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一项用于评估下丘脑-垂体-肾上腺轴功能的低剂量促肾上腺皮质激素(ACTH)试验。

A low dose ACTH test to assess the function of the hypothalamic-pituitary-adrenal axis.

作者信息

Rasmuson S, Olsson T, Hagg E

机构信息

Department of Internal Medicine, University Hospital of Northern Sweden, Umea.

出版信息

Clin Endocrinol (Oxf). 1996 Feb;44(2):151-6. doi: 10.1046/j.1365-2265.1996.600482.x.

Abstract

OBJECTIVE

The insulin tolerance test (ITT) has long been used to assess the hypothalamic-pituitary-adrenal axis, but may be hazardous. The standard synthetic ACTH (Synacthen) test has been advocated as a substitute but is sometimes insensitive. In this study the ITT has been compared to a low dose ACTH stimulation test (1 microg) and the standard ACTH stimulation test (250 microg).

SUBJECTS

Twenty-seven subjects were studied, 24 with verified or suspected hypothalamic-pituitary disorders and three on long-term glucocorticoid therapy.

DESIGN

Insulin tolerance, low dose ACTH and standard ACTH tests were performed in all patients. The ITT was performed less than 48 hours after the ACTH tests. Synacthen was administered as an intravenous bolus.

MEASUREMENTS

Serum cortisol values were determined by radioimmunoassay. The peak cortisol value during ITT was compared to the cortisol levels during the ACTH tests.

RESULTS

There was a highly significant correlation between peak cortisol values during ITT and cortisol levels after 20-60 minutes in the low dose ACTH test (r(s) = 0.91-0.93; P < 0.0001) and after 30 and 60 minutes in the standard ACTH test (r(s) = 0.85 and 0.89 respectively; P < 0.0001). Four patients showed discrepancies between the three tests.

CONCLUSIONS

The 1-microg ACTH test follows the ITT more closely and may be more sensitive than the standard ACTH test in detecting more subtle insufficiency of the hypothalamic-pituitary-adrenal axis. The standard ACTH test and the insulin tolerance test may thus be replaced by the 1-microg ACTH test in screening for secondary cortisol insufficiency. We recommend that serum cortisol is measured before and 30 and 40 minutes after the ACTH injection.

摘要

目的

胰岛素耐量试验(ITT)长期以来一直用于评估下丘脑 - 垂体 - 肾上腺轴,但可能存在风险。标准的合成促肾上腺皮质激素(赛可强)试验已被提倡作为替代方法,但有时不敏感。在本研究中,将ITT与低剂量促肾上腺皮质激素刺激试验(1微克)和标准促肾上腺皮质激素刺激试验(250微克)进行了比较。

受试者

对27名受试者进行了研究,其中24名患有已证实或疑似下丘脑 - 垂体疾病,3名正在接受长期糖皮质激素治疗。

设计

对所有患者进行了胰岛素耐量、低剂量促肾上腺皮质激素和标准促肾上腺皮质激素试验。ITT在促肾上腺皮质激素试验后不到48小时进行。赛可强作为静脉推注给药。

测量

通过放射免疫测定法测定血清皮质醇值。将ITT期间的皮质醇峰值与促肾上腺皮质激素试验期间的皮质醇水平进行比较。

结果

ITT期间的皮质醇峰值与低剂量促肾上腺皮质激素试验中20 - 60分钟后的皮质醇水平(r(s)=0.91 - 0.93;P < 0.0001)以及标准促肾上腺皮质激素试验中30和60分钟后的皮质醇水平(分别为r(s)=0.85和0.89;P < 0.0001)之间存在高度显著的相关性。4名患者在这三项试验中表现出差异。

结论

1微克促肾上腺皮质激素试验比标准促肾上腺皮质激素试验更接近ITT,并且在检测下丘脑 - 垂体 - 肾上腺轴更细微的功能不全方面可能更敏感。因此,在筛查继发性皮质醇功能不全时,标准促肾上腺皮质激素试验和胰岛素耐量试验可能会被1微克促肾上腺皮质激素试验所取代。我们建议在促肾上腺皮质激素注射前以及注射后30和40分钟测量血清皮质醇。

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