Gravelle Madelaine N K, Vandewouw Marlee M, Young Julia M, Dunkley Benjamin T, Shroff Manohar M, Taylor Margot J
Department of Diagnostic Imaging, Hospital for Sick Children, Toronto, Ontario, Canada; Neurosciences & Mental Health Program, Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Diagnostic Imaging, Hospital for Sick Children, Toronto, Ontario, Canada; Neurosciences & Mental Health Program, Hospital for Sick Children, Toronto, Ontario, Canada; Department of Psychology, University of Toronto, Toronto, Ontario, Canada.
Neuroimage Clin. 2020;28:102373. doi: 10.1016/j.nicl.2020.102373. Epub 2020 Aug 6.
Anophthalmia, characterized by the absence of an eye(s), is a rare major birth defect with a relatively unexplored neuroanatomy. Longitudinal comparison of white matter development in an anophthalmic (AC) very preterm (VPT) child with both binocular VPT and full-term (FT) children provides unique insights into early neurodevelopment of the visual system. VPT-born neonates (<32wks gestational age), including the infant with unilateral anophthalmia, underwent neuroimaging every two years from birth until 8 years. DTI images (N = 168) of the optic radiation (OR) and a control track, the posterior limb of the internal capsule (PLIC), were analysed. The diameter of the optic nerves (ON) were analysed using T1-weighted images. Significant group differences in FA and AD were found bilaterally in the OR and PLIC. This extends the literature on altered white matter development in VPT children, being the first longitudinal study showing stable group differences across the 4, 6 and 8 year timepoints. AC showed greater deficits in FA and AD bilaterally, but recovered towards VPT group means from 4 to 8 years-of-age. Complete lack of binocular input would be responsible for these early deficits; compensatory mechanisms may facilitate structural improvement over time. AC's ON exhibited significant atrophy ipsilateral to the anophthalmic eye. Functionally, AC displayed normal visual acuity and form perception, but naso-temporal bias in motion perception. Following these groups and AC longitudinally enabled novel understanding of the joint influence of monocular vision and VPT birth on neurodevelopment.
无眼畸形,其特征为一只或两只眼睛缺失,是一种罕见的严重出生缺陷,其神经解剖结构相对未被充分探索。对一名患有无眼畸形的极早产儿(AC)与双眼极早产儿和足月儿的白质发育进行纵向比较,为视觉系统的早期神经发育提供了独特的见解。极早产出生的新生儿(胎龄<32周),包括患有单侧无眼畸形的婴儿,从出生到8岁每两年接受一次神经影像学检查。分析了视辐射(OR)和一个对照轨迹——内囊后肢(PLIC)的扩散张量成像(DTI)图像(N = 168)。使用T1加权图像分析视神经(ON)的直径。在OR和PLIC双侧均发现FA和AD存在显著的组间差异。这扩展了关于极早产儿白质发育改变的文献,是第一项显示在4年、6年和8年时间点上存在稳定组间差异的纵向研究。AC在双侧FA和AD方面表现出更大的缺陷,但在4至8岁时向极早产组均值恢复。双眼输入的完全缺失可能是这些早期缺陷的原因;随着时间的推移,代偿机制可能促进结构改善。AC的患侧视神经表现出明显萎缩。在功能上,AC表现出正常的视力和形状感知,但在运动感知上存在鼻颞侧偏差。对这些组和AC进行纵向跟踪,能够对单眼视觉和极早产出生对神经发育的联合影响有新的认识。