Low-dose spironolactone reduces plasma fibulin-1 levels in patients with type 2 diabetes and resistant hypertension.

1] Research Unit for Cardiovascular and Metabolic Prevention, Department of Endocrinology, Odense University Hospital, Odense C, Denmark [2] Centre for individualized Medicine in Arterial Diseases, Odense University Hospital, Odense C, Denmark. 1] Centre for individualized Medicine in Arterial Diseases, Odense University Hospital, Odense C, Denmark [2] Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense C, Denmark. Research Unit for Cardiovascular and Metabolic Prevention, Department of Endocrinology, Odense University Hospital, Odense C, Denmark. Department of Endocrinology, Esbjerg, Denmark. Department of Medicine, Fredericia, Denmark. Steno Diabetes Centre, Gentofte, Denmark. Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC, USA. 1] Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense C, Denmark [2] Department of Endocrinology, Esbjerg, Denmark.

Journal of human hypertension. 2015;(1):28-32

Abstract

Diabetic patients with hypertension are at particularly high risk of vascular damage and consequently cardiovascular and renal disease. Fibulin-1, an extracellular matrix glycoprotein, is increased in arterial tissue and plasma from individuals with type 2 diabetes. This study aimed to evaluate whether antihypertensive treatment with spironolactone changes plasma fibulin-1 levels. In a multicenter, double-blind, randomized, placebo-controlled study, 119 patients with type 2 diabetes and resistant hypertension were included. A dose of spironolactone 25 mg or matching placebo was added to previous treatment at randomization. Blood pressure (BP) and plasma fibulin-1 were measured at baseline and at 16 weeks follow-up. Overall, 112 patients completed the study. All measures of BP were reduced in the spironolactone group at follow-up. Plasma fibulin-1 was significantly reduced after spironolactone treatment (P=0.009), but increased after placebo (P=0.017). Baseline plasma fibulin-1 correlated with BP and estimated glomerular filtration rate. Increased levels of plasma fibulin-1 (P=0.004) were observed in diabetic participants reporting erectile dysfunction as compared with participants who did not. Treatment with low-dose spironolactone reduced plasma fibulin-1 levels in patients with type 2 diabetes and resistant hypertension. This supports the hypothesis that the antihypertensive effect of the mineralocorticoid receptor blocker in part may be due to regression of vascular remodeling.

Methodological quality

Metadata