Age-dependent decrease in 11β-hydroxysteroid dehydrogenase type 2 (11β-HSD2) activity in hypertensive patients

被引:51
作者
Henschkowski, Jana [2 ,3 ]
Stuck, Andreas E. [2 ,3 ]
Frey, Brigitte M. [1 ,4 ]
Gillmann, Gerhard [5 ]
Dick, Bernhard [1 ]
Frey, Felix J. [1 ]
Mohaupt, Markus G. [1 ]
机构
[1] Univ Hosp Bern, Dept Hypertens & Nephrol, CH-3010 Bern, Switzerland
[2] Univ Hosp Bern, Inselspital, Dept Geriatr, Bern, Switzerland
[3] Univ Bern, Dept Geriatr, Bern, Switzerland
[4] Univ Hosp Bern, Dept Clin Res, CH-3010 Bern, Switzerland
[5] Univ Bern, Inst Social & Prevent Med, Bern, Switzerland
关键词
D O I
10.1038/ajh.2008.152
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
BACKGROUND The prevalence of arterial hypertension lacking a defined underlying cause increases with age. Age-related arterial hypertension is insufficiently understood, yet known characteristics suggest an aldosterone-independent activation of the mineralocorticoid receptor. Therefore, we hypothesized that 11 beta-HSD2 activity is age-dependently impaired, resulting in a compromised intracellular inactivation of cortisol (F) with F-mediated mineralocorticoid hypertension. METHODS Steroid hormone metabolites in 24-h urine samples of 165 consecutive hypertensive patients were analyzed for F and cortisone (E), and their TH-metabolites tetrahydro-F (THF), 5 alpha THF, TH-deoxycortisol (THS), and THE by gas chromatography-mass spectroscopy. Apparent 11 beta-HSD2 and 11 beta-hydroxylase activity and excretion of F metabolites were assessed. RESULTS In 72 female and 93 male patients aged 18-84 years, age correlated positively with the ratios of (THF + 5 alpha THF)/THE (P = 0.065) and F/E (P < 0.002) suggesting an age-dependent reduction in the apparent 11 beta-HSD2 activity, which persisted (F/E; P = 0.020) after excluding impaired renal function. Excretion of F metabolites remained age-independent most likely as a consequence of an age-dependent diminished apparent 11 beta-hydroxylase activity (P = 0.038). CONCLUSION Reduced 11 beta-HSD2 activity emerges as a previously unrecognized risk factor contributing to the rising prevalence of arterial hypertension in elderly. This opens new perspectives for targeted treatment of age-related hypertension.
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页码:644 / 649
页数:6
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