The Vision Center, Children's Hospital Los Angeles, Los Angeles, California, USA.
Department of Ophthalmology, King Saud bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia.
Horm Res Paediatr. 2017;88(3-4):251-257. doi: 10.1159/000479029. Epub 2017 Aug 22.
Optic nerve hypoplasia (ONH), a leading cause of pediatric blindness, is associated with brain malformations and hypopituitarism in the constellation known as septo-optic dysplasia. Neuroimaging is used to anticipate hypopituitarism, but with unconfirmed reliability. We report prospective findings on the association of hypopituitarism with brain malformations.
Children (<24 months) with ONH (n = 146; 87% bilateral) underwent baseline MRI and annual examinations and hormonal testing. Hypopituitarism status at age 5 years was classified.
A total of 74% had brain malformation(s). Hypopituitarism (69%) was not associated with brain malformations (p = 0.351); this persisted after adjusting for the laterality of ONH and the timing of MRI (padj = 0.869). No association was noted for absent septum pellucidum (38%; p = 0.073), corpus callosum abnormality (51%; p = 0.625), and major malformations (22%; p = 0.407). A malformation conferred a positive predictive value of 71% (95% CI: 62%, 80%), and a negative predictive value of 37% (95% CI: 22%, 54%). Overall, 10% (n = 15) of the cohort presented with a triad of absent septum pellucidum, corpus callosum abnormality, and other major malformation; only half (n = 8) of these had hypopituitarism. All 13 subjects with pituitary malformations manifested hypopituitarism, conferring predictive values of 100% (positive) and 34% (negative).
Hypopituitarism and brain malformations are highly prevalent, but have unrelated associations with ONH. Brain MRI in infants and toddlers with ONH is an unreliable screen for hypopituitarism risk.
视神经发育不全(ONH)是儿童失明的主要原因,与被称为视隔发育不良的脑畸形和垂体功能减退有关。神经影像学用于预测垂体功能减退症,但可靠性尚未得到证实。我们报告了关于垂体功能减退症与脑畸形之间关联的前瞻性发现。
患有 ONH(n=146;87%为双侧)的儿童(<24 个月)接受基线 MRI 和年度检查及激素检测。5 岁时的垂体功能减退症状态进行分类。
共有 74%的儿童存在脑畸形。垂体功能减退症(69%)与脑畸形无关(p=0.351);在调整 ONH 的侧位和 MRI 的时间后,这种情况仍然存在(padj=0.869)。未见透明隔缺失(38%;p=0.073)、胼胝体异常(51%;p=0.625)和主要畸形(22%;p=0.407)与垂体功能减退症相关。一种畸形的阳性预测值为 71%(95%CI:62%,80%),阴性预测值为 37%(95%CI:22%,54%)。总体而言,该队列中有 10%(n=15)的儿童出现透明隔缺失、胼胝体异常和其他主要畸形三联征;只有一半(n=8)的儿童患有垂体功能减退症。所有 13 名垂体畸形患者均出现垂体功能减退症,阳性预测值为 100%(阳性)和 34%(阴性)。
垂体功能减退症和脑畸形非常普遍,但与 ONH 无关。ONH 婴儿和幼儿的脑 MRI 是垂体功能减退症风险的不可靠筛查方法。