Tu Chun-Hsien, Wu Wei-Chi, Chin Wei-Chih, Hsu Shih-Chieh, Tang I, Hsu Jen-Fu, Chou Hung-Da, Kang Eugene Yu-Chuan, Huang Yu-Shu
Department of Psychiatry, New Taipei Municipal Tucheng Hospital, New Taipei City 236, Taiwan.
Department of Psychiatry, Chang Gung Memorial Hospital (Linkou Branch), Taoyuan 33305, Taiwan.
Children (Basel). 2024 Jul 25;11(8):894. doi: 10.3390/children11080894.
Premature children with retinopathy of prematurity (ROP) have been reported to an have increased risk of visual and neurocognitive impairments, yet little is known about whether vision could affect specific neurocognition. This study aimed to clarify the correlations between neurocognition and vision in premature children.
This is a nonrandomized, cross-sectional, observational study in a pediatric cohort with five groups: (1) full-term (n = 25), (2) prematurity without ROP (n = 154), (3) prematurity with ROP but without treatment (n = 39), (4) prematurity with ROP and with bevacizumab (IVB) treatment (n = 62), and (5) prematurity with ROP and with laser/laser + IVB treatment (n = 20). Neurocognitive function was evaluated by the Wechsler Preschool and Primary Scale of Intelligence, Fourth Edition (WPPSI-IV) around the age of 4 years. Visual acuity (VA) and refractive errors were tested. Correlations between WPPSI parameters and visual outcomes were analyzed across five groups.
Among the 300 recruited children (mean age = 4.02 + 0.97 years, male = 56.3%), 297 were assessed by WPPSI-IV and 142 were assessed by vision tests. The Full-Scale Intelligence Quotient (FSIQ) index was worse in the premature groups. After adjusting for covariates, seven items, including FSIQ-Index ( = 0.047), fluid-reasoning index ( = 0.004), FR-percentile ranking ( = 0.008), object assembly ( = 0.034), picture concept ( = 0.034), zoo locations ( = 0.014) and bug search ( = 0.020), showed significant differences between groups. The better the best corrected VA (BCVA), the higher the scores on Verbal Comprehension Index (VCI), VCI-PR, and the subtest of information.
Specific cognitive dysfunctions are related to the BCVA in this large cohort. Subtest performance profiles in WPPSI can be affected by prematurity, ROP treatment, and different ROP treatment. FSIQ is generally lower in premature children and even lower in children with ROP.
据报道,患有早产儿视网膜病变(ROP)的早产儿出现视力和神经认知障碍的风险增加,但对于视力是否会影响特定的神经认知知之甚少。本研究旨在阐明早产儿神经认知与视力之间的相关性。
这是一项针对儿科队列的非随机、横断面观察性研究,分为五组:(1)足月儿(n = 25),(2)无ROP的早产儿(n = 154),(3)患有ROP但未接受治疗的早产儿(n = 39),(4)患有ROP且接受贝伐单抗(IVB)治疗的早产儿(n = 62),以及(5)患有ROP且接受激光/激光+IVB治疗的早产儿(n = 20)。在4岁左右通过韦氏学前和小学智力量表第四版(WPPSI-IV)评估神经认知功能。测试视力(VA)和屈光不正。分析五组中WPPSI参数与视力结果之间的相关性。
在招募的300名儿童中(平均年龄 = 4.02 + 0.97岁,男性占56.3%),297名儿童通过WPPSI-IV进行评估,142名儿童通过视力测试进行评估。早产儿组的全量表智商(FSIQ)指数较差。在调整协变量后,包括FSIQ指数( = 0.047)、流体推理指数( = 0.004)、FR百分位排名( = 0.008)、图形拼凑( = 0.034)、图片概念( = 0.034)、动物园位置( = 0.014)和昆虫搜索( = 0.020)在内的七个项目在组间显示出显著差异。最佳矫正视力(BCVA)越好,言语理解指数(VCI)、VCI-PR和信息子测试的得分越高。
在这个大型队列中,特定的认知功能障碍与BCVA相关。WPPSI中的子测试表现概况可能会受到早产、ROP治疗和不同ROP治疗的影响。早产儿的FSIQ通常较低,患有ROP的儿童更低。