97例3 ~ 16岁精神科住院儿童地塞米松抑制试验皮质醇动态及测试表现

MAIRIN B. DOHERTY M.D., DEBORAH MADANSKY M.D., JOHN KRAFT L.I.C.S.W., LINDA L. CARTER-AKE R.N., M.S.N., C.S., PERIHAN A. ROSENTHAL M.D., BRET F. COUGHLIN M.D.
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引用次数: 27

摘要

本报告回顾了基线皮质醇动态和地塞米松抑制试验(DST)在97名3-16岁精神病住院儿童的研究人群中的测试表现。只有5%的抑郁症患者未能维持皮质醇分泌的日变化,而在一些抑郁症儿童和非抑郁症对照中,基础皮质醇升高是一种非特异性发现。34名符合DSM-III重度情感性障碍标准的儿童中,有15名在给予1mg地塞米松治疗后血清皮质醇未能抑制在5μg/dl以下,检测灵敏度为44%,特异性为88%,诊断信度为68%。在广泛的非抑郁诊断类别中,非抑制是可以忽略不计的(3%(1/34)),但21%(4/19)的抑制性神经症患儿和33%(2/6)的抑郁情绪适应障碍患儿也未能抑制。只有1/22或4.5%的DST阳性结果会在下午4点抽取一个皮质醇样本而被遗漏尽管这些儿童的体重范围在15-83公斤之间,但当所有儿童都使用1毫克标准剂量时,在每公斤体重高、中、低剂量地塞米松未能抑制的抑郁儿童的百分比没有显著差异。然而,当高剂量儿童按年龄分组时,0 - 6岁范围内的9名幼儿的敏感性和特异性较差,表明需要进一步研究剂量、年龄、体重和诊断变量对该人群的影响。
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Cortisol Dynamics and Test Performance of the Dexamethasone Suppression Test in 97 Psychiatrically Hospitalized Children Aged 3–16 Years

This report reviews baseline cortisol dynamics and the test performance of the dexamethasone suppression test (DST) in a study population of 97 psychiatrically hospitalized children aged 3–16 years. Only 5% of depressed patients failed to maintain a diurnal variation in cortisol secretion and elevated basal cortisols were a nonspecific finding in some depressed children and nondepressed controls. Fifteen of 34 children who met DSM-III criteria for Major Affective Disorder failed to suppress their serum cortisol below 5μg/dl following 1 mg of dexamethasone giving test sensitivity of 44%, specificity of 88% and diagnostic confidence of 68%. Nonsuppression was negligible (3% (1/34) in a wide range of nondepressed diagnostic categories), but 21% (4/19) children with Depressive Neurosis and 33% (2/6) with Adjustment Disorder with depressed mood also failed to suppress. Only 1/22 or 4.5% of the positive DST results would have been missed by drawing a single cortisol sample at 4:00 P.M. In spite of a weight range of 15–83 kg in the children, there was no significant difference in the percentage of depressed children who failed to suppress at high, medium or low dose of dexamethasone per kg body weight when a 1 mg standard dose was used in all children. However, when the high dose children were grouped by age, 9 young children in the 0–6-year age range showed poor sensitivity and specificity, indicating a need for further study of the effects of dose, age, weight and diagnostic variables in this population.

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