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11β-羟化酶缺乏所致经典型和非经典型先天性肾上腺皮质增生症患者球状带功能的特征分析

Characterization of zona glomerulosa function in patients with classic and non-classic forms of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.

作者信息

Castro-Magana M, Angulo M, Canas J A, Mazur B, Sarrantonio M, Vitollo P, Palekar A, Fuentes B, Lee A

机构信息

Division of Pediatric Endocrinology and Genetics, Winthrop-University Hospital, Mineola, NY 11501, USA.

出版信息

J Pediatr Endocrinol Metab. 1995 Jan-Mar;8(1):19-25. doi: 10.1515/jpem.1995.8.1.19.

Abstract

The function of the adrenal zona glomerulosa was studied in 18 patients with 11-hydroxylase deficiency confirmed by elevated plasma levels of 11-deoxycortisol. Patients were divided into two groups. Group I (4 males, 7 females; aged 1.2-2.8 yrs) had symptoms at birth or shortly after (classic form), and Group II (4 males, 3 females; aged 7.3-20.1 yrs) had their first clinical manifestation during childhood (non-classic form). To study zona glomerulosa function, patients were given dexamethasone p.o. 2 mg/m2/day x6 days, thus suppressing the zona fasciculata. Six hours after the last dose of dexamethasone, the zona glomerulosa was stimulated by i.v. administration of furosemide 1.0 mg/kg as a single dose. Blood was drawn 2 h later. In the untreated state, all patients had striking elevation of ACTH (Group I: 1,070 +/- 380 pg/ml; Group II: 764 +/- 180 pg/ml), 11-deoxycortisol (Group I: 63,000 +/- 22,000 ng/dl; Group II: 17,200 +/- 5,200 ng/dl) and deoxycorticosterone (Group I: 1,100 +/- 67 ng/dl; Group II: 499 +/- 27 ng%) while plasma renin activity (< 0.5 ng/ml/h in both groups) and aldosterone (Group I: 3.0 +/- 1.8 ng/dl; Group II: 2.3 +/- 1.8 ng/dl) were markedly suppressed. After the administration of furosemide 4 patients in Group I were unable to increase aldosterone (2.8 +/- 0.9 ng/dl) secretion in spite of marked elevation of plasma renin activity (28 +/- 7 ng/ml/h), suggesting an impairment of 11-hydroxylase in the zona glomerulosa.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对18例经血浆11 - 脱氧皮质醇水平升高确诊为11β-羟化酶缺乏症的患者的肾上腺球状带功能进行了研究。患者被分为两组。第一组(4名男性,7名女性;年龄1.2 - 2.8岁)在出生时或出生后不久出现症状(典型形式),第二组(4名男性,3名女性;年龄7.3 - 20.1岁)在儿童期首次出现临床表现(非典型形式)。为研究球状带功能,给予患者口服地塞米松2 mg/m²/天,共6天,从而抑制束状带。在最后一剂地塞米松给药6小时后,通过静脉注射1.0 mg/kg速尿作为单次剂量刺激球状带。2小时后采血。在未治疗状态下,所有患者的促肾上腺皮质激素(第一组:1,070±380 pg/ml;第二组:764±180 pg/ml)、11 - 脱氧皮质醇(第一组:63,000±22,000 ng/dl;第二组:17,200±5,200 ng/dl)和脱氧皮质酮(第一组:1,100±67 ng/dl;第二组:499±27 ng%)显著升高,而血浆肾素活性(两组均<0.5 ng/ml/h)和醛固酮(第一组:3.0±1.8 ng/dl;第二组:2.3±1.8 ng/dl)明显受到抑制。给予速尿后,第一组中有4名患者尽管血浆肾素活性显著升高(28±7 ng/ml/h),但醛固酮分泌无法增加(2.8±0.9 ng/dl),提示球状带中11β-羟化酶存在损害。(摘要截短于250字)

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