视网膜中央的一个凹陷，是最关键的区域决定视力。中央凹周围有三层毛细血管吻合，形成中央凹无血管区。众所周知，有早产史的儿童和成人的早产率较小。或中心凹无血管区缺失、中心凹视网膜内层保留以及感光功能下降，并且这些异常在有 ROP 治疗史的个体中更为严重。的发展然而，人类中心凹周围脉管系统很难研究，因为最容易研究的地方没有中心凹。妊娠晚期可获得的动物模型和人类组织病理学样本的稀有性。我们具有互补专业知识的多学科团队将共同努力使用先进的床边手持设备光学相干断层扫描（OCT）血管造影成像填补了我们对中心凹周围知识的空白婴儿血管发育。我们建议通过以下方式阐明人类中心凹周围血管的发育具体目标如下： 1) 优化床边手持式婴儿 OCT 血管造影以可视化中心凹周围血管发育； 2) 确定早产儿的中心凹周围血管发育是否延迟对于足月婴儿，ROP 进一步延迟，并与外视网膜成熟不良相关； 3) 确定黄斑水肿与中心凹周围深部血管复合体形成和视网膜外层减少的关联早产儿的成熟。这项研究将扩大我们对人类中心凹发育的认识了解黄斑和视网膜血管发育疾病的病理生理学。