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本文引用的文献

1
Corticotropin tests for hypothalamic-pituitary- adrenal insufficiency: a metaanalysis.促肾上腺皮质激素检测下丘脑-垂体-肾上腺功能不全:一项荟萃分析。
J Clin Endocrinol Metab. 2008 Nov;93(11):4245-53. doi: 10.1210/jc.2008-0710. Epub 2008 Aug 12.
2
Low-dose and high-dose adrenocorticotropin testing: indications and shortcomings.低剂量和高剂量促肾上腺皮质激素检测:适应证与不足
Curr Opin Endocrinol Diabetes Obes. 2008 Jun;15(3):244-9. doi: 10.1097/MED.0b013e3282fdf16d.
3
Secondary hypoadrenalism.继发性肾上腺功能减退症
Pituitary. 2008;11(2):147-54. doi: 10.1007/s11102-008-0108-4.
4
Factors influencing the adrenocorticotropin test: role of contemporary cortisol assays, body composition, and oral contraceptive agents.影响促肾上腺皮质激素试验的因素:当代皮质醇检测方法、身体组成及口服避孕药的作用
J Clin Endocrinol Metab. 2007 Apr;92(4):1326-33. doi: 10.1210/jc.2006-1791. Epub 2007 Jan 23.
5
The long-term predictive accuracy of the short synacthen (corticotropin) stimulation test for assessment of the hypothalamic-pituitary-adrenal axis.用于评估下丘脑-垂体-肾上腺轴的短程促肾上腺皮质激素(合成促皮质素)刺激试验的长期预测准确性。
J Clin Endocrinol Metab. 2006 Jan;91(1):43-7. doi: 10.1210/jc.2005-1131. Epub 2005 Oct 25.
6
Measurements of serum free cortisol in critically ill patients.危重症患者血清游离皮质醇的测定
N Engl J Med. 2004 Apr 15;350(16):1629-38. doi: 10.1056/NEJMoa020266.
7
Dynamic evaluation of adrenal hypofunction.肾上腺功能减退的动态评估
J Endocrinol Invest. 2003;26(7 Suppl):74-82.
8
A RAPID TEST OF ADRENOCORTICAL FUNCTION.肾上腺皮质功能的快速检测
Lancet. 1965 Jan 30;1(7379):243-5. doi: 10.1016/s0140-6736(65)91526-6.
9
Use of the low-dose corticotropin stimulation test for the diagnosis of secondary adrenocortical insufficiency.使用低剂量促肾上腺皮质激素刺激试验诊断继发性肾上腺皮质功能不全。
Hong Kong Med J. 2002 Dec;8(6):427-34.
10
The low dose (1 microg) ACTH stimulation test for assessment of the hypothalamo-pituitary-adrenal axis.用于评估下丘脑-垂体-肾上腺轴的低剂量(1微克)促肾上腺皮质激素刺激试验。
Neth J Med. 2000 Mar;56(3):91-9. doi: 10.1016/s0300-2977(99)00111-4.

技术细节影响 1μg ACTH 刺激试验的诊断准确性。

Technical details influence the diagnostic accuracy of the 1 microg ACTH stimulation test.

机构信息

Program in Reproductive and Adult Endocrinology, National Institute of Child Health and Human Development Pharmacy Department, National Institutes of Health, Clinical Center, Bethesda, Maryland, USA.

出版信息

Eur J Endocrinol. 2010 Jan;162(1):109-13. doi: 10.1530/EJE-09-0746. Epub 2009 Oct 1.

DOI:10.1530/EJE-09-0746
PMID:19797501
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2941345/
Abstract

OBJECTIVE

To examine the factors causing inadequate cortisol responses to the 1 microg ACTH stimulation test.

DESIGN

Random test assignment (by age and gender) at 0800 or 1600 h.

METHODS

We recruited 20 healthy adults to each of the three age groups (<40 years, 40-55 years, and >55 years; half females in each group). ACTH stimulation tests were performed in an outpatient clinic at the NIH Clinical Research Center. Plasma cortisol was measured just before, and 30 and 60 min after the administration of 1 microg ACTH (1-24). The ACTH concentration in diluted and administered solutions was measured.

RESULTS

Twenty-five volunteers (19 at 1600 h) had a subnormal cortisol response (peak cortisol 10.4-17.5 microg/dl), using a criterion <18 microg/dl (497 nmol/l), for a specificity of 58% (confidence interval (CI) 45-71%). Afternoon testing had a significant impact on failure rates (odds ratio 6.98, CI 2.17-22.43), while gender and age did not. The stock solution contained 1 microg ACTH, but after administration through tubing it contained only 0.5-0.8 microg.

CONCLUSIONS

The high rate of abnormal results, especially in the afternoon, and loss of ACTH through tubing suggest that morning testing and minimal tubing should be adopted to avoid an inappropriate diagnosis of adrenal insufficiency. Earlier time points and standardized protocols would facilitate comparison of studies.

摘要

目的

探讨导致 1μgACTH 刺激试验皮质醇反应不足的因素。

设计

0800 或 1600 时按年龄和性别随机分组进行检测。

方法

我们招募了 20 名健康成年人,每个年龄组(<40 岁、40-55 岁和>55 岁;每组各有一半女性)各 20 名。ACTH 刺激试验在 NIH 临床研究中心的门诊进行。在给予 1μgACTH(1-24)前、后 30 和 60 分钟测量血浆皮质醇。测量了稀释和给予的溶液中的 ACTH 浓度。

结果

25 名志愿者(19 名在 1600 时)的皮质醇反应异常(峰值皮质醇 10.4-17.5μg/dl),采用<18μg/dl(497nmol/l)的标准,特异性为 58%(置信区间 45-71%)。下午检测对失败率有显著影响(比值比 6.98,置信区间 2.17-22.43),而性别和年龄没有。储备溶液中含有 1μgACTH,但通过管道给药后仅含有 0.5-0.8μg。

结论

异常结果的高发生率,尤其是下午,以及通过管道丢失 ACTH,提示应采用上午检测和最小化管道以避免不适当的肾上腺功能不全诊断。更早的时间点和标准化方案将有助于比较研究。