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首页> 外文期刊>Hormone research >Significance of low-dose and standard-dose ACTH tests compared to overnight metyrapone test in the diagnosis of adrenal insufficiency in childhood.
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Significance of low-dose and standard-dose ACTH tests compared to overnight metyrapone test in the diagnosis of adrenal insufficiency in childhood.

机译:低剂量和标准剂量ACTH试验与隔夜甲吡酮试验相比对诊断儿童肾上腺功能不全具有重要意义。

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OBJECTIVE: To discover the value of low-dose (LDAT) and standard-dose ACTH tests (SDAT) as compared with the metyrapone test in the diagnosis of secondary adrenal insufficiency. PATIENTS AND METHODS: LDAT (0.5 microg/m2), SDAT (250 microg/m2) and overnight metyrapone (30 mg/kg) tests were carried out in 29 patients with suspected adrenal insufficiency. LDAT and SDAT were also performed in 36 control subjects. RESULTS: 18 of 29 patients were grouped in the adrenal-sufficient (AS) group and 11 of 29 patients in the adrenal-deficient (AD) group according to the metyrapone test results. The control group had significantly higher cortisol responses than the AS and AD groups during LDAT. The control group had similar cortisol responses to the AS group but higher cortisol responses than the AD group during SDAT. The AS group was divided into 2 subgroups: AS patients with multiple pituitary hormone deficiencies (AS-multiple) and AS patients with idiopathic growth hormone deficiencies (AS-isolated). The AS-multiple group had statistically lower cortisol responses than the control group during LDAT. Receiver-operating characteristics analysis revealed that the cortisol cutoff value in LDAT was 19.8 microg/dl (100% sensitivity, 89% specificity) and 30.4 microg/dl in SDAT (82% sensitivity, 78% specificity). CONCLUSION: LDAT is capable of identifying patients with adrenal insufficiency more effectively than SDAT. The cortisol cutoff value in LDAT was calculated as 19.8 microg/dl with 100% sensitivity. AS patients with multiple pituitary hormone deficiencies had lower cortisol responses to LDAT than the control group implying that these patients might have a lower cortisol secretory capacity than healthy subjects.
机译:目的:发现低剂量(LDAT)和标准剂量ACTH试验(SDAT)与甲吡酮试验相比在诊断继发性肾上腺皮质功能不全中的价值。患者和方法:对29名怀疑肾上腺功能不全的患者进行了LDAT(0.5 microg / m2),SDAT(250 microg / m2)和隔夜甲吡酮(30 mg / kg)测试。 LDAT和SDAT也对36名对照受试者进行。结果:根据甲吡酮测试结果,将29例患者中的18例归入肾上腺皮质激素(AS)组,将29例患者中的11例纳入肾上腺皮质激素(AD)组。 LDAT期间,对照组的皮质醇反应明显高于AS和AD组。在SDAT期间,对照组的皮质醇反应与AS组相似,但皮质醇反应高于AD组。 AS组分为两个亚组:患有多种垂体激素缺乏症的AS患者(AS-multiple)和患有特发性生长激素缺乏症的AS患者(AS-isolated)。在LDAT期间,AS多元组的皮质醇反应在统计学上低于对照组。接受者操作特征分析显示,LDAT中的皮质醇截止值是19.8 microg / dl(100%灵敏度,89%特异性)和SDAT中的30.4 microg / dl(82%灵敏度,78%特异性)。结论:LDAT比SDAT能够更有效地识别肾上腺功能不全的患者。 LDAT中的皮质醇截止值经计算为19.8 microg / dl,灵敏度为100%。患有多种垂体激素缺乏症的AS患者对LDAT的皮质醇反应比对照组低,这意味着这些患者的皮质醇分泌能力可能比健康受试者低。

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