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首页> 外文期刊>Pediatric Research >DETERMINATIONS OF PLASMA TESTOSTERONE (T) , 17-OH ROGESTERONE(17-OHP), ACTH & RENIN ACTIVITY (R.A) in THE TREATMENT CONTROL OF CONGENITAL ADRENAL HYPERPLASIA DUE TO C-21 HYDROXYLASE DEFICIENCY (C-21 AH)
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DETERMINATIONS OF PLASMA TESTOSTERONE (T) , 17-OH ROGESTERONE(17-OHP), ACTH & RENIN ACTIVITY (R.A) in THE TREATMENT CONTROL OF CONGENITAL ADRENAL HYPERPLASIA DUE TO C-21 HYDROXYLASE DEFICIENCY (C-21 AH)

机译:C-21羟化酶缺乏症(C-21 AH)治疗先天性肾上腺皮质增生症的血浆中睾丸激素(T),17-OH雄激素(17-OHP),ACT和肾素活性(R.A)的测定

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These parameters were determined in 34 children and adolescents with C-21 AH, during 2 years period. Blood samples were obtained between 6 and 9 a.m. on fasting individuals after one night of rest at the hospital. Elevated levels of T were observed before treatment or when the glucocorticoid doses were in sufficient. In some cases, starting or raising the mineralocorticoid treatment (9 alpha fluorocortisol) was followed by a decrease in T levels. High levels of R. A. were constantly found before treatment, even in the absence of salt losing syndrome. In some cases treated by glucocorticoid and salt. R.A. levels remained elevated: appropriated doses of 9 alpha|fluorocortisol induced a marked decrease in R.A. levels. Elevated 17-OH levels were always present before treatment, but frequently failed to normalize under therapy. Important individual variations were ibserved from day today and in the same day. As far as ACTH is concerned, our data are too inconsistnet to take into account this parameter. Regular determinations of plasma T and R. A. allow us a better control of glucocorticoid therapy (our mean dose being 19 mg hydrocortisone/m2/day which is lower than dosages usually published) and of skeletal maturation (however, none of this infants followed since birth are older than two years).
机译:在2年期间,对34名C-21 AH的儿童和青少年确定了这些参数。在医院休息一晚后,在上午6点至9点之间的空腹患者身上采集血液样本。在治疗之前或当糖皮质激素剂量足够时,观察到T水平升高。在某些情况下,开始或增加盐皮质激素治疗(9α氟皮质醇),然后降低T水平。即使在没有失盐综合症的情况下,治疗前也经常发现高水平的RA。在某些情况下用糖皮质激素和盐治疗。 R.A.血红蛋白水平仍然升高:适当剂量的9氟皮质醇引起R.A明显降低。水平。治疗前总会出现17-OH升高的水平,但在治疗下经常无法正常化。从今天的当天和同一天开始观察重要的个体差异。就ACTH而言,我们的数据不一致,无法考虑此参数。定期测定血浆T和RA可让我们更好地控制糖皮质激素治疗(我们的平均剂量为19毫克氢化可的松/平方米/天,低于通常公布的剂量)和骨骼成熟(但是,自出生以来没有随访的婴儿是超过两年)。

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