Concurrent primary aldosteronism and subclinical cortisol hypersecretion: a prospective study

被引:52
作者
Fallo, Francesco [1 ]
Bertello, Chiara [2 ]
Tizzani, Davide [2 ]
Fassina, Ambrogio [3 ]
Boulkroun, Sheerazed [4 ]
Sonino, Nicoletta [5 ]
Monticone, Silvia [2 ]
Viola, Andrea [2 ]
Veglio, Franco [2 ]
Mulatero, Paolo [2 ]
机构
[1] Univ Padua, Dept Med & Surg Sci, I-35128 Padua, Italy
[2] Univ Turin, Div Internal Med & Hypertens, Dept Med & Expt Oncol, Turin, Italy
[3] Univ Padua, Surg Pathol & Cytopathol Unit, Padua, Italy
[4] Univ Paris 05, INSERM, U970, Paris Cardiovasc Res Ctr, Paris, France
[5] Univ Padua, Dept Stat Sci, Padua, Italy
关键词
adrenal tumor; hypercortisolism; primary aldosteronism; CLINICAL-PRACTICE GUIDELINE; CUSHINGS-SYNDROME; DIFFERENTIAL-DIAGNOSIS; CARDIOVASCULAR RISK; CRITERIA; HYPERTENSION; HYPERPLASIA; ADENOMAS; SUBTYPES;
D O I
10.1097/HJH.0b013e32834937f3
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Background Primary aldosteronism is the most frequent cause of secondary hypertension and is responsible for an increased risk of cardiometabolic complications. A concomitant subtle cortisol hyperproduction could enhance cardiovascular risk. We prospectively estimated the occurrence of subclinical hypercortisolism in primary aldosteronism patients. Methods In a large population of hypertensive patients without clinical signs of hypercortisolism, 76 consecutive patients with primary aldosteronism were investigated. Differential diagnosis between unilateral and bilateral aldosterone hypersecretion was made by computed tomography/MRI and/or adrenal venous sampling (AVS). Subclinical hypercortisolism was defined as failure to suppress plasma cortisol to less than 50 nmol/l after 1 mg-overnight dexamethasone, used as screening test, and at least one of two other abnormal hormonal parameters, that is, adrenocorticotrophin (ACTH) less than 2 pmol/l and urinary cortisol more than 694 nmol/24 h. Results Three out of 76 patients had postdexamethasone plasma cortisol more than 50 nmol/l. Only one also showed low-normal ACTH and mildly elevated urinary cortisol. The patient had a right 4cm adrenal mass. Laparoscopic adrenalectomy was followed by short-term steroid replacement to prevent adrenal insufficiency. In-situ hybridization showed CYP11B1 expression exclusively in tumoral tissue, whereas CYP11B2 was expressed only in a peritumoral region composed of zona glomerulosa-like cells, suggesting the co-existence of a cortisol-producing adenoma and an aldosterone-producing hyperplasia in the same adrenal. The restoration of hormone abnormalities to normal levels was confirmed at 12 months of follow-up. Conclusion Concurrent aldosterone and subclinical cortisol hypersecretion seems to be a rare event in primary aldosteronism patients; however, its detection by appropriate testing is important to avoid AVS misinterpretation. J Hypertens 29:1773-1777 (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
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收藏
页码:1773 / 1777
页数:5
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