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脑畸形不会预测伴有视神经发育不良的幼儿的垂体功能减退症。

Brain Malformations Do Not Predict Hypopituitarism in Young Children with Optic Nerve Hypoplasia.

机构信息

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.

出版信息

Horm Res Paediatr. 2017;88(3-4):251-257. doi: 10.1159/000479029. Epub 2017 Aug 22.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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)。

结论

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。

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