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一小时促肾上腺皮质激素试验在诊断轻型21-羟化酶缺乏症中的评估

Assessment of the one hour adrenocorticotrophic hormone test in the diagnosis of attenuated 21-hydroxylase deficiency.

作者信息

Innanen V T, Vale J M

机构信息

Division of Clinical Biochemistry, Women's College Hospital, Toronto, Canada.

出版信息

J Clin Pathol. 1990 Jun;43(6):493-5. doi: 10.1136/jcp.43.6.493.

DOI:10.1136/jcp.43.6.493
PMID:2166094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC502504/
Abstract

Attenuated or partial 21-hydroxylase deficiency is one of several biochemical defects in steroid metabolism that can lead to hirsutism in young women after puberty. The diagnosis is made through the exaggerated response of 17 alpha-hydroxyprogesterone (17-OH) to adrenocorticotrophic hormone (ACTH). To provide reference data 72 mild to moderately hirsute patients aged 18 to 35 were studied (over two years) with the ACTH test. Four patients with an exaggerated response were found. The mean (+/- 1SD) for zero time was 2.4 (0.96) nmol/l and for the 60 minute time was 7.2 (2.04) nmol/l. A subpopulation was found with a significantly higher baseline at 6.2 (1.3) nmol/l but a blunted 60 minute response at 8.7 (2.5) nmol/l. This is important because of the potential confusion arising from the known variability in baseline values in previously reported patients with partial 21-hydroxylase deficiency. Extending the test to 90 minutes did not show further increase in the 17-OH response to ACTH, thus confirming the validity of the 60 minutes ACTH test. The cortisol response to ACTH was also studied. One patient with presumptive partial 21-hydroxylase deficiency overlapped in cortisol response with eight of the reference population. Theoretically, a blunted cortisol response would be expected because of the postulated enzyme block, and these results suggest that other steroid enzyme defects should also be considered when an exaggerated 17-OH response to ACTH is seen.

摘要

轻度或部分21 - 羟化酶缺乏是类固醇代谢中的几种生化缺陷之一,可导致青春期后年轻女性多毛症。诊断通过17α - 羟孕酮(17 - OH)对促肾上腺皮质激素(ACTH)的过度反应来进行。为提供参考数据,对72名年龄在18至35岁的轻度至中度多毛患者进行了为期两年的ACTH试验研究。发现4名患者有过度反应。零时间的平均值(±1标准差)为2.4(0.96)nmol/L,60分钟时为7.2(2.04)nmol/L。发现一个亚组,其基线值显著更高,为6.2(1.3)nmol/L,但60分钟反应迟钝,为8.7(2.5)nmol/L。这很重要,因为在先前报道的部分21 - 羟化酶缺乏患者中,已知基线值存在变异性,可能会引起混淆。将试验延长至90分钟并未显示17 - OH对ACTH的反应进一步增加,从而证实了60分钟ACTH试验的有效性。还研究了皮质醇对ACTH的反应。一名疑似部分21 - 羟化酶缺乏的患者在皮质醇反应方面与8名参照人群重叠。理论上,由于假定的酶阻断,预期皮质醇反应会迟钝,这些结果表明,当看到17 - OH对ACTH的过度反应时,还应考虑其他类固醇酶缺陷。

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引用本文的文献

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Int J Pediatr Endocrinol. 2010;2010:625105. doi: 10.1155/2010/625105. Epub 2010 Jun 30.
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Non-classic adrenal hyperplasia in hyperandrogenism: a reappraisal.高雄激素血症中的非经典型肾上腺增生:重新评估
J Endocrinol Invest. 1998 Nov;21(10):707-20. doi: 10.1007/BF03350803.

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Clinical assessment of body hair growth in women.女性体毛生长的临床评估
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