Severity of hypertension in familial hyperaldosteronism type I: Relationship to gender and degree of biochemical disturbance


Autoria(s): Stowasser, M.; Bachmann, A. W.; Huggard, P. R.; Rossetti, T. R.; Gordon, R. D.
Data(s)

01/01/2000

Resumo

In familial hyperaldosteronism type I (FH-I), inheritance of a hybrid 11 beta-hydroxylase/aldosterone synthase gene causes ACTH-regulated aldosterone overproduction. In an attempt to understand the marked variability in hypertension severity in FH-I, we compared clinical and biochemical characteristics of 9 affected individuals with mild hypertension (normotensive or onset of hypertension after 15 yr, blood pressure never >160/100 mm Hg, less than or equal to 1 medication required to control hypertension, no history of stroke, age >18 yr when studied) with those of 17 subjects with severe hypertension (onset before 15 yr, or systolic blood pressure >180 mm Hg or diastolic blood pressure >120 mm Hg at least once, or greater than or equal to 2 medications, or history of stroke). Severe hypertension was more frequent in males (11 of 13 males vs. 6 of 13 females; P

Identificador

http://espace.library.uq.edu.au/view/UQ:36577

Idioma(s)

eng

Publicador

Endocrine Society

Palavras-Chave #Endocrinology & Metabolism #Glucocorticoid-remediable Aldosteronism #Suppressible Hyper-aldosteronism #Plasma-renin Activity #Hybrid Gene #Dexamethasone #Diagnosis #Phenotype #Individuals #321004 Endocrinology #730105 Endocrine organs and diseases (incl. diabetes) #C1
Tipo

Journal Article