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Prevalence and risk factors for disrupted circadian rhythmicity in children with optic nerve hypoplasia.

机译:视神经发育不良儿童的昼夜节律紊乱的患病率和危险因素。

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BACKGROUND/AIMS: Children with optic nerve hypoplasia (ONH) have visual impairment and may have hypopituitarism and developmental delay. Children with ONH have also been reported to have abnormal sleep-wake cycles. We assessed the incidence and nature of sleep-wake abnormalities in children with ONH. METHODS: Rest-activity patterns were assessed in 23 children with ONH using actigraphy, which is a non-invasive method for continuously monitoring activity. The children also had formal assessment of pituitary function, visual acuity measurements, assessment of papillary responsiveness, MRI scans of the head and assessment of neurocognitive function. RESULTS: Sufficient actigraphy data were obtained on 19 of the children. Analysis of expressed rhythmicity revealed normal rest-activity patterns in 13 children (68%). Of the six children (32%) with abnormal rhythmicity, three had fragmented sleep, one had free-running rest-activity cycles and two were arrhythmic. Of the children with normal rhythmicity, the following were found: hypoplastic corpus callosum in 30%, growth hormone deficiency in 53%, hypothyroidism in 23%, adrenal insufficiency in 30%, diabetes insipidus in 0% and developmental delay in 15%. Of the children with abnormal rhythmicity, the following were found: hypoplastic corpus callosum in 66% (p>0.05), severe visual impairment in 100% (p=0.006), abnormal pupillary responsiveness in 85% (p=0.0084), cognitive impairment in 100% (p=0.04) and multiple hormonal deficiencies in 66% (p=0.03). CONCLUSIONS: Abnormal rest-activity rhythmicity patterns are present in 30% of children with ONH. The best predictors of abnormal rhythmicity are severe vision impairment, abnormal pupillary responsiveness, developmental delay and multiple hormonal deficiencies.
机译:背景/目的:视神经发育不全(ONH)的儿童有视觉障碍,可能患有垂体功能低下和发育迟缓。据报道,ONH患儿有异常的睡眠-觉醒周期。我们评估了ONH患儿觉醒异常的发生率和性质。方法:采用活动照相法对23名ONH儿童的休息活动模式进行了评估,这是一种连续监测活动的非侵入性方法。这些孩子还进行了垂体功能的正式评估,视力测量,乳头反应性评估,头部的MRI扫描以及神经认知功能评估。结果:19名儿童获得了足够的书法记录数据。表达的节律性分析显示13名儿童(68%)的正常休息活动模式。在6名儿童(32%)的节律异常中,有3名睡眠不足,1名自由活动的休息活动周期,还有2名心律不齐。在节律正常的儿童中,发现以下情况:发育不良的hypo体占30%,生长激素缺乏症占53%,甲状腺功能减退症占23%,肾上腺功能不全占30%,尿崩症占0%,发育迟缓占15%。在节律异常的儿童中,发现以下情况:发育不良的call体占66%(p> 0.05),严重视力障碍占100%(p = 0.006),瞳孔反应异常占85%(p = 0.0084),认知障碍100%(p = 0.04)和66%(p = 0.03)的多种激素缺乏症。结论:30%的ONH患儿存在异常的休息活动节律模式。节律异常的最佳预测指标是严重视力障碍,瞳孔反应异常,发育迟缓和多种激素缺乏。

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