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Efficacy and safety of the selective 11β-HSD-1 inhibitors MK-0736 and MK-0916 in overweight and obese patients with hypertension.

Authors :
Shah S
Hermanowski-Vosatka A
Gibson K
Ruck RA
Jia G
Zhang J
Hwang PM
Ryan NW
Langdon RB
Feig PU
Source :
Journal of the American Society of Hypertension : JASH [J Am Soc Hypertens] 2011 May-Jun; Vol. 5 (3), pp. 166-76. Date of Electronic Publication: 2011 Mar 21.
Publication Year :
2011

Abstract

11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) may be involved in several abnormalities associated with the metabolic syndrome. This study evaluated the antihypertensive efficacy and safety of two 11β-HSD1 inhibitors, MK-0736 and MK-0916, in overweight-to-obese hypertensive patients. Patients aged 18-75 years with sitting diastolic blood pressure (SiDBP) 90-104 mm Hg, systolic BP <160 mm Hg (after washout of prior antihypertensive medications), and BMI ≥27 to <41 kg/m(2) were randomized to receive 2 or 7 mg/d MK-0736, 6 mg/d MK-0916, or placebo for 12 weeks (n = 51-54/group). Patients with BMI ≥20 to <27 kg/m(2) received 6 mg/d MK-0916 or placebo for 24 weeks (n = 19/group). The primary endpoint was placebo-adjusted change from baseline in trough SiDBP in patients treated for 12 weeks with 7 mg/d MK-0736. The primary endpoint was not met (placebo-adjusted reduction = 2.2 mm Hg; P = .157). With 7 mg/d MK-0736, placebo-adjusted LDL-C decreased by 12.3%, high-density lipoprotein cholesterol by 6.3%, and body weight by 1.4 kg. Both 11β-HSD1 inhibitors were generally well tolerated. In overweight-to-obese patients with hypertension, reduction in SiDBP with MK-0736 was not statistically significant. Nonetheless, MK-0736 was well tolerated and did appear to modestly improve other BP endpoints, LDL-C, and body weight.<br /> (Copyright © 2011 American Society of Hypertension. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1933-1711
Volume :
5
Issue :
3
Database :
MEDLINE
Journal :
Journal of the American Society of Hypertension : JASH
Publication Type :
Academic Journal
Accession number :
21419745
Full Text :
https://doi.org/10.1016/j.jash.2011.01.009