Hypertension in Cushing's syndrome

被引:95
作者
Magiakou, Maria Alexandra [1 ]
Smyrnaki, Penelope [1 ]
Chrousos, George P. [1 ]
机构
[1] Univ Athens, Sch Med, Agia Sophia Childrens Hosp, Dept Pediat 1,Unit Endocrinol Metab & Diabet, GR-11527 Athens, Greece
关键词
Cushing's syndrome; glucocorticoids; mineralocorticoids; aldosterone; renin-angiotensin system; hypertension;
D O I
10.1016/j.beem.2006.07.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cushing's syndrome can be exogenous, resulting from the administration of glucocorticoids or adrenocorticotrophic hormone (ACTH), or endogenous, secondary to increased secretion of cortisol or ACTH. Hypertension is one of the most distinguishing features of endogenous Cushing's syndrome, as it is present in about 80% of adult patients and in almost half of children and adolescents patients. Hypertension results from the interplay of several pathophysiological mechanisms regulating plasma volume, peripheral vascular resistance and cardiac output, all of which may be increased. The therapeutic goal is to find and remove the cause of excess glucocorticoids, which, in most cases of endogenous Cushing's syndrome, is achieved surgically. Treatment of Cushing's syndrome usually results in resolution or amelioration of hypertension. However, some patients may not achieve normotension or may require a prolonged period of time for the correction of hypercortisolism. Therefore, therapeutic strategies for Cushing's-specific hypertension (to normalise blood pressure and decrease the duration of hypertension) are necessary to decrease the morbidity and mortality associated with this disorder. The various pathogenetic mechanisms that have been proposed for the development of glucocorticoid-induced hypertension in Cushing's syndrome and its management are discussed.
引用
收藏
页码:467 / 482
页数:16
相关论文
共 77 条
[1]  
ALEVIZAKI M, 2004, 86 ANN M END SOC NEW, P418
[2]   Direct evidence of leukocyte adhesion in arterioles by angiotensin II [J].
Alvarez, A ;
Cerda-Nicolás, M ;
Nabah, YNA ;
Mata, M ;
Issekutz, AC ;
Panés, J ;
Lobb, RR ;
Sanz, MJ .
BLOOD, 2004, 104 (02) :402-408
[3]   Effects of chronic administration of PPAR-γ ligand rosiglitazone in Cushing's disease [J].
Ambrosi, B ;
Dall'Asta, C ;
Cannavò, S ;
Libé, R ;
Vigo, T ;
Epaminonda, P ;
Chiodini, L ;
Ferrero, S ;
Trimarchi, F ;
Arosio, M ;
Beck-Peccoz, P .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2004, 151 (02) :173-178
[4]   Tissue renin-angiotensin systems:: new insights from experimental animal models in hypertension research [J].
Bader, J ;
Peters, J ;
Baltatu, O ;
Müller, DN ;
Luft, FC ;
Ganten, D .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2001, 79 (2-3) :76-102
[5]   Glucocorticoid excess and hypertension [J].
Baid, S ;
Nieman, LK .
CURRENT HYPERTENSION REPORTS, 2004, 6 (06) :493-499
[6]   Adrenocortical hypertension [J].
Capricchione, A ;
Winer, N ;
Sowers, JR .
CURRENT HYPERTENSION REPORTS, 2004, 6 (03) :224-229
[7]  
Cheng ZJ, 2005, MED SCI MONITOR, V11, pRA194
[8]   Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure [J].
Chobanian, AV ;
Bakris, GL ;
Black, HR ;
Cushman, WC ;
Green, LA ;
Izzo, JL ;
Jones, DW ;
Materson, BJ ;
Oparil, S ;
Wright, JT ;
Roccella, EJ .
HYPERTENSION, 2003, 42 (06) :1206-1252
[9]   Persistence of increased cardiovascular risk in patients with Cushing's disease after five years of successful cure [J].
Colao, A ;
Pivonello, R ;
Spiezia, S ;
Faggiano, A ;
Ferone, D ;
Filippella, M ;
Marzullo, P ;
Cerbone, G ;
Siciliani, M ;
Lombardi, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (08) :2664-2672
[10]  
Cylwik D, 2005, PHARMACOL REP, V57, P14