CONTINUING NEED FOR MINERALOCORTICOID THERAPY IN SALT-LOSING CONGENITAL ADRENAL-HYPERPLASIA

被引:23
作者
HUGHES, IA
WILTON, A
LOLE, CA
GRAY, OP
机构
[1] UNIV WALES WELSH NATL SCH MED, TENOVUS INST CANC RES, Cardiff CF4 4XX, S Glam, WALES
[2] UNIV WALES WELSH NATL SCH MED, ROYAL INFIRM,KRUF INST RENAL DIS, Cardiff CF4 4XN, S Glam, WALES
关键词
D O I
10.1136/adc.54.5.350
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Four patients with salt-losing congenital adrenal hyperplasia (CAH) who had stopped mineralocorticoid therapy for several years, showed raised plasma concentrations of 17OH-progesterone and plasma renin activity, despite adequate glucocorticoid therapy. One patient was able to reduce urinary sodium excretion when the sodium intake was restricted. Another patient who was a salt-loser, developed signs of an adrenal crisis when salt deprived. In comparison, 1 nonsalt-loser and 2 normal subjects decreased urinary sodium excretion in response to sodium restriction. The addiction of fludrocortisone (100 μg) to usual maintenance doses of glucocorticoid, resulted in normal levels of plasma 17OH-progesterone and plasma renin activity in all 4 salt-losers. Two female salt-losers, with raised plasma testosterone concentrations, began menstruating when their plasma testosterone concentrations returned to normal after treatment with fludrocortisone. It is recommended that salt-losing CAH patients should be given mineralocorticoid, in addition to glucocorticoid therapy, at least until adult life.
引用
收藏
页码:350 / 355
页数:6
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