Choi Young-Jin, Hong Eun Hee, Shin Yong Un, Bae Gi Hwan, Kim Inah, Cho Heeyoon
Department of Pediatrics, Hanyang University Guri Hospital, Guri, South Korea.
Department of Ophthalmology, Hanyang University Guri Hospital, Guri, South Korea.
Front Pediatr. 2022 Feb 9;10:816409. doi: 10.3389/fped.2022.816409. eCollection 2022.
This study aimed to investigate whether severe retinopathy of prematurity (ROP) could be an association factor for neurodevelopmental disorders in premature infants without other risk factors-such as congenital anomalies, birth injuries, and neurological diseases-that may cause developmental delay.
We used health claims data recorded between 2007 and 2018 in the Korean National Health Insurance Service (KNHIS) database. We recruited a total of 18,256 premature infant born between 2007 and 2008 without congenital anomaly or birth injury (with ROP 6,995, without ROP 11,261) and divided them into four groups as follows: Group A, 209 extremely premature infants [gestational age (GA) < 28] with mild ROP; Group B, 75 extremely premature infants (GA < 28) with severe ROP; Group C, 6,510 other premature infants (28 ≤ GA <37)with mild ROP; and Group D, 201 other premature infants (28 ≤ GA < 37) with severe ROP. Using regression analysis, we analyzed whether there was a correlation between ROP prevalence, severity, and developmental delay in premature infants without other risk factors.
The prevalence of developmental delay, according to GA and ROP severity, was higher in patients with severe ROP than in the other patients. The prevalence gradually decreased after birth. Among extremely premature infants with ROP, those with severe ROP had a 3.082-fold higher association with neurodevelopmental complications than those with mild ROP ( < 0.001). Compared with other premature infants with ROP, those with severe ROP had a 3.269-fold higher association with neurodevelopmental complications than those with mild ROP.
The severity of ROP may be associated with neurodevelopmental disorders in premature infants.
本研究旨在调查在没有其他可能导致发育迟缓的危险因素(如先天性异常、出生损伤和神经系统疾病)的早产儿中,重度早产儿视网膜病变(ROP)是否可能是神经发育障碍的关联因素。
我们使用了韩国国民健康保险服务(KNHIS)数据库中2007年至2018年记录的健康保险理赔数据。我们共招募了18256名2007年至2008年出生、无先天性异常或出生损伤的早产儿(有ROP的6995名,无ROP的11261名),并将他们分为以下四组:A组,209名患有轻度ROP的极早产儿[胎龄(GA)<28周];B组,75名患有重度ROP的极早产儿(GA<28周);C组,6510名患有轻度ROP的其他早产儿(28≤GA<37周);D组,201名患有重度ROP的其他早产儿(28≤GA<37周)。通过回归分析,我们分析了在没有其他危险因素的早产儿中,ROP患病率、严重程度与发育迟缓之间是否存在相关性。
根据GA和ROP严重程度,重度ROP患者的发育迟缓患病率高于其他患者。出生后患病率逐渐下降。在患有ROP的极早产儿中,重度ROP患者发生神经发育并发症的关联度比轻度ROP患者高3.082倍(P<0.001)。与其他患有ROP的早产儿相比,重度ROP患者发生神经发育并发症的关联度比轻度ROP患者高3.269倍。
ROP的严重程度可能与早产儿的神经发育障碍有关。